Tova Hershkovitz

Nahariyya, Z, Israel

Last Updated: 09/26/2026

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Found 37 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

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson syndrome.

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson syndrome.

Journal: American journal of human genetics

Published: June 05, 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

Monogenic and SLE-like disorders in the pediatric population: insights from a Northern Israel cohort.

Monogenic and SLE-like disorders in the pediatric population: insights from a Northern Israel cohort.

Journal: Lupus

Published: January 14, 2026

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

Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND).

Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND).

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 23, 2025

Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND).

Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND).

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 23, 2025

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson Syndrome.

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson Syndrome.

Journal: medRxiv : the preprint server for health sciences

Published: May 19, 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

Impaired Wnt/Planar Cell Polarity Signaling in Yellow Nail Syndrome.

Impaired Wnt/Planar Cell Polarity Signaling in Yellow Nail Syndrome.

Journal: Annals of internal medicine

Published: December 23, 2024

Showing 1-12 of 37

Last Updated: 09/26/2026