Neonatal screening for sickle cell disease, glucose-6-phosphate dehydrogenase deficiency and a-thalassemia in Qatif and Al Hasa

Autor: Al Aqib A, Al Jame A, Al Qatari G, Abu Srair H, Nasserullah Z, Mokhtar M, Al Naim S

Publikováno v: Annals of Saudi medicine. 18(4)

Screening programs to determine the frequency of sickle cell, glucose-6-phosphate dehydrogenase deficiency and alpha-thalassemia gene are available in Saudi Arabia, although not used frequently. Greater use of these programs will decrease the morbidi

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https://pubmed.ncbi.nlm.nih.gov/17344674

Demands and challenges for patients with sickle-cell disease requiring hematopoietic stem cell transplantation in Saudi Arabia.

Autor: Alsultan A; Department of Pediatrics and Sickle Cell Disease Research Center, College of Medicine, King Saud University, Riyadh, Saudi Arabia.; Department of Pediatric Hematology/Oncology, King Abdullah Specialist Children's Hospital, Riyadh, Saudi Arabia., Jastaniah W; King Abdulaziz Medical City, Jeddah, Saudi Arabia.; Department of Pediatrics, College of Medicine, Umm alQura University, Makkah, Saudi Arabia., Al Afghani S; King Fahad Specialist Hospital, Dammam, Saudi Arabia., Al Bagshi MH; Maternity and Children's Hospital, Hofuf, Saudi Arabia., Nasserullah Z; Maternity & Children's Hospital, Dammam, Saudi Arabia., Al-Suliman AM; King Fahad Hospital, Hofuf, Saudi Arabia., Alabdulaali MK; King Fahad Hospital, Hofuf, Saudi Arabia.

Publikováno v: Pediatric transplantation [Pediatr Transplant] 2016 Sep; Vol. 20 (6), pp. 831-5. Date of Electronic Publication: 2016 Jul 31.

Molecular patterns of alpha-thalassemia in the kingdom of Saudi Arabia: identification of prevalent genotypes and regions with high incidence.

Autor: Alhuthali, Hayaa M.¹ (AUTHOR) hmhuthali@tu.edu.sa, Ataya, Eman F.^2,3 (AUTHOR), Alsalmi, Alaa¹ (AUTHOR), Elmissbah, Triq E¹ (AUTHOR), Alsharif, Khalaf F¹ (AUTHOR), Alzahrani, Hind A.² (AUTHOR), Alsaiari, Ahad Amer¹ (AUTHOR), Allahyani, Mamdouh¹ (AUTHOR), Gharib, Amal F.¹ (AUTHOR), Qanash, Husam^4,5 (AUTHOR), Elmasry, Heba M.^6,7 (AUTHOR), Hassanein, Doha Elsayed^6,8 (AUTHOR)

Publikováno v: Thrombosis Journal. 11/10/2023, Vol. 21 Issue 1, p1-8. 8p.

Spectrum of α-thalassemia mutations in transfusion-dependent β-thalassemia patients from the Eastern Province of Saudi Arabia.

Autor: Akhtar MS; Department of Biochemistry, University of Dammam, Dammam 31441, Saudi Arabia. makhtar@ud.edu.sa, Qaw F, Borgio JF, Albuali W, Suliman A, Nasserullah Z, Al-Jarrash S, Al-Ali A

Publikováno v: Hemoglobin [Hemoglobin] 2013; Vol. 37 (1), pp. 65-73.

Neonatal screening for sickle cell disease, glucose-6-phosphate dehydrogenase deficiency and a-thalassemia in Qatif and Al Hasa.

Autor: Nasserullah Z; Department of Pediatrics, Qatif Central Hospital, Dammam Central Laboratory, Qatif Primary Care Center, King Fahad Hospital, Hofuf., Al Jame A, Abu Srair H, Al Qatari G, Al Naim S, Al Aqib A, Mokhtar M

Publikováno v: Annals of Saudi medicine [Ann Saudi Med] 1998 Jul-Aug; Vol. 18 (4), pp. 289-92.