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Inherited risk factors for thrombophilia in children with nephrotic syndrome
(Springer VerlagNew YorkEUA, 1998)
Inherited risk factors for thrombophilia among children with Legg-Calve-Perthes disease
(Lippincott Williams & WilkinsPhiladelphiaEUA, 1999)
MTHFR Polymorphic Variant C677T Is Associated to Vascular Complications in Sickle-Cell Disease
(Mary Ann Liebert IncNew RochelleEUA, 2012)
Lack Of Association Between The Prothrombin Rs1799963 Polymorphism And Juvenile Myoclonic Epilepsy
(ASSOC ARQUIVOS NEURO- PSIQUIATRIASAO PAULO SP, 2015)
Molecular analysis of homocystinuria in Brazilian patients
(Elsevier B.V., 2005-12-01)
Background: Cystathionine beta-synthase (CBS) deficiency is the most common cause of homocystinuria. However, no data are available concerning the molecular basis of this disease in Brazilian populations.Methods: We studied ...
Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults
(F K Schattauer Verlag GmbhStuttgartAlemanha, 2000)