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Headache|August 12, 2000
Assessing the relative incidence of mitochondrial DNA A3243G in migraine without aura with maternal inheritanceG Di Gennaro, M G Buzzi, O Ciccarelli, et al.Journal of the Neurological Sciences|June 17, 1999
The mitochondrial DNA A3243G mutation in Portugal: clinical and molecular studies in 5 familiesL Vilarinho, F M Santorelli, I Coelho, et al.Neurogenetics|December 20, 2023
Dem-Aging: autophagy-related pathologies and the "two faces of dementia"N Gammaldi, S Doccini, S Bernardi, et al.Neurology|January 14, 2004
A novel mutation in SACS gene in a family from southern ItalyC Criscuolo, S Banfi, M Orio, et al.Journal of the Neurological Sciences|April 16, 2024
Clinical and genetic features of dominant Essential Tremor in Tuscany, Italy: FUS, CAMTA1, ATXN1 and beyondD Orsucci, A Tessa, E Caldarazzo Ienco, et al.Neurology|May 6, 2009
Mitochondrial DNA haplogroups influence the therapeutic response to riboflavin in migraineursC Di Lorenzo, F Pierelli, G Coppola, et al.Neurology|July 27, 2001
Fatal infantile leukodystrophy: a severe variant of CACH/VWM syndrome, allelic to chromosome 3q27P Francalanci, E Eymard-Pierre, C Dionisi-Vici, et al.European Journal of Neurology|May 15, 2014
Large deletion mutation of SPAST in a multi-generation family from SardiniaL Racis, R Di Fabio, A Tessa, et al.Neurology|September 12, 2001
Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndromeS Salvi, F M Santorelli, E Bertini, et al.Neurology|December 25, 2002
SPG3A: An additional family carrying a new atlastin mutationA Tessa, C Casali, M Damiano, et al.Pageof 13