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Last Updated: 10/31/2025
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Found 292 publications
Pearls & Oy-sters: Acute Obstructive Hydrocephalus Co-Occurrence With Vigabatrin-Associated MRI Changes in an Infant With LIS1-Related Classical Lissencephaly.
Journal: Neurology
Published: September 26, 2025
Diagnosis of Lissencephaly in a Neonate After Antenatal Polyhydramnios and Suspicion of Fetal Esophageal Atresia: A Case Report.
Journal: Cureus
Published: September 17, 2025
Understanding the Molecular Basis of Miller-Dieker Syndrome.
Journal: International journal of molecular sciences
Published: July 01, 2025
Multiple roles of EML1 in microtubule stabilization and vesicle transport in the nervous system.
Journal: Biochimica et biophysica acta. Molecular cell research
Published: May 13, 2025
Corpus Callosotomy for Atonic Drop Seizures in Bilateral Malformations of Cortical Development: A Systematic Review of Literature.
Journal: Cureus
Published: March 27, 2025
"Hair-on-end" appearance in thickened cortex in a case of classic lissencephaly due to DCX gene mutation.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: February 12, 2025
Diffuse subcortical band heterotopia: Expanding the phenotype associated with the loss of the YWHAE gene.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: January 19, 2025
Prenatal Diagnosis of KBG Syndrome: Phenotypic and Genotypic Features of 12 Fetal Cases With the Disorder.
Journal: Prenatal diagnosis
Published: November 04, 2024
Lissencephaly with subcortical band heterotopia in an East African child: A case report.
Journal: Radiology case reports
Published: September 21, 2024
TUBGCP2 variants cause lissencephaly spectrum disorders: a case report and literature review.
Journal: Frontiers in pediatrics
Published: August 05, 2024
Last Updated: 10/31/2025