-
1
-
-
34347266509
-
Changes in causes of death in systemic sclerosis, 1972-2002
-
DOI 10.1136/ard.2006.066068
-
Steen VD, Medsger TA. Changes in causes of death in systemic sclerosis, 1972-2002. Ann Rheum Dis 2007;66 :940-4. (Pubitemid 46999798)
-
(2007)
Annals of the Rheumatic Diseases
, vol.66
, Issue.7
, pp. 940-944
-
-
Steen, V.D.1
Medsger, T.A.2
-
2
-
-
33645319446
-
Genetic association of the serotonin transporter in pulmonary arterial hypertension
-
Machado RD, Koehler R, Glissmeyer E, et al. Genetic association of the serotonin transporter in pulmonary arterial hypertension. Am J Respir Crit Care Med 2006;173:793-7.
-
(2006)
Am J Respir Crit Care Med
, vol.173
, pp. 793-797
-
-
Machado, R.D.1
Koehler, R.2
Glissmeyer, E.3
-
3
-
-
33748314526
-
High frequency of BMPR2 exonic deletions/duplications in familial pulmonary arterial hypertension
-
DOI 10.1164/rccm.200602-165OC
-
Cogan JD, Pauciulo MW, Batchman AP, et al. High frequency of BMPR2 exonic deletions/duplications in familial pulmonary arterial hypertension. Am J Respir Crit Care Med 2006;174:590-8. (Pubitemid 44330553)
-
(2006)
American Journal of Respiratory and Critical Care Medicine
, vol.174
, Issue.5
, pp. 590-598
-
-
Cogan, J.D.1
Pauciulo, M.W.2
Batchman, A.P.3
Prince, M.A.4
Robbins, I.M.5
Hedges, L.K.6
Stanton, K.C.7
Wheeler, L.A.8
Phillips III, J.A.9
Loyd, J.E.10
Nichols, W.C.11
-
4
-
-
67649573380
-
Genetics and genomics of pulmonary arterial hypertension
-
Machado RD, Eickelberg O, Elliott CG, et al. Genetics and genomics of pulmonary arterial hypertension. J Am Coll Cardiol 2009;54(Suppl 1):S32-42.
-
(2009)
J Am Coll Cardiol
, vol.54
, Issue.SUPPL. 1
-
-
Machado, R.D.1
Eickelberg, O.2
Elliott, C.G.3
-
5
-
-
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 identi fies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia. J Med Genet 2003;40:865-71. (Pubitemid 38117534)
-
(2003)
Journal of Medical Genetics
, vol.40
, Issue.12
, pp. 865-871
-
-
Harrison, R.E.1
Flanagan, J.A.2
Sankelo, M.3
Abdalla, S.A.4
Rowell, J.5
Machado, R.D.6
Elliott, C.G.7
Robbins, I.M.8
Olschewski, H.9
McLaughlin, V.10
Gruenig, E.11
Kermeen, F.12
Laitinen, T.13
Morrell, N.W.14
Halme, M.15
Raisanen-Sakolowski16
Trembath, R.C.17
-
6
-
-
65549132025
-
Genetics of systemic sclerosis-associated pulmonary arterial hypertension: Recent progress and current concepts
-
Shah SJ. Genetics of systemic sclerosis-associated pulmonary arterial hypertension: recent progress and current concepts. Curr Rheumatol Rep 2009;11:89-96.
-
(2009)
Curr Rheumatol Rep
, vol.11
, pp. 89-96
-
-
Shah, S.J.1
-
7
-
-
0036822548
-
Mutations of bone morphogenetic protein receptor type II are not found in patients with pulmonary hypertension and underlying connective tissue diseases [6]
-
DOI 10.1002/art.10487
-
Tew MB, Arnett FC, Reveille JD, et al. Mutations of bone morphogenetic protein receptor type II are not found in patients with pulmonary hypertension and underlying connective tissue diseases. Arthritis Rheum 2002;46:2829-30. (Pubitemid 36118956)
-
(2002)
Arthritis and Rheumatism
, vol.46
, Issue.10
, pp. 2829-2830
-
-
Tew, M.B.1
Arnett, F.C.2
Reveille, J.D.3
Tan, F.K.4
-
8
-
-
0036844311
-
Pulmonary hypertension in scleroderma spectrum of disease: Lack of bone morphogenetic protein receptor 2 mutations
-
Morse J, Barst R, Horn E, et al. Pulmonary hypertension in scleroderma spectrum of disease: lack of bone morphogenetic protein receptor 2 mutations. J Rheumatol 2002;29:2379-81. (Pubitemid 35266029)
-
(2002)
Journal of Rheumatology
, vol.29
, Issue.11
, pp. 2379-2381
-
-
Morse, J.1
Barst, R.2
Horn, E.3
Cuervo, N.4
Deng, Z.5
Knowles, J.6
-
9
-
-
34250768373
-
Mutations of activin-receptor-like kinase 1 (ALK-1) are not found in patients with pulmonary hypertension and underlying connective tissue disease
-
DOI 10.1007/s10067-006-0388-x
-
Selva-O'Callaghan A, Balada E, Serrano-Acedo S, et al. Mutations of activin-receptor-like kinase 1 (ALK-1) are not found in patients with pulmonary hypertension and underlying connective tissue disease. Clin Rheumatol 2007;26:947-9. (Pubitemid 46951295)
-
(2007)
Clinical Rheumatology
, vol.26
, Issue.6
, pp. 947-949
-
-
Selva-O'Callaghan, A.1
Balada, E.2
Serrano-Acedo, S.3
Simeon, A.C.P.4
Ordi-Ros, J.5
-
10
-
-
79960934301
-
Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis
-
Allanore Y, Saad M, Dieudé P, et al. Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis. PLoS Genet 2011;7:e1002091.
-
(2011)
PLoS Genet
, vol.7
-
-
Allanore, Y.1
Saad, M.2
Dieudé, P.3
-
11
-
-
0023854176
-
Scleroderma (systemic sclerosis): classification, subsets and pathogenesis
-
editorial
-
LeRoy EC, Black C, Fleischmajer R, et al. Scleroderma (systemic sclerosis): classification, subsets and pathogenesis [editorial]. J Rheumatol 1988;15:202-5.
-
(1988)
J Rheumatol
, vol.15
, pp. 202-205
-
-
LeRoy, E.C.1
Black, C.2
Fleischmajer, R.3
-
12
-
-
80052339811
-
Prediction of pulmonary hypertension related to systemic sclerosis by an index based on simple clinical observations
-
Meune C, Avouac J, Airò P, et al. Prediction of pulmonary hypertension related to systemic sclerosis by an index based on simple clinical observations. Arthritis Rheum 2011; 63:2790-6.
-
(2011)
Arthritis Rheum
, vol.63
, pp. 2790-2796
-
-
Meune, C.1
Avouac, J.2
Airò, P.3
-
13
-
-
79953687390
-
Association of the CD226 Ser(307) variant with systemic sclerosis: Evidence of a contribution of costimulation pathways in systemic sclerosis pathogenesis
-
Dieudé P, Guedj M, Truchetet ME, et al. Association of the CD226 Ser(307) variant with systemic sclerosis: evidence of a contribution of costimulation pathways in systemic sclerosis pathogenesis. Arthritis Rheum 2011;63:1097-105.
-
(2011)
Arthritis Rheum
, vol.63
, pp. 1097-1105
-
-
Dieudé, P.1
Guedj, M.2
Truchetet, M.E.3
-
14
-
-
33144462810
-
Hereditary haemorrhagic telangiectasia: Current views on genetics and mechanisms of disease
-
DOI 10.1136/jmg.2005.030833
-
Abdalla SA, Letarte M. Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease. J Med Genet 2006;43:97-110. (Pubitemid 43262964)
-
(2006)
Journal of Medical Genetics
, vol.43
, Issue.2
, pp. 97-110
-
-
Abdalla, S.A.1
Letarte, M.2
-
15
-
-
34047123228
-
Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension
-
DOI 10.1093/rheumatology/kel378
-
Wipff J, Kahan A, Hachulla E, et al. Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension. Rheumatology 2007;46:622-5. (Pubitemid 46523307)
-
(2007)
Rheumatology
, vol.46
, Issue.4
, pp. 622-625
-
-
Wipff, J.1
Kahan, A.2
Hachulla, E.3
Sibilia, J.4
Cabane, J.5
Meyer, O.6
Mouthon, L.7
Guillevin, L.8
Junien, C.9
Boileau, C.10
Allanore, Y.11
-
16
-
-
81255136932
-
Molecular genetic characterization of SMAD signaling molecules in pulmonary arterial hypertension
-
Nasim MT, Ogo T, Ahmed M, et al. Molecular genetic characterization of SMAD signaling molecules in pulmonary arterial hypertension. Hum Mutat 2011;32:1385-9.
-
(2011)
Hum Mutat
, vol.32
, pp. 1385-1389
-
-
Nasim, M.T.1
Ogo, T.2
Ahmed, M.3
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