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Parkinsonism & Related Disorders|February 7, 2017
Deconstructing Fahr's disease/syndrome of brain calcification in the era of new genesAmit Batla, Xin You Tai, Lucia Schottlaender, et al.Neurobiology of Aging|October 30, 2016
Analysis of the prion protein gene in multiple system atrophyViorica Chelban, Andreea Manole, Lasse Pihlstrøm, et al.Journal of Neurology|October 31, 2012
The frequency of spinocerebellar ataxia type 23 in a UK populationKatherine Fawcett, Mohadeseh Mehrabian, Yo-Tsen Liu, et al.Neuromuscular Disorders : NMD|January 17, 2021
Feeding difficulties in children and adolescents with spinal muscular atrophy type 2Renske I Wadman, Ramona De Amicis, Chiara Brusa, et al.Acta Neuropathologica Communications|December 25, 2019
Investigation of somatic CNVs in brains of synucleinopathy cases using targeted SNCA analysis and single cell sequencingDiego Perez-Rodriguez, Maria Kalyva, Melissa Leija-Salazar, et al.Neurology. Genetics|March 27, 2020
MYORG-related disease is associated with central pontine calcifications and atypical parkinsonismViorica Chelban, Miryam Carecchio, Gillian Rea, et al.JAMA Neurology|May 8, 2013
Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R geneRita Guerreiro, Eleanna Kara, Isabelle Le Ber, et al.Brain : a Journal of Neurology|May 25, 2016
Genetic and phenotypic characterization of complex hereditary spastic paraplegiaEleanna Kara, Arianna Tucci, Claudia Manzoni, et al.Neurology|November 8, 2014
LRRK2 exonic variants and risk of multiple system atrophyMichael G Heckman, Lucia Schottlaender, Alexandra I Soto-Ortolaza, et al.Neurology|September 16, 2016
A genome-wide association study in multiple system atrophyAnna Sailer, Sonja W Scholz, Michael A Nalls, et al.Pageof 1