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.
Inherited bisalbuminemia with growth hormone deficiency.
Clin Chem Lab Med
; 57(9): e226-e229, 2019 08 27.
Artigo
Inglês
| MEDLINE | ID: mdl-30763259
3.
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
4.
Hyperbaric Oxygen Therapy for Mumps-Associated Outer Retinitis with Frosted Branch Angiitis.
Ocul Immunol Inflamm
; 30(4): 1001-1004, 2022 May 19.
Artigo
Inglês
| MEDLINE | ID: mdl-33545017
5.
Prevalence and risk factors of overweight and obesity in elementary schoolchildren in the metropolitan region of Tunis, Tunisia.
Tunis Med
; 89(1): 50-4, 2011 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-21267829
6.
A rare cause of cyanosis: Congenital methemoglobinemia.
Clin Case Rep
; 9(7): e04422, 2021 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-34267908
7.
Abdominal tuberculosis in children.
J Pediatr Gastroenterol Nutr
; 50(6): 634-8, 2010 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-20386326
8.
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
9.
Extra-pulmonary tuberculosis in children: a study of 41 cases.
Tunis Med
; 87(10): 693-8, 2009 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-20187360
10.
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
11.
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
12.
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
13.
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
14.
3M Syndrome: A Rare Cause of Short Stature.
Indian Pediatr
; 56(9): 799, 2019 09 15.
Artigo
Inglês
| MEDLINE | ID: mdl-31638017
15.
Central system nervous tuberculosis in infants.
J Child Neurol
; 25(1): 102-6, 2010 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-20032518