Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Khaled Eid"'
Autor:
Amal El-Beshlawy, Azza A. G. Tantawy, Rabah M. Shawky, Solaf M. Elsayed, Iman M. Marzouk, S. Elgawhary, Hadeer Abdelghaffar, Usama El Safy, Khaled Eid, Khalid I. EISayh, Ahmed Megahed, Amira Adly, Eman M. Sherif, Mervat A. M. Youssef, Manar Mohamed Fathy, Nouran Yousef Salah, Sherine M. Elzeiny, Eslam Rabie Abdel Aziz EI Bakky, Ekram Fateen
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-16 (2024)
Abstract Background Gaucher disease (GD), an autosomal recessive, lysosomal storage disorder, is caused due to mutations in the glucocerebrosidase (GBA) gene. GD can occur at any age and is classified as type 1 (non-neurologic), type 2 (infantile for
Externí odkaz:
https://doaj.org/article/40af8925d1554eb7ab90e6b492f1c684
Publikováno v:
Al-Azhar Assiut Medical Journal, Vol 20, Iss 1, Pp 67-71 (2022)
Background and aim Eradication of Helicobacter pylori becomes an ongoing challenge worldwide because eradication rates of H. pylori are declining to less than 60% in some countries. As there is no acceptable definite long-standing used therapeutic re
Externí odkaz:
https://doaj.org/article/f53ffbb211e648a28fb88c6aebd01f30
Autor:
Magd A. Kotb, Mona Hamdy, Khaled Eid, Mona Aziz, Mai Abd El Salam, Hend Abd El Baky, Nabil Lotfi, Niveen Salama
Publikováno v:
Pediatric Sciences Journal, Vol 1, Iss 2, Pp 98-106 (2021)
Background: Children with β-thalassemia major differ regarding age at presentation, transfusion requirements and unpredictable timing, rate and severity of hemolytic crisis. The blood transfusions are associated with iron overload. Glutathione S tra
Externí odkaz:
https://doaj.org/article/acd5c11354cc417596e2ae33f816a157
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 20, Iss , Pp - (2019)
Advanced liver disease complicated by hepatopulmonary syndrome is a recognized complication of Gaucher disease. Macrophage-targeted, recombinant enzyme replacement therapy is effective in reversing clinical manifestations attributed to the accumulati
Externí odkaz:
https://doaj.org/article/451df5782a794624832f356d8124b2f3
Autor:
Omar Mohammed A Alrashedi, Adil Mohammad Almaqati, Majed abdulaziz bin hassan, Khaled eid alotaibi, Saad Abdulazez Alabodi, Thamer Dawas Aldajani, Meshal Suwailem Alotaibi, Nasser Ali Al Abdullah, Mustafa Saleh Mohammad Alsaad
Background: In recent years, the healthcare system has undergone rapid transformation. Nonetheless, a recent Quality and Patient Safety Report highlighted declining levels of patient safety and quality culture among healthcare professionals. This hig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27e4bc03cb452b3c53a2bc482fdb1ae7
Autor:
Nabil Lotfi, Mona Hamdy, Mai Abd El Salam, Magd A. Kotb, Niveen Salama, Hend Abd El Baky, Mona Aziz, Khaled Eid
Publikováno v:
Pediatric Sciences Journal. 1:98-106
Background: Children with β-thalassemia major differ regarding age at presentation, transfusion requirements and unpredictable timing, rate and severity of hemolytic crisis. The blood transfusions are associated with iron overload. Glutathione S tra
Publikováno v:
International Journal of Business and Management. 18:24
The research aims to develop the internal control system in Gaza's municipalities in accordance with the proposed COSO model to achieve the goal for which it was found. The research used the analytical descriptive curriculum to prepare the applied as
Autor:
Khaled Eid, Susan Christensen, Jennifer Hoff, Diane Drake, Kartik Yadav, Paige Burtson, Mebin Kuriakose, Harold Patton, Adey Nyamathi
Publikováno v:
Clinical Journal of Oncology Nursing. 24:E50-E56
Background Cancer treatment has a significant impact on a patient's sexual health and function. However, numerous communication barriers deter healthcare professionals from initiating a sexual health conversation with patients. Objectives This study
Publikováno v:
Egyptian Dental Journal. 65:2299-2305
Background: Gaucher disease (GD) is a lysosomal storage disease caused by an autosomal recessive inherited deficiency of the lysosomal enzyme glucocerebrosidase. The aim of this study was to describe jaw bones involvement and dental radiographic feat
Autor:
Noha Talha, Mervat M. Khorshied, Salwa Bakr, Nohair Soliman, Karim Yahia Jaffer, Khaled Eid, Mona El-Ghamrawy
Publikováno v:
Annals of Hematology. 98:1805-1812
Sickle cell disease (SCD) is a relatively common inherited hemolytic anemia among individuals of African descent. Genetic factors might clarify clinical diversity of the disease and variations in treatment response. Some researchers investigated heme