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Fraqueza Muscular Na Infância E Síndrome Do Lactente Hipotônico: Guia Para Avaliação Clínica E Propedêutica Diagnóstica
(Universidade Federal de São Paulo (UNIFESP), 2017-06-29)
On daily practice, besides having a sedimented theoretical knowledge, a neurologist must be capable of executing and interpreting a thorough neurological exam, leading to a better disclosure of patient’s complaints. This ...
Hydroanencephalia in a newborn due to congenital toxoplasmosis
(2011)
Se presenta el caso de un recién nacido de término con hidranencefalia por toxoplasmosis congénita con diagnóstico prenatal, el cual habría adquirido su infección en forma precoz durante el embarazo. Destaca madre con ...
Congenital fiber-type disproportion myopathy: a case study
(UANL. Facultad de Medicina, 2015)
Evento com aparente risco de morte recorrente como manifestação inicial de síndrome miastênica congênitaEvento con aparente riesgo de muerte recurrente como manifestación inicial de síndrome miasténico congénitoRecurrent apparent life-threatening event as the first manifestation of congenital myasthenia
(Sociedade de Pediatria de São Paulo, 2013)
Fukuyama-type congenital muscular dystrophy: a case report in the Japanese population living in Brazil
(Blackwell Munksgaard, 2002-08-01)
Introduction We present herein clinical, histological and magnetic resonance imaging (MRI) findings in a patient with Fukuyama-type congenital muscular dystrophy ( FCMD). He is the first case report in the Japanese population ...
Multi-minicore disease revisited
(Assoc Arquivos De Neuro- PsiquiatriaSao Paulo SpBrasil, 2004)
Análise da expressão do colágeno VI na distrofia muscular congênita
(Academia Brasileira de Neurologia - ABNEURO, 2005-06-01)
Congenital muscular dystrophy (CMD) composes a group of disorders characterized by hypotonia and muscular weakness noticed in the first year of life. The Ullrich's form is characterized by proximal joint contractures and ...