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Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion.
Not available
S-EPMC3733662
|
biostudies-literature
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The association between cardiac physiology, acquired brain injury, and postnatal brain growth in critical congenital heart disease.
Not available
S-EPMC5732841
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biostudies-literature
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Fetal Cerebral Oxygenation Is Impaired in Congenital Heart Disease and Shows Variable Response to Maternal Hyperoxia.
Not available
S-EPMC7955474
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biostudies-literature
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Astroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus Callosum.
Not available
S-EPMC5094913
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biostudies-literature
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Long-Term Safety, Immunologic Response, and Imaging Outcomes following Neural Stem Cell Transplantation for Pelizaeus-Merzbacher Disease.
Not available
S-EPMC6700500
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biostudies-literature
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Deficient activity of alanyl-tRNA synthetase underlies an autosomal recessive syndrome of progressive microcephaly, hypomyelination, and epileptic encephalopathy.
Not available
S-EPMC5599341
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biostudies-literature
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Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia.
Not available
S-EPMC4471336
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biostudies-literature
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Somatic mutations in cerebral cortical malformations.
Not available
S-EPMC4274952
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biostudies-literature
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The clinicopathologic spectrum of focal cortical dysplasias: a consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission.
Not available
S-EPMC3058866
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biostudies-literature
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Neural stem cell engraftment and myelination in the human brain.
Not available
S-EPMC3893824
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biostudies-literature
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