Noura Elleuch-Bougacha

Sfax, Tunisia

Last Updated: 09/26/2026

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Found 13 publications

Pustular psoriasis of pregnancy: Clinical and genetic characteristics in a series of eight patients and review of the literature.

Pustular psoriasis of pregnancy: Clinical and genetic characteristics in a series of eight patients and review of the literature.

Journal: Dermatologic therapy

Published: March 11, 2022

Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype-phenotype correlation.

Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype-phenotype correlation.

Journal: BMC medical genomics

Published: September 09, 2021

Occurrence of Hypopituitarism in Tunisian Turner Syndrome patients: familial versus sporadic cases.

Occurrence of Hypopituitarism in Tunisian Turner Syndrome patients: familial versus sporadic cases.

Journal: Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology

Published: June 14, 2021

Potential role of liver enzyme levels as predictive markers of glucose metabolism disorders in a Tunisian population.

Potential role of liver enzyme levels as predictive markers of glucose metabolism disorders in a Tunisian population.

Journal: Canadian journal of physiology and pharmacology

Published: March 13, 2018

Affinity kinetics of leptin-reactive immunoglobulins are associated with plasma leptin and markers of obesity and diabetes.

Affinity kinetics of leptin-reactive immunoglobulins are associated with plasma leptin and markers of obesity and diabetes.

Journal: Nutrition & diabetes

Published: January 05, 2018

Potential Predictive Role of Lipid Peroxidation Markers for Type 2 Diabetes in the Adult Tunisian Population.

Potential Predictive Role of Lipid Peroxidation Markers for Type 2 Diabetes in the Adult Tunisian Population.

Journal: Canadian journal of diabetes

Published: April 25, 2017

Erratum to: Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect.

Erratum to: Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect.

Journal: European journal of pediatrics

Published: November 15, 2015

Unusual association of turner syndrome and hypopituitarism in a Tunisian family.

Unusual association of turner syndrome and hypopituitarism in a Tunisian family.

Journal: Current research in translational medicine

Published: July 11, 2015

Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect.

Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect.

Journal: European journal of pediatrics

Published: March 18, 2015

A 20 year history of clinical and genetic study of thyroid autoimmunity in a Tunisian multigenerational family: Evidence for gene interaction.

A 20 year history of clinical and genetic study of thyroid autoimmunity in a Tunisian multigenerational family: Evidence for gene interaction.

Journal: Meta gene

Published: October 22, 2013

IL-1β a potential factor for discriminating between thyroid carcinoma and atrophic thyroiditis.

IL-1β a potential factor for discriminating between thyroid carcinoma and atrophic thyroiditis.

Journal: European cytokine network

Published: September 22, 2012

IL-1β and TSH disturb thyroid epithelium integrity in autoimmune thyroid diseases.

IL-1β and TSH disturb thyroid epithelium integrity in autoimmune thyroid diseases.

Journal: Immunobiology

Published: November 17, 2011

Showing 1-12 of 13

Last Updated: 09/26/2026