Bruria B. Zeev

Ramat Gan, TA 52620, Israel

Last Updated: 09/26/2026

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Found 12 publications

High-dose diazepam as a long-term treatment strategy for epileptic encephalopathy and developmental epileptic encephalopathy spike-and-wave activation in sleep: A tertiary center's experience.

High-dose diazepam as a long-term treatment strategy for epileptic encephalopathy and developmental epileptic encephalopathy spike-and-wave activation in sleep: A tertiary center's experience.

Journal: Epilepsy & behavior : E&B

Published: December 28, 2024

Development of an International Standard Set of Outcomes and Measurement Methods for Routine Practice for Adults with Epilepsy: The International Consortium for Health Outcomes Measurement Consensus Recommendations.

Development of an International Standard Set of Outcomes and Measurement Methods for Routine Practice for Adults with Epilepsy: The International Consortium for Health Outcomes Measurement Consensus Recommendations.

Journal: Epilepsia

Published: October 03, 2023

PRDM16 co-operates with LHX2 to shape the human brain.

PRDM16 co-operates with LHX2 to shape the human brain.

Journal: Oxford open neuroscience

Published: August 12, 2023

Corrigendum to: Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes.

Corrigendum to: Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes.

Journal: Molecular genetics and metabolism

Published: July 15, 2023

DNA methylation episignatures are sensitive and specific biomarkers for detection of patients with KAT6A/KAT6B variants.

DNA methylation episignatures are sensitive and specific biomarkers for detection of patients with KAT6A/KAT6B variants.

Journal: Epigenomics

Published: May 30, 2023

Gene therapy for aromatic L-amino acid decarboxylase deficiency: Requirements for safe application and knowledge-generating follow-up.

Gene therapy for aromatic L-amino acid decarboxylase deficiency: Requirements for safe application and knowledge-generating follow-up.

Journal: Journal of inherited metabolic disease

Published: April 26, 2023

Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes.

Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes.

Journal: Molecular genetics and metabolism

Published: March 14, 2023

4-Aminopyridine is a promising treatment option for patients with gain-of-function KCNA2-encephalopathy.

4-Aminopyridine is a promising treatment option for patients with gain-of-function KCNA2-encephalopathy.

Journal: Science translational medicine

Published: September 13, 2021

Unique findings of subependymal giant cell astrocytoma within cortical tubers in patients with tuberous sclerosis complex: a histopathological evaluation.

Unique findings of subependymal giant cell astrocytoma within cortical tubers in patients with tuberous sclerosis complex: a histopathological evaluation.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Published: October 31, 2016

Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency.

Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency.

Journal: Journal of inherited metabolic disease

Published: March 11, 2015

CAOS-Episodic Cerebellar Ataxia, Areflexia, Optic Atrophy, and Sensorineural Hearing Loss: A Third Allelic Disorder of the ATP1A3 Gene.

CAOS-Episodic Cerebellar Ataxia, Areflexia, Optic Atrophy, and Sensorineural Hearing Loss: A Third Allelic Disorder of the ATP1A3 Gene.

Journal: Journal of child neurology

Published: August 18, 2014

The phenotype associated with a large deletion on MECP2.

The phenotype associated with a large deletion on MECP2.

Journal: European journal of human genetics : EJHG

Published: April 05, 2012

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Last Updated: 09/26/2026