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Latest Articles

Resident & Fellow Section
Child Neurology: Maternal Transmission of Congenital Myotonic Dystrophy Type 2: Case Report
Alide A. Tieleman, Manon J. Damen, Aad Verrips, et al.

Neurology September 30, 2022
Clinical/Scientific Note
Biallelic COX10 Mutations and PMP22 Deletion in a Family With Leigh Syndrome and Hereditary Neuropathy With Liability to Pressure Palsy
Yasuko Kuroha, Takanobu Ishiguro, Mari Tada, et al.

Neurology Genetics September 27, 2022
Research Article
Genetic Testing for Malformations of Cortical DevelopmentA Clinical Diagnostic Study
Barbora Straka, Barbora Hermanovska, Lenka Krskova, et al.

Neurology Genetics September 27, 2022
Resident & Fellow Section
Clinical Reasoning: A Teenage Girl With Progressive Hyperkinetic Movements, Seizures, and Encephalopathy
Sonia Khamis, Maria R Mitakidou, Michael Champion, et al.

Neurology September 21, 2022