Detalhe da pesquisa
1.
SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype.
Am J Hum Genet
; 108(11): 2112-2129, 2021 11 04.
Artigo
Inglês
| MEDLINE | ID: mdl-34626534
2.
Turner syndrome: results of the first Tunisian study group on Turner syndrome (TuSGOT).
J Pediatr Endocrinol Metab
; 36(6): 577-583, 2023 Jun 27.
Artigo
Inglês
| MEDLINE | ID: mdl-37084413
3.
C677t polymorphism of MTHFR and G80A polymorphism of RFC genes and their relation with homocysteine levels in obese Tunisian children.
Tunis Med
; 89(6): 565-8, 2011 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-21681722
4.
A rare cause of cyanosis: Congenital methemoglobinemia.
Clin Case Rep
; 9(7): e04422, 2021 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-34267908
5.
Characteristics and etiologies of short stature in children: Experience of an endocrine clinic in a Tunisian tertiary care hospital.
Int J Pediatr Adolesc Med
; 7(2): 74-77, 2020 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-32642540
6.
Validation of the Arabic and Tunisian Arabic version of the KINDL questionnaires for children with diabetes type 1.
Libyan J Med
; 14(1): 1537457, 2019 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-30481145
7.
Congenital hypothyroidism presenting with reversible renal impairment: an under-recognised problem?
J Diabetes Metab Disord
; 18(2): 733-738, 2019 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-31890699
8.
Congenital lobar emphysema. Report of 17 cases.
Tunis Med
; 86(4): 373-7, 2008 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-19476142
9.
Implementation of effective transition from pediatric to adult diabetes care: epidemiological and clinical characteristics-a pioneering experience in North Africa.
Acta Diabetol
; 55(11): 1163-1169, 2018 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-30074090
10.
A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients.
Mol Immunol
; 90: 57-63, 2017 10.
Artigo
Inglês
| MEDLINE | ID: mdl-28704707
11.
Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome.
Arch Med Res
; 47(2): 105-10, 2016 02.
Artigo
Inglês
| MEDLINE | ID: mdl-27133709
12.
[Autoimmune polyglandular syndrome type I]. / Polyendocrinopathie autoimmune de type I.
Tunis Med
; 86(5): 519-20, 2008 May.
Artigo
Francês
| MEDLINE | ID: mdl-19469319