University research records
University of Monastir
9 imported, source-linked research records. Published in the last five years.
Published in the last five years
Back to university profile →9 matching research records
Topic: Mitochondrial DNA mutations. Only records linked to University of Monastir are included. Historical ingestion is still running; these are imported records, not a count of all research worldwide.
Showing 1–9 of 9 matching records. Counts update as records arrive.
The Tolerability of Metformin in Carriers of the m.3243A G Mutation Depends on the Genetic Determinants of the Phenotype
June 1, 2026 · 0 citations · Open access
Open original record →Respiratory Chain Complex I Deficiency in Leber Hereditary Optic Neuropathy: Insights from Ophthalmologic and Molecular Investigations in Tunisia
November 22, 2024 · 1 citations · Open access
Open original record →To prevent sudden death in m.3243A G carriers, comprehensive neurologic, cardiac, and pulmological examinations are required
September 1, 2024 · 0 citations · Open access
Open original record →MIDD Patients Should Not Be Confused with MELAS Patients, Even Though Both Carry the m.3243A G Variant
July 28, 2024 · 1 citations · Open access
Open original record →Seizure phenomenology in MELAS
October 1, 2023 · 0 citations · Open access
Open original record →Mitochondrial disorders due to m.3243A G not meeting diagnostic criteria for MELAS require comprehensive work-up
July 3, 2023 · 1 citations · Open access
Open original record →Milder Phenotype of Homoplasmic Versus Heteroplasmic m.8344A G Variant in the Same Family: A Case Report
August 28, 2022 · 3 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
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