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1.
Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians.
Cell Physiol Biochem
; 55(1): 117-129, 2021 Mar 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-33667330
2.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-31688634
3.
Hb Moscva [ß24(B6)GlyâAsp (GGT>GAT), HBB: c.74G>A]: An Unstable Hemoglobin Newly Detected as a De Novo Mutation in a Mauritanian Patient.
Hemoglobin
; 42(1): 7-10, 2018 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-29564956
4.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-28592168
5.
Dynamics of SARS-CoV-2 antibodies after natural infection: insights from a study on Pasteur Institute of Tunis employees.
Libyan J Med
; 19(1): 2348233, 2024 Dec 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-38693671
6.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-33421605
7.
The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients.
Hematology
; 22(3): 178-182, 2017 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-27869039
8.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-27077760
9.
Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1.
Hematology
; 21(2): 121-5, 2016 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26146896
10.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-26125973
11.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-24263212
12.
Rapid and inexpensive detection of common HBB gene mutations in Tunisian population by high-resolution melting analysis: implication for molecular diagnosis.
Hematology
; 19(2): 80-4, 2014 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-23683733
13.
Implication of genetic variation at the promoter and exon1 of UGT1A1 in occurrence of cholelithiasis in Tunisia.
Ann Biol Clin (Paris)
; 70(6): 702-6, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-23207817
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