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Annals of Neurology|February 26, 2005
Vascular endothelial growth factor gene variability is associated with increased risk for ADRoberto Del Bo, Marina Scarlato, Serena Ghezzi, et al.Human Mutation|August 16, 2005
Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophiesRachele Cagliani, Francesca Magri, Antonio Toscano, et al.Parkinsonism & Related Disorders|March 10, 2019
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathyEdoardo Monfrini, Letizia Straniero, Sara Bonato, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 17, 2012
Progranulin gene (GRN) promoter methylation is increased in patients with sporadic frontotemporal lobar degenerationDaniela Galimberti, Claudio D'Addario, Bernardo Dell'osso, et al.Frontiers in Neurology|July 15, 2021
Early Findings in Neonatal Cases of RYR1-Related Congenital MyopathiesEleonora Mauri, Daniela Piga, Alessandra Govoni, et al.BMC Neurology|November 8, 2020
A case report of late-onset cerebellar ataxia associated with a rare p.R342W TGM6 (SCA35) mutationArianna Manini, Tommaso Bocci, Alice Migazzi, et al.Journal of Alzheimer'S Disease : JAD|January 25, 2011
Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindredAnna M Pietroboni, Giorgio G Fumagalli, Laura Ghezzi, et al.European Journal of Human Genetics : EJHG|December 23, 2011
The novel mitochondrial tRNAAsn gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairmentDario Ronchi, Monica Sciacco, Andreina Bordoni, et al.Neuroscience Letters|November 1, 2005
SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosisChiara Fenoglio, Daniela Galimberti, Maria Ban, et al.Journal of Alzheimer'S Disease : JAD|June 5, 2009
MCP-1 A-2518G polymorphism: effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levelsDaniela Galimberti, Eliana Venturelli, Chiara Villa, et al.Pageof 34