Zobrazeno 1 - 10
of 562
pro vyhledávání: '"Mona, Hassan"'
Publikováno v:
Iranian Journal of Nursing and Midwifery Research, Vol 29, Iss 4, Pp 460-465 (2024)
Background: Chronic kidney disease is the biggest problem in health care today, and the primary replacement therapy, hemodialysis, has a severe impact on both self-management and quality of life. This study aimed to evaluate the effect of educational
Externí odkaz:
https://doaj.org/article/021dcccc189d4122acb52a767293b7de
Autor:
Mona Hassan Eltagui, Christine William S. Basanti, Magd Ahmed Kotb, Toka Emad Eldin Saad, Mai Mohamed Abd El Salam
Publikováno v:
Pediatric Sciences Journal, Vol 4, Iss 2, Pp 49-56 (2024)
Background: β-thalassemia syndromes are a group of hereditary blood diseases characterized by reduced or absent β-globin chain synthesis, resulting in reduced hemoglobin in red blood cells. Pulmonary dysfunction ranging from restrictive to obstruct
Externí odkaz:
https://doaj.org/article/7e3869c547f044a99069030145fdf73e
Autor:
Awad, Nancy Naser1, Mohammed, Mona Hassan1, Mahmoud, Omayma Mahfouz1, Wahab Almallah, Amani Abdel1 amanialmallah32@gmail.com
Publikováno v:
Egyptian Journal of Histology. Sep2024, Vol. 47 Issue 3, p1138-1156. 19p.
Autor:
Galhom, Rania A., Ali, Saleh Nasser Saleh, El-Fark, Magdy Mohamed Omar, Ali, Mona Hassan Mohammed, Hussein, Hoda Hassan
Publikováno v:
In Tissue and Cell October 2024 90
Publikováno v:
Microbes and Infectious Diseases, Vol 5, Iss 1, Pp 260-269 (2024)
Background: New Delhi Metallo-b-lactamase (NDM- 1) and Klebsiella pneumoniae carbapenemase (KPC) are enzymes associated with resistance to many β- lactam agents. Their early detection is very important for controlling the spread of drug- resistant b
Externí odkaz:
https://doaj.org/article/24398469d35540308f03adb090c2dcb8
Autor:
Esraa Elmorsi Abdelaziz Elderini, Amira Mohamed ELTohamy, Mona Hassan EL-Tagui, Mariam Saad Nassim
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 24, Iss 1, Pp 1-8 (2023)
Abstract Background Thalassemia is a commonly occurring genetic hemoglobinopathy worldwide. Periodic and routine blood transfusions, iron chelation therapy and splenectomy procedures are all required for the treatment of thalassemia. Numerous organs
Externí odkaz:
https://doaj.org/article/7c8133751bfa4cb0a97321c62323a93e
Autor:
Abdelrazik, Rania Mahmoud, Ali, Mona Hassan Mohammed, Atef, Reham Mohammed, Abdel Fattah, Islam Omar
Publikováno v:
In Tissue and Cell December 2024 91
Autor:
Mona Hassan Eltagui, Hadeel M. Seif Eldein, Marwa Abd Elhady, Dalia El-Sayed, Nouran Momen, Yasmeen M. M. Selim, Mai Mohammed Abd EL Salam
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 71, Iss 1, Pp 1-7 (2023)
Abstract Objective Early identification of sickle renovascular changes via renal Doppler sonography among sickle cell disease patients to help in early diagnosis and interventions to prevent progression to end-stage renal disease. Methods Forty-five
Externí odkaz:
https://doaj.org/article/c62a6fb0a2874b478695aef6ba4d1f88
Autor:
Rania Sobhy Abou Khadrah, Mona Hassan Abedelmalik, Mohammed Abed Elhameed Alameldeen, Aly Aly Elbarbary
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 54, Iss 1, Pp 1-11 (2023)
Abstract Background Hepatic arterial anatomy is important in performing many surgical and endovascular procedures. Familiarity with variations in the hepatic arterial anatomy is essential to achieving adequate embolization. In some patients, in addit
Externí odkaz:
https://doaj.org/article/55151d4d236943bdbf7757e83d6b0049
Autor:
Abdel Mohsen Soliman, Rehab Fawzy, El Ghobashy, Mohamed Hamdna Allah, Hafez, Mona Hassan, Abdel Latif, Hend Mehawed, Elbarbary, Menna, Ibrahim, Amany
Publikováno v:
In Pediatrics & Neonatology April 2024