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Annals of the Child Neurology Society|August 7, 2026
Charcot-Marie-Tooth disease in childrenEzgi Saylam, Praveen Kumar Ramani, Ruthwik Duvuru, et al.Annals of the Child Neurology Society|August 7, 2026
The use of dynamic magnetic resonance angiography in the diagnosis of rotational vertebral artery syndromeChrisoula Cheronis, Grant L Lin, Andrew Silverman, et al.Annals of the Child Neurology Society|August 7, 2026
Postconcussive symptom severity, risk factors for prolonged recovery, and mental health history: Pathways of influence in a diverse pediatric sampleLaura K Winstone-Weide, Kelly Gettig, Cynthia A AustinAnnals of the Child Neurology Society|August 7, 2026
Burden of illness in aromatic l-amino acid decarboxylase deficiencyMelissa L DiBacco, Jordan Hinahara, Thomas F Goss, et al.Annals of the Child Neurology Society|August 7, 2026
Communication about sudden unexpected death in epilepsy: Understanding the caregiver perspectiveIsabella K Pallotto, Renée A Shellhaas, Kayli Maney, et al.Annals of the Child Neurology Society|August 7, 2026
Neonatal Seizures in Tuberous Sclerosis Complex: A Case SeriesKristina Jülich, Kristen ArredondoAnnals of the Child Neurology Society|August 7, 2026
Raising awareness of TBC1 domain-containing kinase (TBCK) epileptic encephalopathy among Puerto Rican childrenJohanna De Luca-Ramirez, Sofia Rosado Fernández, Orlando A TorresAnnals of the Child Neurology Society|August 7, 2026
Saccade and pupil changes in children recovering from opsoclonus-myoclonus ataxia syndrome reveal midbrain alterations in oculomotor circuitsDouglas P Munoz, Brian J White, Donald C Brien, et al.Annals of the Child Neurology Society|August 7, 2026
Complex epilepsy phenotype associated with chromosome 2q24.2-q24.3 deletion involving sodium channel gene clusterRima Madan, Fiorella S Guido, Nicole BresciaAnnals of the Child Neurology Society|August 7, 2026
The congenital muscular dystrophiesHaluk Topaloğlu, Bita PoorshiriPageof 11