-
1
-
-
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.116 A
, Issue.4
, pp. 324-328
-
-
Westermann, C.J.1
Rosina, A.F.2
de Vries, V.3
de Coteau, P.A.4
-
2
-
-
0024394433
-
Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population
-
Plauchu H, de Chadarévian 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 Chadarévian, J.P.2
Bideau, A.3
Robert, J.M.4
-
3
-
-
0026683949
-
Hereditary haemorrhagic telangiectasia: A clinical analysis
-
Porteous ME, Burn J, Proctor SJ. Hereditary haemorrhagic telangiectasia: a clinical analysis. J Med Genet. 1992;29(8):527-530.
-
(1992)
J Med Genet.
, vol.29
, Issue.8
, pp. 527-530
-
-
Porteous, M.E.1
Burn, J.2
Proctor, S.J.3
-
4
-
-
0028171579
-
Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1
-
McAllister KA, Grogg KM, Johnson DW, et al. Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1. Nat Genet. 1994;8(4):345-351.
-
(1994)
Nat Genet.
, vol.8
, Issue.4
, pp. 345-351
-
-
McAllister, K.A.1
Grogg, K.M.2
Johnson, D.W.3
-
5
-
-
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(1):21-28.
-
(1995)
Genome Res.
, vol.5
, Issue.1
, pp. 21-28
-
-
Johnson, D.W.1
Berg, J.N.2
Gallione, C.J.3
-
6
-
-
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(1):29-32.
-
(2003)
Acta Haematol.
, vol.110
, Issue.1
, pp. 29-32
-
-
Cirulli, A.1
Liso, A.2
D'Ovidio, F.3
-
7
-
-
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(5):325-334.
-
(2001)
N Engl J Med.
, vol.345
, Issue.5
, pp. 325-334
-
-
Trembath, R.C.1
Thomson, J.R.2
Machado, R.D.3
-
8
-
-
0027126057
-
Hereditary hemorrhagic telangiectasia (Osler's disease) [in German]
-
Römer W, Burk M, Schneider W. Hereditary hemorrhagic telangiectasia (Osler's disease) [in German]. Dtsch Med Wochenschr. 1992;117(17):669-675.
-
(1992)
Dtsch Med Wochenschr.
, vol.117
, Issue.17
, pp. 669-675
-
-
Römer, W.1
Burk, M.2
Schneider, W.3
-
9
-
-
67249096183
-
Transillumination of the fingers for vascular anomalies: A novel method for evaluating hereditary hemorrhagic telangiectasia
-
Mohler ER III, et al. Transillumination of the fingers for vascular anomalies: a novel method for evaluating hereditary hemorrhagic telangiectasia. Genet Med. 2009;11(5):356-358.
-
(2009)
Genet Med.
, vol.11
, Issue.5
, pp. 356-358
-
-
Mohler III, E.R.1
-
10
-
-
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
-
11
-
-
0032809791
-
Pulmonary arteriovenous malformations: Screening procedures and pulmonary angiography in patients with hereditary hemorrhagic telangiectasia
-
Kjeldsen AD, Oxhøj 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(2):432-439.
-
(1999)
Chest.
, vol.116
, Issue.2
, pp. 432-439
-
-
Kjeldsen, A.D.1
Oxhøj, H.2
Andersen, P.E.3
Elle, B.4
Jacobsen, J.P.5
Vase, P.6
-
12
-
-
0035150362
-
Contrast echocardiography for detection of pulmonary arteriovenous malformations
-
Nanthakumar K, Graham AT, Robinson TI, et al. Contrast echocardiography for detection of pulmonary arteriovenous malformations. Am Heart J. 2001;141(2):243-246.
-
(2001)
Am Heart J.
, vol.141
, Issue.2
, pp. 243-246
-
-
Nanthakumar, K.1
Graham, A.T.2
Robinson, T.I.3
-
13
-
-
0037331163
-
The role of echocardiography in screening for pulmonary arteriovenous malformations
-
Gossage JR. The role of echocardiography in screening for pulmonary arteriovenous malformations. Chest. 2003;123(2):320-322.
-
(2003)
Chest.
, vol.123
, Issue.2
, pp. 320-322
-
-
Gossage, J.R.1
-
14
-
-
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
-
15
-
-
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 JE, 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.E.5
Sheppard, M.N.6
-
16
-
-
0027970430
-
Life-threatening pulmonary hemorrhage with pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia
-
Ference BA, Shannon TM, White RI Jr, Zawin M, Burdge CM. Life-threatening pulmonary hemorrhage with pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia. Chest. 1994;106(5):1387-1390.
-
(1994)
Chest.
, vol.106
, Issue.5
, pp. 1387-1390
-
-
Ference, B.A.1
Shannon, T.M.2
White Jr., R.I.3
Zawin, M.4
Burdge, C.M.5
-
17
-
-
0037286297
-
Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): A view from the 21st century
-
Begbie ME, Wallace GM, Shovlin CL. Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century. Postgrad Med J. 2003;79(927):18-24.
-
(2003)
Postgrad Med J.
, vol.79
, Issue.927
, pp. 18-24
-
-
Begbie, M.E.1
Wallace, G.M.2
Shovlin, C.L.3
-
18
-
-
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
-
19
-
-
33750133796
-
Liver involvement in hereditary hemorrhagic telangiectasia: CT and clinical findings do not correlate in symptomatic patients
-
Wu JS, Saluja S, Garcia-Tsao G, Chong A, Henderson KJ, White RI Jr. Liver involvement in hereditary hemorrhagic telangiectasia: CT and clinical findings do not correlate in symptomatic patients. AJR Am J Roentgenol. 2006;187(4):W399-405.
-
(2006)
AJR Am J Roentgenol.
, vol.187
, Issue.4
-
-
Wu, J.S.1
Saluja, S.2
Garcia-Tsao, G.3
Chong, A.4
Henderson, K.J.5
White Jr., R.I.6
-
20
-
-
52949131377
-
Hepatic vascular malformations in hereditary hemorrhagic telangiectasia
-
Khalid SK, Garcia-Tsao G. Hepatic vascular malformations in hereditary hemorrhagic telangiectasia. Semin Liver Dis. 2008;28(3):247-258.
-
(2008)
Semin Liver Dis.
, vol.28
, Issue.3
, pp. 247-258
-
-
Khalid, S.K.1
Garcia-Tsao, G.2
-
21
-
-
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
-
22
-
-
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
-
23
-
-
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
-
24
-
-
77649191005
-
International guidelines for the diagnosis and management of hereditary hemorrhagic telangiectasia
-
[published online ahead of print June 29, 2009]
-
Faughnan ME, Palda VA, Garcia-Tsao G, et al. International guidelines for the diagnosis and management of hereditary hemorrhagic telangiectasia [published online ahead of print June 29, 2009]. J Med Genet.
-
J Med Genet
-
-
Faughnan, M.E.1
Palda, V.A.2
Garcia-Tsao, G.3
-
25
-
-
33646810085
-
Screening for children from families with Rendu-Osler-Weber disease: From geneticist to clinician
-
Giordano P, Nigro A, Lenato GM, et al. Screening for children from families with Rendu-Osler-Weber disease: from geneticist to clinician. J Thromb Haemost. 2006;4(6):1237-1245.
-
(2006)
J Thromb Haemost.
, vol.4
, Issue.6
, pp. 1237-1245
-
-
Giordano, P.1
Nigro, A.2
Lenato, G.M.3
-
26
-
-
8644283490
-
The value of screening for multiple arterio-venous malformations in hereditary hemorrhagic telangiectasia: A diagnostic study
-
Folz BJ, Wollstein AC, Alfke H, et al. The value of screening for multiple arterio-venous malformations in hereditary hemorrhagic telangiectasia: a diagnostic study. Eur Arch Otorhinolaryngol. 2004;261(9):509-516.
-
(2004)
Eur Arch Otorhinolaryngol.
, vol.261
, Issue.9
, pp. 509-516
-
-
Folz, B.J.1
Wollstein, A.C.2
Alfke, H.3
-
27
-
-
0038016648
-
Should asymptomatic patients with hereditary haemorrhagic telangiectasia (HHT) be screened for cerebral vascular malformations? Data from 22,061 years of HHT patient life
-
Easey AJ, Wallace GM, Hughes JM, Jackson JE, Taylor WJ, Shovlin CL. Should asymptomatic patients with hereditary haemorrhagic telangiectasia (HHT) be screened for cerebral vascular malformations? Data from 22,061 years of HHT patient life. J Neurol Neurosurg Psychiatry. 2003;74(6):743-748.
-
(2003)
J Neurol Neurosurg Psychiatry.
, vol.74
, Issue.6
, pp. 743-748
-
-
Easey, A.J.1
Wallace, G.M.2
Hughes, J.M.3
Jackson, J.E.4
Taylor, W.J.5
Shovlin, C.L.6
-
28
-
-
21944442052
-
Hereditary haemorrhagic telangiectasia: State of the art
-
Fiorella ML, Ross DA, White RI, Sabbà C, Fiorella R. Hereditary haemorrhagic telangiectasia: state of the art. Acta Otorhinolaryngol Ital. 2004;24(6):330-336.
-
(2004)
Acta Otorhinolaryngol Ital.
, vol.24
, Issue.6
, pp. 330-336
-
-
Fiorella, M.L.1
Ross, D.A.2
White, R.I.3
Sabbà, C.4
Fiorella, R.5
-
29
-
-
42449163015
-
The impact of septodermoplasty and potassium-titanyl-phosphate (KTP) laser therapy in the treatment of hereditary hemorrhagic telangiectasia-related epistaxis
-
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(2):182-187.
-
(2008)
Am J Rhinol.
, vol.22
, Issue.2
, pp. 182-187
-
-
Harvey, R.J.1
Kanagalingam, J.2
Lund, V.J.3
-
30
-
-
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
-
31
-
-
0027968607
-
Angiographic embolization for the treatment of epistaxis: A review of 108 cases
-
Elden L, Montanera W, Terbrugge K, Willinsky R, Lasjaunias P, Charles D. Angiographic embolization for the treatment of epistaxis: a review of 108 cases. Otolaryngol Head Neck Surg. 1994;111(1):44-50.
-
(1994)
Otolaryngol Head Neck Surg.
, vol.111
, Issue.1
, pp. 44-50
-
-
Elden, L.1
Montanera, W.2
Terbrugge, K.3
Willinsky, R.4
Lasjaunias, P.5
Charles, D.6
-
34
-
-
79956362223
-
Neurologic decompression illness in a scuba diver with hereditary hemorrhagic telangiectasia
-
Potkin R. Neurologic decompression illness in a scuba diver with hereditary hemorrhagic telangiectasia. Undersea Hyperb Med. 2008;35(4).
-
(2008)
Undersea Hyperb Med.
, vol.35
, Issue.4
-
-
Potkin, R.1
-
35
-
-
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
-
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(2):210-213.
-
(2008)
Liver Transpl.
, vol.14
, Issue.2
, pp. 210-213
-
-
Mitchell, A.1
Adams, L.A.2
McQuillan, G.3
Tibballs, J.4
vanden Driesen, R.5
Delriviere, L.6
-
37
-
-
76749171642
-
Thalidomide for the treatment of chronic gastrointestinal bleeding from angiodysplasias: A case series
-
Kamalaporn P, Saravanan R, Cirocco M, et al. Thalidomide for the treatment of chronic gastrointestinal bleeding from angiodysplasias: a case series. Eur J Gastroenterol Hepatol. 2009;21(12):1347-1350.
-
(2009)
Eur J Gastroenterol Hepatol.
, vol.21
, Issue.12
, pp. 1347-1350
-
-
Kamalaporn, P.1
Saravanan, R.2
Cirocco, M.3
|