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Prefrontal syndrome as a manifestation of intracranial dural arterio-venous mal...

Cerqueira, L; Serviço de Neurorradiologia, Hospital de Santo António dos Capuchos, Lisboa.; Coimbra, J; Matos, E; Reis, F C; Beirão, J C

The authors present a clinical case of an intracranial dural arteriovenous malformation with clinical manifestations of a prefrontal syndrome, documented with its respective diagnostic tests, including imaging studies. A number of considerations are being enlarged upon, concerning possible pathophysiological mechanisms. ; The authors present a clinical case of an intracranial dural arteriovenous malformation w...

Data: 1992   |   Origem: Acta Médica Portuguesa

Orphan diseases and drugs.

Beirão, J C

Data: 1970   |   Origem: Acta Médica Portuguesa

The semiology and classification of myoclonias.

Almeida, R; Serviço de Neurologia, Hospital de Sto António dos Capuchos, Lisboa.; Gonçalves, M; Viana, J P; Beirão, J C

Myoclonus can present itself in various distinct clinical contexts. The authors review the possible different types of myoclonus, as a single manifestation or included in a syndrome, based on a semiological and aetiological classification. Special emphasis is given to the group of progressive myoclonus epilepsies. ; Myoclonus can present itself in various distinct clinical contexts. The authors review the poss...

Data: 1970   |   Origem: Acta Médica Portuguesa


Cerebrovascular disorders in young subjects and deficit of protein S.

Gonçalves, M; Serviço de Neurologia, Hospital de Santo António dos Capuchos.; Beirão, J C

The authors describe a right hemiparesis and global aphasia, suddenly developed in a 33-Year-old woman, with a previous aphasia, 7 years ago, from which she recovered without sequels. They discuss the relationship between protein inhibitor of blood coagulation and arterial thrombosis, and make references to what has been published about it. ; The authors describe a right hemiparesis and global aphasia, suddenl...

Data: 1970   |   Origem: Acta Médica Portuguesa

Familial peripheral neuropathy caused by susceptibility to entrapment (tomaculo...

Viana, J P; Serviço de Neurologia, Hospital de Santo António dos Capuchos, Lisboa.; Coimbra, J; Goulart, Z; de Almeida, L B; Beirão, J C

The authors describe a case of hereditary neuropathy with liability to pressure palsies (entrapment), and compare it to reports from literature. The main characteristics are: autosomal dominant inheritance, recurrent mononeuropathies (ulnar, median, peroneal, brachial plexus), and specific features at nerve biopsy. The sensory nerve reveals predominantly demyelinating alterations, having the remaining myelin fi...

Data: 1970   |   Origem: Acta Médica Portuguesa

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Fundação para a Ciência e a Tecnologia Universidade do Minho   Governo Português Ministério da Educação e Ciência Programa Operacional da Sociedade do Conhecimento União Europeia