Fattoum S - 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: fattoum s. 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

Detection of two rare beta-thalassemia alleles found in the Tunisian population: codon 47 (+A) and codons 106/107 (+G).

Bibi A, Messaoud T, Beldjord C, Fattoum S. Bibi A, et al. Among authors: fattoum s. Hemoglobin. 2006;30(4):437-47. doi: 10.1080/03630260600867933. Hemoglobin. 2006. PMID: 16987798

3

Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults.

Jouini L, Bibi A, Ouali F, Hadj Fredj S, Ouennich F, Siala H, Messaoud T, Fattoum S. Jouini L, et al. Among authors: fattoum s. Mol Biol Rep. 2012 Apr;39(4):4619-25. doi: 10.1007/s11033-011-1253-9. Epub 2011 Sep 27. Mol Biol Rep. 2012. PMID: 21947948

4

Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC).

Sahli CA, Ben Salem I, Jouini L, Laouini N, Dabboubi R, Hadj Fredj S, Siala H, Othmeni R, Dakhlaoui B, Fattoum S, Bibi A, Messaoud T. Sahli CA, et al. Among authors: fattoum s. J Clin Lab Anal. 2016 Sep;30(5):392-8. doi: 10.1002/jcla.21867. Epub 2016 Apr 18. J Clin Lab Anal. 2016. PMID: 27086580 Free PMC article.

5

alpha-Thalassaemia in Tunisia: some epidemiological and molecular data.

Siala H, Ouali F, Messaoud T, Bibi A, Fattoum S. Siala H, et al. Among authors: fattoum s. J Genet. 2008 Dec;87(3):229-34. doi: 10.1007/s12041-008-0036-0. J Genet. 2008. PMID: 19147907 Free article.

6

Glucose-6-phosphate dehydrogenase deficiency in Tunisia: molecular data and phenotype-genotype association.

Laouini N, Bibi A, Ammar H, Kazdaghli K, Ouali F, Othmani R, Amdouni S, Haloui S, Sahli CA, Jouini L, Hadj Fredj S, Siala H, Ben Romdhane N, Toumi NE, Fattoum S, Messsaoud T. Laouini N, et al. Among authors: fattoum s. Mol Biol Rep. 2013 Feb;40(2):851-6. doi: 10.1007/s11033-012-2124-8. Epub 2012 Oct 14. Mol Biol Rep. 2013. PMID: 23065279

7

Molecular basis of beta-thalassemia in the population of Tunisia.

Fattoum S, Messaoud T, Bibi A. Fattoum S, et al. Hemoglobin. 2004 Aug;28(3):177-87. doi: 10.1081/hem-120040307. Hemoglobin. 2004. PMID: 15481884

8

A novel alpha-thalassemia nonsense mutation in codon 23 of the alpha2-globin gene (GAG-->TAG) in a Tunisian family.

Siala H, Fattoum S, Messaoud T, Ouali F, Gerard N, Krishnamoorthy R. Siala H, et al. Among authors: fattoum s. Hemoglobin. 2004 Aug;28(3):249-54. doi: 10.1081/hem-120040258. Hemoglobin. 2004. PMID: 15481894

9

First description in Tunisia of a point mutation at codon 119 (CCT-->TCT) in the alpha1-globin gene: Hb Groene Hart in association with the -alpha3.7 deletion.

Siala H, Ouali F, Messaoud T, Sfar R, Fattoum S. Siala H, et al. Among authors: fattoum s. Hemoglobin. 2005;29(4):263-8. doi: 10.1080/03630260500308053. Hemoglobin. 2005. PMID: 16370486

10

Haplotypes linked to three rare beta-thalassemia mutations, originally reported in Tunisia.

Bibi A, Messaoud T, Fattoum S. Bibi A, et al. Among authors: fattoum s. Hemoglobin. 2006;30(2):175-81. doi: 10.1080/03630260600642427. Hemoglobin. 2006. PMID: 16798642

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