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European Neurology|February 28, 2004
Mitochondrial abnormalities in genetically assessed oculopharyngeal muscular dystrophyS Gambelli, A Malandrini, F Ginanneschi, et al.Annals of Neurology|August 12, 1999
Ataxin 1 and ataxin 3 in neuronal intranuclear inclusion diseaseA P Lieberman, J Q Trojanowski, D G Leonard, et al.Neuromuscular Disorders : NMD|February 5, 2003
Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 geneG Siciliano, A Tessa, S Petrini, et al.Neurology|January 14, 2004
Clinical and molecular findings in patients with giant axonal neuropathy (GAN)C Bruno, E Bertini, A Federico, et al.Neurology|March 14, 2001
The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndromeR Carrozzo, A Tessa, M E Vázquez-Memije, et al.Acta Neuropathologica|January 28, 1998
Localization of laminin alpha 2 chain in normal human central nervous system: an immunofluorescence and ultrastructural studyM Villanova, A Malandrini, P Sabatelli, et al.Acta Neuropathologica|August 1, 1996
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathyA Malandrini, P Carrera, S Palmeri, et al.Neurology|January 14, 2004
Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay typeG S Grieco, A Malandrini, G Comanducci, et al.American Journal of Medical Genetics. Part A|April 27, 2004
Hypertelorism, ptosis, and myopia associated with drug-resistant epilepsy, mental delay, growth deficiency, ectodermal defects, and osteopeniaR Zannolli, S Buoni, F Macucci, et al.American Journal of Human Genetics|October 23, 1997
Chorea-acanthocytosis: genetic linkage to chromosome 9q21J P Rubio, A Danek, C Stone, et al.Pageof 11