Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Reham Abdel Haleem"'
Autor:
Reham Abdel Haleem Abo El Wafa, Mohamed Ibrahim Sayed Ahmed, Mona Wagdy Ayad, Omar Mohamed Ghallab, Dalia Mohamed Tarek Farghaly
Publikováno v:
Alexandria Journal of Medicine, Vol 60, Iss 1, Pp 301-311 (2024)
Background Acute myeloid leukemia (AML) is a challenging heterogenous hematologic malignancy characterized by suboptimal outcomes. Genetic characterization of AML enhanced the understanding of individualized patient’s risk and led to the developmen
Externí odkaz:
https://doaj.org/article/6deeb67ecef648428c526baf147f5dcb
Autor:
Salma Said Ibrahim Elsayed, Akram Abdel-Moneim Deghady, Dalia AbdElmoat Elneily, Reham Abdel Haleem AboElwafa
Publikováno v:
Alexandria Journal of Medicine, Vol 60, Iss 1, Pp 186-191 (2024)
Background AML is a complex and heterogeneous disease. The KRAS gene is one of the important genes in the pathogenesis of acute myeloid leukemia (AML). Mutant RAS can promote oncogenesis via different mechanisms including oncogenic transcription, cel
Externí odkaz:
https://doaj.org/article/3f9dac918b53405088820124ca87689a
Autor:
Islam Moheb, Ehab Moustafa Hassouna, Iman Ezzat El-Gohary, Reham Abdel Haleem Abo Elwafa, Ahmed Kamal
Publikováno v:
Alexandria Journal of Medicine, Vol 60, Iss 1, Pp 92-98 (2024)
Background Diagnosing spontaneous bacterial peritonitis (SBP) requires a high clinical index of suspicion because the clinical presentation varies widely. Early detection and treatment of SBP are crucial for improving survival rates. Ascitic fluid ne
Externí odkaz:
https://doaj.org/article/65ba1e133761419e89860055a1d986c7
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 3, Pp n/a-n/a (2024)
Abstract Background Familial hypercholesterolemia (MIM: PS143890) is a genetic disorder characterized by an increase in blood cholesterol. LDLR is one of the genes which their defect contributes to the disorder. Affected individuals may carry a heter
Externí odkaz:
https://doaj.org/article/6a7477e0eda544abb134fe80cbc0d97a
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 11, Iss 1, Pp e2019013-e2019013 (2019)
Background: Low bone mineral density (BMD) is a characteristic feature of Beta thalassemia major (βTM) patients. Vitamin D is important for bone mineralization. Vitamin D receptors (VDR) genetic variants may be related to vitamin D status and BMD.
Externí odkaz:
https://doaj.org/article/837ddec3abbe4b5b8df408dec8fe294d
Autor:
Song, Yongjun1 (AUTHOR), Elwafa, Reham Abdel Haleem Abo2 (AUTHOR), Omar, Omneya Magdy3 (AUTHOR), Seo, Go Hun1 (AUTHOR), Lee, Hane1 (AUTHOR) hlee@3billion.io
Publikováno v:
Molecular Genetics & Genomic Medicine. Mar2024, Vol. 12 Issue 3, p1-6. 6p.
Autor:
El-Nawawy, Ahmed1 (AUTHOR), Elwafa, Reham Abdel Haleem Abo2 (AUTHOR), Khalil Abouahmed, Ahmed1 (AUTHOR), Rasheed, Rehab Atef1 (AUTHOR), Omar, Omneya Magdy1 (AUTHOR) O_magdy09@alexmed.edu.eg
Publikováno v:
European Journal of Pediatrics. Feb2024, Vol. 183 Issue 2, p769-778. 10p.
Autor:
Abo El Wafa, Reham Abdel Haleem, Ahmed, Mohamed Ibrahim Sayed, Ayad, Mona Wagdy, Ghallab, Omar Mohamed, Farghaly, Dalia Mohamed Tarek
Publikováno v:
Alexandria Journal of Medicine; Dec2024, Vol. 60 Issue 1, p301-311, 11p
Autor:
Ibrahim Elsayed, Salma Said, Deghady, Akram Abdel-Moneim, Elneily, Dalia AbdElmoat, AboElwafa, Reham Abdel Haleem
Publikováno v:
Alexandria Journal of Medicine; Dec2024, Vol. 60 Issue 1, p186-191, 6p
Autor:
Moheb, Islam, Hassouna, Ehab Moustafa, El-Gohary, Iman Ezzat, Elwafa, Reham Abdel Haleem Abo, Kamal, Ahmed
Publikováno v:
Alexandria Journal of Medicine; Dec2024, Vol. 60 Issue 1, p92-98, 7p