Uso de sugamadex em doença de Strumpell-Lorrain: relato de dois casos

Uso de sugamadex em doença de Strumpell-Lorrain: relato de dois casos

CONTEÚDO: A doença de Strumpell-Lorrain, ou paraparesia espástica familiar (PEF), é uma doença hereditária neurológica rara, caracterizada principalmente por graus variáveis de rigidez e enfraquecimento dos músculos, com comprometimento cognitivo, surdez e ataxia nos casos mais graves. Descrevemos o...

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Bibliographic Details
Main Authors:	José Antonio Franco-Hernández, Luis Munoz Rodríguez, Pilar Jubera Ortiz de Landázuri, Alejandra Garcia Hernández
Format:	Article
Language:	English
Published:	Sociedade Brasileira de Anestesiologia 2013-02-01
Series:	Revista Brasileira de Anestesiologia
Subjects:	BLOQUEO NEUROMUSCULAR, Rocurónio ENFERMIDAD, Pocos Paraplejia Espástica Hereditaria
Online Access:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0034-70942013000100010&lng=en&tlng=en

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