Abdelhamid Slama

Paris, France

Last Updated: 09/26/2026

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Found 43 publications

Mitochondrial DNA or Genomic DNA Variant(s): Utility of Exhaustive Sequencing in Leigh Syndrome.

Mitochondrial DNA or Genomic DNA Variant(s): Utility of Exhaustive Sequencing in Leigh Syndrome.

Journal: American journal of medical genetics. Part A

Published: October 03, 2024

MPC2 variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathy.

MPC2 variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathy.

Journal: Brain : a journal of neurology

Published: July 01, 2022

Association of the CAG repeat polymorphism in mitochondrial polymerase gamma (POLG1) with male infertility: a case-control study in an Algerian population.

Association of the CAG repeat polymorphism in mitochondrial polymerase gamma (POLG1) with male infertility: a case-control study in an Algerian population.

Journal: African journal of reproductive health

Published: June 02, 2021

Adenosine kinase deficiency: Three new cases and diagnostic value of hypermethioninemia.

Adenosine kinase deficiency: Three new cases and diagnostic value of hypermethioninemia.

Journal: Molecular genetics and metabolism

Published: August 05, 2020

Mitochondrial dysfunction caused by novel ATAD3A mutations.

Mitochondrial dysfunction caused by novel ATAD3A mutations.

Journal: Molecular genetics and metabolism

Published: July 09, 2020

Clinical, neuroimaging and biochemical findings in patients and patient fibroblasts expressing ten novel GFM1 mutations.

Clinical, neuroimaging and biochemical findings in patients and patient fibroblasts expressing ten novel GFM1 mutations.

Journal: Human mutation

Published: June 16, 2019

Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature review.

Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature review.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: June 04, 2019

Mitochondrial myopathy associated with anti-programmed cell death 1 therapy.

Mitochondrial myopathy associated with anti-programmed cell death 1 therapy.

Journal: European journal of cancer (Oxford, England : 1990)

Published: December 12, 2018

Life-threatening lactic acidosis occurring in adults with mitochondrial disorders.

Life-threatening lactic acidosis occurring in adults with mitochondrial disorders.

Journal: Revue neurologique

Published: August 31, 2018

Steroids in Stroke with Special Reference to Progesterone.

Steroids in Stroke with Special Reference to Progesterone.

Journal: Cellular and molecular neurobiology

Published: July 24, 2018

Expanding and Underscoring the Hepato-Encephalopathic Phenotype of QIL1/MIC13.

Expanding and Underscoring the Hepato-Encephalopathic Phenotype of QIL1/MIC13.

Journal: Hepatology (Baltimore, Md.)

Published: June 14, 2018

Intranasal administration of progesterone: A potential efficient route of delivery for cerebroprotection after acute brain injuries.

Intranasal administration of progesterone: A potential efficient route of delivery for cerebroprotection after acute brain injuries.

Journal: Neuropharmacology

Published: April 10, 2018

Showing 1-12 of 43

Last Updated: 09/26/2026