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Molecular and Cellular Probes|April 9, 2001
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff diseaseM Gomez-Lira, M Mottes, C Perusi, et al.Human Genetics|May 26, 1998
Molecular genetic characterization of two metachromatic leukodystrophy patients who carry the T799G mutation and show different phenotypes; description of a novel null-type mutationM Gomez-Lira, C Perusi, M Mottes, et al.Journal of Neurology|May 1, 1996
Sensory involvement in X-linked spino-bulbar muscular atrophy (Kennedy's syndrome): an electrophysiological studyA Polo, F Teatini, S D'Anna, et al.Journal of the Neurological Sciences|July 30, 1999
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patientsM Gomez-Lira, C Perusi, M Mottes, et al.Human Genetics|October 1, 1995
A common beta hexosaminidase gene mutation in adult Sandhoff disease patientsM Gomez-Lira, A Sangalli, M Mottes, et al.Journal of Neuroimmunology|November 26, 2002
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosisM Gomez-Lira, G Moretto, D Bonamini, et al.International Journal of Immunogenetics|March 22, 2007
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease riskS Mazzola, M Gomez Lira, M D Benedetti, et al.European Journal of Neurology|January 3, 2013
Prevalence of multiple sclerosis in Verona, Italy: an epidemiological and genetic studyA Gajofatto, A Stefani, M Turatti, et al.Italian Journal of Neurological Sciences|December 1, 1992
AZT-induced mitochondrial myopathyG Tomelleri, P Tonin, M Spadaro, et al.Human Mutation|September 12, 2000
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutationsM G Lira, M Mottes, P F Pignatti, et al.Pageof 3