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Late onset familial dystonia: could mitochondrial deficits induce a diffuse lesioning process of the whole basal ganglia system?

BACKGROUND—Striatal necrosis has been related to various clinical syndromes, with acute or chronic progression, and juvenile or late occurrence, but the most common type is Leigh's encephalopathy.
METHODS—Between 1967 and 1995, six out of seven related patients with chronic familial dystonia we...

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Detalhes bibliográficos
Main Authors: Caparros-Lefebvre, D, Destee, A, Petit, H
Formato: Artigo
Idioma:English
Publicado em: BMJ Group 1997
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2169679/
https://ncbi.nlm.nih.gov/pubmed/9285458
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