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UnknownMedullary Tegmental Cap Dysplasia: Fetal and Postnatal Presentations of a Unique Brainstem Malformation.
Not available
S-EPMC10187821 | biostudies-literature
UnknownIdentification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy.
Not available
S-EPMC5569911 | biostudies-literature
UnknownCombined BRAFV600E and MEK blockade for BRAFV600E-mutant gliomas.
Not available
S-EPMC5560871 | biostudies-literature
UnknownDe novo PIK3R2 variant causes polymicrogyria, corpus callosum hyperplasia and focal cortical dysplasia.
Not available
S-EPMC4989218 | biostudies-literature
UnknownDe Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions.
Not available
S-EPMC4863473 | biostudies-literature
UnknownShared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia.
Not available
S-EPMC5429027 | biostudies-literature
UnknownTargeted therapy for BRAFV600E malignant astrocytoma.
Not available
S-EPMC3638050 | biostudies-literature
UnknownRegulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival.
Not available
S-EPMC7272323 | biostudies-literature
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