P. Nicolao

Intravenous thrombolysis for ischemic stroke in the Veneto region: the gap between eligibility and reality

D. Idone, G. Zanette, F. Ferracci, 2018, Journal of Thrombosis and Thrombolysis.

Do patients’ and referral centers’ characteristics influence multiple sclerosis phenotypes? Results from the Italian multiple sclerosis and related disorders register

M. Ulivelli, G. Marfia, M. Rovaris, 2022, Neurological Sciences.

DHPLC analysis of the MECP2 gene in Italian Rett patients

S. Bortoluzzi, P. Gasparini, B. Giometto, 2001, Human mutation.

Do patients’ and referral centers’ characteristics influence multiple sclerosis phenotypes? Results from the Italian multiple sclerosis and related disorders register

M. Ulivelli, G. Marfia, M. Rovaris, 2022, Neurological Sciences.

Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2q.

B. Giometto, L. Edström, M. Anvret, 1999, American journal of human genetics.

A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21

F. Chapon, L. Edström, M. Anvret, 1999, Neuromuscular Disorders.

Mutation screening in Rett syndrome patients

M. Anvret, M. Bailey, S. Buervenich, 2000, Journal of medical genetics.

Muscle histopathology in upper motor neuron-dominant amyotrophic lateral sclerosis

F. Piccione, C. Angelini, E. Pegoraro, 2008, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.