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Mostrando ítems 11-20 de 38
Aneurisma roto de aorta torácica descendente: tratamiento endovascular
(Sociedad Médica de Santiago, 2001)
Modified 'Stent-Graft Sandwich' Technique for Treatment of Isolated Common Iliac Artery Aneurysm in Patient With Marfan Syndrome
(Elsevier B.V., 2012-04-01)
Isolated iliac artery aneurysms are rare in the general population (0.03%) and represent 2% of all abdominal aneurysms, and the association with Marfan syndrome is even rarer. We report a Marfan syndrome case with an ...
Immediate effects of submaximal effort on pulse wave velocity in patients with Marfan syndrome
(Associação Brasileira de Divulgação Científica, 2010-04-01)
Marfan syndrome (MS) is a dominant autosomal disease caused by mutations in chromosome 15, the locus controlling fibrillin 1 synthesis, and may exhibit skeletal, ocular, cardiovascular, and other manifestations. Pulse wave ...
Syndromic and non-syndromic aneurysms of the human ascending aorta share activation of the Smad2 pathway
(JOHN WILEY & SONS LTD, 2009)
Common features such as elastic fibre destruction, mucoid accumulation, and smooth muscle cell apoptosis are co-localized in aneurysms of the ascending aorta of various aetiologies. Recent experimental studies reported an ...
Avaliação antropométrica e músculo esquelética de pacientes com síndrome de MarfanAnthropometric and musculoskeletal assessment of patients with Marfan syndrome
(Associação Brasileira de Pesquisa e Pós-Graduação em Fisioterapia, 2012)
Avaliação clínico-cardiológica e ecocardiográfica, seqüencial, em crianças portadoras da síndrome de Marfan
(Sociedade Brasileira de Cardiologia - SBC, 2005-11-01)
OBJECTIVE: To describe the clinical cardiac manifestations and temporal evolution of Marfan syndrome in children; to estimate the incidence of annuloaortic ectasia and mitral valve prolapse; and to evaluate tolerability ...
CorrectionBraz J Med Biol Res 2011; 44(8): 793-800Candidate gene linkage analysis indicates genetic heterogeneity in Marfan syndrome
(Associação Brasileira de Divulgação Científica, 2011-10-01)
CorrectionBraz J Med Biol Res 2011; 44(8): 793-800Candidate gene linkage analysis indicates genetic heterogeneity in Marfan syndrome
(Associação Brasileira de Divulgação Científica, 2011)
Estrategias terapéuticas de aneurisma abdominal en sindrome de Marfan a propósito de un caso
(Universidad de Cuenca. Facultad de Ciencias Médicas, 2014)
Avaliação antropométrica e musculoesquelética de pacientes com síndrome de Marfan
(Associação Brasileira de Pesquisa e Pós-Graduação em Fisioterapia, 2011-08-01)
BACKGROUND: Marfan syndrome (MS) is an autosomic dominant condition of the connective tissue that involves the ocular, cardiovascular and musculoskeletal systems. MS is caused by mutations in the fibrillin-1 gene, leading ...