Late-Onset Glycogen Storage Disease Type 2. | Curr Mol Med;14(8): 971-978, 2014. | MEDLINE

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Late-Onset Glycogen Storage Disease Type 2.

Filosto, M; Cotelli, M S; Vielmi, V; Todeschini, A; Rinaldi, F; Rota, S; Scarpelli, M; Padovani, A.

Affiliation

Filosto M; Clinical Neurology, University Hospital "Spedali Civili", Pz.le Spedali Civili 1, 25100 Brescia, Italy.

Curr Mol Med ; 14(8): 971-978, 2014.

Article in En | MEDLINE | ID: mdl-25323875

Key words

Autophagia; GAA; GSDII; Pompe's disease; enzymatic replacement therapy; glycogen storage disease; glycogenosis II; lysosomal disease

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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Curr Mol Med Journal subject: BIOLOGIA MOLECULAR Year: 2014 Document type: Article Affiliation country: Italy Country of publication: Netherlands

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Curr Mol Med Journal subject: BIOLOGIA MOLECULAR Year: 2014 Document type: Article Affiliation country: Italy Country of publication: Netherlands