Author

F. Ouali

Observed names: F Ouali, Fadiq Ouali, OUALI, F.

Observed institution: Children's Hospital

OpenAlex ID: A5111594638

α-Thalassaemia in Tunisia: some epidemiological and molecular data

2008 · H. Siala, F. Ouali, et al. · Journal of Genetics · 23

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

2013 · L. Jouini, C. A. Sahli, et al. · Molecular Biology Reports · 16

Prenatal diagnosis of hemoglobinopathies in Tunisia: an 18 years of experience

2016 · F. Ouali, H. Siala, et al. · International Journal of Laboratory Hematology · 14

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

2012 · N. Laouini, A. Bibi, et al. · Molecular Biology Reports · 13

A Novel α‐Thalassemia Nonsense Mutation in Codon 23 of the α2‐Globin Gene (GAG→TAG) in a Tunisian Family

2004 · Hajer Siala, Slaheddine Fattoum, et al. · Hemoglobin · 10

Prenatal diagnosis of cystic fibrosis: 10-years experience

2015 · S. Hadj Fredj, F. Ouali, et al. · Pathologie Biologie · 7

[Children's accidents in rural environment: study of 324 cases].

2003 · F Ghribi, F Ouali, et al. · PubMed · 4

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

2006 · A Bibi, S Benmoussa, et al. · PubMed · 1

IL-10 promoter polymorphisms (−1082G > A, −819C > T and − 592 C > A) and pediatric asthma susceptibility in a Mauritanian population

2026 · Salka Boghale, Sondess Hadj fredj, et al. · Journal of Asthma

Clinical expression of patients with the E1104X cystic fibrosis mutation in Tunisian and Libyan population

2024 · S. Hadj Fredj, C. Sahli, et al. · Clinica Chimica Acta

Study of haptoglobin gene polymorphism in in patients with sickle cell syndromes: Findings from a Tunisian cohort study

2024 · F. Ouali, R. Dabboubi, et al. · Clinica Chimica Acta

Neonatal screening for hemoglobinopathies in tunisia over a period of 18 years (2005- 2023)

2024 · O. Sassi, F. Ouenniche, et al. · Clinica Chimica Acta

Study of haplotypes in sickle cell subjects in a Tunisian population

2024 · C. Sahli, W. Affes, et al. · Clinica Chimica Acta

Kernicterus secondary to henna application in a neonate with G6PD deficiency: A case report

2024 · R. Dabboubi, F. Ouali, et al. · Clinica Chimica Acta

Works count: 15

Citation count: 88

H-index: 6

I10-index: 5