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Neurology. Genetics|November 17, 2021
CSF MicroRNAs Reveal Impairment of Angiogenesis and Autophagy in Parkinson DiseaseAlan J Fowler, Jaeil Ahn, Michaeline Hebron, et al.
Neurology. Genetics|November 17, 2021
Body Mass Index and Height in the Friedreich Ataxia Clinical Outcome Measures StudyMaya Patel, Ashley McCormick, Jaclyn Tamaroff, et al.
Neurology. Genetics|November 17, 2021
Progressive Myoclonus Epilepsies: Diagnostic Yield With Next-Generation Sequencing in Previously Unsolved CasesLaura Canafoglia, Silvana Franceschetti, Antonio Gambardella, et al.
Neurology. Genetics|December 20, 2021
Homozygous SOD1 Variation L144S Produces a Severe Form of Amyotrophic Lateral Sclerosis in an Iranian FamilyDelia Gagliardi, Minoo Ahmadinejad, Roberto Del Bo, et al.
Neurology. Genetics|March 12, 2021
Polygenic Risk Scores Augment Stroke SubtypingJiang Li, Durgesh P Chaudhary, Ayesha Khan, et al.
Neurology. Genetics|November 18, 2021
PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic SpectrumKatrine M Johannesen, Elena Gardella, Cathrine E Gjerulfsen, et al.
Neurology. Genetics|December 8, 2021
Novel Variations in the KDM5C Gene Causing X-Linked Intellectual DisabilityPo-Ming Wu, Wen-Hao Yu, Chi-Wu Chiang, et al.
Neurology. Genetics|March 10, 2021
Cumulative Genetic Risk and APOE ε4 Are Independently Associated With Dementia Status in a Multiethnic, Population-Based CohortKelly M Bakulski, Harita S Vadari, Jessica D Faul, et al.
Neurology. Genetics|October 31, 2022
Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral SclerosisAndrea Calvo, Antonio Canosa, Cristina Moglia, et al.
Neurology. Genetics|September 1, 2022
RFC1-Related Disease: Molecular and Clinical InsightsKayli Davies, David J Szmulewicz, Louise A Corben, et al.
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