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Journal of Neurology|August 5, 2020
Neurological comorbidity and severity of COVID-19Alberto Romagnolo, Roberta Balestrino, Gabriele Imbalzano, et al.Journal of the Neurological Sciences|April 16, 2015
Two families with novel missense mutations in COL4A1: When diagnosis can be missedElisa Giorgio, Giovanna Vaula, Giovanni Bosco, et al.Human Molecular Genetics|February 22, 2015
A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD)Elisa Giorgio, Daniel Robyr, Malte Spielmann, et al.Annals of Neurology|July 30, 2024
Structural Variants at the LMNB1 Locus: Deciphering Pathomechanisms in Autosomal Dominant Adult-Onset Demyelinating LeukodystrophyPaola Dimartino, Mariia Zadorozhna, Verónica Yumiceba, et al.Annals of Neurology|August 10, 2022
Heterozygous NOTCH1 Variants Cause CNS Immune Activation and MicroangiopathyGuy Helman, Parand Zarekiani, Samantha A M Tromp, et al.American Journal of Human Genetics|July 29, 2014
ELOVL5 mutations cause spinocerebellar ataxia 38Eleonora Di Gregorio, Barbara Borroni, Elisa Giorgio, et al.Human Mutation|May 8, 2013
Analysis of LMNB1 duplications in autosomal dominant leukodystrophy provides insights into duplication mechanisms and allele-specific expressionElisa Giorgio, Harshvardhan Rolyan, Laura Kropp, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|May 26, 2023
Sars-CoV2 infection in pregnant women with multiple sclerosisMaria Grazia Aprea, Irene Schiavetti, Emilio Portaccio, et al.Pageof 2