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Neurology. Genetics|November 8, 2024
Progressive Apraxia of Speech as a Manifestation of Spinocerebellar Ataxia 2: Case ReportAudrey M Blazek, Gabriela Meade, Lauren M Jackson, et al.
Neurology. Genetics|February 25, 2025
The Spastic Paraplegia-Centers of Excellence Research Network (SP-CERN): Clinical Trial Readiness for Hereditary Spastic ParaplegiaLuca Schierbaum, Vicente Quiroz, Kathryn Yang, et al.
Neurology. Genetics|November 14, 2025
Expanding the Phenotype Spectrum of β-MannosidosisAngela M Martin Rios, Liliane H Gibbs, Karolina M Stepien, et al.
Neurology. Genetics|November 14, 2025
Parkinson Disease SNCA Risk Variants Are Associated With Higher Asymmetric Putamen Dopaminergic DysfunctionSaud Alhusaini, Gabriel Dayanim, Mohamed Kandil, et al.
Neurology. Genetics|November 13, 2025
Novel ATXN10 Repeat Motif Patterns in Peruvian Families Modify Disease OnsetKamilla Sedov, Carla Manrique-Enciso, Madison James Yang, et al.
Neurology. Genetics|November 3, 2025
Serum NOTCH3 Extracellular Domain in Patients With CADASILHyesung Kim, Yumi Yamamoto, Young Ree Kim, et al.
Neurology. Genetics|September 29, 2025
Targeted Therapy of GRIA1-Related Epilepsy and Intellectual Disability With Perampanel: A Case Report and Literature ReviewElisabetta Cesaroni, Claudia Passamonti, Carla Marini
Neurology. Genetics|December 16, 2020
Practical guidelines to manage discordant situations of SMN2 copy number in patients with spinal muscular atrophyIvon Cuscó, Sara Bernal, Laura Blasco-Pérez, et al.
Neurology. Genetics|December 30, 2020
Who and Why? Requests for Presymptomatic Genetic Testing for Amyotrophic Lateral Sclerosis/Frontotemporal Dementia vs Huntington DiseaseMaria Del Mar Amador, Marcela Gargiulo, Christilla Boucher, et al.
Neurology. Genetics|December 25, 2019
GNA11 brain somatic pathogenic variant in an individual with phacomatosis pigmentovascularisJoseph M Sliepka, Sarah C McGriff, Linda Z Rossetti, et al.
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