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Recently, COL4A1 mutations have been reported in porencephaly and other cerebral vascular diseases, often associated with ocular… Expand The development of the human cerebral cortex is an orchestrated process involving the generation of neural progenitors in the… Expand Purposes: To describe the clinical spectrum and to evaluate the efficacy of different therapeutic agents in children with… Expand Schizencephaly is a rare congenital brain defect characterized by gray matter lined clefts of the cerebral mantle, frequently… Expand Schizencephaly is an uncommon structural disorder of cerebral cortical development, characterized by congenital clefts spanning… Expand inding a unifying concept behind the diversity of signs and symptoms in schizophrenia is a central challenge to contemporary… Expand We describe two brothers aged 8 and 10 affected by severe bilateral schizencephaly, carrying an identical point mutation of the… Expand Schizencephaly is an uncommon congenital disorder of cerebral cortical development. Although a well-recognized cause of seizures… Expand Schizencephaly1 is an extremely rare human congenital disorder characterized by a full-thickness cleft within the cerebral… Expand PURPOSE
To correlate clinical outcome with the size and location of clefts in patients with schizencephaly.
PATIENTS AND… Expand