Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Hayam Ghazy"'
Autor:
Fatma Abozeid, Maysaa Zaki, Wafaa Nagah, Amany Ragab, Aya fathy, Dina Elhammady, Hayam Ghazy, Ahmed Yassen, Mohamed Serria, Omar Ammar, Maha Ragab, Manal Nomir
Publikováno v:
Egyptian Liver Journal, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Liver serves as a hub for key metabolic pathways such as folate cycle that provides one-carbon units for a network of metabolic reactions. Methylenetetrahydrofolate reductase (MTHFR) is a rate limiting enzyme in folate metabolism and thus it
Externí odkaz:
https://doaj.org/article/78d1b9f9873f4636bf16992df8cc344a
Autor:
Adel El-Badrawy, Ahmed Tawfik, Gehad Saleh, Mai Abdel-Naby, Hayam Ghazy, Ziad Emarah, Ahmed Ramez, Mohamed A. Elfatah, Ahmed Eltantawy, Mona M. Taalab, Noha Eisa, Shaimaa El-Ashwah, Yasmine Essam, Basma Atef, Shahira Ali El-Etreby, Monir H. Bahgat, Ahmed Deiab, Hatem Elalfy, Tarek Besheer, Ahmed El-Mesery, Mohamed Mahmoud Sarhan, Suzy Abd Elmabood, Ahmed Megahed, Mohamed Farouk Akl, Khaled Abouelkhair, Hanan Wahba, Amal Halim, Nirmeen Megahed, Eman Omar Khashaba
Publikováno v:
Cardiovascular Disorder and Medicine. :1-6
Objective: The aim of this work was to evaluate Multidetector Computed Tomography (MDCT) findings of hepatic manifestation in common malignant hematological disorders. Materials and Methods: This retrospective study included 300 patients with differe
Autor:
Shaimaa El-Ashwah, Noreen Elbayoumi, May Denewer, Mohamed ELboghdady, Emad Azmy, Mohamed Mabed, Gehad Saleh, M.A. ElBaiomy, Maha Elzaafarany, Mohamed A. Ebrahim, Manal A. Salah-Eldin, Tawfik ElKhodary, Hayam Ghazy, Sameh Shamaa
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 22:S362-S363
Autor:
Shaimaa El-Ashwah, Noreen Elbayoumi, May Denewer, Mohamed ELboghdady, Emad Azmy, Mohamed Mabed, Gehad Saleh, M.A. ElBaiomy, Maha Elzaafarany, Mohamed A. Ebrahim, Manal A. Salah-Eldin, Tawfik ElKhodary, Hayam Ghazy, Sameh Shamaa
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 22:S171
Publikováno v:
International Journal of Cancer and Biomedical Research.
Background: Little is known about characteristics of young patients with gastric carcinoma (GC) in Egypt. Aim: The purpose of this study was to define the clinicopathological features and survival of young GC patients in our population. Patients and
Autor:
Sameh Shamaa, Adel El-Badrawy, Nadia Atwan, Ziad Emarah, Tamer Akl, Sherif Refaat, Khaled Abdelwahab, Abd Al-Rahman Mohammad Foda, Tawfik Elkhodary, Hayam Ghazy
Publikováno v:
Breast disease. 40(2)
BACKGROUND: Transforming growth factor–β (TGFβ) has a dual function in breast cancer, having a tumor suppressor activity in early carcinomas while enhancing tumor metastasis in advanced breast carcinoma. Consequently, the prognostic role of TGFβ
Publikováno v:
Journal of gastrointestinal cancer. 53(2)
Worldwide, esophageal cancer is the eighth most common cancer and the sixth leading cause of cancer-related death. At initial diagnosis, about 50% of esophageal cancer patients present with metastasis. The prognosis of metastatic esophageal cancer is
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 21:S430-S431
Context The biological behavior of multiple myeloma is determined by genetics and the marrow microenvironment. Inflammatory cells are the major sources of cytokines in MM-infiltrated bone marrow, and they can mediate immune suppression in MM. The cur
Autor:
Ziad Emarah, Mohammed M.H. Al-Gayyar, Hayam Ghazy, Reham Alghandour, Mohamed A. Ebrahim, Sameh Shamaa
Publikováno v:
Cureus
Syndecan-1 (also known as SDC-1 or CD138) is a transmembrane proteoglycan that is expressed in many hematological and solid tumors and affects the prognosis of those cancers. We conducted this study to investigate the prognostic role of syndecan-1 in
Autor:
Ahmed Shaban, Afaf Elsaid, Hayam Ghazy, Amoura M. Abou-El-Naga, Ahmad Settin, Rami M. Elshazli
Publikováno v:
Meta Gene. 15:35-41
Background The three founder mutations of BRCA1/2 (185delAG, 5382insC and 6174delT) have been reported to be associated with breast cancer. This work was designed to check for the frequency of these genetic mutations in Egyptian women affected with b