Galit Tal

Haifa, HA, Israel

Last Updated: 09/26/2026

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Found 47 publications

Corrigendum to "Glutaminase deficiency provides insight to the role of glutamine accumulation and neurotoxicity" [Mol. Genet. Metab. 148(2) (2026) 109906].

Corrigendum to "Glutaminase deficiency provides insight to the role of glutamine accumulation and neurotoxicity" [Mol. Genet. Metab. 148(2) (2026) 109906].

Journal: Molecular genetics and metabolism

Published: June 08, 2026

X-Linked Cerebral Adrenoleukodystrophy Presenting With Acute Encephalitis-Like Illness and Optic Neuropathy in a Child.

X-Linked Cerebral Adrenoleukodystrophy Presenting With Acute Encephalitis-Like Illness and Optic Neuropathy in a Child.

Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society

Published: May 14, 2026

Erratum to "Glutaminase deficiency provides insight to the role of glutamine accumulation and neurotoxicity" [Mol Genet Metab. (2026) Vol. 148 Issue 2 109906].

Erratum to "Glutaminase deficiency provides insight to the role of glutamine accumulation and neurotoxicity" [Mol Genet Metab. (2026) Vol. 148 Issue 2 109906].

Journal: Molecular genetics and metabolism

Published: April 07, 2026

Glutaminase deficiency provides insight to the role of glutamine accumulation and neurotoxicity.

Glutaminase deficiency provides insight to the role of glutamine accumulation and neurotoxicity.

Journal: Molecular genetics and metabolism

Published: January 21, 2026

From genotype to outcome: Zygosity-specific insights in 63 cases of CLPB-related mitochondrial disease.

From genotype to outcome: Zygosity-specific insights in 63 cases of CLPB-related mitochondrial disease.

Journal: Molecular genetics and metabolism

Published: November 25, 2025

Impact of Rapid Exome Sequencing on Pediatric Patients With Cardiomyopathy and Acute Heart Failure.

Impact of Rapid Exome Sequencing on Pediatric Patients With Cardiomyopathy and Acute Heart Failure.

Journal: American journal of medical genetics. Part A

Published: July 15, 2025

Impact of Rapid Exome Sequencing on Pediatric Patients With Cardiomyopathy and Acute Heart Failure.

Impact of Rapid Exome Sequencing on Pediatric Patients With Cardiomyopathy and Acute Heart Failure.

Journal: American journal of medical genetics. Part A

Published: July 15, 2025

The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.

The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.

Journal: Brain : a journal of neurology

Published: July 01, 2025

The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.

The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.

Journal: Brain : a journal of neurology

Published: July 01, 2025

Proliferative retinopathy in a patient with mutation in the CLCN2 gene.

Proliferative retinopathy in a patient with mutation in the CLCN2 gene.

Journal: European journal of ophthalmology

Published: February 21, 2025

Using chanarin-dorfman syndrome patient fibroblasts to explore disease mechanisms and new treatment avenues.

Using chanarin-dorfman syndrome patient fibroblasts to explore disease mechanisms and new treatment avenues.

Journal: Orphanet journal of rare diseases

Published: November 09, 2024

Sengers syndrome caused by biallelic TIMM29 variants and RNAi silencing in Drosophila orthologue recapitulates the human phenotype.

Sengers syndrome caused by biallelic TIMM29 variants and RNAi silencing in Drosophila orthologue recapitulates the human phenotype.

Journal: Human genomics

Published: November 01, 2024

Showing 1-12 of 47

Last Updated: 09/26/2026