Cortical Dysplasia Latest Advances

Find the Latest Research About Cortical Dysplasia

Last Updated: 04/28/2026

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Found 22357 publications

Deficiency of pnkp in zebrafish causes microcephaly, seizures, and developmental delay through mitochondrial dysfunction.

Deficiency of pnkp in zebrafish causes microcephaly, seizures, and developmental delay through mitochondrial dysfunction.

Journal: Zoological research
Published: April 15, 2026

Miller-Dieker Syndrome: Genetic Etiology, Neurocognitive Impact, and Clinical Implications in a Neuronal Migration Disorder.

Miller-Dieker Syndrome: Genetic Etiology, Neurocognitive Impact, and Clinical Implications in a Neuronal Migration Disorder.

Journal: Developmental neuropsychology
Published: April 14, 2026

American Epilepsy Society Clinical Practice Guideline: Infantile Epilepsy.

American Epilepsy Society Clinical Practice Guideline: Infantile Epilepsy.

Journal: Epilepsy currents
Published: April 13, 2026

hTERT-immortalized mesenchymal stem cell-derived EV treatment reduces ZIKV-induced cortical neuronal death, infection, and exosome-mediated transmission.

hTERT-immortalized mesenchymal stem cell-derived EV treatment reduces ZIKV-induced cortical neuronal death, infection, and exosome-mediated transmission.

Journal: Microbiology spectrum
Published: April 13, 2026

Genotype-Phenotype Correlation in Tuberous Sclerosis Complex: Insights from Thirty-three Patients from North Macedonia.

Genotype-Phenotype Correlation in Tuberous Sclerosis Complex: Insights from Thirty-three Patients from North Macedonia.

Journal: Balkan medical journal
Published: April 10, 2026

STRADA deficiency impairs cortical interneuron development in humans and mice.

STRADA deficiency impairs cortical interneuron development in humans and mice.

Journal: bioRxiv : the preprint server for biology
Published: April 10, 2026

Camurati-Engelmann disease with bilateral proptosis and optic neuropathy: a case report and literature review.

Camurati-Engelmann disease with bilateral proptosis and optic neuropathy: a case report and literature review.

Journal: Orbit (Amsterdam, Netherlands)
Published: April 08, 2026

Expanding the Phenotypic Spectrum of SLC1A4-Related Spastic Tetraplegia: A Case With Novel Multisystem Features.

Expanding the Phenotypic Spectrum of SLC1A4-Related Spastic Tetraplegia: A Case With Novel Multisystem Features.

Journal: Journal of investigative medicine high impact case reports
Published: April 04, 2026

Malformations of Cortical Development.

Malformations of Cortical Development.

Journal: Neuroimaging clinics of North America
Published: April 03, 2026

Growth Faltering: Definitions and References for Typical Ranges.

Growth Faltering: Definitions and References for Typical Ranges.

Journal: Pediatric annals
Published: April 02, 2026

A Stepwise Approach to Macrocephaly: Clinical Clues to the Rare Diagnosis of PTEN Hamartoma Tumor Syndrome.

A Stepwise Approach to Macrocephaly: Clinical Clues to the Rare Diagnosis of PTEN Hamartoma Tumor Syndrome.

Journal: Pediatric annals
Published: April 02, 2026

Genetic analysis of a de novo EFTUD2 variant causing Mandibulofacial dysostosis with microcephaly in a fetus

Genetic analysis of a de novo EFTUD2 variant causing Mandibulofacial dysostosis with microcephaly in a fetus

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 01, 2026
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Last Updated: 04/28/2026