Objective: The major form of magnetic resonance imaging–defined white matter injury (WMI)
comprises diffuse lesions where the burden of small necrotic foci (microscopic necrosis) is …

Purpose: To describe seizure control, complications, adaptive function and language skills
following hemispheric surgery for epilepsy. Methods: Retrospective chart review of patients …

See Cannon (doi: 10.1093/brain/awv400 ) for a scientific commentary on this article. Congenital
myopathies are a clinically and genetically heterogeneous group of muscle disorders …

Mucopolysaccharidosis type I (MPS I) is an autosomal recessive disease resulting from
deficiency of the lysosomal enzyme α‐L‐iduronidase. A murine model which shows complete …

Alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV) is a lethal lung
developmental disorder caused by heterozygous point mutations or genomic deletion copy-…

BACKGROUND. Surgical removal and radiation therapy are associated with significant risk
for morbidity in the pediatric population with craniopharyngioma. Intracystic therapies have …

Nestin is an intermediate filament protein (IFP) expressed in undifferentiated cells during CNS
development and in CNS tumors. Previous studies have arrived at different conclusions in …

CK syndrome (CKS) is an X-linked recessive intellectual disability syndrome characterized
by dysmorphism, cortical brain malformations, and an asthenic build. Through an X …

Mosaic KRAS variants and other RASopathy genes cause oculoectodermal, encephalo‐cranio‐cutaneous
lipomatosis, and Schimmelpenning‐Feuerstein‐Mims syndromes, and a …

Introduction Spontaneous regression of pilocytic astrocytoma after incomplete resection is
well recognized, especially for cerebellar and optic pathway tumors, and tumors associated …