Ayalla Fedida
Nahariyya, Z, Israel
Last Updated: 09/26/2026
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Found 12 publications
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
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.
Journal: Molecular genetics and metabolism
Published: January 21, 2026
Long term ophthalmic complications of distal arthrogryposis type 5D.
Journal: Ophthalmic genetics
Published: December 02, 2022
A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness.
Journal: Journal of the American Society of Nephrology : JASN
Published: October 06, 2021
COG6-CDG: Expanding the phenotype with emphasis on glycosylation defects involved in the causation of male disorders of sex development.
Journal: Clinical genetics
Published: June 16, 2020
Sedaghatian-type spondylometaphyseal dysplasia: Whole exome sequencing in neonatal dry blood spots enabled identification of a novel variant in GPX4.
Journal: European journal of medical genetics
Published: September 02, 2019
Newborn screening for cerebrotendinous xanthomatosis is the solution for early identification and treatment.
Journal: Journal of lipid research
Published: July 03, 2018
Two Synechococcus genes, Two Different Effects on Cyanophage Infection.
Journal: Viruses
Published: April 07, 2017
Transcriptome dynamics of a broad host-range cyanophage and its hosts.
Journal: The ISME journal
Published: June 07, 2015
Showing 1-12 of 12
Last Updated: 09/26/2026