Tiziana Cavallaro

Two novel mutations in dynamin-2 cause axonal Charcot–Marie–Tooth disease

R. Cerini, N. Rizzuto, G. Fabrizi, 2007, Neurology.

Giant axon and neurofilament accumulation in Charcot–Marie–Tooth disease type 2E

C. Angiari, N. Rizzuto, G. Fabrizi, 2004, Neurology.

MELAS: clinical phenotype and morphological brain abnormalities

L. Morelli, L. Bartolomei, A. Simonati, 2003, Acta Neuropathologica.

Hereditary neuropathy with liability to pressure palsies: electrophysiological and genetic study of a family with carpal tunnel syndrome as only clinical manifestation

N. Rizzuto, G. Fabrizi, T. Cavallaro, 2003, Neurological Sciences.

A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B

A. Polo, N. Rizzuto, G. Fabrizi, 2001, Neurology.

PMP22 related congenital hypomyelination neuropathy

M. Mostacciuolo, A. Pini, A. Simonati, 2001, Journal of neurology, neurosurgery, and psychiatry.

Conduction slowing, conduction block and temporal dispersion in demyelinating, dysmyelinating and axonal neuropathies: Electrophysiology meets pathology

F. Manganelli, A. Uncini, Tiziana Cavallaro, 2024, Journal of the peripheral nervous system : JPNS.