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Journal of Medical Genetics|February 9, 2000
Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutationsR Barresi, C Di Blasi, T Negri, et al.Neurology|April 13, 2005
Sequential antibodies to potassium channels and glutamic acid decarboxylase in neuromyotoniaC Antozzi, C Frassoni, A Vincent, et al.Gene Therapy|April 22, 2003
Dystrophic phenotype of canine X-linked muscular dystrophy is mitigated by adenovirus-mediated utrophin gene transferM Cerletti, T Negri, F Cozzi, et al.Neuroepidemiology|August 7, 2004
Prevalence of inherited ataxias in the province of Padua, ItalyM Zortea, M Armani, E Pastorello, et al.Archives of Neurology|February 20, 1999
Clinical correlations in 16 patients with total or partial laminin alpha2 deficiency characterized using antibodies against 2 fragments of the proteinL Morandi, C Di Blasi, L Farina, et al.Neurology|April 7, 2010
Detection of poliovirus-infected macrophages in thymus of patients with myasthenia gravisP Cavalcante, M Barberis, M Cannone, et al.European Neurology|July 15, 2000
Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian familiesA Filla, C Mariotti, G Caruso, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 10, 2004
Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian familiesC Mariotti, C Gellera, M Rimoldi, et al.ESMO Open|June 11, 2025
Clinical relevance and methodological approach for the assessment of drug-drug interactions in cancer patients: a position statement from the Italian Association of Medical Oncology (AIOM) and the Italian Society of Pharmacology (SIF)M Del Re, R Roncato, A Argentiero, et al.Neuroscience Letters|March 17, 2011
Whole body cholesterol metabolism is impaired in Huntington's diseaseV Leoni, C Mariotti, L Nanetti, et al.Pageof 16