-
1
-
-
0036164129
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
21
-
-
2142703735
-
Pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia
-
Cottin V, Plauchu H, Bayle JY, Barthelet M, Revel D, Cordier JF. Pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia. Am J Respir Crit Care Med. 2004;169(9):994–1000.
-
(2004)
Am J Respir Crit Care Med
, vol.169
, Issue.9
, pp. 994-1000
-
-
Cottin, V.1
Plauchu, H.2
Bayle, J.Y.3
Barthelet, M.4
Revel, D.5
Cordier, J.F.6
-
22
-
-
34250753845
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
‘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
-
58
-
-
84905567897
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
-
[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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
127
-
-
0023680793
-
Hereditary hemorrhagic telangiectasia and danazol
-
Haq AU, Glass J, Netchvolodoff CV, Bowen LM. Hereditary hemorrhagic telangiectasia and danazol. Ann Intern Med. 1988; 109(2):171.
-
(1988)
Ann Intern Med
, vol.109
, Issue.2
, pp. 171
-
-
Haq, A.U.1
Glass, J.2
Netchvolodoff, C.V.3
Bowen, L.M.4
-
128
-
-
84857645067
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
153
-
-
85011580459
-
Embolisation for pulmonary arteriovenous malformation
-
Hsu CC, Kwan GN, Thompson SA, Evans-Barns H, van Driel ML. Embolisation for pulmonary arteriovenous malformation. Cochrane Database Syst Rev. 2012;8:CD008017.
-
(2012)
Cochrane Database Syst Rev
, vol.8
-
-
Hsu, C.C.1
Kwan, G.N.2
Thompson, S.A.3
Evans-Barns, H.4
Van Driel, M.L.5
-
154
-
-
33646125437
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
161
-
-
0034016138
-
Bleeding risk of cerebrovascular malformations in hereditary hemorrhagic telangiectasia
-
Willemse RB, Mager JJ, Westermann CJ, Overtoom TT, Mauser H, Wolbers JG. Bleeding risk of cerebrovascular malformations in hereditary hemorrhagic telangiectasia. J Neurosurg. 2000;92(5):779–784.
-
(2000)
J Neurosurg
, vol.92
, Issue.5
, pp. 779-784
-
-
Willemse, R.B.1
Mager, J.J.2
Westermann, C.J.3
Overtoom, T.T.4
Mauser, H.5
Wolbers, J.G.6
-
162
-
-
0037407959
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
169
-
-
13244287695
-
Natural history, evaluation, and management of intracranial vascular malformations
-
Brown RD Jr, Flemming KD, Meyer FB, Cloft HJ, Pollock BE, Link ML. Natural history, evaluation, and management of intracranial vascular malformations. Mayo Clin Proc. 2005;80(2):269–281.
-
(2005)
Mayo Clin Proc
, vol.80
, Issue.2
, pp. 269-281
-
-
Brown, R.D.1
Flemming, K.D.2
Meyer, F.B.3
Cloft, H.J.4
Pollock, B.E.5
Link, M.L.6
-
170
-
-
33749588150
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
|