Isabella Moroni

Phenotypic clustering of lamin A/C mutations in neuromuscular patients

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

A fourth case of POMT2-related limb girdle muscle dystrophy with mild reduction of α-dystroglycan glycosylation.

L. Morandi, F. Blàsevich, M. Mora, 2014, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain disease

C. Pantaleoni, L. Morandi, M. Mora, 2012, Journal of the Neurological Sciences.

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

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