Mohamed T. Sfar

Mahdia, Tunisia

Last Updated: 09/26/2026

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Found 13 publications

Turner syndrome: results of the first Tunisian study group on Turner syndrome (TuSGOT).

Turner syndrome: results of the first Tunisian study group on Turner syndrome (TuSGOT).

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: July 15, 2022

A cost-effectiveness analysis of PHiD-CV compared to PCV13 in a national immunization program setting in Tunisia.

A cost-effectiveness analysis of PHiD-CV compared to PCV13 in a national immunization program setting in Tunisia.

Journal: Human vaccines & immunotherapeutics

Published: June 15, 2022

Phenotypic variability in Tunisian PFIC3 patients harboring a complex genotype with a differential clinical outcome of UDCA treatment.

Phenotypic variability in Tunisian PFIC3 patients harboring a complex genotype with a differential clinical outcome of UDCA treatment.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: January 24, 2018

Poikiloderma with neutropenia in a Tunisian patient with a novel C16orf57 gene mutation.

Poikiloderma with neutropenia in a Tunisian patient with a novel C16orf57 gene mutation.

Journal: Pediatric blood & cancer

Published: December 28, 2017

Hospital cost of invasive pneumococcal disease in children aged under 15 years old in Tunisia.

Hospital cost of invasive pneumococcal disease in children aged under 15 years old in Tunisia.

Journal: Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit

Published: December 22, 2016

Enterovirus meningitis in Tunisia (Monastir, Mahdia, 2011-2013): identification of virus variants cocirculating in France.

Enterovirus meningitis in Tunisia (Monastir, Mahdia, 2011-2013): identification of virus variants cocirculating in France.

Journal: Diagnostic microbiology and infectious disease

Published: December 29, 2014

Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesis.

Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesis.

Journal: Indian journal of endocrinology and metabolism

Published: June 19, 2013

Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Journal: Indian journal of endocrinology and metabolism

Published: December 11, 2012

High frequency of W1327X mutation in glycogen storage disease type III patients from central Tunisia.

High frequency of W1327X mutation in glycogen storage disease type III patients from central Tunisia.

Journal: Annales de biologie clinique

Published: December 05, 2012

Antioxidant enzymes activities in obese Tunisian children.

Antioxidant enzymes activities in obese Tunisian children.

Journal: Nutrition journal

Published: October 06, 2012

Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: characterization of three novel polymorphisms.

Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: characterization of three novel polymorphisms.

Journal: Gene

Published: May 05, 2012

Long-term outcome of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Long-term outcome of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Journal: The American journal of the medical sciences

Published: January 25, 2012

Showing 1-12 of 13

Last Updated: 09/26/2026