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Neurology. Genetics|April 28, 2020
Erratum: Heritability of cervical spinal cord structure
Neurology. Genetics|April 28, 2020
Acute encephalopathy after head trauma in a patient with a RHOBTB2 mutationAnnemarie C S Knijnenburg, Joost Nicolai, Levinus A Bok, et al.
Neurology. Genetics|September 3, 2021
Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish CohortAyşe Candayan, Arman Çakar, Gulshan Yunisova, et al.
Neurology. Genetics|July 20, 2016
APOE polymorphisms influence longitudinal lipid trends preceding intracerebral hemorrhageChia-Ling Phuah, Miriam R Raffeld, Alison M Ayres, et al.
Neurology. Genetics|July 20, 2016
Progressive myoclonus epilepsy associated with SACS gene mutationsFábio A Nascimento, Laura Canafoglia, Danah Aljaafari, et al.
Neurology. Genetics|June 18, 2020
Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophyMajida Charif, Arnaud Chevrollier, Naïg Gueguen, et al.
Neurology. Genetics|August 19, 2016
Pathogenic mtDNA mutations causing mitochondrial myopathy: The need for muscle biopsySteven A Hardy, Emma L Blakely, Andrew I Purvis, et al.
Neurology. Genetics|September 5, 2025
Vascular NOTCH3 Deposition Load: Association With NOTCH3 Genotype and CADASIL Disease SeverityYu-Wen Cheng, Chih-Hao Chen, Chi-Chao Chao, et al.
Neurology. Genetics|May 12, 2021
Expanding the Spectrum of Movement Disorders Associated With C9orf72 Hexanucleotide ExpansionsCarlos Estevez-Fraga, Francesca Magrinelli, Davina Hensman Moss, et al.
Neurology. Genetics|May 14, 2021
Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor SubtypesIsabel Alfradique-Dunham, Rami Al-Ouran, Rainer von Coelln, et al.
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