Enrico Bertini

发表

Congenital muscular dystrophies with defective glycosylation of dystroglycan

G. Comi, G. Vasco, M. Pane, 2009, Neurology.

Hammersmith Functional Motor Scale and Motor Function Measure-20 in non ambulant SMA patients

M. Main, E. Mazzone, C. Palermo, 2014, Neuromuscular Disorders.

Phenotypic clustering of lamin A/C mutations in neuromuscular patients

E. Bertini, G. Comi, R. Caldara, 2007, Neurology.

CONGENITAL MUSCULAR DYSTROPHY WITH DEFECTIVE α-DYSTROGLYCAN, CEREBELLAR HYPOPLASIA, AND EPILEPSY

E. Mercuri, A. D’Amico, C. Bruno, 2009, Neurology.

POMT2 mutation in a patient with ‘MEB-like’ phenotype

M. Pane, E. Mercuri, F. Muntoni, 2006, Neuromuscular Disorders.

Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiency

G. Comi, G. Vasco, F. Bianco, 2012, Neuromuscular Disorders.

Revisiting mitochondrial ocular myopathies: a study from the Italian Network

G. Comi, M. Zeviani, M. Mancuso, 2017, Journal of Neurology.

Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases

G. Comi, M. Zeviani, M. Mancuso, 2012, Neuromuscular Disorders.