Saayda Ben Becher
Tunis, Tunisia
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
Turner syndrome: results of the first Tunisian study group on Turner syndrome (TuSGOT).
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: July 15, 2022
SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype.
Journal: American journal of human genetics
Published: July 21, 2021
A rare cause of cyanosis: Congenital methemoglobinemia.
Journal: Clinical case reports
Published: February 04, 2021
Characteristics and etiologies of short stature in children: Experience of an endocrine clinic in a Tunisian tertiary care hospital.
Journal: International journal of pediatrics & adolescent medicine
Published: April 22, 2019
Congenital hypothyroidism presenting with reversible renal impairment: an under-recognised problem?
Journal: Journal of diabetes and metabolic disorders
Published: April 12, 2019
Validation of the Arabic and Tunisian Arabic version of the KINDL questionnaires for children with diabetes type 1.
Journal: The Libyan journal of medicine
Published: November 28, 2018
Implementation of effective transition from pediatric to adult diabetes care: epidemiological and clinical characteristics-a pioneering experience in North Africa.
Journal: Acta diabetologica
Published: June 14, 2018
Drug Reaction With Eosinophilia and Systemic Symptoms (DRESS) Syndrome in Children: A Case Report.
Journal: Journal of investigational allergology & clinical immunology
Published: April 12, 2017
Rare splicing defects of FAS underly severe recessive autoimmune lymphoproliferative syndrome.
Journal: Clinical immunology (Orlando, Fla.)
Published: November 07, 2016
Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome.
Journal: Archives of medical research
Published: October 09, 2015
Showing 1-10 of 10
Last Updated: 09/26/2026