Epilepsy in Children Latest Advances

Pyridoxine-Dependent Epilepsy in Newborn - A Rare and Challenging Diagnosis.

Journal: Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki)

Published: December 09, 2025

A comparative cohort study of epilepsy in children in Greenland and Denmark.

Journal: International journal of circumpolar health

Published: December 05, 2025

Functional consequence of pathogenic GABRA3 variants determines whether X-linked inheritance is dominant or recessive.

Journal: The Journal of clinical investigation

Published: November 25, 2025

Developmental epileptic encephalopathy caused by a de novo mutation in the SCN8A gene

Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

Published: November 24, 2025

Genetic and clinical characteristics in epilepsy patients with ATP6V1A gene variants

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: November 13, 2025

Analysis of clinical phenotypes and genotypic characteristics in children with epilepsy

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: November 13, 2025

Probiotics restore GABAergic neurons and attenuate postnatal seizures in periventricular leukomalacia.

Journal: Nutritional neuroscience

Published: November 11, 2025

One Center's Experience With Outpatient Initiation of Ketogenic Therapy in Infants 18 Months or Younger.

Journal: Journal of child neurology

Published: November 11, 2025

Complete Pancreatic Agenesis Presenting With Neonatal Diabetes and Exocrine Insufficiency: A Case Report.

Journal: Cureus

Published: November 09, 2025

Sex Disparities in Neonatal Arterial Ischemic Stroke: Larger Lesion Volume and More Severe Long-Term Disability in Male Infants.

Journal: Pediatric neurology

Published: November 08, 2025

Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review.

Journal: Balkan journal of medical genetics : BJMG

Published: November 07, 2025

Congenital disorder of glycosylation type IIb in an infant with developmental and epileptic encephalopathy.

Journal: BMJ case reports

Published: November 05, 2025

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Pyridoxine-Dependent Epilepsy in Newborn - A Rare and Challenging Diagnosis.

Pyridoxine-Dependent Epilepsy in Newborn - A Rare and Challenging Diagnosis.

A comparative cohort study of epilepsy in children in Greenland and Denmark.

A comparative cohort study of epilepsy in children in Greenland and Denmark.

Functional consequence of pathogenic GABRA3 variants determines whether X-linked inheritance is dominant or recessive.

Functional consequence of pathogenic GABRA3 variants determines whether X-linked inheritance is dominant or recessive.

Developmental epileptic encephalopathy caused by a de novo mutation in the SCN8A gene

Developmental epileptic encephalopathy caused by a de novo mutation in the SCN8A gene

Genetic and clinical characteristics in epilepsy patients with ATP6V1A gene variants

Genetic and clinical characteristics in epilepsy patients with ATP6V1A gene variants

Analysis of clinical phenotypes and genotypic characteristics in children with epilepsy

Analysis of clinical phenotypes and genotypic characteristics in children with epilepsy

Probiotics restore GABAergic neurons and attenuate postnatal seizures in periventricular leukomalacia.

Probiotics restore GABAergic neurons and attenuate postnatal seizures in periventricular leukomalacia.

One Center's Experience With Outpatient Initiation of Ketogenic Therapy in Infants 18 Months or Younger.

One Center's Experience With Outpatient Initiation of Ketogenic Therapy in Infants 18 Months or Younger.

Complete Pancreatic Agenesis Presenting With Neonatal Diabetes and Exocrine Insufficiency: A Case Report.

Complete Pancreatic Agenesis Presenting With Neonatal Diabetes and Exocrine Insufficiency: A Case Report.

Sex Disparities in Neonatal Arterial Ischemic Stroke: Larger Lesion Volume and More Severe Long-Term Disability in Male Infants.

Sex Disparities in Neonatal Arterial Ischemic Stroke: Larger Lesion Volume and More Severe Long-Term Disability in Male Infants.

Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review.

Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review.

Congenital disorder of glycosylation type IIb in an infant with developmental and epileptic encephalopathy.

Congenital disorder of glycosylation type IIb in an infant with developmental and epileptic encephalopathy.