-
1
-
-
36349008161
-
Practice parameter: evaluating an apparent unprovoked first seizure in adults (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology and the American Epilepsy Society
-
Ksrumholz A, Wiebe S, Gronseth G, et al. Practice parameter: evaluating an apparent unprovoked first seizure in adults (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology and the American Epilepsy Society. Neurology 2007; 69:1996-2007.
-
(2007)
Neurology
, vol.69
, pp. 1996-2007
-
-
Ksrumholz, A.1
Wiebe, S.2
Gronseth, G.3
-
2
-
-
0032720393
-
A murine model of hereditary hemorrhagic telangiectasia
-
Bourdeau A, Dumont DJ, Letarte M. A murine model of hereditary hemorrhagic telangiectasia. J Clin Invest 1999; 104:1343-1351.
-
(1999)
J Clin Invest
, vol.104
, pp. 1343-1351
-
-
Bourdeau, A.1
Dumont, D.J.2
Letarte, M.3
-
3
-
-
0036164129
-
Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan
-
Dakeishi M, Shioya T, Wada Y, et al. Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan. Hum Mutat 2002; 19:140-148.
-
(2002)
Hum Mutat
, vol.19
, pp. 140-148
-
-
Dakeishi, M.1
Shioya, T.2
Wada, Y.3
-
5
-
-
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; 91:66-67.
-
(2000)
Am J Med Genet
, vol.91
, pp. 66-67
-
-
Shovlin, C.L.1
Guttmacher, A.E.2
Buscarini, E.3
-
6
-
-
31144450942
-
Emergencies in hereditary haemorrhagic telangiectasia
-
Gallitelli M, Pasculli G, Fiore T, Carella A, Sabbà C. Emergencies in hereditary haemorrhagic telangiectasia. QJM 2006; 99:15-22.
-
(2006)
QJM
, vol.99
, pp. 15-22
-
-
Gallitelli, M.1
Pasculli, G.2
Fiore, T.3
Carella, A.4
Sabbà, C.5
-
9
-
-
0032799731
-
Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms
-
Shovlin CL, Letarte M. Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms. Thorax 1999; 54:714-729.
-
(1999)
Thorax
, vol.54
, pp. 714-729
-
-
Shovlin, C.L.1
Letarte, M.2
-
10
-
-
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 R.I. Jr3
-
11
-
-
0028585971
-
Genetic heterogenicity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype
-
McAllister KA, Lennon F, Bowles-Biesecker B, et al. Genetic heterogenicity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype. J Med Genet 1994; 31:927-932.
-
(1994)
J Med Genet
, vol.31
, pp. 927-932
-
-
McAllister, K.A.1
Lennon, F.2
Bowles-Biesecker, B.3
-
12
-
-
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; 32:291-297.
-
(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
-
13
-
-
40649111657
-
Primary determinants of ischaemic stroke/brain abscess risks are independent of severity of pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia
-
Shovlin CL, Jaskson JE, Bamford KB, et al. Primary determinants of ischaemic stroke/brain abscess risks are independent of severity of pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia. Thorax 2008; 63:259-266.
-
(2008)
Thorax
, vol.63
, pp. 259-266
-
-
Shovlin, C.L.1
Jaskson, J.E.2
Bamford, K.B.3
-
14
-
-
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; 343:931-936.
-
(2000)
N Engl J Med
, vol.343
, pp. 931-936
-
-
Garcia-Tsao, G.1
Korzenik, J.R.2
-
15
-
-
77952817788
-
-
Cooper DH, Krainik AJ, Lubner SJ, Reno HEL, editors. Philadelphia: Lippincott Williams & Wilkins, Critical care. 32nd ed
-
Kolleft MH, Micek ST. Critical care. In: Cooper DH, Krainik AJ, Lubner SJ, Reno HEL, editors. Washington Manual of Medical Therapeutics. 32nd ed. Philadelphia: Lippincott Williams & Wilkins, 2007:224-230.
-
(2007)
Washington Manual of Medical Therapeutics
, pp. 224230
-
-
Kolleft, M.H.1
Micek, S.T.2
-
16
-
-
0033065276
-
Pulmonary arteriovenous fistulas: Mayo linic experience: 1872-1997
-
Swanson KL, Prakash UB, Stanson AW. Pulmonary arteriovenous fistulas: Mayo linic experience: 1872-1997. Mayo Clin Proc 1999; 74:671-680.
-
(1999)
Mayo Clin Proc
, vol.74
, pp. 671-680
-
-
Swanson, K.L.1
Prakash, U.B.2
Stanson, A.W.3
-
18
-
-
0014558712
-
Pulmonary arteriovenous fistula: diagnosis and prognosis in noncompliant patients
-
Sluiter-Eringa H, Orie NG, Sluiter HJ. Pulmonary arteriovenous fistula: diagnosis and prognosis in noncompliant patients. Am Rev Respir Dis 1969; 100:177-188.
-
(1969)
Am Rev Respir Dis
, vol.100
, pp. 177-188
-
-
Sluiter-Eringa, H.1
Orie, N.G.2
Sluiter, H.J.3
-
20
-
-
33745314873
-
Clinical and anatomic outcomes after embolotherapy of pulmonary arteriovenous malformations
-
Pollak JS, Saluja S, Thabet A, Henderson KJ, Denbow N, White RI Jr. Clinical and anatomic outcomes after embolotherapy of pulmonary arteriovenous malformations. J Vasc Interv Radio 2006; 17:35-44.
-
(2006)
J Vasc Interv Radio
, vol.17
, pp. 35-44
-
-
Pollak, J.S.1
Saluja, S.2
Thabet, A.3
Henderson, K.J.4
Denbow, N.5
White R.I. Jr6
-
21
-
-
0030813490
-
The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2
-
Berg JN, Gallion CJ, Stenzel TT, et al. The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2. Am J Hum Genet 1997; 61:60-67.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 60-67
-
-
Berg, J.N.1
Gallion, C.J.2
Stenzel, T.T.3
-
22
-
-
0028171579
-
Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary hemorrhagic telangiectasias type 1
-
McAllister KA, Grogg KM, Johnson DW, et al. Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary hemorrhagic telangiectasias type 1. Nat Genet 1994; 8:345-351.
-
(1994)
Nat Genet
, vol.8
, pp. 345-351
-
-
McAllister, K.A.1
Grogg, K.M.2
Johnson, D.W.3
-
23
-
-
0030050973
-
Mutations in the activin receptor-like kinase gene in hereditary haemorrhagic telangeictasia type 2
-
Johnson DW, Berg JN, Baldwin MA, et al. Mutations in the activin receptor-like kinase gene in hereditary haemorrhagic telangeictasia type 2. Nat Genet 1996; 13:189-195.
-
(1996)
Nat Genet
, vol.13
, pp. 189-195
-
-
Johnson, D.W.1
Berg, J.N.2
Baldwin, M.A.3
-
24
-
-
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
-
25
-
-
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; 6:175-191.
-
(2004)
Genet Med
, vol.6
, pp. 175-191
-
-
Bayrak-Toydemir, P.1
Mao, R.2
Lewin, S.3
McDonald, J.4
-
26
-
-
24344507129
-
Cost comparison of genetic and clinical screening in families with hereditary hemorrhagic telangiectasia
-
Cohen JH, Faughnan ME, Letarte M, Vandezande K, Kennedy SJ, Krahn MD. Cost comparison of genetic and clinical screening in families with hereditary hemorrhagic telangiectasia. Am J Med Genet A 2005; 137:153-160.
-
(2005)
Am J Med Genet A
, vol.137
, pp. 153-160
-
-
Cohen, J.H.1
Faughnan, M.E.2
Letarte, M.3
Vandezande, K.4
Kennedy, S.J.5
Krahn, M.D.6
-
27
-
-
56849104879
-
Post-NICE 2008: Antibiotic prophylaxis prior to dental procedures for patients with pulmonary arteriovenous malformations (PAVMs) and hereditary haemorrhagic telangiectasia
-
Shovlin C, Bamfort K, Wray D. Post-NICE 2008: Antibiotic prophylaxis prior to dental procedures for patients with pulmonary arteriovenous malformations (PAVMs) and hereditary haemorrhagic telangiectasia. Br Dent J 2008; 205:531-533.
-
(2008)
Br Dent J
, vol.205
, pp. 531-533
-
-
Shovlin, C.1
Bamfort, K.2
Wray, D.3
-
28
-
-
16644380662
-
Desbaric air embolism during diving: an unusual complication of Osler-Weber-Rendu disease
-
Hsu YL, Wang HC, Yang PC. Desbaric air embolism during diving: an unusual complication of Osler-Weber-Rendu disease. Br J Sports Med 2004; 38:E6.
-
(2004)
Br J Sports Med
, vol.38
-
-
Hsu, Y.L.1
Wang, H.C.2
Yang, P.C.3
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