Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Sonia Adolf Habib"'
Autor:
Doaa El Demerdash, Mohamed Talaat El Kholy, Alia Abdel-Aziz Ayad, Noha Tawfik, Magda Rakha, Sonia Adolf Habib, Manal Hamdy EL Said, George Sobhy, Maha Yacoub
Publikováno v:
The Egyptian Journal of Internal Medicine, Vol 36, Iss 1, Pp 1-9 (2024)
Abstract Background Heavy menstrual bleeding is an important health problem in women of reproductive age and is also one of the most common symptoms in women with bleeding disorders. Data about the frequency of rare bleeding disorders are limited, an
Externí odkaz:
https://doaj.org/article/476db0b8352f4a21ac38e237c9343165
Autor:
Galila Mokhtar, Ahmed Youssef, Ashraf Abdel Baky, Ehab Khairy El Khashab, Enas Raafat, Ilham Youssry, Iman Ragab, Laila Sherief, Manar Mohamed Fathy, Mervat Abdallah Hesham, Nouran Yousef Salah, Rasha AbdelRaouf AbdelAziz Afifi, Sherein Abdelhamid Shalaby, Sonia Adolf Habib, Tarek Omar, Yasmin Gamal El Gendy
Publikováno v:
Bulletin of the National Research Centre, Vol 47, Iss 1, Pp 1-10 (2023)
Abstract Background Iron deficiency (ID) is the most common nutritional disorder affecting all age groups. Infants and young children are vulnerable to anemia especially iron deficiency anemia (IDA), which represents a public health problem with defi
Externí odkaz:
https://doaj.org/article/a9166828c45c4eafac1dfe4196911001
Autor:
Galila Mokhtar, Ashraf Abdel Baky, Ilham Youssry, Iman Ragab, Laila Sherief, Marwa Zakaria, Mervat Hesham, Nouran Salah, Rasha Abdel-Raouf, Sara Makkeyah, Sherein Shalaby, Sonia Adolf Habib, Tarek Omar, Yasser Amer, Niveen M. Salama
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 71, Iss 1, Pp 1-9 (2023)
Abstract Background Acute hemolytic anemia (AHA) is a common emergency in pediatric emergency departments, hence the need to adapt pre-existing high-quality practice guidelines for the diagnosis, management, and prevention of AHA to be available for
Externí odkaz:
https://doaj.org/article/0f720bb0f3134caab15ad9431688ac59
Publikováno v:
Open Access Macedonian Journal of Medical Sciences, Vol 8, Iss B (2020)
Open Access Macedonian Journal of Medical Sciences; Vol. 8 No. B (2020): B-Clinical Sciences; 26-30
Open Access Macedonian Journal of Medical Sciences; Vol. 8 No. B (2020): B-Clinical Sciences; 26-30
BACKGROUND: Iron overload is the main cause of oxidative stress in beta-thalassemia (βT) by the increased production of free radicals and reactive oxygen species. Antioxidants counteract the toxic effects of oxidative stress. AIM: This study aims to
Publikováno v:
Open Access Macedonian Journal of Medical Sciences
Open Access Macedonian Journal of Medical Sciences, Vol 7 (2019)
Open Access Macedonian Journal of Medical Sciences; Vol 7 No 15 (2019): Aug 15 (OAMJMS); 2434-2439
Open Access Macedonian Journal of Medical Sciences, Vol 7 (2019)
Open Access Macedonian Journal of Medical Sciences; Vol 7 No 15 (2019): Aug 15 (OAMJMS); 2434-2439
BACKGROUND: Hepcidin, a small peptide hormone, is established as the main regulator of iron homeostasis. AIM: To estimate serum hepcidin, ferritin, and hepcidin: ferritin ratio in β-thalassemia patients and to determine the effect of splenectomy and
Autor:
Azza M.O. Abdel Rahman, Howayda E Gomaa, Sonia Adolf Habib, Hanan M Ibrahim, Aser A Khattab, Sally A.F. El-Sahrigy, Mohamed G. Shouman, Naiven A Helmy
Publikováno v:
Open Access Macedonian Journal of Medical Sciences, Vol 7, Iss 11 (2019)
Open Access Macedonian Journal of Medical Sciences; Vol 7 No 11 (2019): Jun 15 (OAMJMS); 1744-1749
Open Access Macedonian Journal of Medical Sciences
Open Access Macedonian Journal of Medical Sciences; Vol 7 No 11 (2019): Jun 15 (OAMJMS); 1744-1749
Open Access Macedonian Journal of Medical Sciences
BACKGROUND: Hospital-acquired (nosocomial) infection is a common serious health problem worldwide, especially in pediatric intensive care units and is associated with high mortality and morbidity, prolonged hospital stays and high cost.AIM: To determ
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 2, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 2, Pp n/a-n/a (2021)
Background Hemophilia A (HA) is an inherited X‐linked recessive coagulation disorder caused by factor VIII (F8) deficiency. F8 rearrangements involving intron 22 (int22) and intron 1 (int1) account for almost half of severe HA phenotype also a hots
Autor:
Solaf Kamel, Eman A Albostany, Sonia Adolf Habib, Eman ElTahlawy, Neveen A Helmy, Eman H. Thabet, Neveen Salama, Eman A. Elghoroury, Shereen H Abd El Aziz
Publikováno v:
Journal of The Arab Society for Medical Research. 15:1
Background/aim Iron overload is the main concern in treatment of hemolytic diseases with repeated blood transfusion, especially sickle cell disease (SCD). Hepcidin has appeared as the key iron metabolism regulator. Erythroferrone (ERFE) is postulated
Autor:
Mona H. Ibrahim, Zeinab S. Sleem, Fatina I. Fadel, Hafez M. Bazaraa, Azza M. O. Abdel Rahman, Sonia Adolf Habib, Mohamed Farouk Mohamed, Mohamed M.A. Soliman
Publikováno v:
Archives of Medical Science : AMS
Introduction Cardiopulmonary bypass (CPB) surgery is considered one of the most frequent surgical procedures in which acute kidney injury (AKI) represents a frequent and serious complication. The aim of the present study was to evaluate the efficienc
Red cell alloimmunization and autoantibodies in Egyptian transfusion-dependent thalassaemia patients
Autor:
Nahed A. Emara, Shadia Ragab, Azza M. Ahmed, Sonia Adolf Habib, Azza A. Aly, Nehal Salah Hasan
Publikováno v:
Archives of Medical Science : AMS
Introduction: The objective of this study was to explore the frequency of red cell alloantibodies and autoantibodies among β-thalassaemia patients who received regular transfusions. Material and methods: This study included 501 patients with β-thal