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Acta Neuropathologica|February 9, 2000
Hepatitis C virus infection and myositis: a polymerase chain reaction studyM Villanova, C Caudai, P Sabatelli, et al.
Neuromuscular Disorders : NMD|March 1, 1997
Intracellular detection of laminin alpha 2 chain in skin by electron microscopy immunocytochemistry: comparison between normal and laminin alpha 2 chain deficient subjectsS Squarzoni, M Villanova, P Sabatelli, et al.
European Neurology|January 1, 1990
Congenital lactic acidosis due to a defect of pyruvate dehydrogenase complex (E1). Clinical, biochemical, nerve biopsy study and effect of therapyA Federico, M T Dotti, G M Fabrizi, et al.
Acta Neuropathologica|January 1, 1993
Choreo-acanthocytosis like phenotype without acanthocytes: clinicopathological case report. A contribution to the knowledge of the functional pathology of the caudate nucleusA Malandrini, G M Fabrizi, S Palmeri, et al.
Acta Neuropathologica|January 1, 1996
Neuronal intranuclear inclusion disease: polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new caseA Malandrini, G M Fabrizi, T Cavallaro, et al.
Journal of Submicroscopic Cytology and Pathology|July 1, 1997
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one caseK Plewnia, M T Dotti, A Malandrini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1996
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndromeG M Fabrizi, E Cardaioli, G S Grieco, et al.
Neuromuscular Disorders : NMD|July 19, 2000
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiencyL Santoro, R Carrozzo, A Malandrini, et al.
Journal of Clinical Forensic Medicine|September 15, 2004
A syndrome of bilateral hemorrhage of the thalamus and myocarditis with fatal courseA Malandrini, D Luchini, S Gambelli, et al.
European Neurology|September 28, 1998
CAG repeat expansion in an italian family with spinocerebellar ataxia type 2 (SCA2): a clinical and genetic studyA Malandrini, L Galli, M Villanova, et al.
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