F. Martinello

发表

Myocardial involvement is very frequent among patients affected with subclinical Becker's muscular dystrophy.

G. Danieli, C. Angelini, M. Miorelli, 1996, Circulation.

Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations.

E. Hoffman, C. Angelini, M. Mostacciuolo, 1997, Journal of medical genetics.

Prognostic factors in mild dystrophinopathies

G. Danieli, C. Angelini, G. Siciliano, 1996, Journal of the Neurological Sciences.

Laminin α2 muscular dystrophy

T. Crawford, E. Hoffman, R. Zimmerman, 1998, Neurology.

Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: Characterization of sub-clinical phenotypes

C. Angelini, M. Cadaldini, E. Pegoraro, 1994, Neuromuscular Disorders.

Genetic epidemiology of congenital muscular dystrophy in a sample from north-east Italy

C. Angelini, M. Mostacciuolo, P. Perini, 1996, Human Genetics.

Brain alterations in the classical form of congenital muscular dystrophy

M. Chevallay, F. Tomé, M. Fanin, 1996, Child's Nervous System.

The Brain Involvement in Congenital Myotonic Dystrophy: a Review

C. Trevisan, F. Martinello, 1997 .

Genetic epidemiology ofmuscular dystrophies resulting fromsarcoglycan genemutations

C. Angelini, M. Mostacciuolo, G. Soraru', 1997 .

Alterations of the retino-cortical conduction in patients affected by Classical Congenital Muscular Dystrophy (Cl-CMD) with merosin deficiency

A. Tormene, C. Trevisan, E. Pastorello, 2004, Documenta Ophthalmologica.

Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients.

T. Crawford, E. Hoffman, R. Zimmerman, 1998, Neurology.

Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-up.

C. Angelini, E. Ferruzza, C. Trevisan, 1995, European neurology.

Rasagiline and Rapid Symptomatic Motor Effect in Parkinson’s Disease: Review of Literature

M. Gioulis, S. Zambito Marsala, F. Martinello, 2013, Neurology and Therapy.