Rania Mohamed Samy

Cairo University — Egypt

Medicine · Health Sciences

8h-index113citations19works0.02yr avg
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Research Topics

Hemoglobinopathies and Related Disorders(5), Iron Metabolism and Disorders(3), Neonatal Respiratory Health Research(3), Pregnancy and preeclampsia studies(2), Blood Coagulation and Thrombosis Mechanisms(2)

Publications19 total

Combined central nervous system tuberculosis and neurocryptococcosis in a non-HIV patient following severe psychological trauma
The Egyptian Journal of Internal Medicine·2024Open Access
Assessment of haemophilic joints in a low‐resourced area using clinical tools: The effect of different types of prophylaxis
Haemophilia·2024Open Access
Multidrug resistance Gene-1 polymorphisms (C3435T and G2677T) and the risk of inflammatory bowel disease in Egyptian patients
Arab Journal of Gastroenterology·2024
Alteration in apoptosis and ataxia telangiectasia mutated (ATM) gene expression in mesenchymal stem cells in patients with idiopathic acquired aplastic anemia
Comparative Clinical Pathology·2023
The association between growth differentiation factor-15, erythroferrone, and iron status in thalassemic patients
Pediatric Research·2023· 12 citedOpen Access
Bone health in pediatric transfusion‐dependent beta‐thalassemia: Circulating osteoprotegerin and RANKL system
Pediatric Blood & Cancer·2021· 7 cited
Lymphocyte mosaicism in Fanconi anemia: diagnosis and clinical correlation
Middle East Journal of Medical Genetics·2020
Apolipoprotein E and plasminogen activator inhibitor 1 gene polymorphism in children with chronic renal insufficiency associated with cardiovascular disease
Egyptian Pediatric Association Gazette·2019Open Access
Prevalence of α-Thalassemia in the Egyptian Population
Hemoglobin·2018· 10 cited
Molecular characterization of patients with clinical suspicion of 22q11.2 deletion syndrome
Middle East Journal of Medical Genetics·2018
Enhancing Effect of Hydroxyurea on Hb F in Sickle Cell Disease: Ten-Year Egyptian Experience
Hemoglobin·2017· 8 cited
Circulating microparticles and the risk of thromboembolic events in Egyptian beta thalassemia patients
Annals of Hematology·2017· 17 cited
Association of TLR polymorphisms with bronchopulmonary dysplasia
Gene·2016· 11 cited
Polymorphisms of Vascular Endothelial Growth Factor and Retinopathy of Prematurity
Journal of Pediatric Ophthalmology & Strabismus·2015· 15 cited
Relationship between angiotensin‐converting enzyme gene polymorphism and respiratory distress syndrome in premature neonates
The Clinical Respiratory Journal·2014· 2 cited
Plasma myeloperoxidase enzyme assay in cases of neonatal sepsis
El Mednifico Journal·2014
CDX2 gene expression in acute lymphoblastic leukemia
Journal of the Egyptian National Cancer Institute·2014· 2 citedOpen Access
G6PD Deficiency and G6PD (Mediterranean and Silent) Polymorphisms in Egyptian Infants with Neonatal Hyperbilirubinemia
Laboratory Medicine·2013· 18 cited
Study of fibromodulin gene expression in B-cell chronic lymphocytic leukemia
Journal of the Egyptian National Cancer Institute·2011· 11 citedOpen Access

Frequent Co-authors

Ilham Youssry(7), Rayan Bou‐Fakhredin(2), Alì Taher(2), Niveen Salama(2), Dalia Abd Elaziz(2), Samia Rizk(2), Eman Abdel Ghany Abdel Ghany(2), Hoda M Abd El-Ghany(2), Zahraa M. Ezz El-Deen(1), Nouran F. Hussin(1), Tamer A. Abdel Hamid(1), Osman R. Abdel Migeed(1), Nohair Soliman(1), Mona El-Ghamrawy(1), Amal Nasr(1), Mohamed Abdel Mohsen(1), Mohamed ElShahaat(1), Aliaa A. Ali(1), Nouran F. Hussien(1), Khalid Al Husseiny(1)