au.\*:("GIDARO, T")
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Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathyBROCCOLINI, A; GIDARO, T; TASCA, G et al.Neurology. 2010, Vol 75, Num 3, pp 265-272, issn 0028-3878, 8 p.Article
NCAM is hyposialylated in hereditary inclusion body myopathy due to GNE mutationsRICCI, E; BROCCOLINI, A; GIDARO, T et al.Neurology. 2006, Vol 66, Num 5, pp 755-758, issn 0028-3878, 4 p.Article
The mitotic clock in skeletal muscle regeneration, disease and cell mediated gene therapyMOULY, V; AAMIRI, A; PERIE, S et al.Acta physiologica scandinavica. 2005, Vol 184, Num 1, pp 3-15, issn 0001-6772, 13 p.Article