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New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level.
J Pediatr Hematol Oncol. 2020 Jan;42(1):20-22. doi: 10.1097/MPH.0000000000001626.
J Pediatr Hematol Oncol. 2020.
PMID: 31688634
rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.
Chaouch L, Moumni I, Ouragini H, Darragi I, Kalai M, Chaouachi D, Boudrigua I, Hafsia R, Abbes S.
Chaouch L, et al. Among authors: boudrigua i.
Hematology. 2016 Mar 3:1-5. doi: 10.1179/1607845415Y.0000000026. Online ahead of print.
Hematology. 2016.
PMID: 26125973
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rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.
Chaouch L, Moumni I, Ouragini H, Darragi I, Kalai M, Chaouachi D, Boudrigua I, Hafsia R, Abbes S.
Chaouch L, et al. Among authors: boudrigua i.
Hematology. 2016 Aug;21(7):425-9. doi: 10.1080/10245332.2015.1107275. Epub 2016 Jan 22.
Hematology. 2016.
PMID: 27077760
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The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients.
Kalai M, Dridi M, Chaouch L, Moumni I, Ouragini H, Darragi I, Boudrigua I, Chaouachi D, Mellouli F, Bejaoui M, Abbes S.
Kalai M, et al. Among authors: boudrigua i.
Hematology. 2017 Apr;22(3):178-182. doi: 10.1080/10245332.2016.1253253. Epub 2016 Nov 20.
Hematology. 2017.
PMID: 27869039
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Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1.
Chaouch L, Kalai1 M, Darragi I, Boudrigua I, Chaouachi D, Ammar SB, Mellouli F, Bjaoui M, Abbes S.
Chaouch L, et al. Among authors: boudrigua i.
Hematology. 2016 Mar;21(2):121-5. doi: 10.1179/1607845415Y.0000000030. Epub 2015 Jul 6.
Hematology. 2016.
PMID: 26146896
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Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions.
Zitouni S, Bouatrous E, Laabidi O, Boudrigua I, Chaouachi D, Saidani N, Kraiem I, Ayachi A, Abbes S, Mourali M, Menif S, Ouragini H.
Zitouni S, et al. Among authors: boudrigua i.
Am J Perinatol. 2022 Aug;39(11):1241-1247. doi: 10.1055/s-0040-1722199. Epub 2020 Dec 29.
Am J Perinatol. 2022.
PMID: 33374024
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Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia.
Trabelsi N, Chaouch L, Haddad F, Jaouani M, Barkaoui E, Darragi I, Chaouachi D, Boudrigua I, Menif S, Abbes S.
Trabelsi N, et al. Among authors: boudrigua i.
Eur J Med Genet. 2021 Feb;64(2):104139. doi: 10.1016/j.ejmg.2021.104139. Epub 2021 Jan 7.
Eur J Med Genet. 2021.
PMID: 33421605
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Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians.
Trabelsi N, Bouguerra G, Haddad F, Ouederni M, Darragi I, Boudrigua I, Chaouachi D, Barmat M, Fouzai C, Bejaoui M, Menif S, Kraiem I, Abbes S.
Trabelsi N, et al. Among authors: boudrigua i.
Cell Physiol Biochem. 2021 Mar 6;55(1):117-129. doi: 10.33594/000000333.
Cell Physiol Biochem. 2021.
PMID: 33667330
Free article.
Clinical Trial.
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