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Volumn 5, Issue , 2014, Pages 191-206

Optimal management of hereditary hemorrhagic telangiectasia

Author keywords

Arteriovenous malformations; Bevacizumab; Embolization; Epistaxis; Guidelines; Review; Screening

Indexed keywords

ACETYLCYSTEINE; ACTIVIN RECEPTOR LIKE KINASE 1; ANTIFIBRINOLYTIC AGENT; BEVACIZUMAB; BLOOD CLOTTING FACTOR 8; BONE MORPHOGENETIC PROTEIN 9; DANAZOL; ENDOGLIN; ESTROGEN; ETHINYLESTRADIOL; INTERFERON; LENALIDOMIDE; NORETHISTERONE; PROGESTERONE; PROPRANOLOL; RAPAMYCIN; SEROTONIN; SMAD4 PROTEIN; TAMOXIFEN; THALIDOMIDE; TIMOLOL; TRANEXAMIC ACID; TRANSFORMING GROWTH FACTOR BETA; VASCULOTROPIN;

EID: 85018603044     PISSN: None     EISSN: 11792736     Source Type: Journal    
DOI: 10.2147/JBM.S45295     Document Type: Review
Times cited : (86)

References (191)
  • 1
    • 0036164129 scopus 로고    scopus 로고
    • Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan
    • Dakeishi M, Shioya T, Wada Y, et al. Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan. Hum Mutat. 2002;19(2):140–148.
    • (2002) Hum Mutat , vol.19 , Issue.2 , pp. 140-148
    • Dakeishi, M.1    Shioya, T.2    Wada, Y.3
  • 2
    • 0033007057 scopus 로고    scopus 로고
    • Hereditary haemorrhagic telangiectasia: A population-based study of prevalence and mortality in Danish patients
    • Kjeldsen AD, Vase P, Green A. Hereditary haemorrhagic telangiectasia: a population-based study of prevalence and mortality in Danish patients. J Intern Med. 1999;245(1):31–39.
    • (1999) J Intern Med , vol.245 , Issue.1 , pp. 31-39
    • Kjeldsen, A.D.1    Vase, P.2    Green, A.3
  • 3
    • 0042130535 scopus 로고    scopus 로고
    • The prevalence and manifestations of hereditary hemorrhagic telangiectasia in the Afro-Caribbean population of The Netherlands Antilles: A family screening
    • Westermann CJ, Rosina AF, De Vries V, de Coteau PA. The prevalence and manifestations of hereditary hemorrhagic telangiectasia in the Afro-Caribbean population of The Netherlands Antilles: a family screening. Am J Med Genet A. 2003;116A(4):324–328.
    • (2003) Am J Med Genet A , vol.116A , Issue.4 , pp. 324-328
    • Westermann, C.J.1    Rosina, A.F.2    De Vries, V.3    De Coteau, P.A.4
  • 4
    • 0024394433 scopus 로고
    • Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population
    • Plauchu H, de Chadarevian JP, Bideau A, Robert JM. Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population. Am J Med Genet. 1989;32(3):291–297.
    • (1989) Am J Med Genet , vol.32 , Issue.3 , pp. 291-297
    • Plauchu, H.1    De Chadarevian, J.P.2    Bideau, A.3    Robert, J.M.4
  • 5
    • 84861888864 scopus 로고    scopus 로고
    • A long diagnostic delay in patients with hereditary haemorrhagic telangiectasia: A questionnaire-based retrospective study
    • Pierucci P, Lenato GM, Suppressa P, et al. A long diagnostic delay in patients with hereditary haemorrhagic telangiectasia: a questionnaire-based retrospective study. Orphanet J Rare Dis. 2012;7:33.
    • (2012) Orphanet J Rare Dis , vol.7 , pp. 33
    • Pierucci, P.1    Lenato, G.M.2    Suppressa, P.3
  • 6
    • 84893581613 scopus 로고    scopus 로고
    • The use of US health insurance data for surveillance of rare disorders: Hereditary hemorrhagic telangiectasia
    • Grosse SD, Boulet SL, Grant AM, Hulihan MM, Faughnan ME. The use of US health insurance data for surveillance of rare disorders: hereditary hemorrhagic telangiectasia. Genet Med. 2014;16(1):33–39.
    • (2014) Genet Med , vol.16 , Issue.1 , pp. 33-39
    • Grosse, S.D.1    Boulet, S.L.2    Grant, A.M.3    Hulihan, M.M.4    Faughnan, M.E.5
  • 7
    • 80052578272 scopus 로고    scopus 로고
    • Why is genetic screening for autosomal dominant disorders underused in families? The case of hereditary hemorrhagic telangiectasia
    • Bernhardt BA, Zayac C, Pyeritz RE. Why is genetic screening for autosomal dominant disorders underused in families? The case of hereditary hemorrhagic telangiectasia. Genet Med. 2011;13(9):812–820.
    • (2011) Genet Med , vol.13 , Issue.9 , pp. 812-820
    • Bernhardt, B.A.1    Zayac, C.2    Pyeritz, R.E.3
  • 8
    • 79551624460 scopus 로고    scopus 로고
    • International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia
    • Faughnan ME, Palda VA, Garcia-Tsao G, et al. International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia. J Med Genet. 2011;48(2):73–87.
    • (2011) J Med Genet , vol.48 , Issue.2 , pp. 73-87
    • Faughnan, M.E.1    Palda, V.A.2    Garcia-Tsao, G.3
  • 9
    • 0025939367 scopus 로고
    • The natural history of epistaxis in hereditary hemorrhagic telangiectasia
    • AAssar OS, Friedman CM, White RI Jr. The natural history of epistaxis in hereditary hemorrhagic telangiectasia. Laryngoscope. 1991;101(9): 977–980.
    • (1991) Laryngoscope , vol.101 , Issue.9 , pp. 977-980
    • Aassar, O.S.1    Friedman, C.M.2    White, R.I.3
  • 10
    • 0041326362 scopus 로고    scopus 로고
    • Hereditary haemorrhagic telangiectasia: A questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations
    • Berg J, Porteous M, Reinhardt D, et al. Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations. J Med Genet. 2003;40(8):585–590.
    • (2003) J Med Genet , vol.40 , Issue.8 , pp. 585-590
    • Berg, J.1    Porteous, M.2    Reinhardt, D.3
  • 11
    • 84921861731 scopus 로고    scopus 로고
    • Dysphonia and vocal fold telangiectasia in hereditary hemorrhagic telangiectasia
    • Epub June 9
    • Chang J, Yung KC. Dysphonia and vocal fold telangiectasia in hereditary hemorrhagic telangiectasia. Ann Otol Rhinol Laryngol. Epub June 9, 2014.
    • (2014) Ann Otol Rhinol Laryngol
    • Chang, J.1    Yung, K.C.2
  • 12
    • 0033953054 scopus 로고    scopus 로고
    • Gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia
    • Kjeldsen AD, Kjeldsen J. Gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia. Am J Gastroenterol. 2000;95(2): 415–418.
    • (2000) Am J Gastroenterol , vol.95 , Issue.2 , pp. 415-418
    • Kjeldsen, A.D.1    Kjeldsen, J.2
  • 13
    • 0037256839 scopus 로고    scopus 로고
    • Diagnosis and management of gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia
    • Longacre AV, Gross CP, Gallitelli M, Henderson KJ, White RI Jr, Proctor DD. Diagnosis and management of gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia. Am J Gastroenterol. 2003;98(1):59–65.
    • (2003) Am J Gastroenterol , vol.98 , Issue.1 , pp. 59-65
    • Longacre, A.V.1    Gross, C.P.2    Gallitelli, M.3    Henderson, K.J.4    White, R.I.5    Proctor, D.D.6
  • 14
    • 10444238514 scopus 로고    scopus 로고
    • Evidence of small-bowel involvement in hereditary hemorrhagic telangiectasia: A capsule-endoscopic study
    • Ingrosso M, Sabba C, Pisani A, et al. Evidence of small-bowel involvement in hereditary hemorrhagic telangiectasia: a capsule-endoscopic study. Endoscopy. 2004;36(12):1074–1079.
    • (2004) Endoscopy , vol.36 , Issue.12 , pp. 1074-1079
    • Ingrosso, M.1    Sabba, C.2    Pisani, A.3
  • 15
    • 84890295970 scopus 로고    scopus 로고
    • Role of transthoracic contrast echocardiography in the clinical diagnosis of hereditary hemorrhagic telangiectasia
    • Velthuis S, Vorselaars VM, van Gent MW, et al. Role of transthoracic contrast echocardiography in the clinical diagnosis of hereditary hemorrhagic telangiectasia. Chest. 2013;144(6):1876–1882.
    • (2013) Chest , vol.144 , Issue.6 , pp. 1876-1882
    • Velthuis, S.1    Vorselaars, V.M.2    Van Gent, M.W.3
  • 16
    • 67650388734 scopus 로고    scopus 로고
    • Contrast echocardiography for pulmonary arteriovenous malformations screening: Does any bubble matter?
    • Gazzaniga P, Buscarini E, Leandro G, et al. Contrast echocardiography for pulmonary arteriovenous malformations screening: does any bubble matter? Eur J Echocardiogr. 2009;10(4):513–518.
    • (2009) Eur J Echocardiogr , vol.10 , Issue.4 , pp. 513-518
    • Gazzaniga, P.1    Buscarini, E.2    Leandro, G.3
  • 17
    • 84863522255 scopus 로고    scopus 로고
    • Prevalence of pulmonary arteriovenous malformations as estimated by low-dose thoracic CT screening
    • Nakayama M, Nawa T, Chonan T, et al. Prevalence of pulmonary arteriovenous malformations as estimated by low-dose thoracic CT screening. Intern Med. 2012;51(13):1677–1681.
    • (2012) Intern Med , vol.51 , Issue.13 , pp. 1677-1681
    • Nakayama, M.1    Nawa, T.2    Chonan, T.3
  • 18
    • 33745314873 scopus 로고    scopus 로고
    • Clinical and anatomic outcomes after embolotherapy of pulmonary arteriovenous malformations
    • quiz 45
    • Pollak JS, Saluja S, Thabet A, Henderson KJ, Denbow N, White RI Jr. Clinical and anatomic outcomes after embolotherapy of pulmonary arteriovenous malformations. J Vasc Interv Radiol. 2006;17(1):35–44; quiz 45.
    • (2006) J Vasc Interv Radiol , vol.17 , Issue.1 , pp. 35-44
    • Pollak, J.S.1    Saluja, S.2    Thabet, A.3    Henderson, K.J.4    Denbow, N.5    White, R.I.6
  • 19
    • 80051535927 scopus 로고    scopus 로고
    • Idiopathic pulmonary arteriovenous malformations: Clinical and imaging characteristics
    • Wong HH, Chan RP, Klatt R, Faughnan ME. Idiopathic pulmonary arteriovenous malformations: clinical and imaging characteristics. Eur Respir J. 2011;38(2):368–375.
    • (2011) Eur Respir J , vol.38 , Issue.2 , pp. 368-375
    • Wong, H.H.1    Chan, R.P.2    Klatt, R.3    Faughnan, M.E.4
  • 20
    • 77957841685 scopus 로고    scopus 로고
    • Real prevalence of pulmonary right-to-left shunt according to genotype in patients with hereditary hemorrhagic telangiectasia: A transthoracic contrast echocardiography study
    • van Gent MW, Post MC, Snijder RJ, Westermann CJ, Plokker HW, Mager JJ. Real prevalence of pulmonary right-to-left shunt according to genotype in patients with hereditary hemorrhagic telangiectasia: a transthoracic contrast echocardiography study. Chest. 2010;138(4): 833–839.
    • (2010) Chest , vol.138 , Issue.4 , pp. 833-839
    • Van Gent, M.W.1    Post, M.C.2    Snijder, R.J.3    Westermann, C.J.4    Plokker, H.W.5    Mager, J.J.6
  • 22
    • 34250753845 scopus 로고    scopus 로고
    • Pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia: Follow-up and pathophysiologic considerations
    • author reply 939
    • Cottin V, Plauchu H, Dupuis-Girod S, Cordier JF. Pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia: follow-up and pathophysiologic considerations. J Vasc Interv Radiol. 2007;18(7):938–939; author reply 939.
    • (2007) J Vasc Interv Radiol , vol.18 , Issue.7 , pp. 938-939
    • Cottin, V.1    Plauchu, H.2    Dupuis-Girod, S.3    Cordier, J.F.4
  • 23
    • 0031846341 scopus 로고    scopus 로고
    • Pulmonary arteriovenous malformations. A state of the art review
    • Gossage JR, Kanj G. Pulmonary arteriovenous malformations. A state of the art review. Am J Respir Crit Care Med. 1998;158(2):643–661.
    • (1998) Am J Respir Crit Care Med , vol.158 , Issue.2 , pp. 643-661
    • Gossage, J.R.1    Kanj, G.2
  • 24
    • 84898657842 scopus 로고    scopus 로고
    • Arterial oxygen content is precisely maintained by graded erythrocytotic responses in settings of high/normal serum iron levels, and predicts exercise capacity: An observational study of hypoxaemic patients with pulmonary arteriovenous malformations
    • Santhirapala V, Williams LC, Tighe HC, Jackson J., Shovlin CL. Arterial oxygen content is precisely maintained by graded erythrocytotic responses in settings of high/normal serum iron levels, and predicts exercise capacity: an observational study of hypoxaemic patients with pulmonary arteriovenous malformations. PLoS One. 2014;9(3):e90777.
    • (2014) PLoS One , vol.9 , Issue.3
    • Santhirapala, V.1    Williams, L.C.2    Tighe, H.C.3    Jackson, J.4    Shovlin, C.L.5
  • 25
    • 84897365712 scopus 로고    scopus 로고
    • Orthodeoxia and postural orthostatic tachycardia in patients with pulmonary arteriovenous malformations: A prospective 8-year series
    • Epub April 8
    • Santhirapala V, Chamali B, McKernan H, et al. Orthodeoxia and postural orthostatic tachycardia in patients with pulmonary arteriovenous malformations: a prospective 8-year series. Thorax. Epub April 8, 2014.
    • (2014) Thorax
    • Santhirapala, V.1    Chamali, B.2    McKernan, H.3
  • 26
    • 84870231106 scopus 로고    scopus 로고
    • Platypnea-orthodeoxia syndrome as a presentation of hereditary hemorrhagic telangiectasia
    • Kumar N, Kraemer RR, Murthy RK, Hartig JR. Platypnea-orthodeoxia syndrome as a presentation of hereditary hemorrhagic telangiectasia. Circulation. 2012;126(22):2645–2647.
    • (2012) Circulation , vol.126 , Issue.22 , pp. 2645-2647
    • Kumar, N.1    Kraemer, R.R.2    Murthy, R.K.3    Hartig, J.R.4
  • 27
    • 0032926941 scopus 로고    scopus 로고
    • Sensitivity and specificity of radioisotope right-left shunt measurements and pulse oximetry for the early detection of pulmonary arteriovenous malformations
    • Thompson RD, Jackson J, Peters AM, Dore CJ, Hughes JM. Sensitivity and specificity of radioisotope right-left shunt measurements and pulse oximetry for the early detection of pulmonary arteriovenous malformations. Chest. 1999;115(1):109–113.
    • (1999) Chest , vol.115 , Issue.1 , pp. 109-113
    • Thompson, R.D.1    Jackson, J.2    Peters, A.M.3    Dore, C.J.4    Hughes, J.M.5
  • 28
    • 0023684756 scopus 로고
    • Pulmonary arteriovenous malformations: Techniques and long-term outcome of embolotherapy
    • White RI Jr, Lynch-Nyhan A, Terry P, et al. Pulmonary arteriovenous malformations: techniques and long-term outcome of embolotherapy. Radiology. 1988;169(3):663–669.
    • (1988) Radiology , vol.169 , Issue.3 , pp. 663-669
    • White, R.I.1    Lynch-Nyhan, A.2    Terry, P.3
  • 29
    • 52749098193 scopus 로고    scopus 로고
    • Embolisation of pulmonary arteriovenous malformations: No consistent effect on pulmonary artery pressure
    • Shovlin CL, Tighe HC, Davies RJ, Gibbs JS, Jackson JE. Embolisation of pulmonary arteriovenous malformations: no consistent effect on pulmonary artery pressure. Eur Respir J. 2008;32(1):162–169.
    • (2008) Eur Respir J , vol.32 , Issue.1 , pp. 162-169
    • Shovlin, C.L.1    Tighe, H.C.2    Davies, R.J.3    Gibbs, J.S.4    Jackson, J.E.5
  • 30
    • 47349107056 scopus 로고    scopus 로고
    • Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): Suggested approach for obstetric services
    • Shovlin CL, Sodhi V, McCarthy A, Lasjaunias P, Jackson J., Sheppard MN. Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): suggested approach for obstetric services. BJOG. 2008; 115(9):1108–1115.
    • (2008) BJOG , vol.115 , Issue.9 , pp. 1108-1115
    • Shovlin, C.L.1    Sodhi, V.2    McCarthy, A.3    Lasjaunias, P.4    Jackson, J.5    Sheppard, M.N.6
  • 31
    • 84874668713 scopus 로고    scopus 로고
    • Pulmonary hypertension in a patient with hereditary haemorrhagic telangiectasia
    • 2013. pii: bcr2012008352
    • Chadha D, Handa A, Kumar A. Pulmonary hypertension in a patient with hereditary haemorrhagic telangiectasia. BMJ Case Rep. 2013;2013. pii: bcr2012008352.
    • (2013) BMJ Case Rep
    • Chadha, D.1    Handa, A.2    Kumar, A.3
  • 32
    • 61649114738 scopus 로고    scopus 로고
    • Fatal rupture of pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasis and severe PAH
    • Montani D, Price LC, Girerd B, et al. Fatal rupture of pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasis and severe PAH. Eur Respir Rev. 2009;18(111):42–46.
    • (2009) Eur Respir Rev , vol.18 , Issue.111 , pp. 42-46
    • Montani, D.1    Price, L.C.2    Girerd, B.3
  • 33
    • 11844294657 scopus 로고    scopus 로고
    • Massive pulmonary hemorrhage from dual circulation pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia
    • Sharma KB, Forkert L. Massive pulmonary hemorrhage from dual circulation pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia. Can Respir J. 2004;11(8):597–598.
    • (2004) Can Respir J , vol.11 , Issue.8 , pp. 597-598
    • Sharma, K.B.1    Forkert, L.2
  • 34
    • 70349644719 scopus 로고    scopus 로고
    • Pulmonary arteriovenous malformations associated with migraine with aura
    • Post MC, van Gent MW, Plokker HW, et al. Pulmonary arteriovenous malformations associated with migraine with aura. Eur Respir J. 2009;34(4):882–887.
    • (2009) Eur Respir J , vol.34 , Issue.4 , pp. 882-887
    • Post, M.C.1    Van Gent, M.W.2    Plokker, H.W.3
  • 35
    • 33644923255 scopus 로고    scopus 로고
    • Embolization of pulmonary arteriovenous malformations and decrease in prevalence of migraine
    • Post MC, Thijs V, Schonewille WJ, et al. Embolization of pulmonary arteriovenous malformations and decrease in prevalence of migraine. Neurology. 2006;66(2):202–205.
    • (2006) Neurology , vol.66 , Issue.2 , pp. 202-205
    • Post, M.C.1    Thijs, V.2    Schonewille, W.J.3
  • 36
    • 27144454299 scopus 로고    scopus 로고
    • A pulmonary right-to-left shunt in patients with hereditary hemorrhagic telangiectasia is associated with an increased prevalence of migraine
    • Post MC, Letteboer TG, Mager JJ, Plokker TH, Kelder JC, Westermann CJ. A pulmonary right-to-left shunt in patients with hereditary hemorrhagic telangiectasia is associated with an increased prevalence of migraine. Chest. 2005;128(4):2485–2489.
    • (2005) Chest , vol.128 , Issue.4 , pp. 2485-2489
    • Post, M.C.1    Letteboer, T.G.2    Mager, J.J.3    Plokker, T.H.4    Kelder, J.C.5    Westermann, C.J.6
  • 37
    • 49949099079 scopus 로고    scopus 로고
    • Pulmonary arteriovenous malformations and migraine: A new vision
    • Post MC, van Gent MW, Snijder RJ, et al. Pulmonary arteriovenous malformations and migraine: a new vision. Respiration. 2008;76(2): 228–233.
    • (2008) Respiration , vol.76 , Issue.2 , pp. 228-233
    • Post, M.C.1    Van Gent, M.W.2    Snijder, R.J.3
  • 38
    • 58149252329 scopus 로고    scopus 로고
    • An association of migraine with hereditary haemorrhagic telangiectasia independently of pulmonary right-to-left shunts
    • Marziniak M, Jung A, Guralnik V, Evers S, Prudlo J, Geisthoff UW. An association of migraine with hereditary haemorrhagic telangiectasia independently of pulmonary right-to-left shunts. Cephalalgia. 2009;29(1):76–81.
    • (2009) Cephalalgia , vol.29 , Issue.1 , pp. 76-81
    • Marziniak, M.1    Jung, A.2    Guralnik, V.3    Evers, S.4    Prudlo, J.5    Geisthoff, U.W.6
  • 39
    • 84903163080 scopus 로고    scopus 로고
    • Relationships between epistaxis, migraines, and triggers in hereditary hemorrhagic telangiectasia
    • Elphick A, Shovlin CL. Relationships between epistaxis, migraines, and triggers in hereditary hemorrhagic telangiectasia. Laryngoscope. 2014;124(7):1521–1528.
    • (2014) Laryngoscope , vol.124 , Issue.7 , pp. 1521-1528
    • Elphick, A.1    Shovlin, C.L.2
  • 40
    • 0028851489 scopus 로고
    • Screening family members of patients with hereditary hemorrhagic telangiectasia
    • Haitjema T, Disch F, Overtoom TT, Westermann CJ, Lammers JW. Screening family members of patients with hereditary hemorrhagic telangiectasia. Am J Med. 1995;99(5):519–524.
    • (1995) Am J Med , vol.99 , Issue.5 , pp. 519-524
    • Haitjema, T.1    Disch, F.2    Overtoom, T.T.3    Westermann, C.J.4    Lammers, J.W.5
  • 41
    • 0032231685 scopus 로고    scopus 로고
    • MR of hereditary hemorrhagic telangiectasia: Prevalence and spectrum of cerebrovascular malformations
    • Fulbright RK, Chaloupka JC, Putman CM, et al. MR of hereditary hemorrhagic telangiectasia: prevalence and spectrum of cerebrovascular malformations. AJNR Am J Neuroradiol. 1998;19(3):477–484.
    • (1998) AJNR Am J Neuroradiol , vol.19 , Issue.3 , pp. 477-484
    • Fulbright, R.K.1    Chaloupka, J.C.2    Putman, C.M.3
  • 42
    • 84855355068 scopus 로고    scopus 로고
    • Brain arteriovenous malformation multiplicity predicts the diagnosis of hereditary hemorrhagic telangiectasia: Quantitative assessment
    • Bharatha A, Faughnan ME, Kim H, et al. Brain arteriovenous malformation multiplicity predicts the diagnosis of hereditary hemorrhagic telangiectasia: quantitative assessment. Stroke. 2012;43(1):72–78.
    • (2012) Stroke , vol.43 , Issue.1 , pp. 72-78
    • Bharatha, A.1    Faughnan, M.E.2    Kim, H.3
  • 43
    • 0035074068 scopus 로고    scopus 로고
    • Cerebrovascular manifestations in 321 cases of hereditary hemorrhagic telangiectasia
    • Maher CO, Piepgras DG, Brown RD Jr, Friedman JA, Pollock BE. Cerebrovascular manifestations in 321 cases of hereditary hemorrhagic telangiectasia. Stroke. 2001;32(4):877–882.
    • (2001) Stroke , vol.32 , Issue.4 , pp. 877-882
    • Maher, C.O.1    Piepgras, D.G.2    Brown, R.D.3    Friedman, J.A.4    Pollock, B.E.5
  • 44
    • 84893842883 scopus 로고    scopus 로고
    • Medical management with or without interventional therapy for unruptured brain arteriovenous malformations (ARUBA): A multicentre, non-blinded, randomised trial
    • Mohr JP, Parides MK, Stapf C, et al. Medical management with or without interventional therapy for unruptured brain arteriovenous malformations (ARUBA): a multicentre, non-blinded, randomised trial. Lancet. 2014;383(9917):614–621.
    • (2014) Lancet , vol.383 , Issue.9917 , pp. 614-621
    • Mohr, J.P.1    Parides, M.K.2    Stapf, C.3
  • 45
    • 20944446296 scopus 로고    scopus 로고
    • Neurovascular phenotypes in hereditary haemorrhagic telangiectasia patients according to age. Review of 50 consecutive patients aged 1 day-60 years
    • Krings T, Ozanne A, Chng SM, Alvarez H, Rodesch G, Lasjaunias PL. Neurovascular phenotypes in hereditary haemorrhagic telangiectasia patients according to age. Review of 50 consecutive patients aged 1 day-60 years. Neuroradiology. 2005;47(10):711–720.
    • (2005) Neuroradiology , vol.47 , Issue.10 , pp. 711-720
    • Krings, T.1    Ozanne, A.2    Chng, S.M.3    Alvarez, H.4    Rodesch, G.5    Lasjaunias, P.L.6
  • 46
    • 0036363130 scopus 로고    scopus 로고
    • Intracranial hemorrhage in infants and children with hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome)
    • Morgan T, McDonald J, Anderson C, et al. Intracranial hemorrhage in infants and children with hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome). Pediatrics. 2002;109(1):E12.
    • (2002) Pediatrics , vol.109 , Issue.1 , pp. E12
    • Morgan, T.1    McDonald, J.2    Anderson, C.3
  • 47
    • 12444268352 scopus 로고    scopus 로고
    • Supratentorial cerebral arteriovenous fistulas (AVFs) in children: Review of 41 cases with 63 non choroidal single-hole AVFs
    • Weon YC, Yoshida Y, Sachet M, et al. Supratentorial cerebral arteriovenous fistulas (AVFs) in children: review of 41 cases with 63 non choroidal single-hole AVFs. Acta Neurochir (Wien). 2005;147(1):17–31.
    • (2005) Acta Neurochir (Wien) , vol.147 , Issue.1 , pp. 17-31
    • Weon, Y.C.1    Yoshida, Y.2    Sachet, M.3
  • 48
    • 3442875883 scopus 로고    scopus 로고
    • Posterior cranial fossa single-hole arteriovenous fistulae in children: 14 consecutive cases
    • Yoshida Y, Weon YC, Sachet M, et al. Posterior cranial fossa single-hole arteriovenous fistulae in children: 14 consecutive cases. Neuroradiology. 2004;46(6):474–481.
    • (2004) Neuroradiology , vol.46 , Issue.6 , pp. 474-481
    • Yoshida, Y.1    Weon, Y.C.2    Sachet, M.3
  • 49
    • 29544449897 scopus 로고    scopus 로고
    • Hereditary hemorrhagic telangiectasia in children: Endovascular treatment of neurovascular malformations: Results in 31 patients
    • Krings T, Chng SM, Ozanne A, Alvarez H, Rodesch G, Lasjaunias PL. Hereditary hemorrhagic telangiectasia in children: endovascular treatment of neurovascular malformations: results in 31 patients. Neuroradiology. 2005;47(12):946–954.
    • (2005) Neuroradiology , vol.47 , Issue.12 , pp. 946-954
    • Krings, T.1    Chng, S.M.2    Ozanne, A.3    Alvarez, H.4    Rodesch, G.5    Lasjaunias, P.L.6
  • 50
    • 58149090066 scopus 로고    scopus 로고
    • Acute paraplegia due to spinal arteriovenous fistula in two patients with hereditary hemorrhagic telangiectasia
    • Poisson A, Vasdev A, Brunelle F, Plauchu H, Dupuis-Girod S; French Italian HHT network. Acute paraplegia due to spinal arteriovenous fistula in two patients with hereditary hemorrhagic telangiectasia. Eur J Pediatr. 2009;168(2):135–139.
    • (2009) Eur J Pediatr , vol.168 , Issue.2 , pp. 135-139
    • Poisson, A.1    Vasdev, A.2    Brunelle, F.3    Plauchu, H.4    Dupuis-Girod, S.5    French Italian, H.H.T.6
  • 51
    • 33748202605 scopus 로고    scopus 로고
    • Spinal arteriovenous shunts presenting before 2 years of age: Analysis of 13 cases
    • Cullen S, Alvarez H, Rodesch G, Lasjaunias P. Spinal arteriovenous shunts presenting before 2 years of age: analysis of 13 cases. Childs Nerv Syst. 2006;22(9):1103–1110.
    • (2006) Childs Nerv Syst , vol.22 , Issue.9 , pp. 1103-1110
    • Cullen, S.1    Alvarez, H.2    Rodesch, G.3    Lasjaunias, P.4
  • 52
    • 0346218098 scopus 로고    scopus 로고
    • Hereditary hemorrhagic telangiectasia: Multi-detector row helical CT assessment of hepatic involvement
    • Ianora AA, Memeo M, Sabba C, Cirulli A, Rotondo A, Angelelli G. Hereditary hemorrhagic telangiectasia: multi-detector row helical CT assessment of hepatic involvement. Radiology. 2004;230(1):250–259.
    • (2004) Radiology , vol.230 , Issue.1 , pp. 250-259
    • Ianora, A.A.1    Memeo, M.2    Sabba, C.3    Cirulli, A.4    Rotondo, A.5    Angelelli, G.6
  • 53
    • 4644353125 scopus 로고    scopus 로고
    • Doppler ultrasonographic grading of hepatic vascular malformations in hereditary hemorrhagic telangiectasia – results of extensive screening
    • Buscarini E, Danesino C, Olivieri C, et al. Doppler ultrasonographic grading of hepatic vascular malformations in hereditary hemorrhagic telangiectasia – results of extensive screening. Ultraschall Med. 2004;25(5):348–355.
    • (2004) Ultraschall Med , vol.25 , Issue.5 , pp. 348-355
    • Buscarini, E.1    Danesino, C.2    Olivieri, C.3
  • 54
    • 79959759416 scopus 로고    scopus 로고
    • Natural history and outcome of hepatic vascular malformations in a large cohort of patients with hereditary hemorrhagic teleangiectasia
    • Buscarini E, Leandro G, Conte D, et al. Natural history and outcome of hepatic vascular malformations in a large cohort of patients with hereditary hemorrhagic teleangiectasia. Dig Dis Sci. 2011;56(7): 2166–2178.
    • (2011) Dig Dis Sci , vol.56 , Issue.7 , pp. 2166-2178
    • Buscarini, E.1    Leandro, G.2    Conte, D.3
  • 55
    • 0034727052 scopus 로고    scopus 로고
    • Liver disease in patients with hereditary hemorrhagic telangiectasia
    • Garcia-Tsao G, Korzenik JR, Young L, et al. Liver disease in patients with hereditary hemorrhagic telangiectasia. N Engl J Med. 2000;343(13):931–936.
    • (2000) N Engl J Med , vol.343 , Issue.13 , pp. 931-936
    • Garcia-Tsao, G.1    Korzenik, J.R.2    Young, L.3
  • 56
    • 0017596791 scopus 로고
    • ‘Pseudocirrhosis’ in hereditary haemorrhagic telangiectasia
    • Cooney T, Sweeney EC, Coll R, Greally M. ‘Pseudocirrhosis’ in hereditary haemorrhagic telangiectasia. J Clin Pathol. 1977;30(12): 1134–1141.
    • (1977) J Clin Pathol , vol.30 , Issue.12 , pp. 1134-1141
    • Cooney, T.1    Sweeney, E.C.2    Coll, R.3    Greally, M.4
  • 57
    • 0007742564 scopus 로고
    • Experimental arterialization of the liver
    • Schwartz SI, Morton JH, McGovern GR. Experimental arterialization of the liver. Surgery. 1961;49:611–617.
    • (1961) Surgery , vol.49 , pp. 611-617
    • Schwartz, S.I.1    Morton, J.H.2    McGovern, G.R.3
  • 58
    • 84905567897 scopus 로고    scopus 로고
    • Appreciating the broad clinical features of SMAD4 mutation carriers: A multicenter chart review
    • Wain KE, Ellingson MS, McDonald J, et al. Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review. Genet Med. 2014;16(8):588–593.
    • (2014) Genet Med , vol.16 , Issue.8 , pp. 588-593
    • Wain, K.E.1    Ellingson, M.S.2    McDonald, J.3
  • 59
    • 84871708823 scopus 로고    scopus 로고
    • Thoracic aortic disease in two patients with juvenile polyposis syndrome and SMAD4 mutations
    • Teekakirikul P, Milewicz DM, Miller DT, et al. Thoracic aortic disease in two patients with juvenile polyposis syndrome and SMAD4 mutations. Am J Med Genet A. 2013;161A(1):185–191.
    • (2013) Am J Med Genet A , vol.161A , Issue.1 , pp. 185-191
    • Teekakirikul, P.1    Milewicz, D.M.2    Miller, D.T.3
  • 60
    • 36049038657 scopus 로고    scopus 로고
    • Elevated factor VIII in hereditary haemorrhagic telangiectasia (HHT): Association with venous thromboembolism
    • Shovlin CL, Sulaiman NL, Govani FS, Jackson J., Begbie ME. Elevated factor VIII in hereditary haemorrhagic telangiectasia (HHT): association with venous thromboembolism. Thromb Haemost. 2007;98(5): 1031–1039.
    • (2007) Thromb Haemost , vol.98 , Issue.5 , pp. 1031-1039
    • Shovlin, C.L.1    Sulaiman, N.L.2    Govani, F.S.3    Jackson, J.4    Begbie, M.E.5
  • 61
    • 84858797729 scopus 로고    scopus 로고
    • Low serum iron levels are associated with elevated plasma levels of coagulation factor VIII and pulmonary emboli/deep venous thromboses in replicate cohorts of patients with hereditary haemorrhagic telangiectasia
    • Livesey JA, Manning RA, Meek JH, et al. Low serum iron levels are associated with elevated plasma levels of coagulation factor VIII and pulmonary emboli/deep venous thromboses in replicate cohorts of patients with hereditary haemorrhagic telangiectasia. Thorax. 2012;67(4):328–333.
    • (2012) Thorax , vol.67 , Issue.4 , pp. 328-333
    • Livesey, J.A.1    Manning, R.A.2    Meek, J.H.3
  • 62
    • 84874366861 scopus 로고    scopus 로고
    • Antiplatelet and anticoagulant agents in hereditary hemorrhagic telangiectasia
    • Devlin HL, Hosman AE, Shovlin CL. Antiplatelet and anticoagulant agents in hereditary hemorrhagic telangiectasia. N Engl J Med. 2013;368(9):876–878.
    • (2013) N Engl J Med , vol.368 , Issue.9 , pp. 876-878
    • Devlin, H.L.1    Hosman, A.E.2    Shovlin, C.L.3
  • 63
    • 33847620295 scopus 로고    scopus 로고
    • Hemorrhagic hereditary telangiectasia (Rendu-Osler disease) and infectious diseases: An underestimated association
    • Dupuis-Girod S, Giraud S, Decullier E, et al. Hemorrhagic hereditary telangiectasia (Rendu-Osler disease) and infectious diseases: an underestimated association. Clin Infect Dis. 2007;44(6):841–845.
    • (2007) Clin Infect Dis , vol.44 , Issue.6 , pp. 841-845
    • Dupuis-Girod, S.1    Giraud, S.2    Decullier, E.3
  • 64
    • 84883741856 scopus 로고    scopus 로고
    • Immunological abnormalities associated with hereditary haemorrhagic telangiectasia
    • Guilhem A, Malcus C, Clarivet B, Plauchu H, Dupuis-Girod S. Immunological abnormalities associated with hereditary haemorrhagic telangiectasia. J Intern Med. 2013;274(4):351–362.
    • (2013) J Intern Med , vol.274 , Issue.4 , pp. 351-362
    • Guilhem, A.1    Malcus, C.2    Clarivet, B.3    Plauchu, H.4    Dupuis-Girod, S.5
  • 65
    • 84890491238 scopus 로고    scopus 로고
    • Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls
    • Hosman AE, Devlin HL, Silva BM, Shovlin CL. Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls. Orphanet J Rare Dis. 2013;8:195.
    • (2013) Orphanet J Rare Dis , vol.8 , pp. 195
    • Hosman, A.E.1    Devlin, H.L.2    Silva, B.M.3    Shovlin, C.L.4
  • 66
    • 0034007163 scopus 로고    scopus 로고
    • Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)
    • Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet. 2000;91(1):66–67.
    • (2000) Am J Med Genet , vol.91 , Issue.1 , pp. 66-67
    • Shovlin, C.L.1    Guttmacher, A.E.2    Buscarini, E.3
  • 67
    • 84874220027 scopus 로고    scopus 로고
    • Hereditary hemorrhagic telangiectasia: How accurate are the clinical criteria?
    • van Gent MW, Velthuis S, Post MC, et al. Hereditary hemorrhagic telangiectasia: how accurate are the clinical criteria? Am J Med Genet A. 2013;161A(3):461–466.
    • (2013) Am J Med Genet A , vol.161A , Issue.3 , pp. 461-466
    • Van Gent, M.W.1    Velthuis, S.2    Post, M.C.3
  • 68
    • 67649199928 scopus 로고    scopus 로고
    • Hereditary haemorrhagic telangiectasia: A clinical and scientific review
    • Govani FS, Shovlin CL. Hereditary haemorrhagic telangiectasia: a clinical and scientific review. Eur J Hum Genet. 2009;17(7):860–871.
    • (2009) Eur J Hum Genet , vol.17 , Issue.7 , pp. 860-871
    • Govani, F.S.1    Shovlin, C.L.2
  • 69
    • 58849092281 scopus 로고    scopus 로고
    • Screening for pulmonary arteriovenous malformations using transthoracic contrast echocardiography: A prospective study
    • van Gent MW, Post MC, Luermans JG, et al. Screening for pulmonary arteriovenous malformations using transthoracic contrast echocardiography: a prospective study. Eur Respir J. 2009;33(1):85–91.
    • (2009) Eur Respir J , vol.33 , Issue.1 , pp. 85-91
    • Van Gent, M.W.1    Post, M.C.2    Luermans, J.G.3
  • 70
    • 85042948902 scopus 로고    scopus 로고
    • [homepage on the Internet]. Available from, Accessed July 7
    • HHT Mutation Database [homepage on the Internet]. Available from: http://arup.utah.edu/database/HHT/. Accessed July 7, 2014.
    • (2014) HHT Mutation Database
  • 71
    • 0031015777 scopus 로고    scopus 로고
    • Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: Doppler sonographic screening in a large family
    • Buscarini E, Buscarini L, Danesino C, et al. Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: Doppler sonographic screening in a large family. J Hepatol. 1997;26(1):111–118.
    • (1997) J Hepatol , vol.26 , Issue.1 , pp. 111-118
    • Buscarini, E.1    Buscarini, L.2    Danesino, C.3
  • 72
    • 0034648503 scopus 로고    scopus 로고
    • Clinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindred
    • McDonald JE, Miller FJ, Hallam SE, Nelson L, Marchuk DA, Ward KJ. Clinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindred. Am J Med Genet. 2000;93(4):320–327.
    • (2000) Am J Med Genet , vol.93 , Issue.4 , pp. 320-327
    • McDonald, J.E.1    Miller, F.J.2    Hallam, S.E.3    Nelson, L.4    Marchuk, D.A.5    Ward, K.J.6
  • 73
    • 0036634625 scopus 로고    scopus 로고
    • Identification of 13 new mutations in the ACVRL1 gene in a group of 52 unselected Italian patients affected by hereditary haemorrhagic telangiectasia
    • Olivieri C, Mira E, Delù G, et al. Identification of 13 new mutations in the ACVRL1 gene in a group of 52 unselected Italian patients affected by hereditary haemorrhagic telangiectasia. J Med Genet. 2002;39(7):E39.
    • (2002) J Med Genet , vol.39 , Issue.7 , pp. E39
    • Olivieri, C.1    Mira, E.2    Delù, G.3
  • 74
    • 12144286738 scopus 로고    scopus 로고
    • A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4)
    • Gallione CJ, Repetto GM, Legius E, et al. A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4). Lancet. 2004;363(9412): 852–859.
    • (2004) Lancet , vol.363 , Issue.9412 , pp. 852-859
    • Gallione, C.J.1    Repetto, G.M.2    Legius, E.3
  • 75
    • 33749260421 scopus 로고    scopus 로고
    • SMAD4 mutations found in unselected HHT patients
    • Gallione CJ, Richards JA, Letteboer TG, et al. SMAD4 mutations found in unselected HHT patients. J Med Genet. 2006;43(10):793–797.
    • (2006) J Med Genet , vol.43 , Issue.10 , pp. 793-797
    • Gallione, C.J.1    Richards, J.A.2    Letteboer, T.G.3
  • 76
    • 22244449292 scopus 로고    scopus 로고
    • A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5
    • Cole SG, Begbie ME, Wallace GM, Shovlin CL. A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5. J Med Genet. 2005;42(7):577–582.
    • (2005) J Med Genet , vol.42 , Issue.7 , pp. 577-582
    • Cole, S.G.1    Begbie, M.E.2    Wallace, G.M.3    Shovlin, C.L.4
  • 77
    • 33749455646 scopus 로고    scopus 로고
    • A fourth locus for hereditary hemorrhagic telangiectasia maps to chromosome 7
    • Bayrak-Toydemir P, McDonald J, Akarsu N, et al. A fourth locus for hereditary hemorrhagic telangiectasia maps to chromosome 7. Am J Med Genet A. 2006;140(20):2155–2162.
    • (2006) Am J Med Genet A , vol.140 , Issue.20 , pp. 2155-2162
    • Bayrak-Toydemir, P.1    McDonald, J.2    Akarsu, N.3
  • 78
    • 84883825716 scopus 로고    scopus 로고
    • BMP9 mutations cause a vascular-anomaly syndrome with phenotypic overlap with hereditary hemorrhagic telangiectasia
    • Wooderchak-Donahue WL, McDonald J, O’Fallon B, et al. BMP9 mutations cause a vascular-anomaly syndrome with phenotypic overlap with hereditary hemorrhagic telangiectasia. Am J Hum Genet. 2013; 93(3):530–537.
    • (2013) Am J Hum Genet , vol.93 , Issue.3 , pp. 530-537
    • Wooderchak-Donahue, W.L.1    McDonald, J.2    O’fallon, B.3
  • 79
    • 85042949729 scopus 로고    scopus 로고
    • HHT Foundation International, Inc. [webpage on the Internet], Available from, Accessed September 5
    • HHT Foundation International, Inc. [webpage on the Internet]. Genetic testing for HHT. Available from: http://www.hht.org/living-with-hht/genetic-testing/. Accessed September 5, 2014.
    • (2014) Genetic testing for HHT
  • 80
    • 33745700371 scopus 로고    scopus 로고
    • Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): Correlation of genotype with phenotype
    • Bossler AD, Richards J, George C, Godmilow L, Ganguly A. Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype. Hum Mutat. 2006;27(7):667–675.
    • (2006) Hum Mutat , vol.27 , Issue.7 , pp. 667-675
    • Bossler, A.D.1    Richards, J.2    George, C.3    Godmilow, L.4    Ganguly, A.5
  • 81
    • 33749239827 scopus 로고    scopus 로고
    • Hereditary haemorrhagic telangiectasia: Mutation detection, test sensitivity and novel mutations
    • Prigoda NL, Savas S, Abdalla SA, et al. Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations. J Med Genet. 2006;43(9):722–728.
    • (2006) J Med Genet , vol.43 , Issue.9 , pp. 722-728
    • Prigoda, N.L.1    Savas, S.2    Abdalla, S.A.3
  • 82
    • 19944426783 scopus 로고    scopus 로고
    • Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients
    • Letteboer TG, Zewald RA, Kamping EJ, et al. Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients. Hum Genet. 2005;116(1–2):8–16.
    • (2005) Hum Genet , vol.116 , Issue.1-2 , pp. 8-16
    • Letteboer, T.G.1    Zewald, R.A.2    Kamping, E.J.3
  • 83
    • 70350453921 scopus 로고    scopus 로고
    • Multiple sequence variants in hereditary hemorrhagic telangiectasia cases: Illustration of complexity in molecular diagnostic interpretation
    • McDonald J, Gedge F, Burdette A, et al. Multiple sequence variants in hereditary hemorrhagic telangiectasia cases: illustration of complexity in molecular diagnostic interpretation. J Mol Diagn. 2009;11(6):569–575.
    • (2009) J Mol Diagn , vol.11 , Issue.6 , pp. 569-575
    • McDonald, J.1    Gedge, F.2    Burdette, A.3
  • 84
    • 77955880114 scopus 로고    scopus 로고
    • Hereditary haemorrhagic telangiectasia: Pathophysiology, diagnosis and treatment
    • Shovlin CL. Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment. Blood Rev. 2010;24(6):203–219.
    • (2010) Blood Rev , vol.24 , Issue.6 , pp. 203-219
    • Shovlin, C.L.1
  • 85
    • 34250172107 scopus 로고    scopus 로고
    • Hereditary hemorrhagic telangiectasia: Clinical features in ENG and ALK1 mutation carriers
    • Sabba C, Pasculli G, Lenato GM, et al. Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers. J Thromb Haemost. 2007;5(6):1149–1157.
    • (2007) J Thromb Haemost , vol.5 , Issue.6 , pp. 1149-1157
    • Sabba, C.1    Pasculli, G.2    Lenato, G.M.3
  • 86
    • 33846208639 scopus 로고    scopus 로고
    • French-Italian-Rendu-Osler Network. Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: Data from the French-Italian HHT network
    • Lesca G, Olivieri C, Burnichon N, et al; French-Italian-Rendu-Osler Network. Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: data from the French-Italian HHT network. Genet Med. 2007;9(1):14–22.
    • (2007) Genet Med , vol.9 , Issue.1 , pp. 14-22
    • Lesca, G.1    Olivieri, C.2    Burnichon, N.3
  • 87
    • 33645786728 scopus 로고    scopus 로고
    • Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia
    • Letteboer TG, Mager JJ, Snijder RJ, et al. Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia. J Med Genet. 2006;43(4):371–377.
    • (2006) J Med Genet , vol.43 , Issue.4 , pp. 371-377
    • Letteboer, T.G.1    Mager, J.J.2    Snijder, R.J.3
  • 88
    • 55849086919 scopus 로고    scopus 로고
    • Genotype-phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia
    • Letteboer TG, Mager HJ, Snijder RJ, et al. Genotype-phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia. Am J Med Genet A. 2008; 146A(21):2733–2739.
    • (2008) Am J Med Genet A , vol.146A , Issue.21 , pp. 2733-2739
    • Letteboer, T.G.1    Mager, H.J.2    Snijder, R.J.3
  • 89
    • 84893540456 scopus 로고    scopus 로고
    • Endoscopic evaluation of gastrointestinal tract in patients with hereditary hemorrhagic telangiectasia and correlation with their genotypes
    • Canzonieri C, Centenara L, Ornati F, et al. Endoscopic evaluation of gastrointestinal tract in patients with hereditary hemorrhagic telangiectasia and correlation with their genotypes. Genet Med. 2014;16(1): 3–10.
    • (2014) Genet Med , vol.16 , Issue.1 , pp. 3-10
    • Canzonieri, C.1    Centenara, L.2    Ornati, F.3
  • 90
    • 25444530657 scopus 로고    scopus 로고
    • Clinical symptoms according to genotype amongst patients with hereditary haemorrhagic telangiectasia
    • Kjeldsen AD, Moller TR, Brusgaard K, Vase P, Andersen PE. Clinical symptoms according to genotype amongst patients with hereditary haemorrhagic telangiectasia. J Intern Med. 2005;258(4):349–355.
    • (2005) J Intern Med , vol.258 , Issue.4 , pp. 349-355
    • Kjeldsen, A.D.1    Moller, T.R.2    Brusgaard, K.3    Vase, P.4    Andersen, P.E.5
  • 91
    • 0036801052 scopus 로고    scopus 로고
    • Guidance on gastrointestinal surveillance for hereditary non-polyposis colorectal cancer, familial adenomatous polypolis, juvenile polyposis, and Peutz-Jeghers syndrome
    • British Society for Gastroenterology; Association of Coloproctology for Great Britain and Ireland
    • Dunlop MG; British Society for Gastroenterology; Association of Coloproctology for Great Britain and Ireland. Guidance on gastrointestinal surveillance for hereditary non-polyposis colorectal cancer, familial adenomatous polypolis, juvenile polyposis, and Peutz-Jeghers syndrome. Gut. 2002;51 Suppl 5:V21–V27.
    • (2002) Gut , vol.51 , pp. V21-V27
    • Dunlop, M.G.1
  • 92
    • 84861223069 scopus 로고    scopus 로고
    • Quality of life in patients with hereditary hemorrhagic telangiectasia in Norway: A population based study
    • Geirdal AO, Dheyauldeen S, Bachmann-Harildstad G, Heimdal K. Quality of life in patients with hereditary hemorrhagic telangiectasia in Norway: a population based study. Am J Med Genet A. 2012;158A(6): 1269–1278.
    • (2012) Am J Med Genet A , vol.158A , Issue.6 , pp. 1269-1278
    • Geirdal, A.O.1    Dheyauldeen, S.2    Bachmann-Harildstad, G.3    Heimdal, K.4
  • 93
    • 34247519602 scopus 로고    scopus 로고
    • Health-related quality of life in hereditary hemorrhagic telangiectasia
    • discussion 734–725
    • Geisthoff UW, Heckmann K, D’Amelio R, et al. Health-related quality of life in hereditary hemorrhagic telangiectasia. Otolaryngol Head Neck Surg. 2007;136(5):726–733; discussion 734–725.
    • (2007) Otolaryngol Head Neck Surg , vol.136 , Issue.5 , pp. 726-733
    • Geisthoff, U.W.1    Heckmann, K.2    D’amelio, R.3
  • 94
    • 13844297132 scopus 로고    scopus 로고
    • Health-related quality of life in a rare disease: Hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease
    • Pasculli G, Resta F, Guastamacchia E, Di Gennaro L, Suppressa P, Sabbà C. Health-related quality of life in a rare disease: hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease. Qual Life Res. Dec 2004;13(10):1715–1723.
    • (2004) Qual Life Res , vol.13 , Issue.10 , pp. 1715-1723
    • Pasculli, G.1    Resta, F.2    Guastamacchia, E.3    Di Gennaro, L.4    Suppressa, P.5    Sabbà, C.6
  • 95
    • 77950813985 scopus 로고    scopus 로고
    • An epistaxis severity score for hereditary hemorrhagic telangiectasia
    • Hoag JB, Terry P, Mitchell S, Reh D, Merlo CA. An epistaxis severity score for hereditary hemorrhagic telangiectasia. Laryngoscope. 2010; 120(4):838–843.
    • (2010) Laryngoscope , vol.120 , Issue.4 , pp. 838-843
    • Hoag, J.B.1    Terry, P.2    Mitchell, S.3    Reh, D.4    Merlo, C.A.5
  • 96
    • 84879306887 scopus 로고    scopus 로고
    • Lifestyle and dietary influences on nosebleed severity in hereditary hemorrhagic telangiectasia
    • Silva BM, Hosman AE, Devlin HL, Shovlin CL. Lifestyle and dietary influences on nosebleed severity in hereditary hemorrhagic telangiectasia. Laryngoscope. 2013;123(5):1092–1099.
    • (2013) Laryngoscope , vol.123 , Issue.5 , pp. 1092-1099
    • Silva, B.M.1    Hosman, A.E.2    Devlin, H.L.3    Shovlin, C.L.4
  • 97
    • 13444258107 scopus 로고    scopus 로고
    • Nd-YAG laser photocoagulation for epistaxis associated with hereditary hemorrhagic telangiectasia
    • Mahoney EJ, Shapshay SM. Nd-YAG laser photocoagulation for epistaxis associated with hereditary hemorrhagic telangiectasia. Laryngoscope. 2005;115(2):373–375.
    • (2005) Laryngoscope , vol.115 , Issue.2 , pp. 373-375
    • Mahoney, E.J.1    Shapshay, S.M.2
  • 98
    • 27744547101 scopus 로고    scopus 로고
    • Management of epistaxis in hereditary hemorrhagic telangiectasia by Nd:YAG laser and quality of life assessment using the HR-QoL questionnaire
    • Karapantzos I, Tsimpiris N, Goulis DG, Van Hoecke H, Van Cauwenberge P, Danielides V. Management of epistaxis in hereditary hemorrhagic telangiectasia by Nd:YAG laser and quality of life assessment using the HR-QoL questionnaire. Eur Arch Otorhinolaryngol. 2005;262(10):830–833.
    • (2005) Eur Arch Otorhinolaryngol , vol.262 , Issue.10 , pp. 830-833
    • Karapantzos, I.1    Tsimpiris, N.2    Goulis, D.G.3    Van Hoecke, H.4    Van Cauwenberge, P.5    Danielides, V.6
  • 99
    • 13444257828 scopus 로고    scopus 로고
    • Outcome of septal dermoplasty in patients with hereditary hemorrhagic telangiectasia
    • Fiorella ML, Ross D, Henderson KJ, White RI Jr. Outcome of septal dermoplasty in patients with hereditary hemorrhagic telangiectasia. Laryngoscope. 2005;115(2):301–305.
    • (2005) Laryngoscope , vol.115 , Issue.2 , pp. 301-305
    • Fiorella, M.L.1    Ross, D.2    Henderson, K.J.3    White, R.I.4
  • 100
    • 0031039508 scopus 로고    scopus 로고
    • Closure of the nasal cavities in the treatment of refractory hereditary haemorrhagic telangiectasia
    • Lund VJ, Howard DJ. Closure of the nasal cavities in the treatment of refractory hereditary haemorrhagic telangiectasia. J Laryngol Otol. 1997;111(1):30–33.
    • (1997) J Laryngol Otol , vol.111 , Issue.1 , pp. 30-33
    • Lund, V.J.1    Howard, D.J.2
  • 101
    • 0027993606 scopus 로고
    • Modified Young’s procedure for refractory epistaxis due to hereditary hemorrhagic telangiectasia
    • Gluckman JL, Portugal LG. Modified Young’s procedure for refractory epistaxis due to hereditary hemorrhagic telangiectasia. Laryngoscope. 1994;104(9):1174–1177.
    • (1994) Laryngoscope , vol.104 , Issue.9 , pp. 1174-1177
    • Gluckman, J.L.1    Portugal, L.G.2
  • 102
    • 84866333870 scopus 로고    scopus 로고
    • The Young’s procedure for severe epistaxis from hereditary hemorrhagic telangiectasia
    • Richer SL, Geisthoff UW, Livada N, et al. The Young’s procedure for severe epistaxis from hereditary hemorrhagic telangiectasia. Am J Rhinol Allergy. 2012;26(5):401–404.
    • (2012) Am J Rhinol Allergy , vol.26 , Issue.5 , pp. 401-404
    • Richer, S.L.1    Geisthoff, U.W.2    Livada, N.3
  • 103
    • 84890048235 scopus 로고    scopus 로고
    • Pilot study of submucosal radiofrequency for epistaxis in hereditary hemorrhagic telangiectasia
    • Mortuaire G, Boute O, Hatron PY, Chevalier D. Pilot study of submucosal radiofrequency for epistaxis in hereditary hemorrhagic telangiectasia. Rhinology. 2013;51(4):355–360.
    • (2013) Rhinology , vol.51 , Issue.4 , pp. 355-360
    • Mortuaire, G.1    Boute, O.2    Hatron, P.Y.3    Chevalier, D.4
  • 104
    • 21244483045 scopus 로고    scopus 로고
    • Patients with hereditary hemorrhagic telangiectasia have increased plasma levels of vascular endothelial growth factor and transforming growth factor-beta1 as well as high ALK1 tissue expression
    • Sadick H, Riedel F, Naim R, et al. Patients with hereditary hemorrhagic telangiectasia have increased plasma levels of vascular endothelial growth factor and transforming growth factor-beta1 as well as high ALK1 tissue expression. Haematologica. 2005;90(6): 818–828.
    • (2005) Haematologica , vol.90 , Issue.6 , pp. 818-828
    • Sadick, H.1    Riedel, F.2    Naim, R.3
  • 105
    • 84857865784 scopus 로고    scopus 로고
    • Bevacizumab in patients with hereditary hemorrhagic telangiectasia and severe hepatic vascular malformations and high cardiac output
    • Dupuis-Girod S, Ginon I, Saurin JC, et al. Bevacizumab in patients with hereditary hemorrhagic telangiectasia and severe hepatic vascular malformations and high cardiac output. JAMA. 2012;307(9):948–955.
    • (2012) JAMA , vol.307 , Issue.9 , pp. 948-955
    • Dupuis-Girod, S.1    Ginon, I.2    Saurin, J.C.3
  • 106
    • 66349137361 scopus 로고    scopus 로고
    • The effect of bevacizumab (Avastin) treatment on epistaxis in hereditary hemorrhagic telangiectasia
    • Simonds J, Miller F, Mandel J, Davidson TM. The effect of bevacizumab (Avastin) treatment on epistaxis in hereditary hemorrhagic telangiectasia. Laryngoscope. 2009;119(5):988–992.
    • (2009) Laryngoscope , vol.119 , Issue.5 , pp. 988-992
    • Simonds, J.1    Miller, F.2    Mandel, J.3    Davidson, T.M.4
  • 107
    • 84857451995 scopus 로고    scopus 로고
    • Treatment of hereditary hemorrhagic telangiectasia with submucosal and topical bevacizumab therapy
    • Karnezis TT, Davidson TM. Treatment of hereditary hemorrhagic telangiectasia with submucosal and topical bevacizumab therapy. Laryngoscope. 2012;122(3):495–497.
    • (2012) Laryngoscope , vol.122 , Issue.3 , pp. 495-497
    • Karnezis, T.T.1    Davidson, T.M.2
  • 108
    • 84859911496 scopus 로고    scopus 로고
    • Bevacizumab nasal spray: Noninvasive treatment of epistaxis in patients with Rendu-Osler disease
    • Guldmann R, Dupret A, Nivoix Y, Schultz P, Debry C. Bevacizumab nasal spray: noninvasive treatment of epistaxis in patients with Rendu-Osler disease. Laryngoscope. 2012;122(5):953–955.
    • (2012) Laryngoscope , vol.122 , Issue.5 , pp. 953-955
    • Guldmann, R.1    Dupret, A.2    Nivoix, Y.3    Schultz, P.4    Debry, C.5
  • 109
    • 79951862329 scopus 로고    scopus 로고
    • Efficacy of intranasal Bevacizumab (Avastin) treatment in patients with hereditary hemorrhagic telangiectasia-associated epistaxis
    • Karnezis TT, Davidson TM. Efficacy of intranasal Bevacizumab (Avastin) treatment in patients with hereditary hemorrhagic telangiectasia-associated epistaxis. Laryngoscope. 2011;121(3):636–638.
    • (2011) Laryngoscope , vol.121 , Issue.3 , pp. 636-638
    • Karnezis, T.T.1    Davidson, T.M.2
  • 110
    • 84857038767 scopus 로고    scopus 로고
    • A retrospective analysis of low dose, intranasal injected bevacizumab (Avastin) in hereditary haemorrhagic telangiectasia
    • Rohrmeier C, Sachs HG, Kuehnel TS. A retrospective analysis of low dose, intranasal injected bevacizumab (Avastin) in hereditary haemorrhagic telangiectasia. Eur Arch Otorhinolaryngol. 2012;269(2): 531–536.
    • (2012) Eur Arch Otorhinolaryngol , vol.269 , Issue.2 , pp. 531-536
    • Rohrmeier, C.1    Sachs, H.G.2    Kuehnel, T.S.3
  • 111
    • 79951890796 scopus 로고    scopus 로고
    • Safety of intranasal Bevacizumab (Avastin) treatment in patients with hereditary hemorrhagic telangiectasia-associated epistaxis
    • Chen S, Karnezis T, Davidson TM. Safety of intranasal Bevacizumab (Avastin) treatment in patients with hereditary hemorrhagic telangiectasia-associated epistaxis. Laryngoscope. 2011;121(3):644–646.
    • (2011) Laryngoscope , vol.121 , Issue.3 , pp. 644-646
    • Chen, S.1    Karnezis, T.2    Davidson, T.M.3
  • 112
    • 84923600344 scopus 로고    scopus 로고
    • Intranasal submucosal bevacizumab for epistaxis in hereditary hemorrhagic telangiectasia: A double-blind, randomized, placebo-controlled trial
    • Epub March 4
    • Riss D, Burian M, Wolf A, Kranebitter V, Kaider A, Arnoldner C. Intranasal submucosal bevacizumab for epistaxis in hereditary hemorrhagic telangiectasia: a double-blind, randomized, placebo-controlled trial. Head Neck. Epub March 4, 2014.
    • (2014) Head Neck
    • Riss, D.1    Burian, M.2    Wolf, A.3    Kranebitter, V.4    Kaider, A.5    Arnoldner, C.6
  • 113
    • 84899713100 scopus 로고    scopus 로고
    • ELLIPSE Study: A Phase 1 study evaluating the tolerance of bevacizumab nasal spray in the treatment of epistaxis in hereditary hemorrhagic telangiectasia
    • Dupuis-Girod S, Ambrun A, Decullier E, et al. ELLIPSE Study: a Phase 1 study evaluating the tolerance of bevacizumab nasal spray in the treatment of epistaxis in hereditary hemorrhagic telangiectasia. MAbs. 2014;6(3):794–799.
    • (2014) MAbs , vol.6 , Issue.3 , pp. 794-799
    • Dupuis-Girod, S.1    Ambrun, A.2    Decullier, E.3
  • 114
    • 84881223902 scopus 로고    scopus 로고
    • Novel treatments for epistaxis in hereditary hemorrhagic telangiectasia: A systematic review of the clinical experience with thalidomide
    • Franchini M, Frattini F, Crestani S, Bonfanti C. Novel treatments for epistaxis in hereditary hemorrhagic telangiectasia: a systematic review of the clinical experience with thalidomide. J Thromb Thrombolysis. 2013;36(3):355–357.
    • (2013) J Thromb Thrombolysis , vol.36 , Issue.3 , pp. 355-357
    • Franchini, M.1    Frattini, F.2    Crestani, S.3    Bonfanti, C.4
  • 115
    • 77950538918 scopus 로고    scopus 로고
    • Thalidomide stimulates vessel maturation and reduces epistaxis in individuals with hereditary hemorrhagic telangiectasia
    • Lebrin F, Srun S, Raymond K, et al. Thalidomide stimulates vessel maturation and reduces epistaxis in individuals with hereditary hemorrhagic telangiectasia. Nat Med. 2010;16(4):420–428.
    • (2010) Nat Med , vol.16 , Issue.4 , pp. 420-428
    • Lebrin, F.1    Srun, S.2    Raymond, K.3
  • 116
    • 77954867089 scopus 로고    scopus 로고
    • Propranolol for infantile haemangiomas: Insights into the molecular mechanisms of action
    • Storch CH, Hoeger PH. Propranolol for infantile haemangiomas: insights into the molecular mechanisms of action. Br J Dermatol. 2010;163(2):269–274.
    • (2010) Br J Dermatol , vol.163 , Issue.2 , pp. 269-274
    • Storch, C.H.1    Hoeger, P.H.2
  • 117
    • 84860371097 scopus 로고    scopus 로고
    • Topical timolol for the treatment of epistaxis in hereditary hemorrhagic telangiectasia
    • Olitsky SE. Topical timolol for the treatment of epistaxis in hereditary hemorrhagic telangiectasia. Am J Otolaryngol. 2012;33(3):375–376.
    • (2012) Am J Otolaryngol , vol.33 , Issue.3 , pp. 375-376
    • Olitsky, S.E.1
  • 118
    • 84862654480 scopus 로고    scopus 로고
    • Local sclerotherapy with polydocanol (Aethoxysklerol®) for the treatment of epistaxis in Rendu-Osler-Weber or hereditary hemorrhagic telangiectasia (HHT): 15 years of experience
    • Morais D, Millás T, Zarrabeitia R, Botella LM, Almaraz A. Local sclerotherapy with polydocanol (Aethoxysklerol®) for the treatment of epistaxis in Rendu-Osler-Weber or hereditary hemorrhagic telangiectasia (HHT): 15 years of experience. Rhinology. Mar 2012;50(1): 80–86.
    • (2012) Rhinology , vol.50 , Issue.1 , pp. 80-86
    • Morais, D.1    Millás, T.2    Zarrabeitia, R.3    Botella, L.M.4    Almaraz, A.5
  • 119
    • 1842505675 scopus 로고    scopus 로고
    • Hormonal and antihormonal therapy for epistaxis in hereditary hemorrhagic telangiectasia
    • Jameson JJ, Cave DR. Hormonal and antihormonal therapy for epistaxis in hereditary hemorrhagic telangiectasia. Laryngoscope. 2004;114(4):705–709.
    • (2004) Laryngoscope , vol.114 , Issue.4 , pp. 705-709
    • Jameson, J.J.1    Cave, D.R.2
  • 120
    • 80051572751 scopus 로고    scopus 로고
    • Anti-estrogen therapy for hereditary hemorrhagic telangiectasia – a long-term clinical trial
    • Yaniv E, Preis M, Shevro J, Nageris B, Hadar T. Anti-estrogen therapy for hereditary hemorrhagic telangiectasia – a long-term clinical trial. Rhinology. 2011;49(2):214–216.
    • (2011) Rhinology , vol.49 , Issue.2 , pp. 214-216
    • Yaniv, E.1    Preis, M.2    Shevro, J.3    Nageris, B.4    Hadar, T.5
  • 121
    • 63249096929 scopus 로고    scopus 로고
    • Antiestrogen therapy for hereditary hemorrhagic telangiectasia: A double-blind placebo-controlled clinical trial
    • Yaniv E, Preis M, Hadar T, Shvero J, Haddad M. Antiestrogen therapy for hereditary hemorrhagic telangiectasia: a double-blind placebo-controlled clinical trial. Laryngoscope. 2009;119(2):284–288.
    • (2009) Laryngoscope , vol.119 , Issue.2 , pp. 284-288
    • Yaniv, E.1    Preis, M.2    Hadar, T.3    Shvero, J.4    Haddad, M.5
  • 122
    • 77749246401 scopus 로고    scopus 로고
    • Estrogen therapy for hereditary haemorrhagic telangiectasia (HHT): Effects of raloxifene, on Endoglin and ALK1 expression in endothelial cells
    • Albiñana V, Bernabeu-Herrero ME, Zarrabeitia R, Bernabéu C, Botella LM. Estrogen therapy for hereditary haemorrhagic telangiectasia (HHT): Effects of raloxifene, on Endoglin and ALK1 expression in endothelial cells. Thromb Haemost. 2010;103(3):525–534.
    • (2010) Thromb Haemost , vol.103 , Issue.3 , pp. 525-534
    • Albiñana, V.1    Bernabeu-Herrero, M.E.2    Zarrabeitia, R.3    Bernabéu, C.4    Botella, L.M.5
  • 123
    • 84923608476 scopus 로고    scopus 로고
    • Treatment of epistaxis in hereditary hemorrhagic telangiectasia with tranexamic acid – a double-blind placebo-controlled cross-over phase IIIB study
    • Geisthoff UW, Seyfert UT, Kübler M, Bieg B, Plinkert PK, König J. Treatment of epistaxis in hereditary hemorrhagic telangiectasia with tranexamic acid – a double-blind placebo-controlled cross-over phase IIIB study. Thromb Res. 2014;134(3):565–571.
    • (2014) Thromb Res , vol.134 , Issue.3 , pp. 565-571
    • Geisthoff, U.W.1    Seyfert, U.T.2    Kübler, M.3    Bieg, B.4    Plinkert, P.K.5    König, J.6
  • 124
    • 0028027438 scopus 로고
    • Treatment of bleeding in hereditary hemorrhagic telangiectasia with aminocaproic acid
    • Korzenik JR, Topazian MD, White R. Treatment of bleeding in hereditary hemorrhagic telangiectasia with aminocaproic acid. N Engl J Med. 1994;331(18):1236.
    • (1994) N Engl J Med , vol.331 , Issue.18 , pp. 1236
    • Korzenik, J.R.1    Topazian, M.D.2    White, R.3
  • 125
    • 62649172211 scopus 로고    scopus 로고
    • The effect of N-acetylcysteine on epistaxis and quality of life in patients with HHT: A pilot study
    • de Gussem EM, Snijder RJ, Disch FJ, Zanen P, Westermann CJ, Mager JJ. The effect of N-acetylcysteine on epistaxis and quality of life in patients with HHT: a pilot study. Rhinology. 2009;47(1):85–88.
    • (2009) Rhinology , vol.47 , Issue.1 , pp. 85-88
    • De Gussem, E.M.1    Snijder, R.J.2    Disch, F.J.3    Zanen, P.4    Westermann, C.J.5    Mager, J.J.6
  • 126
    • 84885738700 scopus 로고    scopus 로고
    • Hemorrhage-adjusted iron requirements, hematinics and hepcidin define hereditary hemorrhagic telangiectasia as a model of hemorrhagic iron deficiency
    • Finnamore H, Le Couteur J, Hickson M, Busbridge M, Whelan K, Shovlin CL. Hemorrhage-adjusted iron requirements, hematinics and hepcidin define hereditary hemorrhagic telangiectasia as a model of hemorrhagic iron deficiency. PLoS One. 2013;8(10):e76516.
    • (2013) PLoS One , vol.8 , Issue.10
    • Finnamore, H.1    Le Couteur, J.2    Hickson, M.3    Busbridge, M.4    Whelan, K.5    Shovlin, C.L.6
  • 128
    • 84857645067 scopus 로고    scopus 로고
    • Iron deficiency anemia related to hereditary hemorrhagic telangiectasia: Response to treatment with bevacizumab
    • Fleagle JM, Bobba RK, Kardinal CG, Freter CE. Iron deficiency anemia related to hereditary hemorrhagic telangiectasia: response to treatment with bevacizumab. Am J Med Sci. 2012;343(3):249–251.
    • (2012) Am J Med Sci , vol.343 , Issue.3 , pp. 249-251
    • Fleagle, J.M.1    Bobba, R.K.2    Kardinal, C.G.3    Freter, C.E.4
  • 129
    • 84873990083 scopus 로고    scopus 로고
    • Bevacizumab as rescue treatment for severe recurrent gastrointestinal bleeding in hereditary hemorrhagic telangiectasia
    • Lupu A, Stefanescu C, Treton X, Attar A, Corcos O, Bouhnik Y. Bevacizumab as rescue treatment for severe recurrent gastrointestinal bleeding in hereditary hemorrhagic telangiectasia. J Clin Gastroenterol. 2013;47(3):256–257.
    • (2013) J Clin Gastroenterol , vol.47 , Issue.3 , pp. 256-257
    • Lupu, A.1    Stefanescu, C.2    Treton, X.3    Attar, A.4    Corcos, O.5    Bouhnik, Y.6
  • 130
    • 84878540326 scopus 로고    scopus 로고
    • Successful treatment of thalidomide for recurrent bleeding due to gastric angiodysplasia in hereditary hemorrhagic telangiectasia
    • Wang XY, Chen Y, Du Q. Successful treatment of thalidomide for recurrent bleeding due to gastric angiodysplasia in hereditary hemorrhagic telangiectasia. Eur Rev Med Pharmacol Sci. 2013;17(8): 1114–1116.
    • (2013) Eur Rev Med Pharmacol Sci , vol.17 , Issue.8 , pp. 1114-1116
    • Wang, X.Y.1    Chen, Y.2    Du, Q.3
  • 131
    • 78851472558 scopus 로고    scopus 로고
    • Low dose intravenous bevacizumab for the treatment of anaemia in hereditary haemorrhagic telangiectasia
    • Suppressa P, Liso A, Sabbà C. Low dose intravenous bevacizumab for the treatment of anaemia in hereditary haemorrhagic telangiectasia. Br J Haematol. 2011;152(4):365.
    • (2011) Br J Haematol , vol.152 , Issue.4 , pp. 365
    • Suppressa, P.1    Liso, A.2    Sabbà, C.3
  • 132
    • 67649998404 scopus 로고    scopus 로고
    • Lenalidomide to control gastrointestinal bleeding in hereditary haemorrhagic telangiectasia: Potential implications for angiodysplasias?
    • Bowcock SJ, Patrick HE. Lenalidomide to control gastrointestinal bleeding in hereditary haemorrhagic telangiectasia: potential implications for angiodysplasias? Br J Haematol. 2009;146(2): 220–222.
    • (2009) Br J Haematol , vol.146 , Issue.2 , pp. 220-222
    • Bowcock, S.J.1    Patrick, H.E.2
  • 133
    • 33644869358 scopus 로고    scopus 로고
    • Regression of cutaneous and gastrointestinal telangiectasia with sirolimus and aspirin in a patient with hereditary hemorrhagic telangiectasia
    • Skaro AI, Marotta PJ, McAlister VC. Regression of cutaneous and gastrointestinal telangiectasia with sirolimus and aspirin in a patient with hereditary hemorrhagic telangiectasia. Ann Intern Med. 2006;144(3):226–227.
    • (2006) Ann Intern Med , vol.144 , Issue.3 , pp. 226-227
    • Skaro, A.I.1    Marotta, P.J.2    McAlister, V.C.3
  • 134
    • 15344347617 scopus 로고    scopus 로고
    • Interferon for metastatic renal cell cancer causing regression of hereditary hemorrhagic telangiectasia
    • Wheatley-Price P, Shovlin C, Chao D. Interferon for metastatic renal cell cancer causing regression of hereditary hemorrhagic telangiectasia. J Clin Gastroenterol. 2005;39(4):344–345.
    • (2005) J Clin Gastroenterol , vol.39 , Issue.4 , pp. 344-345
    • Wheatley-Price, P.1    Shovlin, C.2    Chao, D.3
  • 135
    • 0025230351 scopus 로고
    • Treatment of bleeding gastrointestinal vascular malformations with oestrogen-progesterone
    • van Cutsem E, Rutgeerts P, Vantrappen G. Treatment of bleeding gastrointestinal vascular malformations with oestrogen-progesterone. Lancet. 1990;335(8695):953–955.
    • (1990) Lancet , vol.335 , Issue.8695 , pp. 953-955
    • Van Cutsem, E.1    Rutgeerts, P.2    Vantrappen, G.3
  • 136
    • 0022392050 scopus 로고
    • Endoscopic laser treatment of vascular anomalies of the upper gastrointestinal tract
    • Bown SG, Swain CP, Storey DW, et al. Endoscopic laser treatment of vascular anomalies of the upper gastrointestinal tract. Gut. 1985; 26(12):1338–1348.
    • (1985) Gut , vol.26 , Issue.12 , pp. 1338-1348
    • Bown, S.G.1    Swain, C.P.2    Storey, D.W.3
  • 137
    • 0027526236 scopus 로고
    • Laser ablation of upper gastrointestinal vascular ectasias: Long term results
    • Sargeant IR, Loizou LA, Rampton D, Tulloch M, Bown SG. Laser ablation of upper gastrointestinal vascular ectasias: long term results. Gut. 1993;34(4):470–475.
    • (1993) Gut , vol.34 , Issue.4 , pp. 470-475
    • Sargeant, I.R.1    Loizou, L.A.2    Rampton, D.3    Tulloch, M.4    Bown, S.G.5
  • 138
    • 0023739117 scopus 로고
    • Mucosal vascular malformations of the gastrointestinal tract: Clinical observations and results of endoscopic neodymium: Yttrium-aluminum-garnet laser therapy
    • Gostout CJ, Bowyer BA, Ahlquist DA, Viggiano TR, Balm RK. Mucosal vascular malformations of the gastrointestinal tract: clinical observations and results of endoscopic neodymium: yttrium-aluminum-garnet laser therapy. Mayo Clin Proc. 1988;63(10):993–1003.
    • (1988) Mayo Clin Proc , vol.63 , Issue.10 , pp. 993-1003
    • Gostout, C.J.1    Bowyer, B.A.2    Ahlquist, D.A.3    Viggiano, T.R.4    Balm, R.K.5
  • 139
    • 0034633646 scopus 로고    scopus 로고
    • Pulmonary arteriovenous malformations: Cerebral ischemia and neurologic manifestations
    • Moussouttas M, Fayad P, Rosenblatt M, et al. Pulmonary arteriovenous malformations: cerebral ischemia and neurologic manifestations. Neurology. 2000;55(7):959–964.
    • (2000) Neurology , vol.55 , Issue.7 , pp. 959-964
    • Moussouttas, M.1    Fayad, P.2    Rosenblatt, M.3
  • 140
    • 84902656182 scopus 로고    scopus 로고
    • Pulmonary arteriovenous malformations and embolic complications in patients with hereditary hemorrhagic telangiectasia
    • Angriman F, Ferreyro BL, Wainstein EJ, Serra MM. Pulmonary arteriovenous malformations and embolic complications in patients with hereditary hemorrhagic telangiectasia. Arch Bronconeumol. 2014;50(7):301–304.
    • (2014) Arch Bronconeumol , vol.50 , Issue.7 , pp. 301-304
    • Angriman, F.1    Ferreyro, B.L.2    Wainstein, E.J.3    Serra, M.M.4
  • 141
    • 84865316813 scopus 로고    scopus 로고
    • Silent threat? A retrospective study of screening practices for pulmonary arteriovenous malformations in patients with hereditary haemorrhagic telangiectasia
    • Verkerk MM, Shovlin CL, Lund VJ. Silent threat? A retrospective study of screening practices for pulmonary arteriovenous malformations in patients with hereditary haemorrhagic telangiectasia. Rhinology. 2012;50(3):277–283.
    • (2012) Rhinology , vol.50 , Issue.3 , pp. 277-283
    • Verkerk, M.M.1    Shovlin, C.L.2    Lund, V.J.3
  • 142
    • 0036468088 scopus 로고    scopus 로고
    • Comparison of contrast echocardiography versus cardiac catheterization for detection of pulmonary arteriovenous malformations
    • Feinstein JA, Moore P, Rosenthal DN, Puchalski M, Brook MM. Comparison of contrast echocardiography versus cardiac catheterization for detection of pulmonary arteriovenous malformations. Am J Cardiol. 2002;89(3):281–285.
    • (2002) Am J Cardiol , vol.89 , Issue.3 , pp. 281-285
    • Feinstein, J.A.1    Moore, P.2    Rosenthal, D.N.3    Puchalski, M.4    Brook, M.M.5
  • 143
    • 84881508436 scopus 로고    scopus 로고
    • Grade of pulmonary right-to-left shunt on contrast echocardiography and cerebral complications: A striking association
    • Velthuis S, Buscarini E, van Gent MW, et al. Grade of pulmonary right-to-left shunt on contrast echocardiography and cerebral complications: a striking association. Chest. 2013;144(2):542–548.
    • (2013) Chest , vol.144 , Issue.2 , pp. 542-548
    • Velthuis, S.1    Buscarini, E.2    Van Gent, M.W.3
  • 144
    • 85042949682 scopus 로고    scopus 로고
    • Predicting the size of pulmonary arteriovenous malformations on chest computed tomography: A role for transthoracic contrast echocardiography
    • Velthuis S, Buscarini E, Mager JJ, et al. Predicting the size of pulmonary arteriovenous malformations on chest computed tomography: a role for transthoracic contrast echocardiography. Eur Respir J.
    • Eur Respir J
    • Velthuis, S.1    Buscarini, E.2    Mager, J.J.3
  • 145
    • 84899410049 scopus 로고    scopus 로고
    • Cumulative radiation dose in patients with hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations
    • Hanneman K, Faughnan ME, Prabhudesai V. Cumulative radiation dose in patients with hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations. Can Assoc Radiol J. 2014;65(2): 135–140.
    • (2014) Can Assoc Radiol J , vol.65 , Issue.2 , pp. 135-140
    • Hanneman, K.1    Faughnan, M.E.2    Prabhudesai, V.3
  • 146
    • 42449142638 scopus 로고    scopus 로고
    • MR angiography for detection of pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia
    • Schneider G, Uder M, Koehler M, et al. MR angiography for detection of pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia. AJR Am J Roentgenol. 2008;190(4): 892–901.
    • (2008) AJR Am J Roentgenol , vol.190 , Issue.4 , pp. 892-901
    • Schneider, G.1    Uder, M.2    Koehler, M.3
  • 147
    • 40649111657 scopus 로고    scopus 로고
    • Primary determinants of ischaemic stroke/brain abscess risks are independent of severity of pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia
    • Shovlin CL, Jackson J., Bamford KB, et al. Primary determinants of ischaemic stroke/brain abscess risks are independent of severity of pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia. Thorax. 2008;63(3):259–266.
    • (2008) Thorax , vol.63 , Issue.3 , pp. 259-266
    • Shovlin, C.L.1    Jackson, J.2    Bamford, K.B.3
  • 148
    • 77957865160 scopus 로고    scopus 로고
    • Embolization of pulmonary arteriovenous malformations using the Amplatzer vascular plug: Successful treatment of 69 consecutive patients
    • Hart JL, Aldin Z, Braude P, Shovlin CL, Jackson J. Embolization of pulmonary arteriovenous malformations using the Amplatzer vascular plug: successful treatment of 69 consecutive patients. Eur Radiol. 2010;20(11):2663–2670.
    • (2010) Eur Radiol , vol.20 , Issue.11 , pp. 2663-2670
    • Hart, J.L.1    Aldin, Z.2    Braude, P.3    Shovlin, C.L.4    Jackson, J.5
  • 149
    • 84906935491 scopus 로고    scopus 로고
    • Large pulmonary arteriovenous malformations: Long-term results of embolization with AMPLATZER vascular plugs
    • Kucukay F, Ozdemir M, Senol E, Okten S, Ereren M, Karan A. Large pulmonary arteriovenous malformations: long-term results of embolization with AMPLATZER vascular plugs. J Vasc Interv Radiol. 2014;25(9):1327–1332.
    • (2014) J Vasc Interv Radiol , vol.25 , Issue.9 , pp. 1327-1332
    • Kucukay, F.1    Ozdemir, M.2    Senol, E.3    Okten, S.4    Ereren, M.5    Karan, A.6
  • 150
    • 84859967586 scopus 로고    scopus 로고
    • Novel approach to complex pulmonary arteriovenous malformation embolization using detachable coils and Amplatzer vascular plugs
    • Hundt W, Kalinowski M, Kiessling A, et al. Novel approach to complex pulmonary arteriovenous malformation embolization using detachable coils and Amplatzer vascular plugs. Eur J Radiol. 2012;81(5):e732–e738.
    • (2012) Eur J Radiol , vol.81 , Issue.5 , pp. e732-e738
    • Hundt, W.1    Kalinowski, M.2    Kiessling, A.3
  • 151
    • 2342467411 scopus 로고    scopus 로고
    • Embolotherapy of pulmonary arteriovenous malformations: Long-term results in 112 patients
    • Mager JJ, Overtoom TT, Blauw H, Lammers JW, Westermann CJ. Embolotherapy of pulmonary arteriovenous malformations: long-term results in 112 patients. J Vasc Interv Radiol. 2004;15(5):451–456.
    • (2004) J Vasc Interv Radiol , vol.15 , Issue.5 , pp. 451-456
    • Mager, J.J.1    Overtoom, T.T.2    Blauw, H.3    Lammers, J.W.4    Westermann, C.J.5
  • 152
    • 0036066191 scopus 로고    scopus 로고
    • Pulmonary arteriovenous malformations: Effect of embolization on right-to-left shunt, hypoxemia, and exercise tolerance in 66 patients
    • Gupta P, Mordin C, Curtis J, Hughes JM, Shovlin CL, Jackson JE. Pulmonary arteriovenous malformations: effect of embolization on right-to-left shunt, hypoxemia, and exercise tolerance in 66 patients. AJR Am J Roentgenol. 2002;179(2):347–355.
    • (2002) AJR Am J Roentgenol , vol.179 , Issue.2 , pp. 347-355
    • Gupta, P.1    Mordin, C.2    Curtis, J.3    Hughes, J.M.4    Shovlin, C.L.5    Jackson, J.E.6
  • 154
    • 33646125437 scopus 로고    scopus 로고
    • Pulmonary arteriovenous malformations treated with embolotherapy: Helical CT evaluation of long-term effectiveness after 2–21-year follow-up
    • Remy-Jardin M, Dumont P, Brillet PY, Dupuis P, Duhamel A, Remy J. Pulmonary arteriovenous malformations treated with embolotherapy: helical CT evaluation of long-term effectiveness after 2–21-year follow-up. Radiology. 2006;239(2):576–585.
    • (2006) Radiology , vol.239 , Issue.2 , pp. 576-585
    • Remy-Jardin, M.1    Dumont, P.2    Brillet, P.Y.3    Dupuis, P.4    Duhamel, A.5    Remy, J.6
  • 155
    • 84890041717 scopus 로고    scopus 로고
    • Treated pulmonary arteriovenous malformations: Patterns of persistence and associated retreatment success
    • Woodward CS, Pyeritz RE, Chittams JL, Trerotola SO. Treated pulmonary arteriovenous malformations: patterns of persistence and associated retreatment success. Radiology. 2013;269(3):919–926.
    • (2013) Radiology , vol.269 , Issue.3 , pp. 919-926
    • Woodward, C.S.1    Pyeritz, R.E.2    Chittams, J.L.3    Trerotola, S.O.4
  • 156
    • 84923148612 scopus 로고    scopus 로고
    • Feasibility of time-resolved MR angiography for detecting recanalization of pulmonary arteriovenous malformations treated with embolization with platinum coils
    • Kawai T, Shimohira M, Kan H, et al. Feasibility of time-resolved MR angiography for detecting recanalization of pulmonary arteriovenous malformations treated with embolization with platinum coils. J Vasc Interv Radiol. 2014;25(9):1339–1347.
    • (2014) J Vasc Interv Radiol , vol.25 , Issue.9 , pp. 1339-1347
    • Kawai, T.1    Shimohira, M.2    Kan, H.3
  • 157
    • 0037331686 scopus 로고    scopus 로고
    • Contrast echocardiography remains positive after treatment of pulmonary arteriovenous malformations
    • Lee WL, Graham AF, Pugash RA, et al. Contrast echocardiography remains positive after treatment of pulmonary arteriovenous malformations. Chest. 2003;123(2):351–358.
    • (2003) Chest , vol.123 , Issue.2 , pp. 351-358
    • Lee, W.L.1    Graham, A.F.2    Pugash, R.A.3
  • 158
    • 84888379941 scopus 로고    scopus 로고
    • Successful lung transplantation in a case with diffuse pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia
    • Fukushima H, Mitsuhashi T, Oto T, et al. Successful lung transplantation in a case with diffuse pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia. Am J Transplant. 2013;13(12): 3278–3281.
    • (2013) Am J Transplant , vol.13 , Issue.12 , pp. 3278-3281
    • Fukushima, H.1    Mitsuhashi, T.2    Oto, T.3
  • 159
    • 56849104879 scopus 로고    scopus 로고
    • Post-NICE 2008: Antibiotic prophylaxis prior to dental procedures for patients with pulmonary arteriovenous malformations (PAVMs) and hereditary haemorrhagic telangiectasia
    • Shovlin C, Bamford K, Wray D. Post-NICE 2008: antibiotic prophylaxis prior to dental procedures for patients with pulmonary arteriovenous malformations (PAVMs) and hereditary haemorrhagic telangiectasia. Br Dent J. 2008;205(10):531–533.
    • (2008) Br Dent J , vol.205 , Issue.10 , pp. 531-533
    • Shovlin, C.1    Bamford, K.2    Wray, D.3
  • 160
    • 84855208085 scopus 로고    scopus 로고
    • Flight-related complications are infrequent in patients with hereditary haemorrhagic telangiectasia/pulmonary arteriovenous malformations, despite low oxygen saturations and anaemia
    • Mason CG, Shovlin CL. Flight-related complications are infrequent in patients with hereditary haemorrhagic telangiectasia/pulmonary arteriovenous malformations, despite low oxygen saturations and anaemia. Thorax. 2012;67(1):80–81.
    • (2012) Thorax , vol.67 , Issue.1 , pp. 80-81
    • Mason, C.G.1    Shovlin, C.L.2
  • 162
    • 0037407959 scopus 로고    scopus 로고
    • Neurologic complications of cerebral angiography: Prospective analysis of 2,899 procedures and review of the literature
    • Willinsky RA, Taylor SM, TerBrugge K, Farb RI, Tomlinson G, Montanera W. Neurologic complications of cerebral angiography: prospective analysis of 2,899 procedures and review of the literature. Radiology. 2003;227(2):522–528.
    • (2003) Radiology , vol.227 , Issue.2 , pp. 522-528
    • Willinsky, R.A.1    Taylor, S.M.2    Terbrugge, K.3    Farb, R.I.4    Tomlinson, G.5    Montanera, W.6
  • 163
    • 33746620100 scopus 로고    scopus 로고
    • Three-dimensional dynamic magnetic resonance angiography for the evaluation of radiosurgically treated cerebral arteriovenous malformations
    • Gauvrit JY, Oppenheim C, Nataf F, et al. Three-dimensional dynamic magnetic resonance angiography for the evaluation of radiosurgically treated cerebral arteriovenous malformations. Eur Radiol. 2006;16(3): 583–591.
    • (2006) Eur Radiol , vol.16 , Issue.3 , pp. 583-591
    • Gauvrit, J.Y.1    Oppenheim, C.2    Nataf, F.3
  • 164
    • 0030294008 scopus 로고    scopus 로고
    • MRI in children given gadodiamide injection: Safety and efficacy in CNS and body indications
    • Lundby B, Gordon P, Hugo F. MRI in children given gadodiamide injection: safety and efficacy in CNS and body indications. Eur J Radiol. 1996;23(3):190–196.
    • (1996) Eur J Radiol , vol.23 , Issue.3 , pp. 190-196
    • Lundby, B.1    Gordon, P.2    Hugo, F.3
  • 165
    • 0037268954 scopus 로고    scopus 로고
    • Two-dimensional thick-slice MR digital subtraction angiography in the assessment of small to medium-size intracranial arteriovenous malformations
    • Mori H, Aoki S, Okubo T, et al. Two-dimensional thick-slice MR digital subtraction angiography in the assessment of small to medium-size intracranial arteriovenous malformations. Neuroradiology. 2003;45(1):27–33.
    • (2003) Neuroradiology , vol.45 , Issue.1 , pp. 27-33
    • Mori, H.1    Aoki, S.2    Okubo, T.3
  • 166
    • 0029039478 scopus 로고
    • Intracranial arteriovenous malformations: Quantitative analysis of magnitude contrast MR angiography versus gradient-echo MR imaging versus conventional angiography
    • Mukherji SK, Quisling RG, Kubilis PS, Finn JP, Friedman WA. Intracranial arteriovenous malformations: quantitative analysis of magnitude contrast MR angiography versus gradient-echo MR imaging versus conventional angiography. Radiology. 1995;196(1):187–193.
    • (1995) Radiology , vol.196 , Issue.1 , pp. 187-193
    • Mukherji, S.K.1    Quisling, R.G.2    Kubilis, P.S.3    Finn, J.P.4    Friedman, W.A.5
  • 167
    • 0022465686 scopus 로고
    • A proposed grading system for arteriovenous malformations
    • Spetzler RF, Martin NA. A proposed grading system for arteriovenous malformations. J Neurosurg. 1986;65(4):476–483.
    • (1986) J Neurosurg , vol.65 , Issue.4 , pp. 476-483
    • Spetzler, R.F.1    Martin, N.A.2
  • 168
    • 84864540634 scopus 로고    scopus 로고
    • Stereotactic radiosurgery for arteriovenous malformations after embolization: A case-control study
    • Kano H, Kondziolka D, Flickinger JC, et al. Stereotactic radiosurgery for arteriovenous malformations after embolization: a case-control study. J Neurosurg. 2012;117(2):265–275.
    • (2012) J Neurosurg , vol.117 , Issue.2 , pp. 265-275
    • Kano, H.1    Kondziolka, D.2    Flickinger, J.C.3
  • 170
    • 33749588150 scopus 로고    scopus 로고
    • Liver involvement in hereditary hemorrhagic telangiectasia: Consensus recommendations
    • Buscarini E, Plauchu H, Garcia Tsao G, et al. Liver involvement in hereditary hemorrhagic telangiectasia: consensus recommendations. Liver Int. 2006;26(9):1040–1046.
    • (2006) Liver Int , vol.26 , Issue.9 , pp. 1040-1046
    • Buscarini, E.1    Plauchu, H.2    Garcia Tsao, G.3
  • 171
    • 0038374779 scopus 로고    scopus 로고
    • Sonographic criteria for the diagnosis of hepatic involvement in hereditary hemorrhagic telangiectasia (HHT)
    • Caselitz M, Bahr MJ, Bleck JS, et al. Sonographic criteria for the diagnosis of hepatic involvement in hereditary hemorrhagic telangiectasia (HHT). Hepatology. 2003;37(5):1139–1146.
    • (2003) Hepatology , vol.37 , Issue.5 , pp. 1139-1146
    • Caselitz, M.1    Bahr, M.J.2    Bleck, J.S.3
  • 172
    • 33846564415 scopus 로고    scopus 로고
    • Liver involvement in hereditary hemorrhagic telangiectasia (HHT)
    • Garcia-Tsao G. Liver involvement in hereditary hemorrhagic telangiectasia (HHT). J Hepatol. 2007;46(3):499–507.
    • (2007) J Hepatol , vol.46 , Issue.3 , pp. 499-507
    • Garcia-Tsao, G.1
  • 173
    • 2942558591 scopus 로고    scopus 로고
    • Sonographic findings in hepatic involvement of hereditary haemorrhagic telangiectasia
    • Ocran K, Rickes S, Heukamp I, Wermke W. Sonographic findings in hepatic involvement of hereditary haemorrhagic telangiectasia. Ultraschall Med. 2004;25(3):191–194.
    • (2004) Ultraschall Med , vol.25 , Issue.3 , pp. 191-194
    • Ocran, K.1    Rickes, S.2    Heukamp, I.3    Wermke, W.4
  • 174
    • 3342988244 scopus 로고    scopus 로고
    • Hepatic involvement in hereditary hemorrhagic telangiectasia: Helical computed tomography features in 24 consecutive patients
    • Ravard G, Soyer P, Boudiaf M, et al. Hepatic involvement in hereditary hemorrhagic telangiectasia: helical computed tomography features in 24 consecutive patients. J Comput Assist Tomogr. 2004;28(4): 488–495.
    • (2004) J Comput Assist Tomogr , vol.28 , Issue.4 , pp. 488-495
    • Ravard, G.1    Soyer, P.2    Boudiaf, M.3
  • 175
    • 40949098995 scopus 로고    scopus 로고
    • Liver involvement in a large cohort of patients with hereditary hemorrhagic telangiectasia: Echo-color-Doppler vs multislice computed tomography study
    • Buonamico P, Suppressa P, Lenato GM, et al. Liver involvement in a large cohort of patients with hereditary hemorrhagic telangiectasia: echo-color-Doppler vs multislice computed tomography study. J Hepatol. 2008;48(5):811–820.
    • (2008) J Hepatol , vol.48 , Issue.5 , pp. 811-820
    • Buonamico, P.1    Suppressa, P.2    Lenato, G.M.3
  • 176
    • 77749324908 scopus 로고    scopus 로고
    • Long-term outcome of patients with hereditary hemorrhagic telangiectasia and severe hepatic involvement after orthotopic liver transplantation: A single-center study
    • Dupuis-Girod S, Chesnais AL, Ginon I, et al. Long-term outcome of patients with hereditary hemorrhagic telangiectasia and severe hepatic involvement after orthotopic liver transplantation: a single-center study. Liver Transpl. 2010;16(3):340–347.
    • (2010) Liver Transpl , vol.16 , Issue.3 , pp. 340-347
    • Dupuis-Girod, S.1    Chesnais, A.L.2    Ginon, I.3
  • 177
    • 80054987986 scopus 로고    scopus 로고
    • Successful liver transplantation for Rendu-Weber-Osler disease, a single centre experience
    • Cag M, Audet M, Saouli AC, et al. Successful liver transplantation for Rendu-Weber-Osler disease, a single centre experience. Hepatol Int. 2011;5(3):834–840.
    • (2011) Hepatol Int , vol.5 , Issue.3 , pp. 834-840
    • Cag, M.1    Audet, M.2    Saouli, A.C.3
  • 178
    • 33751346601 scopus 로고    scopus 로고
    • Liver transplantation for hereditary hemorrhagic telangiectasia: Report of the European liver transplant registry
    • discussion 862–854
    • Lerut J, Orlando G, Adam R, et al. Liver transplantation for hereditary hemorrhagic telangiectasia: report of the European liver transplant registry. Ann Surg. 2006;244(6):854–862; discussion 862–854.
    • (2006) Ann Surg , vol.244 , Issue.6 , pp. 854-862
    • Lerut, J.1    Orlando, G.2    Adam, R.3
  • 179
    • 8344222861 scopus 로고    scopus 로고
    • Hepatic artery embolization for treatment of patients with hereditary hemorrhagic telangiectasia and symptomatic hepatic vascular malformations
    • Chavan A, Caselitz M, Gratz KF, et al. Hepatic artery embolization for treatment of patients with hereditary hemorrhagic telangiectasia and symptomatic hepatic vascular malformations. Eur Radiol. 2004;14(11):2079–2085.
    • (2004) Eur Radiol , vol.14 , Issue.11 , pp. 2079-2085
    • Chavan, A.1    Caselitz, M.2    Gratz, K.F.3
  • 180
    • 0031648511 scopus 로고    scopus 로고
    • Hereditary hemorrhagic telangiectasia: Effective protocol for embolization of hepatic vascular malformations – experience in five patients
    • Chavan A, Galanski M, Wagner S, et al. Hereditary hemorrhagic telangiectasia: effective protocol for embolization of hepatic vascular malformations – experience in five patients. Radiology. 1998;209(3): 735–739.
    • (1998) Radiology , vol.209 , Issue.3 , pp. 735-739
    • Chavan, A.1    Galanski, M.2    Wagner, S.3
  • 181
    • 0032725267 scopus 로고    scopus 로고
    • Caution with use of hepatic embolization in the treatment of hereditary hemorrhagic telangiectasia
    • Miller FJ Jr, Whiting JH, Korzenik JR, White RI. Caution with use of hepatic embolization in the treatment of hereditary hemorrhagic telangiectasia. Radiology. 1999;213(3):928–930.
    • (1999) Radiology , vol.213 , Issue.3 , pp. 928-930
    • Miller, F.J.1    Whiting, J.H.2    Korzenik, J.R.3    White, R.I.4
  • 182
    • 84878538170 scopus 로고    scopus 로고
    • Complications and clinical outcome of hepatic artery embolisation in patients with hereditary haemorrhagic telangiectasia
    • Chavan A, Luthe L, Gebel M, et al. Complications and clinical outcome of hepatic artery embolisation in patients with hereditary haemorrhagic telangiectasia. Eur Radiol. 2013;23(4):951–957.
    • (2013) Eur Radiol , vol.23 , Issue.4 , pp. 951-957
    • Chavan, A.1    Luthe, L.2    Gebel, M.3
  • 183
    • 48449084739 scopus 로고    scopus 로고
    • Review article: The hepatic manifestations of hereditary haemorrhagic telangiectasia
    • Sabba C, Pompili M. Review article: the hepatic manifestations of hereditary haemorrhagic telangiectasia. Aliment Pharmacol Ther. 2008;28(5):523–533.
    • (2008) Aliment Pharmacol Ther , vol.28 , Issue.5 , pp. 523-533
    • Sabba, C.1    Pompili, M.2
  • 184
    • 40849130173 scopus 로고    scopus 로고
    • VEGF inhibition and renal thrombotic microangiopathy
    • Eremina V, Jefferson JA, Kowalewska J, et al. VEGF inhibition and renal thrombotic microangiopathy. N Engl J Med. 2008;358(11): 1129–1136.
    • (2008) N Engl J Med , vol.358 , Issue.11 , pp. 1129-1136
    • Eremina, V.1    Jefferson, J.A.2    Kowalewska, J.3
  • 185
    • 0035113551 scopus 로고    scopus 로고
    • Transcatheter embolotherapy of maternal pulmonary arteriovenous malformations during pregnancy
    • Gershon AS, Faughnan ME, Chon KS, et al. Transcatheter embolotherapy of maternal pulmonary arteriovenous malformations during pregnancy. Chest. 2001;119(2):470–477.
    • (2001) Chest , vol.119 , Issue.2 , pp. 470-477
    • Gershon, A.S.1    Faughnan, M.E.2    Chon, K.S.3
  • 186
    • 84902129279 scopus 로고    scopus 로고
    • Risk of cerebral arteriovenous malformation rupture during pregnancy and puerperium
    • Liu XJ, Wang S, Zhao YL, et al. Risk of cerebral arteriovenous malformation rupture during pregnancy and puerperium. Neurology. 2014;82(20):1798–1803.
    • (2014) Neurology , vol.82 , Issue.20 , pp. 1798-1803
    • Liu, X.J.1    Wang, S.2    Zhao, Y.L.3
  • 187
    • 84894450597 scopus 로고    scopus 로고
    • Outcomes of pregnancy in women with hereditary hemorrhagic telangiectasia
    • de Gussem EM, Lausman AY, Beder AJ, et al. Outcomes of pregnancy in women with hereditary hemorrhagic telangiectasia. Obstet Gynecol. 2014;123(3):514–520.
    • (2014) Obstet Gynecol , vol.123 , Issue.3 , pp. 514-520
    • De Gussem, E.M.1    Lausman, A.Y.2    Beder, A.J.3
  • 188
    • 84871008266 scopus 로고    scopus 로고
    • Hereditary hemorrhagic telangiectasia patients can tolerate anticoagulation
    • Edwards CP, Shehata N, Faughnan ME. Hereditary hemorrhagic telangiectasia patients can tolerate anticoagulation. Ann Hematol. 2012;91(12):1959–1968.
    • (2012) Ann Hematol , vol.91 , Issue.12 , pp. 1959-1968
    • Edwards, C.P.1    Shehata, N.2    Faughnan, M.E.3
  • 189
    • 0035139873 scopus 로고    scopus 로고
    • Estimated risks of radiation-induced fatal cancer from pediatric CT
    • Brenner D, Elliston C, Hall E, Berdon W. Estimated risks of radiation-induced fatal cancer from pediatric CT. AJR Am J Roentgenol. 2001;176(2):289–296.
    • (2001) AJR Am J Roentgenol , vol.176 , Issue.2 , pp. 289-296
    • Brenner, D.1    Elliston, C.2    Hall, E.3    Berdon, W.4
  • 190
    • 34548279773 scopus 로고    scopus 로고
    • Excess lifetime cancer mortality risk attributable to radiation exposure from computed tomography examinations in children
    • Chodick G, Ronckers CM, Shalev V, Ron E. Excess lifetime cancer mortality risk attributable to radiation exposure from computed tomography examinations in children. Isr Med Assoc J. 2007;9(8): 584–587.
    • (2007) Isr Med Assoc J , vol.9 , Issue.8 , pp. 584-587
    • Chodick, G.1    Ronckers, C.M.2    Shalev, V.3    Ron, E.4
  • 191
    • 55549115678 scopus 로고    scopus 로고
    • Radiation dose to the brain and subsequent risk of developing brain tumors in pediatric patients undergoing interventional neuroradiology procedures
    • Thierry-Chef I, Simon SL, Land CE, Miller DL. Radiation dose to the brain and subsequent risk of developing brain tumors in pediatric patients undergoing interventional neuroradiology procedures. Radiat Res. 2008;170(5):553–565.
    • (2008) Radiat Res , vol.170 , Issue.5 , pp. 553-565
    • Thierry-Chef, I.1    Simon, S.L.2    Land, C.E.3    Miller, D.L.4


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