Myotonia and the muscle chloride channel: dominant mutations show variable penetrance and founder effect
Koty, P P, Pegoraro, E, Hobson, G, Marks, H G, Turel, A, Flagler, D, Cadaldini, M, Angelini, C, Hoffman, E P
Published in Neurology (01.10.1996)
Published in Neurology (01.10.1996)
Get more information
Journal Article
Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: evidence for failure of dystrophin production in dystrophin-competent myonuclei
Pegoraro, E, Schimke, R N, Garcia, C, Stern, H, Cadaldini, M, Angelini, C, Barbosa, E, Carroll, J, Marks, W A, Neville, H E, Marks, H, Appleton, S, Toriello, H, Wessel, H B, Donnelly, J, Bernes, S M, Taber, J W, Weiss, L, Hoffman, E P
Published in Neurology (01.04.1995)
Published in Neurology (01.04.1995)
Get more information
Journal Article
Molecular characterization of myophosphorylase deficiency in a group of patients from Northern Italy
Martinuzzi, A., Tsujino, S., Vergani, L., Schievano, G., Cadaldini, M., Bartoloni, L., Fanin, M., Siciliano, G., Shanske, S., DiMauro, S., Angelini, C.
Published in Journal of the neurological sciences (01.04.1996)
Published in Journal of the neurological sciences (01.04.1996)
Get full text
Journal Article
Dystrophin-positive fibers in Duchenne dystrophy: origin and correlation to clinical course
Fanin, M, Danieli, G A, Cadaldini, M, Miorin, M, Vitiello, L, Angelini, C
Published in Muscle & nerve (01.10.1995)
Published in Muscle & nerve (01.10.1995)
Get more information
Journal Article