Zobrazeno 1 - 10
of 51 103
pro vyhledávání: '"Thalassemia major"'
Autor:
Beshir, Mohamed Refaat1, Abd-Alaziz, Mahmoud Bakry2 rock148990@gmail.com, Ismail, Weaam Ibrahim3, Baz, Eman Gamal4
Publikováno v:
Zagazig University Medical Journal. Sep2024, Vol. 30 Issue 6, p2280-2289. 10p.
Autor:
abd, Shahad fayiz1 Shahad.Abd2307m@codental.uobaghdad.edu.iq, Mahmood, Maha Adel1 adelmaha70@codental.uobaghdad.edu.iq
Publikováno v:
Misan Journal of Academic Studies. Sep2024, Vol. 23 Issue 51, p173-179. 7p.
Publikováno v:
Turkish Archives of Pediatrics. May2024, Vol. 59 Issue 3, p258-263. 6p.
Autor:
Sari, Teny Tjitra1 (AUTHOR) ludi.dr@gmail.com, Rahmartani, Ludi Dhyani1 (AUTHOR) angga.wirahmadi@gmail.com, Wirahmadi, Angga1 (AUTHOR) foe.stephen@gmail.com, Selene, Nathasha Brigitta2 (AUTHOR) nathasha.selene@gmail.com, Iskandar, Stephen Diah1 (AUTHOR) pustika.amalia@ui.ac.id, Wahidiyat, Pustika Amalia1 (AUTHOR)
Publikováno v:
Thalassemia Reports. Jun2024, Vol. 14 Issue 2, p33-43. 11p.
Autor:
Batouty, Nihal M.1 (AUTHOR), Tawfik, Ahmad M.1 (AUTHOR), Sobh, Donia M.1 (AUTHOR), Gadelhak, Basma N.1 (AUTHOR), El-Ashwah, Shimaa2 (AUTHOR), Hussein, Mohamed Abdelghafar3 (AUTHOR), Gad, Mai4 (AUTHOR), Aziz, A. Ashraf Abd El2 (AUTHOR), El-Shahed, Mahmoud Abd1 (AUTHOR), Karam, Rasha1 (AUTHOR) rasha90karam@mans.edu.eg
Publikováno v:
Journal of Cardiovascular Imaging. 8/3/2024, Vol. 32 Issue 1, p1-13. 13p.
Autor:
Abdo, Ali A.1, Beshir, Mohamed R.1, Hassan, Tamir A.2, Mohamed, Amr A.3 Amr81_elgamal@yahoo.com
Publikováno v:
Zagazig University Medical Journal. May/Jun2024, Vol. 30 Issue 3, p935-945. 11p.
Autor:
Hanna, Diana1 (AUTHOR) menagerges2000@yahoo.com, Nada, Mohamad Gamal2 (AUTHOR), Gohary, Mahmoud M.1 (AUTHOR)
Publikováno v:
Egyptian Pediatric Association Gazette. 9/13/2024, Vol. 72 Issue 1, p1-5. 5p.
Autor:
Sameh M. Nahi, Ferdous A. Jabir
Publikováno v:
Journal of Applied Hematology, Vol 15, Iss 3, Pp 185-191 (2024)
Background: Thalassemia is an inherited disorder that is also called mediterranean anemia and is described by a lack of hemoglobin synthesis. β-thalassemia is more common in people of certain origins, particularly those from the Mediterranean region
Externí odkaz:
https://doaj.org/article/a464c96331744d8b9a9a3c8557e7d26a
Autor:
Shaima’A Dakhel ABDULHASSAN
Publikováno v:
Modern Medicine, Vol 31, Iss 3, Pp 221-226 (2024)
Introduction: Thalassemia, a hereditary autosomal recessive blood disorder, arises from genetic abnormalities leading to a diminished synthesis rate of one of the globin chains constituting hemoglobin. The integration of transfusion and chelation the
Externí odkaz:
https://doaj.org/article/282b8dd2bd024a5fa176c680948a83c8
Autor:
Rohimi, Syarif1 (AUTHOR) syarohmi@yahoo.com, Siswanto, Bambang Budi2 (AUTHOR), Mansyur, Muchtaruddin3 (AUTHOR), Gatot, Djajadiman4 (AUTHOR), Sutanto, Ina5 (AUTHOR), Pandelaki, Jacub6 (AUTHOR), Soesanto, Amiliana M.2 (AUTHOR), Ontoseno, Teddy7 (AUTHOR)
Publikováno v:
Egyptian Pediatric Association Gazette. 8/26/2024, Vol. 72 Issue 1, p1-7. 7p.