-
1
-
-
0023634584
-
Clinical spectrum of hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease)
-
Peery WH. Clinical spectrum of hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease). Am J Med 1987; 82: 989-97.
-
(1987)
Am J Med
, vol.82
, pp. 989-997
-
-
Peery, W.H.1
-
3
-
-
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: 66-7.
-
(2000)
Am J Med Genet
, vol.91
, pp. 66-67
-
-
Shovlin, C.L.1
Guttmacher, A.E.2
Buscarini, E.3
-
4
-
-
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: 31-9.
-
(1999)
J Intern Med
, vol.245
, pp. 31-39
-
-
Kjeldsen, A.D.1
Vase, P.2
Green, A.3
-
5
-
-
0001506230
-
Epistaxis as an indication of impaired nutrition, and of degeneration of the vascular system
-
Sutton H. Epistaxis as an indication of impaired nutrition, and of degeneration of the vascular system. Med Mirror 1864; 1: 769-81.
-
(1864)
Med Mirror
, vol.1
, pp. 769-781
-
-
Sutton, H.1
-
6
-
-
0000990603
-
Épistaxis répétées chez un sujet porteur de petits angiomes cutanés et muqueux
-
Rendu H. Épistaxis répétées chez un sujet porteur de petits angiomes cutanés et muqueux. Gaz Soc Hosp (Paris) 1896; 68: 1322-3.
-
(1896)
Gaz Soc Hosp (Paris)
, vol.68
, pp. 1322-1323
-
-
Rendu, H.1
-
7
-
-
0001210867
-
On a family form of recurring epistaxis, associated with multiple telangiectases of the skin and mucous membranes
-
Osler W. On a family form of recurring epistaxis, associated with multiple telangiectases of the skin and mucous membranes. Bull Johns Hopkins Hosp 1901; 12: 333-7.
-
(1901)
Bull Johns Hopkins Hosp
, vol.12
, pp. 333-337
-
-
Osler, W.1
-
8
-
-
50249209093
-
Multiple hereditary developmental angiomata (telangiectases) of the skin and mucous membranes associated with recurring haemorrhages
-
Weber F. Multiple hereditary developmental angiomata (telangiectases) of the skin and mucous membranes associated with recurring haemorrhages. Lancet 1907; 2: 160-2.
-
(1907)
Lancet
, vol.2
, pp. 160-162
-
-
Weber, F.1
-
9
-
-
0002538614
-
Multiple hereditary telangiectases causing hemorrhage (hereditary hemorrhagic telangiectasia)
-
Hanes F. Multiple hereditary telangiectases causing hemorrhage (hereditary hemorrhagic telangiectasia). Bull Johns Hopkins Hosp 1909; 20: 63-73.
-
(1909)
Bull Johns Hopkins Hosp
, vol.20
, pp. 63-73
-
-
Hanes, F.1
-
10
-
-
0025129826
-
Ultrastructure and three-dimensional organization of the telangiectases of hereditary hemorrhagic telangiectasia
-
Braverman IM, Keh A, Jacobson BS. Ultrastructure and three-dimensional organization of the telangiectases of hereditary hemorrhagic telangiectasia. J Invest Dermatol 1990; 95: 422-7.
-
(1990)
J Invest Dermatol
, vol.95
, pp. 422-427
-
-
Braverman, I.M.1
Keh, A.2
Jacobson, B.S.3
-
11
-
-
2342488852
-
New insights into TGF-beta-Smad signalling
-
Ten Dijke P, Hill CS. New insights into TGF-beta-Smad signalling. Trends Biochem Sci 2004; 29: 265-73.
-
(2004)
Trends Biochem Sci
, vol.29
, pp. 265-273
-
-
Ten Dijke, P.1
Hill, C.S.2
-
12
-
-
0028170226
-
Mechanism of activation of the TGF-beta receptor
-
Wrana JL, Attisano L, Wieser R, Ventura F, Massague J. Mechanism of activation of the TGF-beta receptor. Nature 1994; 370: 341-7.
-
(1994)
Nature
, vol.370
, pp. 341-347
-
-
Wrana, J.L.1
Attisano, L.2
Wieser, R.3
Ventura, F.4
Massague, J.5
-
13
-
-
36448936383
-
TGFbeta-SMAD signal transduction: Molecular specificity and functional flexibility
-
Schmierer B, Hill CS, Schmierer B, Hill CS. TGFbeta-SMAD signal transduction: Molecular specificity and functional flexibility. Nat Rev Mol Cell Biol 2007; 8: 970-82.
-
(2007)
Nat Rev Mol Cell Biol
, vol.8
, pp. 970-982
-
-
Schmierer, B.1
Hill, C.S.2
Schmierer, B.3
Hill, C.S.4
-
14
-
-
0026496172
-
TGF beta signals through a heteromeric protein kinase receptor complex
-
Wrana JL, Attisano L, Carcamo J et al. TGF beta signals through a heteromeric protein kinase receptor complex. Cell 1992; 71: 1003-14.
-
(1992)
Cell
, vol.71
, pp. 1003-1014
-
-
Wrana, J.L.1
Attisano, L.2
Carcamo, J.3
-
15
-
-
0028585971
-
Genetic heterogeneity in hereditary haemorrhagic telangiectasia: Possible correlation with clinical phenotype
-
McAllister KA, Lennon F, Bowles-Biesecker B et al. Genetic heterogeneity in hereditary haemorrhagic telangiectasia: Possible correlation with clinical phenotype. J Med Genet 1994; 31: 927-32.
-
(1994)
J Med Genet
, vol.31
, pp. 927-932
-
-
McAllister, K.A.1
Lennon, F.2
Bowles-Biesecker, B.3
-
16
-
-
0028283454
-
A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33-34
-
McDonald MT, Papenberg KA, Ghosh S et al. A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33-34. Nat Genet 1994; 6: 197-204.
-
(1994)
Nat Genet
, vol.6
, pp. 197-204
-
-
McDonald, M.T.1
Papenberg, K.A.2
Ghosh, S.3
-
17
-
-
0028239861
-
A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3
-
Shovlin CL, Hughes JM, Tuddenham EG et al. A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3. Nat Genet 1994; 6: 205-9.
-
(1994)
Nat Genet
, vol.6
, pp. 205-209
-
-
Shovlin, C.L.1
Hughes, J.M.2
Tuddenham, E.G.3
-
18
-
-
0029125615
-
A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12
-
Johnson DW, Berg JN, Gallione CJ et al. A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12. Genome Res 1995; 5: 21-8.
-
(1995)
Genome Res
, vol.5
, pp. 21-28
-
-
Johnson, D.W.1
Berg, J.N.2
Gallione, C.J.3
-
19
-
-
9144219585
-
Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia
-
Harrison RE, Flanagan JA, Sankelo M et al. Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia. J Med Genet 2003; 40: 865-71.
-
(2003)
J Med Genet
, vol.40
, pp. 865-871
-
-
Harrison, R.E.1
Flanagan, J.A.2
Sankelo, M.3
-
20
-
-
0035797556
-
Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia
-
Trembath RC, Thomson JR, Machado RD et al. Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia. N Engl J Med 2001; 345: 325-34.
-
(2001)
N Engl J Med
, vol.345
, pp. 325-334
-
-
Trembath, R.C.1
Thomson, J.R.2
Machado, R.D.3
-
21
-
-
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: 852-9.
-
(2004)
Lancet
, vol.363
, pp. 852-859
-
-
Gallione, C.J.1
Repetto, G.M.2
Legius, E.3
-
22
-
-
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: 577-82.
-
(2005)
J Med Genet
, vol.42
, pp. 577-582
-
-
Cole, S.G.1
Begbie, M.E.2
Wallace, G.M.3
Shovlin, C.L.4
-
23
-
-
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: 2155-62.
-
(2006)
Am J Med Genet A
, vol.140
, pp. 2155-2162
-
-
Bayrak-Toydemir, P.1
McDonald, J.2
Akarsu, N.3
-
24
-
-
0141453477
-
Vascular endothelial growth factor serum levels are elevated in patients with hereditary hemorrhagic telangiectasia
-
Cirulli A, Liso A, D'Ovidio F et al. Vascular endothelial growth factor serum levels are elevated in patients with hereditary hemorrhagic telangiectasia. Acta Haematol 2003; 110: 29-32.
-
(2003)
Acta Haematol
, vol.110
, pp. 29-32
-
-
Cirulli, A.1
Liso, A.2
D'Ovidio, F.3
-
25
-
-
1042266621
-
Vascular endothelial growth factor induces abnormal microvasculature in the endoglin heterozygous mouse brain
-
Xu B, Wu YQ, Huey M et al. Vascular endothelial growth factor induces abnormal microvasculature in the endoglin heterozygous mouse brain. J Cereb Blood Flow Metab 2004; 24: 237-44.
-
(2004)
J Cereb Blood Flow Metab
, vol.24
, pp. 237-244
-
-
Xu, B.1
Wu, Y.Q.2
Huey, M.3
-
26
-
-
23044480249
-
Plasma level and tissue expression of angiogenic factors in patients with hereditary hemorrhagic telangiectasia
-
Sadick H, Naim R, Sadick M, Hormann K, Riedel F. Plasma level and tissue expression of angiogenic factors in patients with hereditary hemorrhagic telangiectasia. Int J Mol Med 2005; 15: 591-6.
-
(2005)
Int J Mol Med
, vol.15
, pp. 591-596
-
-
Sadick, H.1
Naim, R.2
Sadick, M.3
Hormann, K.4
Riedel, F.5
-
27
-
-
3442883144
-
Hereditary hemorrhagic telangiectasia: An overview of diagnosis and management in the molecular era for clinicians
-
Bayrak-Toydemir P, Mao R, Lewin S, McDonald J. Hereditary hemorrhagic telangiectasia: An overview of diagnosis and management in the molecular era for clinicians. Genet Med 2004; 6: 175-91.
-
(2004)
Genet Med
, vol.6
, pp. 175-191
-
-
Bayrak-Toydemir, P.1
Mao, R.2
Lewin, S.3
McDonald, J.4
-
28
-
-
33144462810
-
Hereditary haemorrhagic telangiectasia: Current views on genetics and mechanisms of disease
-
Abdalla SA, Letarte M. Hereditary haemorrhagic telangiectasia: Current views on genetics and mechanisms of disease. J Med Genet 2006; 43: 97-110.
-
(2006)
J Med Genet
, vol.43
, pp. 97-110
-
-
Abdalla, S.A.1
Letarte, M.2
-
29
-
-
0035875091
-
Analysis of several endoglin mutants reveals no endogenous mature or secreted protein capable of interfering with normal endoglin function
-
Paquet ME, Pece-Barbara N, Vera S et al. Analysis of several endoglin mutants reveals no endogenous mature or secreted protein capable of interfering with normal endoglin function. Hum Mol Genet 2001; 10: 1347-57.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1347-1357
-
-
Paquet, M.E.1
Pece-Barbara, N.2
Vera, S.3
-
30
-
-
33646109750
-
Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1
-
Fernandez LA, Sanz-Rodriguez F, Zarrabeitia R et al. Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1. Hum Mutat 2006; 27: 295.
-
(2006)
Hum Mutat
, vol.27
, pp. 295
-
-
Fernandez, L.A.1
Sanz-Rodriguez, F.2
Zarrabeitia, R.3
-
31
-
-
33344466368
-
Functional analysis of mutations in the kinase domain of the TGF-beta receptor ALK1 reveals different mechanisms for induction of hereditary hemorrhagic telangiectasia
-
Gu Y, Jin P, Zhang L et al. Functional analysis of mutations in the kinase domain of the TGF-beta receptor ALK1 reveals different mechanisms for induction of hereditary hemorrhagic telangiectasia. Blood 2006; 107: 1951-4.
-
(2006)
Blood
, vol.107
, pp. 1951-1954
-
-
Gu, Y.1
Jin, P.2
Zhang, L.3
-
32
-
-
33745008653
-
Hereditary haemorrhagic telangiectasia (HHT): Genetic and molecular aspects
-
Lenato GM, Guanti G. Hereditary haemorrhagic telangiectasia (HHT): genetic and molecular aspects. Curr Pharm Des 2006; 12: 1173-93.
-
(2006)
Curr Pharm Des
, vol.12
, pp. 1173-1193
-
-
Lenato, G.M.1
Guanti, G.2
-
33
-
-
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: 1149-57.
-
(2007)
J Thromb Haemost
, vol.5
, pp. 1149-1157
-
-
Sabba, C.1
Pasculli, G.2
Lenato, G.M.3
-
34
-
-
33646781348
-
DHPLC-based mutation analysis of ENG and ALK-1 genes in HHT Italian population
-
Lenato GM, Lastella P, Di Giacomo MC et al. DHPLC-based mutation analysis of ENG and ALK-1 genes in HHT Italian population. Hum Mutat 2006; 27: 213-4.
-
(2006)
Hum Mutat
, vol.27
, pp. 213-214
-
-
Lenato, G.M.1
Lastella, P.2
Di Giacomo, M.C.3
-
35
-
-
34848865319
-
Analysis of ENG and ACVRL1 genes in 137 HHT Italian families identifies 76 different mutations (24 novel). Comparison with other European studies
-
Olivieri C, Pagella F, Semino L et al. Analysis of ENG and ACVRL1 genes in 137 HHT Italian families identifies 76 different mutations (24 novel). Comparison with other European studies. J Hum Genet 2007; 52: 820-9.
-
(2007)
J Hum Genet
, vol.52
, pp. 820-829
-
-
Olivieri, C.1
Pagella, F.2
Semino, L.3
-
36
-
-
39449109211
-
Bevacizumab reverses need for liver transplantation in hereditary hemorrhagic telangiectasia
-
Mitchell A, Adams LA, Macquillan G, Tibballs J, Vanden Driesen R, Delriviere L. Bevacizumab reverses need for liver transplantation in hereditary hemorrhagic telangiectasia. Liver Transpl 2008; 14: 210-3.
-
(2008)
Liver Transpl
, vol.14
, pp. 210-213
-
-
Mitchell, A.1
Adams, L.A.2
Macquillan, G.3
Tibballs, J.4
Vanden Driesen, R.5
Delriviere, L.6
-
37
-
-
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: 705-9.
-
(2004)
Laryngoscope
, vol.114
, pp. 705-709
-
-
Jameson, J.J.1
Cave, D.R.2
-
38
-
-
0036365786
-
Using thalidomide in a patient with epithelioid leiomyosarcoma and Osler-Weber-Rendu disease
-
Kurstin R. Using thalidomide in a patient with epithelioid leiomyosarcoma and Osler-Weber-Rendu disease. Oncology (Williston Park) 2002; 16: 21-4.
-
(2002)
Oncology (Williston Park)
, vol.16
, pp. 21-24
-
-
Kurstin, R.1
-
39
-
-
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: 344-5.
-
(2005)
J Clin Gastroenterol
, vol.39
, pp. 344-345
-
-
Wheatley-Price, P.1
Shovlin, C.2
Chao, D.3
-
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: 519-24.
-
(1995)
Am J Med
, vol.99
, pp. 519-524
-
-
Haitjema, T.1
Disch, F.2
Overtoom, T.T.3
Westermann, C.J.4
Lammers, J.W.5
-
41
-
-
0032809791
-
Pulmonary arteriovenous malformations: Screening procedures and pulmonary angiography in patients with hereditary hemorrhagic telangiectasia
-
Kjeldsen AD, Oxhoj H, Andersen PE, Elle B, Jacobsen JP, Vase P. Pulmonary arteriovenous malformations: Screening procedures and pulmonary angiography in patients with hereditary hemorrhagic telangiectasia. Chest 1999; 116: 432-9.
-
(1999)
Chest
, vol.116
, pp. 432-439
-
-
Kjeldsen, A.D.1
Oxhoj, H.2
Andersen, P.E.3
Elle, B.4
Jacobsen, J.P.5
Vase, P.6
-
42
-
-
0025939367
-
The natural history of epistaxis in hereditary hemorrhagic telangiectasia
-
Assar O, Friedman CM, White RI Jr. The natural history of epistaxis in hereditary hemorrhagic telangiectasia. Laryngoscope 1991; 101: 977-80.
-
(1991)
Laryngoscope
, vol.101
, pp. 977-980
-
-
Assar, O.1
Friedman, C.M.2
White Jr., R.I.3
-
43
-
-
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: 291-7.
-
(1989)
Am J Med Genet
, vol.32
, pp. 291-297
-
-
Plauchu, H.1
de Chadarevian, J.P.2
Bideau, A.3
Robert, J.M.4
-
44
-
-
0035922440
-
Efficacy of unusually high doses of tranexamic acid for the treatment of epistaxis in hereditary hemorrhagic telangiectasia
-
Sabba C, Gallitelli M, Palasciano G. Efficacy of unusually high doses of tranexamic acid for the treatment of epistaxis in hereditary hemorrhagic telangiectasia. N Engl J Med 2001; 345: 926.
-
(2001)
N Engl J Med
, vol.345
, pp. 926
-
-
Sabba, C.1
Gallitelli, M.2
Palasciano, G.3
-
45
-
-
0035032585
-
Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): Otorhinolaryngological manifestations
-
Pau H, Carney AS, Murty GE. Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): Otorhinolaryngological manifestations. Clin Otolaryngol Allied Sci 2001; 26: 93-8.
-
(2001)
Clin Otolaryngol Allied Sci
, vol.26
, pp. 93-98
-
-
Pau, H.1
Carney, A.S.2
Murty, G.E.3
-
46
-
-
0036617490
-
Hereditary hemorrhagic teleangiectasia (Rendu-Osler-Weber disease)
-
Sabba C, Pasculli G, Cirulli A et al. Hereditary hemorrhagic teleangiectasia (Rendu-Osler-Weber disease). Minerva Cardioangiol 2002; 50: 221-38.
-
(2002)
Minerva Cardioangiol
, vol.50
, pp. 221-238
-
-
Sabba, C.1
Pasculli, G.2
Cirulli, A.3
-
47
-
-
0017275259
-
Percutaneous embolization to control epistaxis in Rendu-Osler-Weber disease
-
Strother CM, Newton TH. Percutaneous embolization to control epistaxis in Rendu-Osler-Weber disease. Arch Otolaryngol 1976; 102: 58-60.
-
(1976)
Arch Otolaryngol
, vol.102
, pp. 58-60
-
-
Strother, C.M.1
Newton, T.H.2
-
48
-
-
0026683949
-
Hereditary haemorrhagic telangiectasia: A clinical analysis
-
Porteous ME, Burn J, Proctor SJ. Hereditary haemorrhagic telangiectasia: a clinical analysis. J Med Genet 1992; 29: 527-30.
-
(1992)
J Med Genet
, vol.29
, pp. 527-530
-
-
Porteous, M.E.1
Burn, J.2
Proctor, S.J.3
-
49
-
-
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: 1074-9.
-
(2004)
Endoscopy
, vol.36
, pp. 1074-1079
-
-
Ingrosso, M.1
Sabba, C.2
Pisani, A.3
-
50
-
-
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: 415-8.
-
(2000)
Am J Gastroenterol
, vol.95
, pp. 415-418
-
-
Kjeldsen, A.D.1
Kjeldsen, J.2
-
51
-
-
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: 953-5.
-
(1990)
Lancet
, vol.335
, pp. 953-955
-
-
van Cutsem, E.1
Rutgeerts, P.2
Vantrappen, G.3
-
52
-
-
1642299483
-
Resolution of hereditary hemorrhagic telangiectasia and anemia with prolonged alpha-interferon therapy for chronic hepatitis C
-
Massoud OI, Youssef WI, Mullen KD. Resolution of hereditary hemorrhagic telangiectasia and anemia with prolonged alpha-interferon therapy for chronic hepatitis C. J Clin Gastroenterol 2004; 38: 377-9.
-
(2004)
J Clin Gastroenterol
, vol.38
, pp. 377-379
-
-
Massoud, O.I.1
Youssef, W.I.2
Mullen, K.D.3
-
53
-
-
0022261163
-
Pulmonary arteriovenous fistulas in hereditary hemorrhagic telangiectasia
-
Vase P, Holm M, Arendrup H. Pulmonary arteriovenous fistulas in hereditary hemorrhagic telangiectasia. Acta Med Scand 1985; 218: 105-9.
-
(1985)
Acta Med Scand
, vol.218
, pp. 105-109
-
-
Vase, P.1
Holm, M.2
Arendrup, H.3
-
54
-
-
0032799731
-
Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: Issues in clinical management and review of pathogenic mechanisms
-
Shovlin CL, Letarte M. Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: Issues in clinical management and review of pathogenic mechanisms. Thorax 1999; 54: 714-29.
-
(1999)
Thorax
, vol.54
, pp. 714-729
-
-
Shovlin, C.L.1
Letarte, M.2
-
55
-
-
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: 477-84.
-
(1998)
AJNR Am J Neuroradiol
, vol.19
, pp. 477-484
-
-
Fulbright, R.K.1
Chaloupka, J.C.2
Putman, C.M.3
-
56
-
-
0034082212
-
Angiographic and clinical characteristics of patients with cerebral arteriovenous malformations associated with hereditary hemorrhagic telangiectasia
-
Matsubara S, Mandzia JL, ter Brugge K, Willinsky RA, Faughnan ME. Angiographic and clinical characteristics of patients with cerebral arteriovenous malformations associated with hereditary hemorrhagic telangiectasia. AJNR Am J Neuroradiol 2000; 21: 1016-20.
-
(2000)
AJNR Am J Neuroradiol
, vol.21
, pp. 1016-1020
-
-
Matsubara, S.1
Mandzia, J.L.2
ter Brugge, K.3
Willinsky, R.A.4
Faughnan, M.E.5
-
57
-
-
0030281252
-
Pulmonary arteriovenous malformations: Diagnosis and transcatheter embolotherapy
-
White RI Jr, Pollak JS, Wirth JA. Pulmonary arteriovenous malformations: diagnosis and transcatheter embolotherapy. J Vasc Interv Radiol 1996; 7: 787-804.
-
(1996)
J Vasc Interv Radiol
, vol.7
, pp. 787-804
-
-
White, R.I.1
Pollak, J.S.2
Wirth, J.A.3
-
58
-
-
0029563707
-
Medical complications of pregnancy in hereditary haemorrhagic telangiectasia
-
Shovlin CL, Winstock AR, Peters AM, Jackson JE, Hughes JM. Medical complications of pregnancy in hereditary haemorrhagic telangiectasia. QJM 1995; 88: 879-87.
-
(1995)
QJM
, vol.88
, pp. 879-887
-
-
Shovlin, C.L.1
Winstock, A.R.2
Peters, A.M.3
Jackson, J.E.4
Hughes, J.M.5
-
59
-
-
0033968624
-
Diffuse pulmonary arteriovenous malformations: Characteristics and prognosis
-
Faughnan ME, Lui YW, Wirth JA et al. Diffuse pulmonary arteriovenous malformations: Characteristics and prognosis. Chest 2000; 117: 31-8.
-
(2000)
Chest
, vol.117
, pp. 31-38
-
-
Faughnan, M.E.1
Lui, Y.W.2
Wirth, J.A.3
-
60
-
-
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: 667-75.
-
(2006)
Hum Mutat
, vol.27
, pp. 667-675
-
-
Bossler, A.D.1
Richards, J.2
George, C.3
Godmilow, L.4
Ganguly, A.5
-
61
-
-
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: E12.
-
(2002)
Pediatrics
, vol.109
-
-
Morgan, T.1
McDonald, J.2
Anderson, C.3
-
62
-
-
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: 1103-10.
-
(2006)
Childs Nerv Syst
, vol.22
, pp. 1103-1110
-
-
Cullen, S.1
Alvarez, H.2
Rodesch, G.3
Lasjaunias, P.4
-
63
-
-
22844447320
-
Endovascular management for intracranial ruptured aneurysms in elderly patients: Outcome and technical aspects
-
Mont'alverne F, Musacchio M, Tolentino V, Riquelme C, Tournade A. Endovascular management for intracranial ruptured aneurysms in elderly patients: Outcome and technical aspects. Neuroradiology 2005; 47: 446-57.
-
(2005)
Neuroradiology
, vol.47
, pp. 446-457
-
-
Mont'alverne, F.1
Musacchio, M.2
Tolentino, V.3
Riquelme, C.4
Tournade, A.5
-
64
-
-
0035149188
-
Stereotactic radiosurgery for motor cortex region arteriovenous malformations
-
Hadjipanayis CG, Levy EI, Niranjan A et al. Stereotactic radiosurgery for motor cortex region arteriovenous malformations. Neurosurgery 2001; 48: 70-6.
-
(2001)
Neurosurgery
, vol.48
, pp. 70-76
-
-
Hadjipanayis, C.G.1
Levy, E.I.2
Niranjan, A.3
-
65
-
-
0034491221
-
Radiosurgery for childhood intracranial arteriovenous malformations
-
Levy EI, Niranjan A, Thompson TP et al. Radiosurgery for childhood intracranial arteriovenous malformations. Neurosurgery 2000; 47: 834-41.
-
(2000)
Neurosurgery
, vol.47
, pp. 834-841
-
-
Levy, E.I.1
Niranjan, A.2
Thompson, T.P.3
-
66
-
-
0027972833
-
Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: Imaging findings
-
Buscarini E, Buscarini L, Civardi G, Arruzzoli S, Bossalini G, Piantanida M. Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: Imaging findings. AJR Am J Roentgenol 1994; 163: 1105-10.
-
(1994)
AJR Am J Roentgenol
, vol.163
, pp. 1105-1110
-
-
Buscarini, E.1
Buscarini, L.2
Civardi, G.3
Arruzzoli, S.4
Bossalini, G.5
Piantanida, M.6
-
67
-
-
33846564415
-
Liver involvement in hereditary hemorrhagic telangiectasia (HHT)
-
Garcia-Tsao G. Liver involvement in hereditary hemorrhagic telangiectasia (HHT). J Hepatol 2007; 46: 499-507.
-
(2007)
J Hepatol
, vol.46
, pp. 499-507
-
-
Garcia-Tsao, G.1
-
68
-
-
1642332403
-
Hepatic involvement in hereditary hemorrhagic telangiectasia: CT findings
-
Memeo M, Stabile Ianora AA, Scardapane A, Buonamico P, Sabba C, Angelelli G. Hepatic involvement in hereditary hemorrhagic telangiectasia: CT findings. Abdom Imaging 2004; 29: 211-20.
-
(2004)
Abdom Imaging
, vol.29
, pp. 211-220
-
-
Memeo, M.1
Stabile Ianora, A.A.2
Scardapane, A.3
Buonamico, P.4
Sabba, C.5
Angelelli, G.6
-
69
-
-
0035077665
-
Hepatic involvement in hereditary hemorrhagic telangiectasia: An unusual indication for liver transplantation
-
Hillert C, Broering DC, Gundlach M, Knoefel WT, Izbicki JR, Rogiers X. Hepatic involvement in hereditary hemorrhagic telangiectasia: An unusual indication for liver transplantation. Liver Transpl 2001; 7: 266-8.
-
(2001)
Liver Transpl
, vol.7
, pp. 266-268
-
-
Hillert, C.1
Broering, D.C.2
Gundlach, M.3
Knoefel, W.T.4
Izbicki, J.R.5
Rogiers, X.6
-
71
-
-
0037712529
-
Large aneurysms of the ascending aorta and major coronary arteries in a patient with hereditary hemorrhagic telangiectasia
-
Hsi DH, Ryan GF, Hellems SO, Cheeran DC, Sheils LA. Large aneurysms of the ascending aorta and major coronary arteries in a patient with hereditary hemorrhagic telangiectasia. Mayo Clin Proc 2003; 78: 774-6.
-
(2003)
Mayo Clin Proc
, vol.78
, pp. 774-776
-
-
Hsi, D.H.1
Ryan, G.F.2
Hellems, S.O.3
Cheeran, D.C.4
Sheils, L.A.5
-
72
-
-
0018578709
-
Ocular lesions in hereditary haemorrhagic telangiectasia
-
Vase I, Vase P. Ocular lesions in hereditary haemorrhagic telangiectasia. Acta Ophthalmol (Copenh) 1979; 57: 1084-90.
-
(1979)
Acta Ophthalmol (Copenh)
, vol.57
, pp. 1084-1090
-
-
Vase, I.1
Vase, P.2
-
73
-
-
0023885429
-
Hereditary hemorrhagic telangiectasia with malignant lymphoma. An autopsy case
-
Kato S, Ichihara K. Hereditary hemorrhagic telangiectasia with malignant lymphoma. An autopsy case. Acta Pathol Jpn 1988; 38: 383-91.
-
(1988)
Acta Pathol Jpn
, vol.38
, pp. 383-391
-
-
Kato, S.1
Ichihara, K.2
-
74
-
-
0027253393
-
Vaginal telangiectasias: Unusual presentation of the Osler-Weber-Rendu syndrome
-
Humphries JE, Frierson HF Jr, Underwood PB Jr. Vaginal telangiectasias: unusual presentation of the Osler-Weber-Rendu syndrome. Obstet Gynecol 1993; 81: 865-6.
-
(1993)
Obstet Gynecol
, vol.81
, pp. 865-866
-
-
Humphries, J.E.1
Frierson, H.F.2
Underwood Jr., P.B.3
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