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Last Updated: 01/07/2026

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Found 281 publications

Pearls & Oy-sters: Acute Obstructive Hydrocephalus Co-Occurrence With Vigabatrin-Associated MRI Changes in an Infant With LIS1-Related Classical Lissencephaly.

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.

Diagnosis of Lissencephaly in a Neonate After Antenatal Polyhydramnios and Suspicion of Fetal Esophageal Atresia: A Case Report.

Journal: Cureus
Published: September 17, 2025

Subcortical band heterotopia: electroclinical, radiological, and prognostic features in adults.

Subcortical band heterotopia: electroclinical, radiological, and prognostic features in adults.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: July 14, 2025

Understanding the Molecular Basis of Miller-Dieker Syndrome.

Understanding the Molecular Basis of Miller-Dieker Syndrome.

Journal: International journal of molecular sciences
Published: July 01, 2025

Corpus Callosotomy for Atonic Drop Seizures in Bilateral Malformations of Cortical Development: A Systematic Review of Literature.

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.

"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.

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.

Prenatal Diagnosis of KBG Syndrome: Phenotypic and Genotypic Features of 12 Fetal Cases With the Disorder.

Journal: Prenatal diagnosis
Published: November 04, 2024

Women With Genetic Epilepsies.

Women With Genetic Epilepsies.

Journal: Neurology. Genetics
Published: October 09, 2024

Lissencephaly with subcortical band heterotopia in an East African child: A case report.

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.

TUBGCP2 variants cause lissencephaly spectrum disorders: a case report and literature review.

Journal: Frontiers in pediatrics
Published: August 05, 2024

Double Cortex Syndrome: An Unusual Cause of Seizures.

Double Cortex Syndrome: An Unusual Cause of Seizures.

Journal: Cureus
Published: June 30, 2024
Showing 1-12 of 281

Last Updated: 01/07/2026