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Neurology. Genetics|May 7, 2021
Erratum: African Americans Have Differences in CSF Soluble TREM2 and Associated Genetic VariantsNeurology. Genetics|April 30, 2021
Biallelic DAB1 Variants Are Associated With Mild Lissencephaly and Cerebellar HypoplasiaDaphne J Smits, Rachel Schot, Martina Wilke, et al.Neurology. Genetics|May 21, 2021
Occurrence of Amyotrophic Lateral Sclerosis in Type 1 Gaucher DiseaseLais M Oliveira, Tara Rastin, Graeme A M Nimmo, et al.Neurology. Genetics|September 17, 2021
Integrative Network-Based Analysis Reveals Gene Networks and Novel Drug Repositioning Candidates for Alzheimer DiseaseZachary F Gerring, Eric R Gamazon, Anthony White, et al.Neurology. Genetics|April 28, 2020
Use of local genetic ancestry to assess TOMM40-523' and risk for Alzheimer diseaseParker L Bussies, Farid Rajabli, Anthony Griswold, et al.Neurology. Genetics|April 28, 2020
Novel EGR2 variant that associates with Charcot-Marie-Tooth disease when combined with lipopolysaccharide-induced TNF-α factor T49M polymorphismMaria Empar Blanco-Cantó, Nikiben Patel, Sergio Velasco-Aviles, et al.Neurology. Genetics|April 28, 2020
Polygenic risk scores of several subtypes of epilepsies in a founder populationClaudia Moreau, Rose-Marie Rébillard, Stefan Wolking, et al.Neurology. Genetics|April 28, 2020
Clinical and pathologic phenotype of a large family with heterozygous STUB1 mutationMerel O Mol, Jeroen G J van Rooij, Esther Brusse, et al.Neurology. Genetics|August 20, 2016
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studiesMichaela F George, Farren B S Briggs, Xiaorong Shao, et al.Neurology. Genetics|August 2, 2021
Miglustat Therapy for SCARB2-Associated Action Myoclonus-Renal Failure SyndromeImran H Quraishi, Anna M Szekely, Anushree C Shirali, et al.Pageof 87