A. Rossi

Axonal motor and sensory neuropathy in myotonic dystrophy

G. Guazzi, A. Malandrini, M. Mondelli, 1993, Acta neurologica Scandinavica.

Mitochondrial Abnormalities in Genetically Assessed Oculopharyngeal Muscular Dystrophy

F. Ginanneschi, A. Malandrini, A. Federico, 2004, European Neurology.

Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL

A. Malandrini, M. Villanova, F. Albani, 2002, Neurology.

Localization of the gene for the intermediate form of Charcot-Marie-Tooth to chromosome 10q24.1-q25.1.

A. Malandrini, K. Verhoeven, V. Timmerman, 2001, American journal of human genetics.

Hypomyelination and Congenital Cataract

F. Zara, C. Bruno, R. Biancheri, 2015 .

GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease

R. Ravazzolo, G. Uziel, D. Pareyson, 2007, Clinical genetics.

Ultrastructural findings in the peripheral nerve in a family with the intermediate form of Charcot-Marie-Tooth disease.

G. Guazzi, A. Malandrini, M. Villanova, 2001, Journal of submicroscopic cytology and pathology.