-
1
-
-
0033767899
-
Severe organ involvement in systemic sclerosis with diffuse scleroderma
-
Steen VD, Medsger TA,Jr. Severe organ involvement in systemic sclerosis with diffuse scleroderma. Arthritis Rheum 2000;43:2437-44.
-
(2000)
Arthritis Rheum
, vol.43
, pp. 2437-2444
-
-
Steen, V.D.1
Medsger Jr., T.A.2
-
2
-
-
4444243652
-
Vascular involvement in systemic sclerosis
-
Kahaleh BM. Vascular involvement in systemic sclerosis. Clin Exp Rheumatol 2004;22(Suppl 33):S19-23.
-
(2004)
Clin Exp Rheumatol
, vol.22
, Issue.SUPPL. 33
-
-
Kahaleh, B.M.1
-
3
-
-
33749329543
-
Clinical differences between idiopathic and scleroderma-related pulmonary hypertension
-
Fisher MR, Mathai SC, Champion HC et al. Clinical differences between idiopathic and scleroderma-related pulmonary hypertension. Arthritis Rheum 2006;54:3043-50.
-
(2006)
Arthritis Rheum
, vol.54
, pp. 3043-3050
-
-
Fisher, M.R.1
Mathai, S.C.2
Champion, H.C.3
-
4
-
-
0035038492
-
Pulmonary hypertension in systemic sclerosis: Risk factors for progression and consequences for survival
-
MacGregor AJ, Canavan R, Knight C et al. Pulmonary hypertension in systemic sclerosis: Risk factors for progression and consequences for survival. Rheumatology 2001;40:453-9.
-
(2001)
Rheumatology
, vol.40
, pp. 453-459
-
-
MacGregor, A.J.1
Canavan, R.2
Knight, C.3
-
5
-
-
23644431874
-
Evaluation and management of the patient with pulmonary arterial hypertension
-
Rubin LJ, Badesch DB. Evaluation and management of the patient with pulmonary arterial hypertension. Ann Intern Med 2005;143: 282-92.
-
(2005)
Ann Intern Med
, vol.143
, pp. 282-292
-
-
Rubin, L.J.1
Badesch, D.B.2
-
6
-
-
27544506082
-
Genetics of scleroderma: Update on single nucleotide polymorphism analysis and microarrays
-
Assassi S, Tan FK. Genetics of scleroderma: Update on single nucleotide polymorphism analysis and microarrays. Curr Opin Rheumatol 2005;17:761-7.
-
(2005)
Curr Opin Rheumatol
, vol.17
, pp. 761-767
-
-
Assassi, S.1
Tan, F.K.2
-
7
-
-
0034965980
-
Familial occurrence frequencies and relative risk for systemic sclerosis (scleroderma) in three United States cohort
-
Arnett FC, Cho M, Chatterjee S et al. Familial occurrence frequencies and relative risk for systemic sclerosis (scleroderma) in three United States cohort. Arthritis Rheum 2001;44:1359-62.
-
(2001)
Arthritis Rheum
, vol.44
, pp. 1359-1362
-
-
Arnett, F.C.1
Cho, M.2
Chatterjee, S.3
-
9
-
-
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;91:66-8.
-
(2000)
Am J Med Genet
, vol.91
, pp. 66-68
-
-
Shovlin, C.L.1
Guttmacher, A.E.2
Buscarini, E.3
-
10
-
-
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
-
11
-
-
33646109750
-
Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1
-
Fernandez A, 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, A.1
Sanz-Rodriguez, F.2
Zarrabeitia, R.3
-
12
-
-
0032926250
-
Polymorphism of the endoglin gene in patients with intracranial saccular aneurysms
-
Takenaka K, Sakai H, Yamakawa H et al. Polymorphism of the endoglin gene in patients with intracranial saccular aneurysms. J Neurosurg 1999;90:935-8.
-
(1999)
J Neurosurg
, vol.90
, pp. 935-938
-
-
Takenaka, K.1
Sakai, H.2
Yamakawa, H.3
-
13
-
-
0035168847
-
Lack of association between endoglin intron 7 insertion polymorphism and intracranial aneurysms in a white population: Evidence of racial/ethnic differences
-
Krex D, Ziegler A, Schackert HK, Schackert G. Lack of association between endoglin intron 7 insertion polymorphism and intracranial aneurysms in a white population: Evidence of racial/ethnic differences. Stroke 2001;32:2689-94.
-
(2001)
Stroke
, vol.32
, pp. 2689-2694
-
-
Krex, D.1
Ziegler, A.2
Schackert, H.K.3
Schackert, G.4
-
14
-
-
0023854176
-
Scleroderma (systemic sclerosis): Classification, subsets and pathogenesis
-
Leroy EC, Black C, Fleischmajer R et al. Scleroderma (systemic sclerosis): Classification, subsets and pathogenesis. J Rheumatol 1988; 15:202-5.
-
(1988)
J Rheumatol
, vol.15
, pp. 202-205
-
-
Leroy, E.C.1
Black, C.2
Fleischmajer, R.3
-
15
-
-
0022465236
-
Development of criteria for the classification and reporting of osteoarthritis. Classification of osteoarthritis of the knee
-
Diagnostic and Therapeutic Criteria Committee of the American Rheumatism Association
-
Altman R, Asch E, Bloch D et al. Development of criteria for the classification and reporting of osteoarthritis. Classification of osteoarthritis of the knee. Diagnostic and Therapeutic Criteria Committee of the American Rheumatism Association. Arthritis Rheum 1986;29:1039-49.
-
(1986)
Arthritis Rheum
, vol.29
, pp. 1039-1049
-
-
Altman, R.1
Asch, E.2
Bloch, D.3
-
16
-
-
23644436719
-
Diagnosis and management of pulmonary arterial hypertension: ACCP evidence-based clinical practice guideline
-
Diagnosis and management of pulmonary arterial hypertension: ACCP evidence-based clinical practice guideline. Chest 2004; 125(Suppl):1S-92S.
-
(2004)
Chest
, vol.125
, Issue.SUPPL.
-
-
-
17
-
-
0142058057
-
Assessment of lung involvement
-
Matucci Cerinic M, D'Angelo S, Denton C, Vlachoyannopoulos P, Silver R. Assessment of lung involvement. Clin Exp Rheumatol 2003;21(Suppl 29):S19.
-
(2003)
Clin Exp Rheumatol
, vol.21
, Issue.SUPPL. 29
-
-
Matucci Cerinic, M.1
D'Angelo, S.2
Denton, C.3
Vlachoyannopoulos, P.4
Silver, R.5
-
18
-
-
0142187600
-
Prevalence and outcome in systemic sclerosis associated pulmonary hypertension: Application of a registry approach
-
Mukerjee D, St George D, Knight C et al. Prevalence and outcome in systemic sclerosis associated pulmonary hypertension: Application of a registry approach. Ann Rheum Dis 2003;62:1088-93.
-
(2003)
Ann Rheum Dis
, vol.62
, pp. 1088-1093
-
-
Mukerjee, D.1
St George, D.2
Knight, C.3
-
19
-
-
4644290657
-
Treatment of pulmonary arterial hypertension
-
Humbert M, Sitbon O, Simonneau G. Treatment of pulmonary arterial hypertension. N Engl J Med 2004;351:1425-36.
-
(2004)
N Engl J Med
, vol.351
, pp. 1425-1436
-
-
Humbert, M.1
Sitbon, O.2
Simonneau, G.3
-
20
-
-
32544458797
-
Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertension
-
Machado RD, Aldred MA, James V et al. Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertension. Hum Mutat 2006;27:121-32.
-
(2006)
Hum Mutat
, vol.27
, pp. 121-132
-
-
Machado, R.D.1
Aldred, M.A.2
James, V.3
-
21
-
-
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
-
22
-
-
2442519516
-
Endoglin germline mutation in a patient with hereditary haemorrhagic telangiectasia and dexfenfluramine associated pulmonary arterial hypertension
-
Chaouat A, Coulet F, Favre C et al. Endoglin germline mutation in a patient with hereditary haemorrhagic telangiectasia and dexfenfluramine associated pulmonary arterial hypertension. Thorax 2004;59:446-8.
-
(2004)
Thorax
, vol.59
, pp. 446-448
-
-
Chaouat, A.1
Coulet, F.2
Favre, C.3
-
23
-
-
13444256185
-
Transforming growth factor-beta receptor mutations and pulmonary arterial hypertension in childhood
-
Harrison RE, Berger R, Haworth SG et al. Transforming growth factor-beta receptor mutations and pulmonary arterial hypertension in childhood. Circulation 2005;111:435-41.
-
(2005)
Circulation
, vol.111
, pp. 435-441
-
-
Harrison, R.E.1
Berger, R.2
Haworth, S.G.3
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