الرئيسية › دليل الباحثين › Rym Dabboubi
Rym Dabboubi
الانتماء : University of Monastir · Children's Hospital
- 28منشورات (انتماء تونسي)
- 33مجموع المنشورات
- 70الاستشهادات
- 4مؤشر h
الملف البحثي
لدى Rym Dabboubi 28 منشور(ات) مفهرسة (2015–2026). تُنشر أعماله أساسًا في «Clinica Chimica Acta»، «Annales de biologie clinique» و«Haemophilia». أكثر مقالاته استشهادًا هو «A new case of congenital atransferrinemia with a novel splice site mutation: c.293-63del» (2020)، وقد استُشهد به 15 مرة. 14 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل.
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Genetic Associations and Epidemiology
- Cystic Fibrosis Research Advances
- Hemoglobinopathies and Related Disorders
- Asthma and respiratory diseases
- Genomics and Rare Diseases
المنشورات (28)
- Inflammatory Biomarkers in Sickle Cell Disease: Understanding Their Role in Predicting the Disease-Related Complications
- Glucose-6-phosphate dehydrogenase activity and genetic variants in tunisian diabetic populations: A case–control study
- Discrepancies in Sigma Metrics Driven by Total Allowable Error Variability: Implications for QC Strategy and Laboratory Efficiency
- Revealing silent alpha-thalassemia: characterization of novel HBA1 deletion and missense mutation in Tunisian families
- Association of Cyp2c19 Genotype with Variability in Clopidogrel Response in Coronary Patients
- Comprehensive analysis of a novel LYST mutation in a Tunisian patient with Chediak-Higashi syndrome
- Challenges in Serum Albumin Measurements: A Comparative Study of the Bromocresol Green and the Capillary Zone Electrophoretic Method
- Study of the Genetic Polymorphisms Involved in the Response of Platelet to Clopidogrel in Coronary Patients
- Assessment of Intra‐ and Intercapillary Variability in HbA1c Measurement Using the Sebia Capillarys OCTA3 Analyzer
- Catalyzing precision: unraveling the diagnostic conundrum of tunisian familial hypophosphatasia case through integrative clinical and molecular approaches
- Clinical expression of patients with the E1104X cystic fibrosis mutation in Tunisian and Libyan population
- Neonatal screening for hemoglobinopathies in tunisia over a period of 18 years (2005- 2023)
- Study of haplotypes in sickle cell subjects in a Tunisian population
- An estimation of fructosamine threshold values for the diagnosis of diabetes in a Tunisian population
- Congenital analbuminemia associated with compound heterozygous novel nucleotide variations in a young adult with coronary thrombosis
- Contribution of common CFTR variants (M470V, T854, and Q1463) to cystic fibrosis in Tunisia: haplotype analysis
- A new case of congenital atransferrinemia with a novel splice site mutation: c.293-63del
- Association analysis of the surfactant protein-C gene to childhood asthma
- Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6‐10_16delTTTG deletion
- Identification of a mild cystic fibrosis mutation 2789+5 G to a for the first time in Tunisian population
- Analysis of IVS8 CFTR gene polymorphism in asthmatic children in a Tunisian population
- Analysis of Two Polymorphic Repeats IVS3 Poly A and IVS10 CA in Tunisian Cystic Fibrosis Patients: Case–Control Study
- Clopidogrel utilization in patients with coronary artery disease and diabetes mellitus: should we determine CYP2C19*2 genotype?
- Association of M470V polymorphism of CFTR gene with variability of clinical expression of asthma: Case-report study
- Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization
- Hypodysfibrinogenemia: A novel abnormal fibrinogen associated with bleeding and thrombotic complications
- Setup of a Protocol of Molecular Diagnosis of β‐Thalassemia Mutations in Tunisia using Denaturing High‐Performance Liquid Chromatography (DHPLC)
- Fortuitous description of haemoglobin A2’ [δ16 (A13) Gly→Arg (GGC→CGC)] in a Tunisian family: study of the molecular defect and its origin
مجلات النشر
- Clinica Chimica Acta × 6
- Annales de biologie clinique × 3
- Haemophilia × 2
- Hemoglobin × 1
- Journal of the National Medical Association × 1
- The Journal of Applied Laboratory Medicine × 1
المنشورات حسب السنة
- 20262
- 20257
- 20245
- 20231
- 20211
- 20203
- 20193
- 20182
- 20171
- 20162
التعاون العلمي
المؤسسات الشريكة : Hospital Fatuma Bourguiba Monastir · Institut National de Nutrition et de Technologie Alimentaire · Military Hospital of Tunis · Hôpital Sahloul · Habib hospital Thameur
المؤلفون المشاركون
- Taieb Ben Messaoud
- Yessine Amri
- Sondess Hadj Fredj
- Chaima Abdelhafidh Sahli
- Sondes Hadj Fredj
- Siwar Chelbi
- Mariem Othmani
- Rim Othmani
- Mohsen Hassine
- Saoussen Chouchène
- Taieb Messaoud
- Hajer Siala
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
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