Tunis El Manar University
20 imported, source-linked research records. All imported publication dates.
20 matching research records
Topic: Mitochondrial DNA mutations. Only records linked to Tunis El Manar University are included. Historical ingestion is still running; these are imported records, not a count of all research worldwide.
Showing 1–20 of 20 matching records. Counts update as records arrive.
m.3243A T carriers require repeated prospective multisystem examinations not to overlook subclinical organ involvement
March 17, 2026 · 0 citations · Open access
Open original record →Delay in diagnosing a patient with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome who presented with status epilepticus and lactic acidosis: a case report
October 10, 2022 · 1 citations · Open access
Open original record →Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment
September 1, 2022 · 7 citations · Open access
Open original record →Fatigue and Exercise Intolerance as Initial Manifestations of a Nonsyndromic Mitochondrial Disorder Due to the Variant m.3243A G
March 23, 2022 · 0 citations · Open access
Open original record →Role of Bioactive Compounds in the Regulation of Mitochondrial Dysfunctions in Brain and Age-Related Neurodegenerative Diseases
January 13, 2022 · 19 citations · Open access
Open original record →Mitochondrial DNA and Alzheimer's Disease: A First Case-control Study of the Tunisian Population
November 2, 2021 · 0 citations · Open access
Open original record →Suspicious MELAS Requires Genetic and Biochemical Confirmation
July 30, 2019 · 0 citations · Open access
Open original record →Relationships Between Ion Channels, Mitochondrial Functions and Inflammation in Human Aging
March 1, 2019 · 61 citations · Open access
Open original record →Vaccination triggering onset of m.8993T G associated Leigh syndrome
April 25, 2018 · 1 citations · Open access
Open original record →Involvement of the Spinal Cord in Mitochondrial Disorders
April 1, 2018 · 27 citations · Open access
Open original record →Low Heteroplasmy Rates of the m.8993T G Variant May Not Be Pathogenic
March 3, 2018 · 0 citations
Open original record →Biomarkers for Detecting Mitochondrial Disorders
January 30, 2018 · 42 citations · Open access
Open original record →Comment on “Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis”
January 1, 2018 · 1 citations · Open access
Open original record →Can MR spectroscopy and muscle biopsy findings be correlated with MELAS and CPEO ?
August 29, 2017 · 0 citations · Open access
Open original record →Psychological morbidity in Leber’s hereditary optic neuropathy depends on phenotypic, social, economic, and genetic factors
May 1, 2017 · 1 citations · Open access
Open original record →Regional cerebral hyperperfusion: A biomarker of upcoming stroke‐like episodes?
April 13, 2017 · 0 citations · Open access
Open original record →Selection on the mitochondrial ATP synthase 6 and the NADH dehydrogenase 2 genes in hares (Lepus capensis L., 1758) from a steep ecological gradient in North Africa
February 7, 2017 · 32 citations · Open access
Open original record →Low blood heteroplasmy-rate may cause late-onset MELAS
February 5, 2017 · 1 citations · Open access
Open original record →Mitochondrial DNA Alterations and Oxidative Stress in Acute Leukemia
April 25, 2013 · 5 citations · Open access
Open original record →Germline HVR-II mitochondrial polymorphisms associated with breast cancer in Tunisian women
January 1, 2010 · 8 citations · Open access
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