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Neurology|October 26, 1999
Transthyretin amyloidosis and superficial siderosis of the CNSM Mascalchi, F Salvi, M G Pirini, et al.
Epilepsia|August 17, 1999
Epilepsy and EEG findings in males with fragile X syndromeS A Musumeci, R J Hagerman, R Ferri, et al.
Neurology|June 12, 2002
Brainstem involvement in Unverricht-Lundborg disease (EPM1): An MRI and (1)H MRS studyM Mascalchi, R Michelucci, M Cosottini, et al.
Lancet (London, England)|May 2, 1992
Identical genetic locus for Baltic and Mediterranean myoclonusA Malafosse, A E Lehesjoki, P Genton, et al.
Neurology|March 23, 2005
Lafora disease due to EPM2B mutations: a clinical and genetic studyC Gómez-Abad, P Gómez-Garre, E Gutiérrez-Delicado, et al.
Clinical Genetics|June 14, 2000
Mutation and transcription analysis of transthyretin gene in Italian families with hereditary amyloidosis: a putative novel hot spot' in codon 47A Ferlini, L Obici, E Manzati, et al.
Human Mutation|January 1, 1992
Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosisM R Almeida, A Ferlini, A Forabosco, et al.
Neurology|August 8, 2007
Neuropathy in multiple myeloma treated with thalidomide: a prospective studyR Plasmati, F Pastorelli, M Cavo, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|December 3, 2003
Atypical familial motor neuropathy in patients with mutant TTR Ile68LeuF Salvi, C Scaglione, R Michelucci, et al.
AJNR. American Journal of Neuroradiology|March 14, 2007
Whole-brain histogram and voxel-based analyses of apparent diffusion coefficient and magnetization transfer ratio in celiac disease, epilepsy, and cerebral calcifications syndromeR Della Nave, A Magaudda, R Michelucci, et al.
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