Absence Seizure Latest Advances

Find the Latest Research About Absence Seizure

Last Updated: 02/24/2026

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Found 71466 publications

Unusual association: Sturge-Weber syndrome with Klippel-Trenaunay syndrome.

Unusual association: Sturge-Weber syndrome with Klippel-Trenaunay syndrome.

Journal: BMJ case reports
Published: January 22, 2026

CTC1 mutation causing cerebro-retinal microangiopathy with calcifications and cysts type 1, masquerading as TORCH Infection.

CTC1 mutation causing cerebro-retinal microangiopathy with calcifications and cysts type 1, masquerading as TORCH Infection.

Journal: BMJ case reports
Published: January 19, 2026

Genotypic and radiological expansion of CONDSIAS.

Genotypic and radiological expansion of CONDSIAS.

Journal: BMJ case reports
Published: January 14, 2026

Recurrent hypocalcaemic seizures: diagnosing 22q11.2 deletion syndrome in early adulthood.

Recurrent hypocalcaemic seizures: diagnosing 22q11.2 deletion syndrome in early adulthood.

Journal: BMJ case reports
Published: January 12, 2026

Posterior reversible encephalopathy syndrome in a child with leptospira-associated glomerulonephritis: the 3 P'S framework.

Posterior reversible encephalopathy syndrome in a child with leptospira-associated glomerulonephritis: the 3 P'S framework.

Journal: BMJ case reports
Published: January 06, 2026

Clinical and genetic analysis of a child with intellectual developmental disorder and seizures associated with variant of AP2M1 gene

Clinical and genetic analysis of a child with intellectual developmental disorder and seizures associated with variant of AP2M1 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: December 26, 2025

Report of a Chinese pedigree affected with Neurodevelopmental disorder with absent language and variable seizures due to variant of WASF1 gene and a literature review

Report of a Chinese pedigree affected with Neurodevelopmental disorder with absent language and variable seizures due to variant of WASF1 gene and a literature review

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: December 26, 2025

Clinical Manifestations.

Clinical Manifestations.

Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: December 25, 2025

Targeting brain hubs of ictal fast ripple activity to reduce seizures in patients with drug-resistant epilepsy.

Targeting brain hubs of ictal fast ripple activity to reduce seizures in patients with drug-resistant epilepsy.

Journal: Science translational medicine
Published: December 24, 2025

Clinical Manifestations.

Clinical Manifestations.

Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: December 24, 2025

Infantile-Onset Unverricht-Lundborg Disease: A Unique Case With Severe Neurological Impairment and Positive Family History.

Infantile-Onset Unverricht-Lundborg Disease: A Unique Case With Severe Neurological Impairment and Positive Family History.

Journal: Journal of investigative medicine high impact case reports
Published: December 23, 2025

Developing Topics.

Developing Topics.

Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: December 23, 2025
Showing 1-12 of 71,466

Last Updated: 02/24/2026