Hafsia R - Search Results

1

Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients.

Jouini L, Sahli CA, Laaouini N, Ouali F, Ben Youssef I, Dakhlaoui B, Othmeni R, Ouennich F, Hadj Fredj S, Siala H, Becher M, Toumi NE, Fattoum S, Hafsia R, Bibi A, Messaoud T. Jouini L, et al. Among authors: hafsia r. Mol Biol Rep. 2013 Nov;40(11):6205-12. doi: 10.1007/s11033-013-2732-y. Epub 2013 Sep 25. Mol Biol Rep. 2013. PMID: 24065537

2

First description of the rs45496295 polymorphism of the C/EBPE gene in β-thalassemia intermedia patients.

Mejri A, Mansri M, Hadj Fredj S, Ouali F, Bibi A, Hafsia R, Messaoud T, Siala H. Mejri A, et al. Among authors: hafsia r. Hemoglobin. 2016 Nov;40(6):411-416. doi: 10.1080/03630269.2016.1252386. Epub 2016 Nov 9. Hemoglobin. 2016. PMID: 27829304

3

Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome.

Haddad F, Trabelsi N, Chaouch L, Darragi I, Oueslati M, Boudriga I, Chaouachi D, El-Borgi W, Hafsia R, Abbes S, Ouragini H. Haddad F, et al. Among authors: hafsia r. Hemoglobin. 2017 Mar;41(2):147-150. doi: 10.1080/03630269.2017.1322610. Epub 2017 Jun 8. Hemoglobin. 2017. PMID: 28592168

4

Hb H disease among Tunisians: molecular characterization of alpha-thalassemia determinants and hematological findings.

Zorai A, Abbes S, Préhu C, Omar S, Gerard N, Hafsia R, Asma B, Guemira F, Dellagi K. Zorai A, et al. Among authors: hafsia r. Hemoglobin. 2003 Feb;27(1):57-61. doi: 10.1081/hem-120018439. Hemoglobin. 2003. PMID: 12603097 No abstract available.

5

Frequency of three polymorphisms of the CCL5 gene (rs2107538, rs2280788 and rs2280789) and their implications for the phenotypic expression of sickle cell anemia in Tunisia.

Kalai M, Chaouch L, Mansour IB, Hafsia R, Ghanem A, Abbes S. Kalai M, et al. Among authors: hafsia r. Pol J Pathol. 2013 Jun;64(2):84-9. doi: 10.5114/pjp.2013.36012. Pol J Pathol. 2013. PMID: 23900864 Free article.

6

[Splenectomy in hereditary hemolytic anemia: 82 Tunisian cases].

Hafsia R, Zriba S, Gouider E, Ben Salah N, Borji W, Zaouche A. Hafsia R, et al. Tunis Med. 2009 May;87(5):323-7. Tunis Med. 2009. PMID: 19927762 Free article. French.

7

[Thalassemia intermedia: 36 cases].

Hafsia R, Ben Salah N, Hafhouf E, Belakhal F, Gouider E, El Borji W, Meddeb B. Hafsia R, et al. Tunis Med. 2010 Feb;88(2):102-4. Tunis Med. 2010. PMID: 20415168 Free article. French.

8

[Hemoglobin C disease: report of 16 Tunisian cases].

Hafsia R, Marrakchi O, Ben Salah N, Gouider E, Ben Lakhal R, Jeddi R, Aissaoui L, Belhadjali Z, Ben Abid H, Meddeb B, Hafsia A. Hafsia R, et al. Among authors: hafsia a. Tunis Med. 2007 Mar;85(3):209-11. Tunis Med. 2007. PMID: 17668575 French.

9

Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among sickle cell aneamia patients.

Chaouch L, Kalai M, Jbara MB, Chaabene AB, Darragi I, Chaouachi D, Mallouli F, Hafsia R, Ghanem A, Abbes S. Chaouch L, et al. Among authors: hafsia r. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2015 Mar;159(1):145-9. doi: 10.5507/bp.2013.080. Epub 2013 Nov 13. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2015. PMID: 24263212 Free article.

10

Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Tunisia.

Daoud BB, Mosbehi I, Préhu C, Chaouachi D, Hafsia R, Abbes S. Daoud BB, et al. Among authors: hafsia r. Pathol Biol (Paris). 2008 Jul;56(5):260-7. doi: 10.1016/j.patbio.2007.08.009. Epub 2008 Jan 15. Pathol Biol (Paris). 2008. PMID: 18226470

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