-
1
-
-
0343157354
-
Prevention of bacterial endocarditis
-
American Heart Association (1997) Prevention of bacterial endocarditis. JAMA 277: 1794-1801
-
(1997)
JAMA
, vol.277
, pp. 1794-1801
-
-
-
2
-
-
50449203878
-
Hereditary epistaxis
-
Babington BG (1865) Hereditary epistaxis. Lancet 2: 362-363
-
(1865)
Lancet
, vol.2
, pp. 362-363
-
-
Babington, B.G.1
-
3
-
-
0032827986
-
Hereditary hemorrhagic telangiectasia with juvenile polyposis - Coincidence or linked autosomal dominant inheritance?
-
Ballauff A, Koletzko S (1999) Hereditary hemorrhagic telangiectasia with juvenile polyposis - coincidence or linked autosomal dominant inheritance? Z Gastroenterol 37: 385-388
-
(1999)
Z Gastroenterol
, vol.37
, pp. 385-388
-
-
Ballauff, A.1
Koletzko, S.2
-
4
-
-
0030047241
-
Clinical heterogenity in hereditary hemorrhagic telangiectasia: Are pulmonary arteriovenous malformations more common in families linked to endoglin?
-
Berg JN, Guttmacher AE, Marchuk DA et al. (1996) Clinical heterogenity in hereditary hemorrhagic telangiectasia: are pulmonary arteriovenous malformations more common in families linked to endoglin? J Med Genet 33: 256-257
-
(1996)
J Med Genet
, vol.33
, pp. 256-257
-
-
Berg, J.N.1
Guttmacher, A.E.2
Marchuk, D.A.3
-
5
-
-
0033003116
-
Hereditary hemorrhagic telangiectasias: A challenge for the clinician
-
Bergler W, Götte K (1999) Hereditary hemorrhagic telangiectasias: a challenge for the clinician. Eur Arch Otorhinolaryngol 256: 10-15
-
(1999)
Eur Arch Otorhinolaryngol
, vol.256
, pp. 10-15
-
-
Bergler, W.1
Götte, K.2
-
6
-
-
0032954559
-
Argon plasma coagulation for the treatment of hereditary hemorrhagic telangiectasia
-
Bergler W, Riedel F, Baker-Schreyer A, Juncker C, Hörmann K (1999) Argon plasma coagulation for the treatment of hereditary hemorrhagic telangiectasia. Laryngoscope 109: 15-20
-
(1999)
Laryngoscope
, vol.109
, pp. 15-20
-
-
Bergler, W.1
Riedel, F.2
Baker-Schreyer, A.3
Juncker, C.4
Hörmann, K.5
-
7
-
-
0032958453
-
Liver transplantation resolves the hyperdynamic circulation in hereditary hemorrhagic telangiectasia with hepatic involvement
-
Boillot O, Bianco F, Viale JP et al. (1999) Liver transplantation resolves the hyperdynamic circulation in hereditary hemorrhagic telangiectasia with hepatic involvement. Gastroenterology 116: 187-192
-
(1999)
Gastroenterology
, vol.116
, pp. 187-192
-
-
Boillot, O.1
Bianco, F.2
Viale, J.P.3
-
8
-
-
0033888018
-
Endoglin expression is reduced in normal vessels but still detectable in arteriovenous malformations of patients with hereditary hemorrhagic telangiectasia type 1
-
Bourdeau A, Cymerman U, Paquet ME et al. (2000) Endoglin expression is reduced in normal vessels but still detectable in arteriovenous malformations of patients with hereditary hemorrhagic telangiectasia type 1. Am J Pathol 156: 911-923
-
(2000)
Am J Pathol
, vol.156
, pp. 911-923
-
-
Bourdeau, A.1
Cymerman, U.2
Paquet, M.E.3
-
9
-
-
0032720393
-
A murine model of hereditary hemorrhagic telangiectasia
-
Bourdeau A, Dumont DJ, Letarte M (1999) A murine model of hereditary hemorrhagic telangiectasia. J Clin Invest 104: 1343-1351
-
(1999)
J Clin Invest
, vol.104
, pp. 1343-1351
-
-
Bourdeau, A.1
Dumont, D.J.2
Letarte, M.3
-
10
-
-
0024370535
-
Ocular manifestations in hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber Disease)
-
Brant AM, Schachat AP, White RI (1989) Ocular manifestations in hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber Disease). Am J Ophtal 107: 642-646
-
(1989)
Am J Ophtal
, vol.107
, pp. 642-646
-
-
Brant, A.M.1
Schachat, A.P.2
White, R.I.3
-
11
-
-
0025129826
-
Ultrastructure and three-dimensional organization of the teleangiectases of hereditary hemorrhagic teleangiectasia
-
Braverman IM, Keh A, Jacobson BS (1990) Ultrastructure and three-dimensional organization of the teleangiectases of hereditary hemorrhagic teleangiectasia. J Invest Dermatol 95: 422-427
-
(1990)
J Invest Dermatol
, vol.95
, pp. 422-427
-
-
Braverman, I.M.1
Keh, A.2
Jacobson, B.S.3
-
12
-
-
0030637701
-
Hereditary hemorrhagic telangiectasia: What the otolaryngologist should know
-
Byahatti SV, Rebeiz EE, Shapshay SM (1997) Hereditary hemorrhagic telangiectasia: what the otolaryngologist should know. Am J Rhinol 11: 55-62
-
(1997)
Am J Rhinol
, vol.11
, pp. 55-62
-
-
Byahatti, S.V.1
Rebeiz, E.E.2
Shapshay, S.M.3
-
13
-
-
0016910663
-
La maladie de Rendu-Osler: À propos de 50 cas suivis à l'Institut Gustave-Roussy
-
Cachin Y, Sauvage JP, Schwaab G (1976) La maladie de Rendu-Osler: à propos de 50 cas suivis à l'Institut Gustave-Roussy. Ann Otol Larngol (Paris) 93: 103-108
-
(1976)
Ann Otol Larngol (Paris)
, vol.93
, pp. 103-108
-
-
Cachin, Y.1
Sauvage, J.P.2
Schwaab, G.3
-
14
-
-
0031959717
-
Clinical outcome of transfemoral embolisation in patients with arteriovenous malformations of the liver in hereditary haemorrhagic telangiectasia (Weber-Rendu-Osler disease)
-
Caselitz M, Wagner S, Chavan A et al. (1998) Clinical outcome of transfemoral embolisation in patients with arteriovenous malformations of the liver in hereditary haemorrhagic telangiectasia (Weber-Rendu-Osler disease). Gut 42: 123-126
-
(1998)
Gut
, vol.42
, pp. 123-126
-
-
Caselitz, M.1
Wagner, S.2
Chavan, A.3
-
15
-
-
0025230351
-
Treatment of bleeding gastrointestinal malformations with oestrogen-progesterone
-
Cutsem van E, Rutgeerts P, Vantrappen G (1990) Treatment of bleeding gastrointestinal malformations with oestrogen-progesterone. Lancet 335: 953-955
-
(1990)
Lancet
, vol.335
, pp. 953-955
-
-
Cutsem van, E.1
Rutgeerts, P.2
Vantrappen, G.3
-
16
-
-
0033977915
-
Identification of hereditary hemorrhagic telangiectasia type 1 in newborns by protein expression and mutation analysis of endoglin
-
Cymerman U, Vera S, Pece-Barbara N, Bourdeau A, White RI, Dunn J, Letarte M (2000) Identification of hereditary hemorrhagic telangiectasia type 1 in newborns by protein expression and mutation analysis of endoglin. Pediatr Res 47: 24-35
-
(2000)
Pediatr Res
, vol.47
, pp. 24-35
-
-
Cymerman, U.1
Vera, S.2
Pece-Barbara, N.3
Bourdeau, A.4
White, R.I.5
Dunn, J.6
Letarte, M.7
-
17
-
-
0034727052
-
Liver disease in patients with hereditary hemorrhagic telangiectasia
-
Garcia-Tsao G, Korzenik JR, Young L et al. (2000) Liver disease in patients with hereditary hemorrhagic telangiectasia. N Engl J Med 28: 931-936
-
(2000)
N Engl J Med
, vol.28
, pp. 931-936
-
-
Garcia-Tsao, G.1
Korzenik, J.R.2
Young, L.3
-
18
-
-
0001165052
-
Hereditary hemorrhagic telangiectasia: A genetic an bibliographic study
-
Garland HG, Anning ST (1950) Hereditary hemorrhagic telangiectasia: A genetic an bibliographic study. Br J Dermatol Syphilis 62: 289-310
-
(1950)
Br J Dermatol Syphilis
, vol.62
, pp. 289-310
-
-
Garland, H.G.1
Anning, S.T.2
-
19
-
-
0027993606
-
Modified Young's procedure for refractory epistaxis due to hereditary hemorrhagic telangiectasia
-
Gluckman JL, Portugal LG (1994) Modified Young's procedure for refractory epistaxis due to hereditary hemorrhagic telangiectasia. Laryngoscope 104: 1174-1177
-
(1994)
Laryngoscope
, vol.104
, pp. 1174-1177
-
-
Gluckman, J.L.1
Portugal, L.G.2
-
21
-
-
0028851489
-
Screening family members of patients with hereditary hemorrhagic telangiectasia
-
Haitjema T, Disch F, Overtoom TT, Westermann CJ, Lammers JW (1995) Screening family members of patients with hereditary hemorrhagic telangiectasia. Am J Med 99: 519-524
-
(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
-
22
-
-
0002538614
-
Multiple hereditary telangiectases cause hemorrhage (hereditary hemorrhagic telangiectasia)
-
Hanes FM (1909) Multiple hereditary telangiectases cause hemorrhage (hereditary hemorrhagic telangiectasia). Johns Hopkins Bull 20: 63-73
-
(1909)
Johns Hopkins Bull
, vol.20
, pp. 63-73
-
-
Hanes, F.M.1
-
23
-
-
0021332591
-
A study of a Caucasian family with variant von Willebrand's disease in association with vascular telangiectasia and haemoglobinopathy
-
Hanna W, McCarroll D, Lin D et al. (1984) A study of a Caucasian family with variant von Willebrand's disease in association with vascular telangiectasia and haemoglobinopathy. Thromb Haemostas 1: 275-278
-
(1984)
Thromb Haemostas
, vol.1
, pp. 275-278
-
-
Hanna, W.1
McCarroll, D.2
Lin, D.3
-
25
-
-
0026681815
-
Hereditary haemorrhagic teleangiectasia: Unsuccessful treatment with the flashlamp-pulsed dye laser
-
Haye R, Austad J (1992) Hereditary haemorrhagic teleangiectasia: unsuccessful treatment with the flashlamp-pulsed dye laser. Rhinology 30: 135-137
-
(1992)
Rhinology
, vol.30
, pp. 135-137
-
-
Haye, R.1
Austad, J.2
-
26
-
-
0028037612
-
Hereditary hemorrhagic telangiectasia: Young's procedure in the management of epistaxis
-
Hosni AA, Innes AJ (1994) Hereditary hemorrhagic telangiectasia: Young's procedure in the management of epistaxis. J Laryngol Otol 108: 754-757
-
(1994)
J Laryngol Otol
, vol.108
, pp. 754-757
-
-
Hosni, A.A.1
Innes, A.J.2
-
27
-
-
0012414555
-
-
Direct Connection, Eigenverlag der HHT Foundation, New Haven, USA, March 2000
-
HHT Foundation International, Inc. (2000) Our most frequently asked questions. Direct Connection, Eigenverlag der HHT Foundation, New Haven, USA, March 2000
-
(2000)
Our Most Frequently Asked Questions
-
-
-
28
-
-
0030050973
-
Mutations in the activin receptor-like kinase 1 gene in hereditary hemorrhagic telangiectasia type 2
-
Johnson DW, Berg JN, Baldwin MA et al. (1996) Mutations in the activin receptor-like kinase 1 gene in hereditary hemorrhagic telangiectasia type 2. Nature Gen 13: 189-195
-
(1996)
Nature Gen
, vol.13
, pp. 189-195
-
-
Johnson, D.W.1
Berg, J.N.2
Baldwin, M.A.3
-
30
-
-
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 (1999) Pulmonary arteriovenous malformations: screening procedures and pulmonary angiography in patients with hereditary hemorrhagic telangiectasia. Chest 116: 432-439
-
(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
-
32
-
-
0033007057
-
Hereditary hemorrhagic telangiectasia: A populationbased study of prevalence and mortality in Danish patients
-
Kjeldsen AD, Vase P, Green A (1999) Hereditary hemorrhagic telangiectasia: a populationbased study of prevalence and mortality in Danish patients. J Intern Med 245: 31-39
-
(1999)
J Intern Med
, vol.245
, pp. 31-39
-
-
Kjeldsen, A.D.1
Vase, P.2
Green, A.3
-
33
-
-
0024442023
-
Coronary artery extasia associated with hereditary hemorrhagic telangiectasia
-
Kurnik PB, Heymann WR (1989) Coronary artery extasia associated with hereditary hemorrhagic telangiectasia. Arch Intern Med 149: 2357-2359
-
(1989)
Arch Intern Med
, vol.149
, pp. 2357-2359
-
-
Kurnik, P.B.1
Heymann, W.R.2
-
34
-
-
0001629660
-
A case of haemophilia complicated with multiple naevi
-
Legg W (1876) A case of haemophilia complicated with multiple naevi. Lancet 2: 856
-
(1876)
Lancet
, vol.2
, pp. 856
-
-
Legg, W.1
-
35
-
-
0031039792
-
A retrospective study of the role of the argon laser in the management of epistaxis secondary to hereditary hemorrhagic telangiectasia
-
Lennox PA, Harries M, Lund VJ, Howard DJ (1997) A retrospective study of the role of the argon laser in the management of epistaxis secondary to hereditary hemorrhagic telangiectasia. J Laryngol Otol 111: 34-37
-
(1997)
J Laryngol Otol
, vol.111
, pp. 34-37
-
-
Lennox, P.A.1
Harries, M.2
Lund, V.J.3
Howard, D.J.4
-
36
-
-
0033612141
-
Defective angiogenesis in mice lacking Endoglin
-
Li DY, Sorensen LK, Brooke BS et al. (1999) Defective angiogenesis in mice lacking Endoglin. Science 284: 1534-1537
-
(1999)
Science
, vol.284
, pp. 1534-1537
-
-
Li, D.Y.1
Sorensen, L.K.2
Brooke, B.S.3
-
37
-
-
0031039508
-
Closure of the nasal cavities in the treatment of refractory hereditary hemorrhagic telangiectasia
-
Lund VJ, Howard DJ (1997) Closure of the nasal cavities in the treatment of refractory hereditary hemorrhagic telangiectasia. J Laryngol Otol 111: 30-33
-
(1997)
J Laryngol Otol
, vol.111
, pp. 30-33
-
-
Lund, V.J.1
Howard, D.J.2
-
38
-
-
0034130826
-
Value of capillary microscopy in the diagnosis of hereditary hemorrhagic telangiectasia
-
Mager JJ, Westermann CJ (2000) Value of capillary microscopy in the diagnosis of hereditary hemorrhagic telangiectasia. Arch Dermatol 136: 732-734
-
(2000)
Arch Dermatol
, vol.136
, pp. 732-734
-
-
Mager, J.J.1
Westermann, C.J.2
-
39
-
-
0031695806
-
Genetic abnormalities in hereditary hemorrhagic telangiectasia
-
Marchuk DA (1998) Genetic abnormalities in hereditary hemorrhagic telangiectasia. Current Opin Hematol 5: 332-338
-
(1998)
Current Opin Hematol
, vol.5
, pp. 332-338
-
-
Marchuk, D.A.1
-
41
-
-
0034082212
-
Angiographic and clinical characteristics of patients with cerebral arteriovenous malformations associated with hereditary hemorrhagic telangiectasia
-
Matsubara S, Manzia JL, ter Brugge K, Willinsky RA, Montanera W, Faughnan ME (2000) Angiographic and clinical characteristics of patients with cerebral arteriovenous malformations associated with hereditary hemorrhagic telangiectasia. AJNR Am J Neuroradiol 21: 1016-1020
-
(2000)
AJNR Am J Neuroradiol
, vol.21
, pp. 1016-1020
-
-
Matsubara, S.1
Manzia, J.L.2
Ter Brugge, K.3
Willinsky, R.A.4
Montanera, W.5
Faughnan, M.E.6
-
42
-
-
0028171579
-
Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary hemorrhagic telangiectasia type 1
-
McAllister KA, Grogg KM, Johnson DW et al. (1994) Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary hemorrhagic telangiectasia type 1. Nature Gen 8: 345-351
-
(1994)
Nature Gen
, vol.8
, pp. 345-351
-
-
McAllister, K.A.1
Grogg, K.M.2
Johnson, D.W.3
-
43
-
-
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 (2000) Clinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindred. Am J Med Genet 93: 320-327
-
(2000)
Am J Med Genet
, vol.93
, 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
-
44
-
-
0015877185
-
Skeletal Hemangiomatosis in association with hereditary hemorrhagic telangiectasia
-
Mirra JM, Arnold WD (1973) Skeletal Hemangiomatosis in association with hereditary hemorrhagic telangiectasia. J Bone Joint Surg 55: 850-854
-
(1973)
J Bone Joint Surg
, vol.55
, pp. 850-854
-
-
Mirra, J.M.1
Arnold, W.D.2
-
45
-
-
0025338575
-
Long-term results of treatment of vascular malformations of the gastrointestinal tract by neodymium YAG laser photocoagulation
-
Naveau S, Aubert A, Poynard T, Chaput JC (1990) Long-term results of treatment of vascular malformations of the gastrointestinal tract by neodymium YAG laser photocoagulation. Dig Dis Sci 35: 821-826
-
(1990)
Dig Dis Sci
, vol.35
, pp. 821-826
-
-
Naveau, S.1
Aubert, A.2
Poynard, T.3
Chaput, J.C.4
-
46
-
-
0001210867
-
On a family form of recurring epistaxis, associated with multiple telangiectases of the skin and mucous membranes
-
Osler W (1901) On a family form of recurring epistaxis, associated with multiple telangiectases of the skin and mucous membranes. Johns Hopkins Hosp Bull 12: 333-337
-
(1901)
Johns Hopkins Hosp Bull
, vol.12
, pp. 333-337
-
-
Osler, W.1
-
47
-
-
0019498858
-
Laser photocoagulation in hereditary hemorrhagic telangiectasia
-
Parkin, JL, Dixon JA (1981) Laser photocoagulation in hereditary hemorrhagic telangiectasia. Otolaryngol. Head Neck Surg 89: 204-208
-
(1981)
Otolaryngol Head Neck Surg
, vol.89
, pp. 204-208
-
-
Parkin, J.L.1
Dixon, J.A.2
-
48
-
-
0030014405
-
Hereditary hemorrhagic telangiectasia with extenxive liver involvment is not caused by either HHT1 or HHT2
-
Piantanida M, Buscarini E, Dellavecchia C, Minelli A, Rossi A, Buscarini L, Danesino C (1996) Hereditary hemorrhagic telangiectasia with extenxive liver involvment is not caused by either HHT1 or HHT2. J Med Gen 33: 441-443
-
(1996)
J Med Gen
, vol.33
, pp. 441-443
-
-
Piantanida, M.1
Buscarini, E.2
Dellavecchia, C.3
Minelli, A.4
Rossi, A.5
Buscarini, L.6
Danesino, C.7
-
49
-
-
0021614384
-
Épidémiologie et constitution d'un registre de population à propos d'une concentration géographique d'une maladie héréditaire rare
-
Plauchu H, Bideau A (1984) Épidémiologie et constitution d'un registre de population à propos d'une concentration géographique d'une maladie héréditaire rare. Population 4: 765-786
-
(1984)
Population
, vol.4
, pp. 765-786
-
-
Plauchu, H.1
Bideau, A.2
-
50
-
-
0024394433
-
Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population
-
Plauchu H, de Chadarevian JP, Bedeau A, Robert JM (1989) Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population. Ame J Med Gen 32: 291-297
-
(1989)
Ame J Med Gen
, vol.32
, pp. 291-297
-
-
Plauchu, H.1
De Chadarevian, J.P.2
Bedeau, A.3
Robert, J.M.4
-
51
-
-
0026683949
-
Hereditary haemorrhagic telangiectasia: A clinical analysis
-
Porteous MEM, Burn J, Proctor SJ(1992) Hereditary haemorrhagic telangiectasia: a clinical analysis. J Med Gen 29: 527-530
-
(1992)
J Med Gen
, vol.29
, pp. 527-530
-
-
Porteous, M.E.M.1
Burn, J.2
Proctor, S.J.3
-
52
-
-
0021318837
-
Clinical manifestations of hereditary hemorrhagic telangiectasia
-
Reilly PJ, Nostrant TT (1984) Clinical manifestations of hereditary hemorrhagic telangiectasia. Am J Gastroent 79: 363-367
-
(1984)
Am J Gastroent
, vol.79
, pp. 363-367
-
-
Reilly, P.J.1
Nostrant, T.T.2
-
53
-
-
0001524076
-
Épistaxis répétées chez un sujet porteur de petits angiomes cutanés et muqueux
-
Rendu M (1896) Épistaxis répétées chez un sujet porteur de petits angiomes cutanés et muqueux. Bull Soc Méd Hôp (Paris) 13: 731-733
-
(1896)
Bull Soc Méd Hôp (Paris)
, vol.13
, pp. 731-733
-
-
Rendu, M.1
-
54
-
-
0034028903
-
Embolotherapy in the bronchial and pulmonary circulations
-
Saluja S, Henderson KJ, White RI Jr (2000) Embolotherapy in the bronchial and pulmonary circulations. Radiol Clin North Am 38: 425-448
-
(2000)
Radiol Clin North Am
, vol.38
, pp. 425-448
-
-
Saluja, S.1
Henderson, K.J.2
White, R.I.3
-
55
-
-
18844464079
-
La fermeture bilaterale des fosses nasales. Une technique chirurgicale originale du traitement des epistaxis recidivantes graves de la maladie de rendu-osler
-
Serrano E, Percodani J, Pessey JJ (1998) La fermeture bilaterale des fosses nasales. Une technique chirurgicale originale du traitement des epistaxis recidivantes graves de la maladie de Rendu-Osler. Ann Otolaryngol Chir Cervicofac 115: 169-73
-
(1998)
Ann Otolaryngol Chir Cervicofac
, vol.115
, pp. 169-173
-
-
Serrano, E.1
Percodani, J.2
Pessey, J.J.3
-
56
-
-
0021720691
-
Treatment of hereditary hemorrhagic telangiectasia by Nd-YAG laser photocoagulation
-
Shapshay MS, Oliver P (1984) Treatment of hereditary hemorrhagic telangiectasia by Nd-YAG laser photocoagulation. Laryngoscope 94: 1554-1556
-
(1984)
Laryngoscope
, vol.94
, pp. 1554-1556
-
-
Shapshay, M.S.1
Oliver, P.2
-
57
-
-
0030878067
-
Molecular defects in rare bleeding disorders: Hereditary hemorrhagic telangiectasia
-
Shovlin CL (1997) Molecular defects in rare bleeding disorders: hereditary hemorrhagic telangiectasia. Thromb Haemostasis 78: 145-150
-
(1997)
Thromb Haemostasis
, vol.78
, pp. 145-150
-
-
Shovlin, C.L.1
-
58
-
-
0034007163
-
Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)
-
Shovlin CL, Guttmacher AE, Buscarini E et al. (2000) Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Gen 91: 66-67
-
(2000)
Am J Med Gen
, vol.91
, pp. 66-67
-
-
Shovlin, C.L.1
Guttmacher, A.E.2
Buscarini, E.3
-
59
-
-
0030860380
-
Characterization of endoglin and identification of novel mutations in hereditary hemorrhagic telangiectasia
-
Shovlin C, Hughes JMB, Scott J, Seidman E, Seidman JG (1997) Characterization of endoglin and identification of novel mutations in hereditary hemorrhagic telangiectasia. Am J Hum Genet 61: 68-79
-
(1997)
Am J Hum Genet
, vol.61
, pp. 68-79
-
-
Shovlin, C.1
Hughes, J.M.B.2
Scott, J.3
Seidman, E.4
Seidman, J.G.5
-
60
-
-
0032799731
-
Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: Issues in clinical management and review of pathogenic mechanisms
-
Shovlin CL, Letarte M (1999) Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms. Thorax 54: 714-29
-
(1999)
Thorax
, vol.54
, pp. 714-729
-
-
Shovlin, C.L.1
Letarte, M.2
-
61
-
-
0029563707
-
Medical complications of pregnancy in hereditary hemorrhagic telangiectasia
-
Shovlin CL, Winstock AR, Peters AM, Jackson JE, Hughes JMB (1995) Medical complications of pregnancy in hereditary hemorrhagic telangiectasia. Quart J Med 88: 879-887
-
(1995)
Quart J Med
, vol.88
, pp. 879-887
-
-
Shovlin, C.L.1
Winstock, A.R.2
Peters, A.M.3
Jackson, J.E.4
Hughes, J.M.B.5
-
62
-
-
0000391083
-
Clinical and experimental. Studies in human inheritance. Is the homozygous form of multiple telangiectasia lethal?
-
Snyder LH, Doan CA (1944) Clinical and experimental. Studies in human inheritance. Is the homozygous form of multiple telangiectasia lethal? J Lab Clin Med 29: 1211-1216
-
(1944)
J Lab Clin Med
, vol.29
, pp. 1211-1216
-
-
Snyder, L.H.1
Doan, C.A.2
-
63
-
-
0030334345
-
Interventionelle endoskopie mit dem argon-plasma-koagulator: Erfahrungen in der allgemeinchirurgie
-
Spies T, Stinner B, Guercio M, Rothmund M (1996) Interventionelle Endoskopie mit dem Argon-Plasma-Koagulator: Erfahrungen in der Allgemeinchirurgie. Langenbecks Arch Chir Kongressbd 113 [Suppl]: 537-539
-
(1996)
Langenbecks Arch Chir Kongressbd
, vol.113
, pp. 537-539
-
-
Spies, T.1
Stinner, B.2
Guercio, M.3
Rothmund, M.4
-
64
-
-
0028968906
-
Recurrent cerebral abscesses 20 years before recognition of multiple pulmonary arteriovenous malformations
-
Suresh CG, Coupe MO, Jegarajah S (1995) Recurrent cerebral abscesses 20 years before recognition of multiple pulmonary arteriovenous malformations. Br J Clin Pract 49: 105-106
-
(1995)
Br J Clin Pract
, vol.49
, pp. 105-106
-
-
Suresh, C.G.1
Coupe, M.O.2
Jegarajah, S.3
-
65
-
-
0001506230
-
Epistaxis as an indication of impaired nutrition, and of degeneration of the vascular system
-
Sutton HG (1864) Epistaxis as an indication of impaired nutrition, and of degeneration of the vascular system. Medical Mirror 1: 769-781
-
(1864)
Medical Mirror
, vol.1
, pp. 769-781
-
-
Sutton, H.G.1
-
66
-
-
0027500608
-
Unruptured intracranial arteriovenous malformations with hereditary haemorrhagic telangiectasia. Neurosurgical treatment or not?
-
Berg JW, Dippel DW, Habbema JD, Westermann CJ, Tulleken CA, Willemse J (1993) Unruptured intracranial arteriovenous malformations with hereditary haemorrhagic telangiectasia. Neurosurgical treatment or not? Acta Neurochir (Wien) 121: 34-42
-
(1993)
Acta Neurochir (Wien)
, vol.121
, pp. 34-42
-
-
Berg, J.W.1
Dippel, D.W.2
Habbema, J.D.3
Westermann, C.J.4
Tulleken, C.A.5
Willemse, J.6
-
67
-
-
0028841271
-
Correlation of the angioarchitectural features of cerebral arteriovenous malformations with clinical presentation of hemorrhage
-
Turjman F, Massoud TF, Vinuela F, Sayre JW, Guglielmi G, Duckwiler G (1995) Correlation of the angioarchitectural features of cerebral arteriovenous malformations with clinical presentation of hemorrhage. Neurosurgery 37: 856-860
-
(1995)
Neurosurgery
, vol.37
, pp. 856-860
-
-
Turjman, F.1
Massoud, T.F.2
Vinuela, F.3
Sayre, J.W.4
Guglielmi, G.5
Duckwiler, G.6
-
68
-
-
0027207868
-
Prominent telangiectasia associated with marked bleeding in CREST syndrome
-
Ueda M, Abe Y, Fujiwara H et al. (1993) Prominent telangiectasia associated with marked bleeding in CREST syndrome. J Dermatol 20: 180-184
-
(1993)
J Dermatol
, vol.20
, pp. 180-184
-
-
Ueda, M.1
Abe, Y.2
Fujiwara, H.3
-
69
-
-
0033910409
-
A hereditary hemorrhagic telangiectasia family with pulmonary involvement is unlinked to the known HHT genes, endoglin and ALK-1
-
Wallace GM, Shovlin CL (2000) A hereditary hemorrhagic telangiectasia family with pulmonary involvement is unlinked to the known HHT genes, endoglin and ALK-1. Thorax 55: 685-690
-
(2000)
Thorax
, vol.55
, pp. 685-690
-
-
Wallace, G.M.1
Shovlin, C.L.2
-
70
-
-
50249209093
-
Multiple hereditary developmental angiomata (teleangiectases) of the skin and mucous membranes associated with recurring haemorrhages
-
Weber FP (1907) Multiple hereditary developmental angiomata (teleangiectases) of the skin and mucous membranes associated with recurring haemorrhages. Lancet 2: 160-162
-
(1907)
Lancet
, vol.2
, pp. 160-162
-
-
Weber, F.P.1
-
71
-
-
0030826815
-
Behandlung der rezidivierenden epistaxis beim morbus rendu-osler-weber
-
Werner JA, Geisthoff UW, Lippert BM, Rudert H (1997) Behandlung der rezidivierenden Epistaxis beim Morbus Rendu-Osler-Weber. HNO 45: 673-681
-
(1997)
HNO
, vol.45
, pp. 673-681
-
-
Werner, J.A.1
Geisthoff, U.W.2
Lippert, B.M.3
Rudert, H.4
-
72
-
-
0026601001
-
Pulmonary arteriovenous malformations: How to diagnose them and why is it important to do so?
-
White RI Jr (1992) Pulmonary arteriovenous malformations: how to diagnose them and why is it important to do so? Radiology 182: 633-635
-
(1992)
Radiology
, vol.182
, pp. 633-635
-
-
White, R.I.1
-
74
-
-
0023684756
-
Pulmonary arteriovenous malformations: Techniques and long-term outcome of embolotherapy
-
White RI Jr, Lynch-Nyhan A, Terry P et al. (1988) Pulmonary arteriovenous malformations: techniques and long-term outcome of embolotherapy. Radiology 169: 663-669
-
(1988)
Radiology
, vol.169
, pp. 663-669
-
-
White, R.I.1
Lynch-Nyhan, A.2
Terry, P.3
-
75
-
-
0025282668
-
Multiple cerebral arteriovenous malformations (AVMs). Review of our experience from 203 patients with cerebral vascular lesions
-
Willinsky RA, Lasjaunias P, Terbrugge K, Burrows P (1990) Multiple cerebral arteriovenous malformations (AVMs). Review of our experience from 203 patients with cerebral vascular lesions. Neuroradiology 32: 207-10
-
(1990)
Neuroradiology
, vol.32
, pp. 207-210
-
-
Willinsky, R.A.1
Lasjaunias, P.2
Terbrugge, K.3
Burrows, P.4
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