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Neurology. Genetics|August 29, 2026
Two Cases of Multiple Sclerosis in a Family With X-Linked Charcot-Marie-Tooth DiseaseMarija Menih, Tanja Hojs Fabjan, Aleš Maver, et al.Neurology. Genetics|September 6, 2026
De Novo Facioscapulohumeral Muscular Dystrophy: A Severe Subtype Driven by D4Z4 Repeat ContractionsQifang He, Xiaodan Lin, Yuhua Lin, et al.Neurology. Genetics|September 6, 2026
Epilepsy Is Part of the CNS Phenotype in Classic Infantile Pompe DiseaseMartha Caterina Faraguna, Alexander Broomfield, Serena Gasperini, et al.Neurology. Genetics|October 24, 2026
Cerebrotendinous Xanthomatosis: Clinical Features of Affected Individuals From Latin AmericaHéctor Rubén Martínez-Hernández, Leonel Villa-Villegas, Carlos Eduardo Piña-Avilés, et al.Neurology. Genetics|October 30, 2026
Caregiver-Reported Signs and Symptoms of Autonomic Dysfunction in Koolen-de Vries SyndromeAhmed N Sahly, Emmanouil Rampakakis, Kenneth A MyersPageof 88