A. Toscano

发表

Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathy

J. Cooper, A. Harding, I. Holt, 1992, Journal of the Neurological Sciences.

Phenotypic clustering of lamin A/C mutations in neuromuscular patients

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

Chronic inflammatory demyelinating polyradiculoneuropathy: can a diagnosis be made in patients not fulfilling electrodiagnostic criteria?

G. Marfia, E. Beghi, L. Santoro, 2020, European journal of neurology.

211th ENMC International Workshop: Development of diagnostic criteria and management strategies for McArdle Disease and related rare glycogenolytic disorders to improve standards of care. 17–19 April 2015, Naarden, The Netherlands

P. Laforêt, J. Vissing, B. Schoser, 2017, Neuromuscular Disorders.

Intrafamilial phenotypic heterogeneity of the Poland complex: a case report.

R. Falsaperla, E. Parano, V. Pavone, 1995, Neuropediatrics.

Hematemesis, a Distended Abdomen, and Pulseless Electrical Activity - An Unusual Presentation of Boerhaave's Syndrome

P. Pancari, M. Nguyen, L. Wilde, 2012 .

POMT1 and POMT2 mutations in CMD patients: A multicentric Italian study

M. Pane, E. Mercuri, A. D’Amico, 2008, Neuromuscular Disorders.

Anti-sulfatide IgM antibodies in peripheral neuropathy

G. Scarlato, P. Marmiroli, S. Monaco, 2000, Journal of the Neurological Sciences.

Highly disabling cerebellar presentation in Huntington disease

F. Squitieri, L. Morgante, G. Tortorella, 2003, European journal of neurology.