Detalhe da pesquisa
1.
Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions.
Am J Perinatol
; 39(11): 1241-1247, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33374024
2.
Enhanced Eryptosis in Glucose-6-Phosphate Dehydrogenase Deficiency.
Cell Physiol Biochem
; 55(6): 761-772, 2021 Dec 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34894207
3.
Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians.
Cell Physiol Biochem
; 55(1): 117-129, 2021 Mar 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33667330
4.
New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level.
J Pediatr Hematol Oncol
; 42(1): 20-22, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31688634
5.
Homozygous Mutation on the ß-Globin Polyadenylation Signal in a Tunisian Patient with ß-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome.
Hemoglobin
; 41(2): 147-150, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28592168
6.
Gilbert syndrome acts as a risk factor of developing gallstone among ß hemoglobinopathy Tunisian patients.
Tunis Med
; 93(4): 237-41, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26375741
7.
Molecular characterization of a novel homozygous deletion in ß-globin cluster causing (δß)0-Thalassemia among Tunisian family.
Ann Clin Biochem
; 60(2): 81-85, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36214153
8.
Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia.
Eur J Med Genet
; 64(2): 104139, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33421605
9.
The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients.
Hematology
; 22(3): 178-182, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-27869039
10.
Fetal Hemoglobin in Tunisian Sickle Cell Disease Patient: Relationship with Polymorphic Sequences Cis to the ß-Globin Gene.
Indian J Hematol Blood Transfus
; 32(1): 114-9, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26855518
11.
rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.
Hematology
; 21(7): 425-9, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27077760
12.
Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1.
Hematology
; 21(2): 121-5, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26146896
13.
rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.
Hematology
; : 1-5, 2016 Mar 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26125973
14.
Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among sickle cell aneamia patients.
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub
; 159(1): 145-9, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24263212
15.
Early complication in sickle cell anemia children due to A(TA)nTAA polymorphism at the promoter of UGT1A1 gene.
Dis Markers
; 35(2): 67-72, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24167350
16.
Early complication in Sickle Cell Anemia children due to A(TA)_n TAA polymorphism at the promoter of UGT1A1 gene.
Dis Markers
; 2013 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-23619273