F. Ouali

发表

Prenatal diagnosis of cystic fibrosis: 10-years experience.

F. Zouari, H. Siala, T. Messaoud, 2015, Pathologie-biologie.

[Difference albumin-transferrin interest in the iron deficiency detection in a cohort of 1288 schoolchildren in the district of Tunis].

A. Torjman, H. Cherif, B. Zouari, 2006, Annales de biologie clinique.

Stroke and inherited thrombophilia in a Tunisian girl with sickle cell anemia

F. Ouali, N. Gritli, R. Nefissi, 2015, Clinical chemistry and laboratory medicine.

Identification of candidate genes involved in clinical variability among Tunisian patients with β-thalassemia.

H. Siala, T. Messaoud, F. Ouali, 2012, Gene.

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

H. Siala, T. Messaoud, S. Hadj Fredj, 2016, Hemoglobin.

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

H. Siala, S. Fredj, F. Ouali, 2013, Molecular Biology Reports.

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia

H. Siala, T. Messaoud, S. Fredj, 2013, Clinical chemistry and laboratory medicine.

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia

H. Siala, T. Messaoud, S. Fredj, 2013, Clinical chemistry and laboratory medicine.

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

H. Siala, T. Messaoud, S. Hadj Fredj, 2012, Molecular Biology Reports.

δ0-Thalassemia in cis of βKnossos globin gene: first homozygous description in thalassemia intermedia Libyans and first combination with codon 39 (C→T) in thalassemia intermedia Tunisian patients

H. Siala, T. Messaoud, S. Fredj, 2012, Clinical chemistry and laboratory medicine.

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

H. Siala, T. Messaoud, S. Hadj Fredj, 2012, Molecular Biology Reports.

α-Thalassaemia in Tunisia: some epidemiological and molecular data

H. Siala, F. Ouali, T. Messaoud, 2008, Journal of Genetics.

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

H. Siala, F. Ouali, T. Messaoud, 2008, Journal of genetics.

Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia

R. Doggui, T. Messaoud, F. Ouali, 2018, Hemoglobin.

First Description in Tunisia of a Point Mutation at Codon 119 (CCT→TCT) in the α1-Globin Gene: Hb Groene Hart in Association with the − α3.7 Deletion

H. Siala, T. Messaoud, F. Ouali, 2005 .

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.

H. Siala, T. Messaoud, F. Ouali, 2005, Hemoglobin.

Detection of a novel splicing mutation causing analbuminemia in a Libyan family.

H. Siala, T. Messaoud, S. Hadj Fredj, 2012, Clinical biochemistry.

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

H. Siala, S. Hadj Fredj, F. Ouali, 2013, Molecular Biology Reports.

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

H. Siala, S. Fredj, F. Ouali, 2013, Molecular Biology Reports.