University research records

University of Monastir

9 imported, source-linked research records. Published in the last five years.

Published in the last five years

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.

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Showing 1–9 of 9 matching records. Counts update as records arrive.

  1. 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

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  2. 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

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  3. To prevent sudden death in m.3243A G carriers, comprehensive neurologic, cardiac, and pulmological examinations are required

    September 1, 2024 · 0 citations · Open access

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  4. 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

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  5. Seizure phenomenology in MELAS

    October 1, 2023 · 0 citations · Open access

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  6. Mitochondrial disorders due to m.3243A G not meeting diagnostic criteria for MELAS require comprehensive work-up

    July 3, 2023 · 1 citations · Open access

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  7. Milder Phenotype of Homoplasmic Versus Heteroplasmic m.8344A G Variant in the Same Family: A Case Report

    August 28, 2022 · 3 citations · Open access

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  8. Role of Bioactive Compounds in the Regulation of Mitochondrial Dysfunctions in Brain and Age-Related Neurodegenerative Diseases

    January 13, 2022 · 19 citations · Open access

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  9. 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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