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Rym Dabboubi
Observed names:
Dabboubi Rym,
R. Dabboubi
Institutions:
University of Monastir,
Children's Hospital
Observed institutions:
University of Monastir,
Children's Hospital
OpenAlex ID:
A5066350533
A new case of congenital atransferrinemia with a novel splice site mutation: c.293-63del
2020
·
Rym Dabboubi
, Yessine Amri
, et al.
·
European Journal of Medical Genetics
·
16
Hypodysfibrinogenemia: A novel abnormal fibrinogen associated with bleeding and thrombotic complications
2016
·
Yessine Amri
, Choumous Kallel
, et al.
·
Clinica Chimica Acta
·
14
Clopidogrel utilization in patients with coronary artery disease and diabetes mellitus: should we determine CYP2C19*2 genotype?
2018
·
Saoussen Chouchene
, Rym Dabboubi
, et al.
·
European Journal of Clinical Pharmacology
·
10
Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization
2017
·
Y. Amri
, H. Jouini
, et al.
·
Haemophilia
·
10
Catalyzing precision: unraveling the diagnostic conundrum of tunisian familial hypophosphatasia case through integrative clinical and molecular approaches
2024
·
Yessine Amri
, Rym Dabboubi
, et al.
·
Molecular Genetics and Genomics
·
4
Association analysis of the surfactant protein-C gene to childhood asthma
2020
·
Malek Nefzi
, Imen Wahabi
, et al.
·
Journal of Asthma
·
4
Discrepancies in Sigma Metrics Driven by Total Allowable Error Variability: Implications for QC Strategy and Laboratory Efficiency
2025
·
Mariem Othmani
, Yessine Amri
, et al.
·
The Journal of Applied Laboratory Medicine
·
3
PDF
Revealing silent alpha-thalassemia: characterization of novel HBA1 deletion and missense mutation in Tunisian families
2025
·
Yessine Amri
, Sondess Hadj Fredj
, et al.
·
Annals of Hematology
·
3
PDF
Setup of a Protocol of Molecular Diagnosis of β‐Thalassemia Mutations in Tunisia using Denaturing High‐Performance Liquid Chromatography (DHPLC)
2016
·
Chaima Abdelhafidh Sahli
, Ikbel Ben Salem
, et al.
·
Journal of Clinical Laboratory Analysis
·
3
PDF
Comprehensive analysis of a novel LYST mutation in a Tunisian patient with Chediak-Higashi syndrome
2025
·
Yessine Amri
, Saoussen Chouchene
, et al.
·
BMC Medical Genomics
·
2
PDF
Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6‐10_16delTTTG deletion
2020
·
Yessine Amri
, Rym Dabboubi
, et al.
·
Haemophilia
·
2
Association of M470V polymorphism of CFTR gene with variability of clinical expression of asthma: Case-report study
2018
·
Imen Wahabi
, Sondess Hadj Fredj
, et al.
·
Allergologia et Immunopathologia
·
2
Inflammatory Biomarkers in Sickle Cell Disease: Understanding Their Role in Predicting the Disease-Related Complications
2026
·
Faida Ouali
, Ahlem Sahli
, et al.
·
Hemoglobin
·
1
Association of Cyp2c19 Genotype with Variability in Clopidogrel Response in Coronary Patients
2025
·
Farah Yacoub
, Saoussen Chouchene
, et al.
·
Indian Journal of Hematology and Blood Transfusion
·
1
Congenital analbuminemia associated with compound heterozygous novel nucleotide variations in a young adult with coronary thrombosis
2023
·
Yessine Amri
, Sana Aboulkacem
, et al.
·
Annales de biologie clinique
·
1
Contribution of common CFTR variants (M470V, T854, and Q1463) to cystic fibrosis in Tunisia: haplotype analysis
2021
·
Malek Nefzi
, Sondess Hadj Fredj
, et al.
·
Annales de biologie clinique
·
1
PDF
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
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.
·
Figshare
Glucose-6-phosphate dehydrogenase activity and genetic variants in tunisian diabetic populations: A case–control study
2026
·
Yessine Amri
, Mariem Othmani
, et al.
·
Journal of the National Medical Association
Assessment of Intra‐ and Intercapillary Variability in HbA1c Measurement Using the Sebia Capillarys OCTA3 Analyzer
2025
·
Meriem Belhedi
, Wiem Lazzem
, et al.
·
Electrophoresis
PDF
Study of the Genetic Polymorphisms Involved in the Response of Platelet to Clopidogrel in Coronary Patients
2025
·
Saoussen Chouchene
, Amani Abderahmene
, et al.
·
Indian Journal of Clinical Biochemistry
Challenges in Serum Albumin Measurements: A Comparative Study of the Bromocresol Green and the Capillary Zone Electrophoretic Method
2025
·
Mariem Othmani
, Yessine Amri
, et al.
·
The Protein Journal
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
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
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Works count:
33
Citation count:
77
H-index:
4
I10-index:
4
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