Abdelbasset Amara

Rue Ibn El Jezzar
Sousse, 4002, Tunisia

Last Updated: 09/26/2026

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Found 13 publications

Association of the OPRM1 and COMT genes' polymorphisms with the efficacy of morphine in Tunisian cancer patients: Impact of the high genetic heterogeneity in Tunisia?

Association of the OPRM1 and COMT genes' polymorphisms with the efficacy of morphine in Tunisian cancer patients: Impact of the high genetic heterogeneity in Tunisia?

Journal: Therapie

Published: January 01, 2016

Genetic study in a tunisian family revealed IVS1+1G>A mutation in the CHM gene.

Genetic study in a tunisian family revealed IVS1+1G>A mutation in the CHM gene.

Journal: Annales de biologie clinique

Published: September 29, 2015

Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent β-Thalassemia Mutations in the Tunisian Population.

Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent β-Thalassemia Mutations in the Tunisian Population.

Journal: Hemoglobin

Published: May 29, 2015

Macrozoospermia: screening for the homozygous c.144delC mutation in AURKC gene in infertile men and estimation of its heterozygosity frequency in the Tunisian population.

Macrozoospermia: screening for the homozygous c.144delC mutation in AURKC gene in infertile men and estimation of its heterozygosity frequency in the Tunisian population.

Journal: Journal of assisted reproduction and genetics

Published: May 26, 2015

Frequency of HNF4A-P.I463V Variant in the Tunisian North-African Population and Its Relation with Diabetes Mellitus.

Frequency of HNF4A-P.I463V Variant in the Tunisian North-African Population and Its Relation with Diabetes Mellitus.

Journal: Iranian journal of public health

Published: December 15, 2014

Multiple self-healing palmoplantar carcinoma: a familial predisposition to skin cancer with primary palmoplantar and conjunctival lesions.

Multiple self-healing palmoplantar carcinoma: a familial predisposition to skin cancer with primary palmoplantar and conjunctival lesions.

Journal: The Journal of investigative dermatology

Published: July 23, 2014

Molecular characterization of piebaldism in a Tunisian family.

Molecular characterization of piebaldism in a Tunisian family.

Journal: Pathologie-biologie

Published: July 11, 2014

Challenges for molecular diagnosis of familial early-onset diabetes in unexplored populations.

Challenges for molecular diagnosis of familial early-onset diabetes in unexplored populations.

Journal: Iranian journal of public health

Published: May 12, 2014

Familial early-onset diabetes is not a typical MODY in several Tunisian patients.

Familial early-onset diabetes is not a typical MODY in several Tunisian patients.

Journal: La Tunisie medicale

Published: December 19, 2012

Reduction of palmoplantar keratoderma Buschke-Fischer-Brauer locus to only 0.967 Mb.

Reduction of palmoplantar keratoderma Buschke-Fischer-Brauer locus to only 0.967 Mb.

Journal: Journal of dermatological science

Published: January 22, 2012

Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III.

Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III.

Journal: Journal of human genetics

Published: November 18, 2011

A c.3216_3217delGA mutation in AGL gene in Tunisian patients with a glycogen storage disease type III: evidence of a founder effect.

A c.3216_3217delGA mutation in AGL gene in Tunisian patients with a glycogen storage disease type III: evidence of a founder effect.

Journal: Clinical genetics

Published: November 01, 2011

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Last Updated: 09/26/2026