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4 resultados
[Clinical and laboratory studies on 28 patients with glutaric aciduria type 1].
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OBJECTIVE
To investigate the clinical, biochemical and genetic profiles of 28 Chinese patients with glutaric aciduria type 1.
METHODS
Twenty-eight patients with glutaric aciduria type 1 seen in the Department of Pediatrics, Peking University First Hospital from July 2003 to October 2013 were
Diagnosis and management of acute movement disorders.
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Most movement disorders, reflecting degenerative disorders, develop in a slowly progressive fashion. Some movement disorders, however, manifest with an acute onset. We wish to give an overview of the management and therapy of those acute-onset movement disorders.Drug-induced movement disorders are
[NMDA receptor encephalitis in the course of recurrent CNS demyelinating disorders: a case report].
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We present the case of a 31-year-old woman who developed N-methyl-d-aspartate (NMDA) receptor encephalitis during the course of relapsing and remitting multiple brain lesions. The patient developed a tingling sensation in the left upper and lower extremities, and was first admitted to our hospital
[The different present-day clinical picture of human African trypanosomiasis caused by T. b. gambiense. Analysis of 300 cases from a focus in Daloa, Ivory Coast].
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300 patients with sleeping sickness have been admitted, at the AHT clinic of Daloa, over a time period of 22 months. The sex ratio of the patients is 1.5 males for 1 female; the mean age is 25.5 years. The most frequent signs and symptoms observed by clinical examination are: fever (30%), nodes
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- Funciona em 55 idiomas
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* Todas as informações são baseadas em pesquisas científicas publicadas
