Mohamed N. Slimane

Monastir, Tunisia

Last Updated: 09/26/2026

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Found 12 publications

Pooling and expanding registries of familial hypercholesterolaemia to assess gaps in care and improve disease management and outcomes: Rationale and design of the global EAS Familial Hypercholesterolaemia Studies Collaboration.

Pooling and expanding registries of familial hypercholesterolaemia to assess gaps in care and improve disease management and outcomes: Rationale and design of the global EAS Familial Hypercholesterolaemia Studies Collaboration.

Journal: Atherosclerosis. Supplements

Published: December 13, 2016

Effect of PPAR-β/δ agonist GW0742 treatment in the acute phase response and blood-brain barrier permeability following brain injury.

Effect of PPAR-β/δ agonist GW0742 treatment in the acute phase response and blood-brain barrier permeability following brain injury.

Journal: Translational research : the journal of laboratory and clinical medicine

Published: March 22, 2016

Correlation of Oxidative Stress Parameters and Inflammatory Markers in Ischemic Stroke Patients.

Correlation of Oxidative Stress Parameters and Inflammatory Markers in Ischemic Stroke Patients.

Journal: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association

Published: November 16, 2015

Gene Variant and Level of IL-1β in Ischemic Stroke Patients With and Without Type 2 Diabetes Mellitus.

Gene Variant and Level of IL-1β in Ischemic Stroke Patients With and Without Type 2 Diabetes Mellitus.

Journal: Journal of molecular neuroscience : MN

Published: May 20, 2015

PCSK9 polymorphism in a Tunisian cohort: identification of a new allele, L8, and association of allele L10 with reduced coronary heart disease risk.

PCSK9 polymorphism in a Tunisian cohort: identification of a new allele, L8, and association of allele L10 with reduced coronary heart disease risk.

Journal: Molecular and cellular probes

Published: June 03, 2014

Effect of the PPARγ C161T gene variant on serum lipids in ischemic stroke patients with and without type 2 diabetes mellitus.

Effect of the PPARγ C161T gene variant on serum lipids in ischemic stroke patients with and without type 2 diabetes mellitus.

Journal: Journal of molecular neuroscience : MN

Published: April 08, 2014

Matrix metalloproteinase-1 and matrix metalloproteinase-12 gene polymorphisms and the risk of ischemic stroke in a Tunisian population.

Matrix metalloproteinase-1 and matrix metalloproteinase-12 gene polymorphisms and the risk of ischemic stroke in a Tunisian population.

Journal: Journal of the neurological sciences

Published: January 19, 2014

Effect of E670G Polymorphism in PCSK9 Gene on the Risk and Severity of Coronary Heart Disease and Ischemic Stroke in a Tunisian Cohort.

Effect of E670G Polymorphism in PCSK9 Gene on the Risk and Severity of Coronary Heart Disease and Ischemic Stroke in a Tunisian Cohort.

Journal: Journal of molecular neuroscience : MN

Published: November 28, 2013

Effect of genetic polymorphism +294T/C in peroxisome proliferator-activated receptor delta on the risk of ischemic stroke in a Tunisian population.

Effect of genetic polymorphism +294T/C in peroxisome proliferator-activated receptor delta on the risk of ischemic stroke in a Tunisian population.

Journal: Journal of molecular neuroscience : MN

Published: January 19, 2013

Genomic characterization of two deletions in the LDLR gene in Tunisian patients with familial hypercholesterolemia.

Genomic characterization of two deletions in the LDLR gene in Tunisian patients with familial hypercholesterolemia.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: June 21, 2012

Autosomal dominant hypercholesterolemia: needs for early diagnosis and cascade screening in the tunisian population.

Autosomal dominant hypercholesterolemia: needs for early diagnosis and cascade screening in the tunisian population.

Journal: Current genomics

Published: June 21, 2012

Effect of mutations in LDLR and PCSK9 genes on phenotypic variability in Tunisian familial hypercholesterolemia patients.

Effect of mutations in LDLR and PCSK9 genes on phenotypic variability in Tunisian familial hypercholesterolemia patients.

Journal: Atherosclerosis

Published: October 16, 2011

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Last Updated: 09/26/2026