-
1
-
-
77955880114
-
Hereditary haemorrhagic telangiectasia: Pathophysiology, diagnosis and treatment
-
Shovlin CL,. Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment. Blood Rev 2010; 24: 203-219.
-
(2010)
Blood Rev
, vol.24
, pp. 203-219
-
-
Shovlin, C.L.1
-
2
-
-
0033007057
-
Hereditary haemorrhagic telangiectasia: A population-based study of prevalence and mortality in Danish patients
-
DOI 10.1046/j.1365-2796.1999.00398.x
-
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: 31-39. (Pubitemid 29049140)
-
(1999)
Journal of Internal Medicine
, vol.245
, Issue.1
, pp. 31-39
-
-
Kjeldsen, A.D.1
Vase, P.2
Green, A.3
-
3
-
-
0036164129
-
Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan
-
DOI 10.1002/humu.10026
-
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: 140-148. (Pubitemid 34121805)
-
(2002)
Human Mutation
, vol.19
, Issue.2
, pp. 140-148
-
-
Dakeishi, M.1
Shioya, T.2
Wada, Y.3
Shindo, T.4
Otaka, K.5
Manabe, M.6
Nozaki, J.-I.7
Inoue, S.8
Koizumi, A.9
-
4
-
-
33144462810
-
Hereditary haemorrhagic telangiectasia: Current views on genetics and mechanisms of disease
-
DOI 10.1136/jmg.2005.030833
-
Abdalla SA, Letarte M,. Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease. J Med Genet 2006; 43: 97-110. (Pubitemid 43262964)
-
(2006)
Journal of Medical Genetics
, vol.43
, Issue.2
, pp. 97-110
-
-
Abdalla, S.A.1
Letarte, M.2
-
5
-
-
70449392400
-
Real-time imaging of de novo arteriovenous malformation in a mouse model of hereditary hemorrhagic telangiectasia
-
Park S, Wankhede M, Lee Y, et al. Real-time imaging of de novo arteriovenous malformation in a mouse model of hereditary hemorrhagic telangiectasia. J Clin Invest 2009; 119: 3487-3496.
-
(2009)
J Clin Invest
, vol.119
, pp. 3487-3496
-
-
Park, S.1
Wankhede, M.2
Lee, Y.3
-
6
-
-
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: 420-428.
-
(2010)
Nat Med
, vol.16
, pp. 420-428
-
-
Lebrin, F.1
Srun, S.2
Raymond, K.3
-
7
-
-
79960845756
-
Hereditary hemorrhagic telangiectasia: An overview of diagnosis, management, and pathogenesis
-
McDonald J, Bayrak-Toydemir P, Pyeritz RE,. Hereditary hemorrhagic telangiectasia: an overview of diagnosis, management, and pathogenesis. Genet Med 2011; 13: 607-616.
-
(2011)
Genet Med
, vol.13
, pp. 607-616
-
-
McDonald, J.1
Bayrak-Toydemir, P.2
Pyeritz, R.E.3
-
8
-
-
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: 977-980.
-
(1991)
Laryngoscope
, vol.101
, pp. 977-980
-
-
Aassar, O.S.1
Friedman, C.M.2
White, Jr.R.I.3
-
9
-
-
17044405510
-
Natural history and control of epistaxis in a group of German patients with Rendu-Osler-Weber disease
-
Folz BJ, Tennie J, Lippert BM, Werner JA,. Natural history and control of epistaxis in a group of German patients with Rendu-Osler-Weber disease. Rhinology 2005; 43: 40-46.
-
(2005)
Rhinology
, vol.43
, pp. 40-46
-
-
Folz, B.J.1
Tennie, J.2
Lippert, B.M.3
Werner, J.A.4
-
10
-
-
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: 1092-1099.
-
(2013)
Laryngoscope
, vol.123
, pp. 1092-1099
-
-
Silva, B.M.1
Hosman, A.E.2
Devlin, H.L.3
Shovlin, C.L.4
-
11
-
-
0024394433
-
Age-related clinical profile of heredity hemorrhagic telangiectasia in an epidemiologically recruited population
-
DOI 10.1002/ajmg.1320320302
-
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: 291-297. (Pubitemid 19146524)
-
(1989)
American Journal of Medical Genetics
, vol.32
, Issue.3
, pp. 291-297
-
-
Plauchu, H.1
De Chadarevian, J.-P.2
Bideau, A.3
Robert, J.-M.4
-
12
-
-
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: 401-404.
-
(2012)
Am J Rhinol Allergy
, vol.26
, pp. 401-404
-
-
Richer, S.L.1
Geisthoff, U.W.2
Livada, N.3
-
13
-
-
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: 73-87.
-
(2011)
J Med Genet
, vol.48
, pp. 73-87
-
-
Faughnan, M.E.1
Palda, V.A.2
Garcia-Tsao, G.3
-
14
-
-
84885738700
-
Hemorrhage-adjusted iron requirements, hematinics and hepcidin define hereditary haemorrhagic 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 haemorrhagic telangiectasia as a model of hemorrhagic iron deficiency. PLoS One 2013; 8: e76516.
-
(2013)
PLoS One
, vol.8
-
-
Finnamore, H.1
Le Couteur, J.2
Hickson, M.3
Busbridge, M.4
Whelan, K.5
Shovlin, C.L.6
-
15
-
-
80051554515
-
Altered quality of life in Rendu-Osler-Weber disease related to recurrent epistaxis
-
Ingrand I, Ingrand P, Gilbert-Dussardier B, et al. Altered quality of life in Rendu-Osler-Weber disease related to recurrent epistaxis. Rhinology 2011; 49: 155-162.
-
(2011)
Rhinology
, vol.49
, pp. 155-162
-
-
Ingrand, I.1
Ingrand, P.2
Gilbert-Dussardier, B.3
-
16
-
-
80051568383
-
Psychosocial quality of life in hereditary haemorrhagic telangiectasia patients
-
Loaec M, Moriniere S, Hitier M, Ferrant O, Plauchu H, Babin E,. Psychosocial quality of life in hereditary haemorrhagic telangiectasia patients. Rhinology 2011; 49: 164-167.
-
(2011)
Rhinology
, vol.49
, pp. 164-167
-
-
Loaec, M.1
Moriniere, S.2
Hitier, M.3
Ferrant, O.4
Plauchu, H.5
Babin, E.6
-
17
-
-
13444258107
-
Nd-YAG laser photocoagulation for epistaxis associated with hereditary hemorrhagic telangiectasia
-
DOI 10.1097/01.mlg.0000154749.09303.e0
-
Mahoney EJ, Shapshay SM,. Nd-YAG laser photocoagulation for epistaxis associated with hereditary hemorrhagic telangiectasia. Laryngoscope 2005; 115: 373-375. (Pubitemid 40216723)
-
(2005)
Laryngoscope
, vol.115
, Issue.2
, pp. 373-375
-
-
Mahoney, E.J.1
Shapshay, S.M.2
-
18
-
-
42449163015
-
The impact of septodermoplasty and potassium-titanyl-phosphate (KTP) laser therapy in the treatment of hereditary hemorrhagic telangiectasia-related epistaxis
-
DOI 10.2500/ajr.2008.22.3145
-
Harvey RJ, Kanagalingam J, Lund VJ,. The impact of septodermoplasty and potassium-titanyl-phosphate (KTP) laser therapy in the treatment of hereditary hemorrhagic telangiectasia-related epistaxis. Am J Rhinol 2008; 22: 182-187. (Pubitemid 351570562)
-
(2008)
American Journal of Rhinology
, vol.22
, Issue.2
, pp. 182-187
-
-
Harvey, R.J.1
Kanagalingam, J.2
Lund, V.J.3
-
19
-
-
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: 284-288.
-
(2009)
Laryngoscope
, vol.119
, pp. 284-288
-
-
Yaniv, E.1
Preis, M.2
Hadar, T.3
Shvero, J.4
Haddad, M.5
-
20
-
-
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: 636-638.
-
(2011)
Laryngoscope
, vol.121
, pp. 636-638
-
-
Karnezis, T.T.1
Davidson, T.M.2
-
21
-
-
84860378849
-
Intravenous and topical intranasal bevacizumab (Avastin) in hereditary hemorrhagic telangiectasia
-
Brinkerhoff BT, Choong NW, Treisman JS, Poetker DM,. Intravenous and topical intranasal bevacizumab (Avastin) in hereditary hemorrhagic telangiectasia. Am J Otolaryngol 2012; 33: 349-351.
-
(2012)
Am J Otolaryngol
, vol.33
, pp. 349-351
-
-
Brinkerhoff, B.T.1
Choong, N.W.2
Treisman, J.S.3
Poetker, D.M.4
-
22
-
-
62649172211
-
The effect of N-acetylcysteine on epistaxis and quality of life in patients with HHT: A pilot study
-
de Gussem E, Snijder R, Disch F, Zanen P, Westermann C, Mager J,. The effect of N-acetylcysteine on epistaxis and quality of life in patients with HHT: a pilot study. Rhinology 2009; 47: 85-88.
-
(2009)
Rhinology
, vol.47
, pp. 85-88
-
-
De Gussem, E.1
Snijder, R.2
Disch, F.3
Zanen, P.4
Westermann, C.5
Mager, J.6
-
23
-
-
0033159168
-
A treatment algorithm for the management of epistaxis in hereditary haemorrhagic telangiectasia
-
Lund V, Howard D,. A treatment algorithm for the management of epistaxis in hereditary haemorrhagic telangiectasia. Am J Rhinol 1999; 13: 319-322.
-
(1999)
Am J Rhinol
, vol.13
, pp. 319-322
-
-
Lund, V.1
Howard, D.2
-
24
-
-
0028453699
-
Migraine prevalence. A review of population-based studies
-
Stewart WF, Shechter A, Rasmussen BK,. Migraine prevalence. A review of population-based studies. Neurology 1994; 44: S17-S23.
-
(1994)
Neurology
, vol.44
-
-
Stewart, W.F.1
Shechter, A.2
Rasmussen, B.K.3
-
25
-
-
70449328805
-
Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous fistula. Study of a large family
-
Hodgson CH, Burchell HB, Good CA, Clagett OT,. Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous fistula. Study of a large family. New Engl J Med 1959; 261: 625-636.
-
(1959)
New Engl J Med
, vol.261
, pp. 625-636
-
-
Hodgson, C.H.1
Burchell, H.B.2
Good, C.A.3
Clagett, O.T.4
-
26
-
-
0027460541
-
An association between migrainous aura and hereditary haemorrhagic telangiectasia
-
Steele JG, Nath PU, Burn J, Porteous ME,. An association between migrainous aura and hereditary haemorrhagic telangiectasia. Headache 1993; 33: 145-148. (Pubitemid 23110624)
-
(1993)
Headache
, vol.33
, Issue.3
, pp. 145-148
-
-
Steele, J.G.1
Nath, P.U.2
Burn, J.3
Porteous, M.E.M.4
-
27
-
-
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: 76-81.
-
(2009)
Cephalalgia
, vol.29
, pp. 76-81
-
-
Marziniak, M.1
Jung, A.2
Guralnik, V.3
Evers, S.4
Prudlo, J.5
Geisthoff, U.W.6
-
28
-
-
77957880743
-
Pulmonary arteriovenous malformations and other vascular abnormalities
-
Mason R.J. Broaddus V.C. Martin T. et al., eds. 5th ed. Philadelphia, PA: Elsevier-Saunders.
-
Shovlin CL, Jackson JE,. Pulmonary arteriovenous malformations and other vascular abnormalities. In:, Mason RJ, Broaddus VC, Martin T, et al., eds. Murray and Nadel's Textbook of Respiratory Medicine. 5th ed. Philadelphia, PA: Elsevier-Saunders; 2010: 1261-1282.
-
(2010)
Murray and Nadel's Textbook of Respiratory Medicine
, pp. 1261-1282
-
-
Shovlin, C.L.1
Jackson, J.E.2
-
29
-
-
33846195431
-
Pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia: A series of 126 patients
-
DOI 10.1097/MD.0b013e31802f8da1, PII 0000579220070100000001
-
Cottin V, Chinet T, Lavole A, et al. Pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia: a series of 126 patients. Medicine (Baltimore) 2007; 86: 1-17. (Pubitemid 46104915)
-
(2007)
Medicine
, vol.86
, Issue.1
, pp. 1-17
-
-
Cottin, V.1
Chinet, T.2
Lavole, A.3
Corre, R.4
Marchand, E.5
Reynaud-Gaubert, M.6
Plauchu, H.7
Cordier, J.-F.8
-
30
-
-
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: 833-839.
-
(2010)
Chest
, vol.138
, 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
-
31
-
-
27144454299
-
A pulmonary right-to-left shunt in patients with hereditary hemorrhagic telangiectasia is associated with an increased prevalence of migraine
-
DOI 10.1378/chest.128.4.2485
-
Post MC, Letteboer TG, Mager JJ, Plokker TH, Kelder JC, Westermann CJ,. A pulmonary right-to-left shunt in patients with hereditary haemorrhagic telangiectasia is associated with an increased prevalence of migraine. Chest 2005; 128: 2485-2489. (Pubitemid 41507598)
-
(2005)
Chest
, vol.128
, Issue.4
, pp. 2485-2489
-
-
Post, M.C.1
Letteboer, T.G.W.2
Mager, J.J.3
Plokker, T.H.4
Kelder, J.C.5
Westermann, C.J.J.6
-
32
-
-
33645063429
-
Migraines linked to intrapulmonary right-to-left shunt
-
Thenganatt J, Schneiderman J, Hyland RH, Edmeads J, Mandzia JL, Faughnan ME,. Migraines linked to intrapulmonary right-to-left shunt. Headache 2006; 46: 439-443.
-
(2006)
Headache
, vol.46
, pp. 439-443
-
-
Thenganatt, J.1
Schneiderman, J.2
Hyland, R.H.3
Edmeads, J.4
Mandzia, J.L.5
Faughnan, M.E.6
-
33
-
-
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: 882-887.
-
(2009)
Eur Respir J
, vol.34
, pp. 882-887
-
-
Post, M.C.1
Van Gent, M.W.2
Plokker, H.W.3
-
34
-
-
33644923255
-
Embolization of pulmonary arteriovenous malformations and decrease in prevalence of migraine
-
DOI 10.1212/01.wnl.0000194257.75559.b0, PII 0000611420060124000013
-
Post MC, Thijs V, Schonewille WJ, et al. Embolization of pulmonary arteriovenous malformations and decrease in prevalence of migraine. Neurology 2006; 66: 202-205. (Pubitemid 43970154)
-
(2006)
Neurology
, vol.66
, Issue.2
, pp. 202-205
-
-
Post, M.C.1
Thijs, V.2
Schonewille, W.J.3
Budts, W.4
Snijder, R.J.5
Plokker, H.W.M.6
Westermann, C.J.J.7
-
35
-
-
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: 876-878.
-
(2013)
N Engl J Med
, vol.368
, pp. 876-878
-
-
Devlin, H.L.1
Hosman, A.E.2
Shovlin, C.L.3
-
36
-
-
84890491238
-
Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls
-
2013, 8:195. DOI: 10.1186/1750-1172-8-195
-
Hosman AE, Devlin HL, Silva BM, Elphick AH, Shovlin CL,. Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls. Orphanet Journal of Rare Diseases. 2013, 8:195. DOI: 10.1186/1750-1172-8-195
-
Orphanet Journal of Rare Diseases
-
-
Hosman, A.E.1
Devlin, H.L.2
Silva, B.M.3
Elphick, A.H.4
Shovlin, C.L.5
-
37
-
-
84903200880
-
-
HHT Foundation International, Inc. Accessed September 30
-
HHT Foundation International, Inc. Available at: www.hht.org Accessed September 30, 2013.
-
(2013)
-
-
-
38
-
-
0034007163
-
Diagnostic criteria for Hereditary Hemorrhagic Telangiectasia (Rendu- Osler-Weber Syndrome)
-
DOI 10.1002/(SICI)1096-8628(20000306) 91:1<66::AID-AJMG12>3.0.CO;2- P
-
Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 2000; 91: 66-67. (Pubitemid 30127562)
-
(2000)
American Journal of Medical Genetics
, vol.91
, Issue.1
, pp. 66-67
-
-
Shovlin, C.L.1
Guttmacher, A.E.2
Buscarini, E.3
Faughnan, M.E.4
Hyland, R.H.5
Westermann, C.J.J.6
Kjeldsen, A.D.7
Plauchu, H.8
-
39
-
-
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; 161: 461-466.
-
(2013)
Am J Med Genet A
, vol.161
, pp. 461-466
-
-
Van Gent, M.W.1
Velthuis, S.2
Post, M.C.3
-
40
-
-
84903180104
-
-
International Headache Society. IHS classification ICHD-2. first accessed for this study 25 March 2013. Reaccessed 20 December 2013
-
International Headache Society. IHS classification ICHD-2. Available at: http://ihs-classification.org/en/, first accessed for this study 25 March 2013. Reaccessed 20 December 2013.
-
-
-
-
41
-
-
84903142735
-
-
Migraine Trust first accessed for this study 25 March 2013. Reaccessed 20 December 2013
-
Migraine Trust. Diagnosing migraine. Available at: http://www. migrainetrust.org/health-professionals/diagnosing-migraine, first accessed for this study 25 March 2013. Reaccessed 20 December 2013.
-
Diagnosing Migraine
-
-
-
42
-
-
1442265540
-
The International Classification of Headache Disorders
-
Headache Classification Subcommittee of the International Headache Society. 2nd ed.
-
Headache Classification Subcommittee of the International Headache Society. The International Classification of Headache Disorders. 2nd ed. Cephalalgia 2004; 24 (suppl 1): 9-160.
-
(2004)
Cephalalgia
, vol.24
, Issue.SUPPL. 1
, pp. 9-160
-
-
-
43
-
-
84860767840
-
Evidence-based guideline update: Pharmacologic treatment for episodic migraine prevention in adults: Report of the Quality Standards Subcommittee of the American Academy of Neurology and the American Headache Society
-
Silberstein SD, Holland S, Freitag F, Dodick DW, Argoff C, Ashman E,. Evidence-based guideline update: pharmacologic treatment for episodic migraine prevention in adults: report of the Quality Standards Subcommittee of the American Academy of Neurology and the American Headache Society. Neurology 2012; 78: 1337-1345.
-
(2012)
Neurology
, vol.78
, pp. 1337-1345
-
-
Silberstein, S.D.1
Holland, S.2
Freitag, F.3
Dodick, D.W.4
Argoff, C.5
Ashman, E.6
-
44
-
-
0000358926
-
Hormonal management of hereditary hemorrhagic telangiectasia
-
Koch HJ, Escher GC, Lewis JS,. Hormonal management of hereditary hemorrhagic telangiectasia. J Am Med Soc 1952; 149: 1376-1380.
-
(1952)
J Am Med Soc
, vol.149
, pp. 1376-1380
-
-
Koch, H.J.1
Escher, G.C.2
Lewis, J.S.3
-
45
-
-
0002179373
-
Familial haemorrhagic telangiectasia
-
Harrison DFN,. Familial haemorrhagic telangiectasia. Q J Med 1964; 129: 25-38.
-
(1964)
Q J Med
, vol.129
, pp. 25-38
-
-
Harrison, D.F.N.1
-
46
-
-
0014957324
-
Hereditary haemorrhagic telangiectasia and oral contraceptives
-
Harris PWR,. Hereditary haemorrhagic telangiectasia and oral contraceptives. Lancet 1970; 1: 615-616.
-
(1970)
Lancet
, vol.1
, pp. 615-616
-
-
Harris, P.W.R.1
-
47
-
-
0017593285
-
Hereditary hemorrhagic telangiectasia (Osler Weber Rendu disease). Management of epistaxis in nine patients using systemic hormone therapy
-
Flessa HC, Glueck HI,. Hereditary hemorrhagic telangiecatsia (Osler-Weber-Rendu disease). Management of epistaxis in nine patients using systemic hormone therapy. Arch Otolaryngol 1977; 103: 148-151. (Pubitemid 8057682)
-
(1977)
Archives of Otolaryngology
, vol.103
, Issue.3
, pp. 148-151
-
-
Flessa, H.C.1
Glueck, H.I.2
-
48
-
-
0025230351
-
Treatment of bleeding gastrointestinal vascular malformations with oestrogen-progesterone
-
DOI 10.1016/0140-6736(90)91010-8
-
van Cutsem E, Rutgeerts P, Vantrappen G,. Treatment of bleeding gastrointestinal vascular malformations with oestrogen-progesterone. Lancet 1990; 335: 953-955. (Pubitemid 20134976)
-
(1990)
Lancet
, vol.335
, Issue.8695
, pp. 953-955
-
-
Van Cutsem, E.1
Rutgeerts, P.2
Vantrappen, G.3
-
49
-
-
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: 284-288.
-
(2009)
Laryngoscope
, vol.119
, pp. 284-288
-
-
Yaniv, E.1
Preis, M.2
Hadar, T.3
Shvero, J.4
Haddad, M.5
-
50
-
-
77749246401
-
Estrogen therapy for hereditary haemorrhagic telangiectasia (HHT): Effects of raloxifene on endoglin and ALK1 expression in endothelial cells
-
Albinana V, Bernabeu-Herrero ME, Zarrabeitia R, Bernabeu 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: 525-534.
-
(2010)
Thromb Haemost
, vol.103
, pp. 525-534
-
-
Albinana, V.1
Bernabeu-Herrero, M.E.2
Zarrabeitia, R.3
Bernabeu, C.4
Botella, L.M.5
-
51
-
-
84864055317
-
Migraine: A disorder of brain excitatory-inhibitory balance?
-
Vecchia D, Pietrobon D,. Migraine: a disorder of brain excitatory-inhibitory balance? Trends Neurosci 2012; 35: 507-520.
-
(2012)
Trends Neurosci
, vol.35
, pp. 507-520
-
-
Vecchia, D.1
Pietrobon, D.2
-
52
-
-
12144286750
-
A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression
-
DOI 10.1016/S0896-6273(04)00085-6, PII S0896627304000856
-
van den Maagdenberg AM, Pietrobon D, Pizzorusso T, et al. A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression. Neuron 2004; 41: 701-710. (Pubitemid 38326833)
-
(2004)
Neuron
, vol.41
, Issue.5
, pp. 701-710
-
-
Van Den Maagdenberg, A.M.J.M.1
Pietrobon, D.2
Pizzorusso, T.3
Kaja, S.4
Broos, L.A.M.5
Cesetti, T.6
Van De Ven, R.C.G.7
Tottene, A.8
Van Der Kaa, J.9
Plomp, J.J.10
Frants, R.R.11
Ferrari, M.D.12
-
53
-
-
43249104681
-
Animal models of migraine headache and aura
-
DOI 10.1097/WCO.0b013e3282fc25de, PII 0001905220080600000013
-
Eikermann-Haerter K, Moskowitz MA,. Animal models of migraine headache and aura. Curr Opin Neurol 2008; 21: 294-300. (Pubitemid 351653979)
-
(2008)
Current Opinion in Neurology
, vol.21
, Issue.3
, pp. 294-300
-
-
Eikermann-Haerter, K.1
Moskowitz, M.A.2
-
54
-
-
33748641238
-
Animal models of migraine: Looking at the component parts of a complex disorder
-
DOI 10.1111/j.1460-9568.2006.05036.x
-
Bergerot A, Holland PR, Akerman S, et al. Animal models of migraine: looking at the component parts of a complex disorder. Eur J Neurosci 2006; 24: 1517-1534. (Pubitemid 44429881)
-
(2006)
European Journal of Neuroscience
, vol.24
, Issue.6
, pp. 1517-1534
-
-
Bergerot, A.1
Holland, P.R.2
Akerman, S.3
Bartsch, T.4
Ahn, A.H.5
MaassenVanDenBrink, A.6
Reuter, U.7
Tassorelli, C.8
Schoenen, J.9
Mitsikostas, D.D.10
Van Den Maagdenberg, A.M.J.M.11
Goadsby, P.J.12
-
55
-
-
84872303333
-
TNFα levels and macrophages expression reflect an inflammatory potential of trigeminal ganglia in a mouse model of familial hemiplegic migraine
-
Franceschini A, Vilotti S, Ferrari MD, van den Maagdenberg AM, Nistri A, Fabbretti E,. TNFα levels and macrophages expression reflect an inflammatory potential of trigeminal ganglia in a mouse model of familial hemiplegic migraine. PLoS One 2013; 8: e52394.
-
(2013)
PLoS One
, vol.8
-
-
Franceschini, A.1
Vilotti, S.2
Ferrari, M.D.3
Van Den Maagdenberg, A.M.4
Nistri, A.5
Fabbretti, E.6
-
56
-
-
2942525883
-
No mutations in CACNA1A and ATP1A2 in probands with common types of migraine
-
DOI 10.1001/archneur.61.6.926
-
Jen JC, Kim GW, Dudding KA, Baloh RW,. No mutations in CACNA1A and ATP1A2 in probands with common types of migraine. Arch Neurol 2004; 61: 926-928. (Pubitemid 38747334)
-
(2004)
Archives of Neurology
, vol.61
, Issue.6
, pp. 926-928
-
-
Jen, J.C.1
Kim, G.W.2
Dudding, K.A.3
Baloh, R.W.4
-
57
-
-
84887239328
-
Cortical spreading depression and migraine
-
Charles AC, Baca SM,. Cortical spreading depression and migraine. Nat Rev Neurol 2013; 9: 637-644.
-
(2013)
Nat Rev Neurol
, vol.9
, pp. 637-644
-
-
Charles, A.C.1
Baca, S.M.2
-
58
-
-
79959721099
-
Genome-wide association study reveals three susceptibility loci for common migraine in the general population
-
Chasman DI, Schurks M, Anttila V, et al. Genome-wide association study reveals three susceptibility loci for common migraine in the general population. Nat Genet 2011; 43: 695-698.
-
(2011)
Nat Genet
, vol.43
, pp. 695-698
-
-
Chasman, D.I.1
Schurks, M.2
Anttila, V.3
-
59
-
-
84862976129
-
Genome-wide association analysis identifies susceptibility loci for migraine without aura
-
Freilinger T, Anttila V, de Vries B, et al. Genome-wide association analysis identifies susceptibility loci for migraine without aura. Nat Genet 2012; 44: 777-782.
-
(2012)
Nat Genet
, vol.44
, pp. 777-782
-
-
Freilinger, T.1
Anttila, V.2
De Vries, B.3
-
60
-
-
33846163129
-
Clinical features in a family with an R460H mutation in transforming growth factor β receptor 2 gene
-
DOI 10.1136/jmg.2006.042176
-
Law C, Bunyan D, Castle B, et al. Clinical features in a family with an R460H mutation in transforming growth factor beta receptor 2 gene. J Med Genet 2006; 43: 908-916. (Pubitemid 46080187)
-
(2006)
Journal of Medical Genetics
, vol.43
, Issue.12
, pp. 908-916
-
-
Law, C.1
Bunyan, D.2
Castle, B.3
Day, L.4
Simpson, I.5
Westwood, G.6
Keeton, B.7
-
61
-
-
33644878471
-
Increased plasma transforming growth factor-β1 in migraine
-
DOI 10.1111/j.1526-4610.2005.00246.x
-
Ishizaki K, Takeshima T, Fukuhara Y, et al. Increased plasma transforming growth factor-beta1 in migraine. Headache 2005; 45: 1224-1228. (Pubitemid 350004912)
-
(2005)
Headache
, vol.45
, Issue.9
, pp. 1224-1228
-
-
Ishizaki, K.1
Takeshima, T.2
Fukuhara, Y.3
Araki, H.4
Nakaso, K.5
Kusumi, M.6
Nakashima, K.7
-
62
-
-
84881503618
-
Evaluation of serum transforming growth factor β1 and C-reactive protein levels in migraine patients
-
Guzel I, Tasdemir N, Celik Y,. Evaluation of serum transforming growth factor β1 and C-reactive protein levels in migraine patients. Neurol Neurochir Pol 2013; 47: 357-362.
-
(2013)
Neurol Neurochir Pol
, vol.47
, pp. 357-362
-
-
Guzel, I.1
Tasdemir, N.2
Celik, Y.3
-
63
-
-
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: 818-828.
-
(2005)
Haematologica
, vol.90
, pp. 818-828
-
-
Sadick, H.1
Riedel, F.2
Naim, R.3
-
64
-
-
24344461857
-
Reduced endothelial secretion and plasma levels of transforming growth factor-β1 in patients with hereditary hemorrhagic telangiectasia type 1
-
DOI 10.1016/j.cardiores.2005.04.028, PII S0008636305002129
-
Letarte M, McDonald ML, Li C, et al. Reduced endothelial secretion and plasma levels of transforming growth factor-beta1 in patients with hereditary hemorrhagic telangiectasia type 1. Cardiovasc Res 2005; 68: 155-164. (Pubitemid 41253566)
-
(2005)
Cardiovascular Research
, vol.68
, Issue.1
, pp. 155-164
-
-
Letarte, M.1
McDonald, M.-L.2
Li, C.3
Kathirkamathamby, K.4
Vera, S.5
Pece-Barbara, N.6
Kumar, S.7
-
65
-
-
77949480911
-
Patients with migraine with aura have increased flow mediated dilation
-
Vernieri F, Moro L, Altamura C, et al. Patients with migraine with aura have increased flow mediated dilation. BMC Neurol 2010; 10: 18.
-
(2010)
BMC Neurol
, vol.10
, pp. 18
-
-
Vernieri, F.1
Moro, L.2
Altamura, C.3
-
66
-
-
78149256335
-
Hypertension and cerebral vasoreactivity: A continuous arterial spin labeling magnetic resonance imaging study
-
Hajjar I, Zhao P, Alsop D, Novak V,. Hypertension and cerebral vasoreactivity: a continuous arterial spin labeling magnetic resonance imaging study. Hypertension 2010; 56: 859-864.
-
(2010)
Hypertension
, vol.56
, pp. 859-864
-
-
Hajjar, I.1
Zhao, P.2
Alsop, D.3
Novak, V.4
-
67
-
-
84884684517
-
Heterogeneous cerebral vasoreactivity dynamics in patients with carotid stenosis
-
Chang TY, Kuan WC, Huang KL, et al. Heterogeneous cerebral vasoreactivity dynamics in patients with carotid stenosis. PLoS One 2013; 8: e76072.
-
(2013)
PLoS One
, vol.8
-
-
Chang, T.Y.1
Kuan, W.C.2
Huang, K.L.3
-
68
-
-
84881534634
-
Cerebral and extracerebral vasoreactivity in symptomatic lacunar stroke patients: A case-control study
-
Deplanque D, Lavallee PC, Labreuche J, et al. Cerebral and extracerebral vasoreactivity in symptomatic lacunar stroke patients: a case-control study. Int J Stroke 2013; 8: 413-421.
-
(2013)
Int J Stroke
, vol.8
, pp. 413-421
-
-
Deplanque, D.1
Lavallee, P.C.2
Labreuche, J.3
-
69
-
-
83455230861
-
Simultaneous impairment of intracranial and peripheral artery vasoreactivity in CADASIL patients
-
Fujiwara Y, Mizuno T, Okuyama C, et al. Simultaneous impairment of intracranial and peripheral artery vasoreactivity in CADASIL patients. Cerebrovasc Dis 2012; 33: 128-134.
-
(2012)
Cerebrovasc Dis
, vol.33
, pp. 128-134
-
-
Fujiwara, Y.1
Mizuno, T.2
Okuyama, C.3
-
70
-
-
84884720532
-
Cerebrovascular reactivity across the menstrual cycle in young healthy women
-
Krejza J, Rudzinski W, Arkuszewski M, Onuoha O, Melhem ER,. Cerebrovascular reactivity across the menstrual cycle in young healthy women. Neuroradiol J 2013; 26: 413-419.
-
(2013)
Neuroradiol J
, vol.26
, pp. 413-419
-
-
Krejza, J.1
Rudzinski, W.2
Arkuszewski, M.3
Onuoha, O.4
Melhem, E.R.5
-
71
-
-
84872115536
-
Nasal arterial vasculature: Medical and surgical applications
-
Saban Y, Amodeo CA, Bouaziz D, Polselli R,. Nasal arterial vasculature: medical and surgical applications. Arch Facial Plast Surg 2012; 14: 429-436.
-
(2012)
Arch Facial Plast Surg
, vol.14
, pp. 429-436
-
-
Saban, Y.1
Amodeo, C.A.2
Bouaziz, D.3
Polselli, R.4
|