Cortical Dysplasia Latest Advances

Understanding septo-optic dysplasia: Endocrine implications and ophthalmic consequences.

Journal: Best practice & research. Clinical endocrinology & metabolism

Published: September 04, 2026

Operational definition, current and emerging pharmacotherapy, and clinical trial considerations in developmental and epileptic encephalopathies.

Journal: Expert opinion on pharmacotherapy

Published: September 03, 2026

Diagnostic Overshadowing in Lennox-Gastaut Syndrome: Immerslund-Gräsbeck Syndrome Unmasked by Radiosurgical Stress.

Journal: Journal of child neurology

Published: August 30, 2026

Timely Surgical Approaches for Pediatric Epilepsy Resistant to Medication.

Journal: Journal of surgery and research

Published: August 29, 2026

Genotype-Driven MRI Re-evaluation Reveals Subtle PAFAH1B1-Related Lissencephaly.

Journal: Journal of child neurology

Published: August 27, 2026

Acute Bilateral Vocal Cord Immobility Secondary to Acute Myopathy.

Journal: Ear, nose, & throat journal

Published: August 25, 2026

Neurophysiological Basis of Mirror Movements in Schizencephaly: A Case Report.

Journal: Journal of child neurology

Published: August 21, 2026

Selective retinal arterial whitening in retinal astrocytic hamartoma in tuberous sclerosis.

Journal: BMJ case reports

Published: August 21, 2026

Rare genetic endocrine tumor syndromes: VHL, NF1, TSC, and Carney complex.

Journal: Best practice & research. Clinical endocrinology & metabolism

Published: August 21, 2026

Congenital hereditary porencephaly in a Limousin calf in Northern Ireland.

Journal: The Veterinary record

Published: August 18, 2026

Biallelic Frameshift Variant in LAMB1 Associated with Occipital Meningoencephalocele and Pansutural Craniosynostosis: A Case Report and Review of the Literature.

Journal: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society

Published: August 13, 2026

Ophthalmic Manifestations of KIF11-Associated Microcephaly With or Without Chorioretinopathy, Lymphedema, or Intellectual Disability: A Case Report of a Novel Variant.

Journal: The American journal of case reports

Published: August 06, 2026

Cortical Dysplasia Latest Advances

Find the Latest Research About Cortical Dysplasia

Understanding septo-optic dysplasia: Endocrine implications and ophthalmic consequences.

Understanding septo-optic dysplasia: Endocrine implications and ophthalmic consequences.

Operational definition, current and emerging pharmacotherapy, and clinical trial considerations in developmental and epileptic encephalopathies.

Operational definition, current and emerging pharmacotherapy, and clinical trial considerations in developmental and epileptic encephalopathies.

Diagnostic Overshadowing in Lennox-Gastaut Syndrome: Immerslund-Gräsbeck Syndrome Unmasked by Radiosurgical Stress.

Diagnostic Overshadowing in Lennox-Gastaut Syndrome: Immerslund-Gräsbeck Syndrome Unmasked by Radiosurgical Stress.

Timely Surgical Approaches for Pediatric Epilepsy Resistant to Medication.

Timely Surgical Approaches for Pediatric Epilepsy Resistant to Medication.

Genotype-Driven MRI Re-evaluation Reveals Subtle PAFAH1B1-Related Lissencephaly.

Genotype-Driven MRI Re-evaluation Reveals Subtle PAFAH1B1-Related Lissencephaly.

Acute Bilateral Vocal Cord Immobility Secondary to Acute Myopathy.

Acute Bilateral Vocal Cord Immobility Secondary to Acute Myopathy.

Neurophysiological Basis of Mirror Movements in Schizencephaly: A Case Report.

Neurophysiological Basis of Mirror Movements in Schizencephaly: A Case Report.

Selective retinal arterial whitening in retinal astrocytic hamartoma in tuberous sclerosis.

Selective retinal arterial whitening in retinal astrocytic hamartoma in tuberous sclerosis.

Rare genetic endocrine tumor syndromes: VHL, NF1, TSC, and Carney complex.

Rare genetic endocrine tumor syndromes: VHL, NF1, TSC, and Carney complex.

Congenital hereditary porencephaly in a Limousin calf in Northern Ireland.

Congenital hereditary porencephaly in a Limousin calf in Northern Ireland.

Biallelic Frameshift Variant in LAMB1 Associated with Occipital Meningoencephalocele and Pansutural Craniosynostosis: A Case Report and Review of the Literature.

Biallelic Frameshift Variant in LAMB1 Associated with Occipital Meningoencephalocele and Pansutural Craniosynostosis: A Case Report and Review of the Literature.

Ophthalmic Manifestations of KIF11-Associated Microcephaly With or Without Chorioretinopathy, Lymphedema, or Intellectual Disability: A Case Report of a Novel Variant.

Ophthalmic Manifestations of KIF11-Associated Microcephaly With or Without Chorioretinopathy, Lymphedema, or Intellectual Disability: A Case Report of a Novel Variant.