Devorah Soiferman
Jerusalem, JM 91120, Israel
Last Updated: 09/26/2026
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Found 10 publications
The Effects of Ascorbate, N-Acetylcysteine, and Resveratrol on Fibroblasts from Patients with Mitochondrial Disorders.
Journal: Journal of clinical medicine
Published: October 21, 2016
Upregulation of Mitochondrial Content in Cytochrome c Oxidase Deficient Fibroblasts.
Journal: PloS one
Published: June 28, 2016
Novel Homozygous Missense Mutation in SPG20 Gene Results in Troyer Syndrome Associated with Mitochondrial Cytochrome c Oxidase Deficiency.
Journal: JIMD reports
Published: January 17, 2016
Postnatal microcephaly and pain insensitivity due to a de novo heterozygous DNM1L mutation causing impaired mitochondrial fission and function.
Journal: American journal of medical genetics. Part A
Published: September 02, 2015
Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation.
Journal: Journal of medical genetics
Published: July 05, 2015
Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy.
Journal: European journal of human genetics : EJHG
Published: November 16, 2013
The effect of small molecules on nuclear-encoded translation diseases.
Journal: Biochimie
Published: June 07, 2013
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy.
Journal: European journal of human genetics : EJHG
Published: March 23, 2013
Agenesis of corpus callosum and optic nerve hypoplasia due to mutations in SLC25A1 encoding the mitochondrial citrate transporter.
Journal: Journal of medical genetics
Published: February 09, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026