Nasserullah Z - Search Results

1

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

Akhtar MS, Qaw F, Borgio JF, Albuali W, Suliman A, Nasserullah Z, Al-Jarrash S, Al-Ali A. Akhtar MS, et al. Among authors: nasserullah z. Hemoglobin. 2013;37(1):65-73. doi: 10.3109/03630269.2012.753510. Hemoglobin. 2013. PMID: 23297837

2

Existence of HbF Enhancer Haplotypes at HBS1L-MYB Intergenic Region in Transfusion-Dependent Saudi β-Thalassemia Patients.

Cyrus C, Vatte C, Borgio JF, Al-Rubaish A, Chathoth S, Nasserullah ZA, Jarrash SA, Sulaiman A, Qutub H, Alsaleem H, Alzahrani AJ, Steinberg MH, Ali AK. Cyrus C, et al. Among authors: nasserullah za. Biomed Res Int. 2017;2017:1972429. doi: 10.1155/2017/1972429. Epub 2017 Feb 9. Biomed Res Int. 2017. PMID: 28280727 Free PMC article.

3

Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β(0) thalassemia.

Alsultan A, Ngo D, Bae H, Sebastiani P, Baldwin CT, Melista E, Suliman AM, Albuali WH, Nasserullah Z, Luo HY, Chui DH, Steinberg MH, Al-Ali AK. Alsultan A, et al. Among authors: nasserullah z. Am J Hematol. 2013 Jun;88(6):531-2. doi: 10.1002/ajh.23434. Epub 2013 May 2. Am J Hematol. 2013. PMID: 23483609 Free article. No abstract available.

4

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

Alsultan A, Jastaniah W, Al Afghani S, Al Bagshi MH, Nasserullah Z, Al-Suliman AM, Alabdulaali MK. Alsultan A, et al. Among authors: nasserullah z. Pediatr Transplant. 2016 Sep;20(6):831-5. doi: 10.1111/petr.12767. Epub 2016 Jul 31. Pediatr Transplant. 2016. PMID: 27477851

5

The effect of alpha-thalassemia on cord blood red cell indices and interaction with sickle cell gene.

Quadri MI, Islam SI, Nasserullah Z. Quadri MI, et al. Among authors: nasserullah z. Ann Saudi Med. 2000 Sep-Nov;20(5-6):367-70. doi: 10.5144/0256-4947.2000.367. Ann Saudi Med. 2000. PMID: 17264624 Free article.

6

Regional experience with newborn screening for sickle cell disease, other hemoglobinopathies and G6PD deficiency.

Nasserullah Z, Alshammari A, Abbas MA, Abu-Khamseen Y, Qadri M, Jafer SA, Wabel MA. Nasserullah Z, et al. Ann Saudi Med. 2003 Nov-Dec;23(6):354-7. doi: 10.5144/0256-4947.2003.354. Ann Saudi Med. 2003. PMID: 16868367 Free article.

7

Hb Bart's levels in cord blood in Hb H disease: follow-up of cases with "probable" Hb H disease.

Quadri MI, Nasserullah Z. Quadri MI, et al. Among authors: nasserullah z. Ann Saudi Med. 2001 Sep-Nov;21(5-6):357-8. doi: 10.5144/0256-4947.2001.357a. Ann Saudi Med. 2001. PMID: 17261953 Free article. No abstract available.

8

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

Nasserullah Z, Al Jame A, Abu Srair H, Al Qatari G, Al Naim S, Al Aqib A, Mokhtar M. Nasserullah Z, et al. Ann Saudi Med. 1998 Jul-Aug;18(4):289-92. doi: 10.5144/0256-4947.1998.289. Ann Saudi Med. 1998. PMID: 17344674 Free article.

9

Splenectomy and acute splenic sequestration crises in sickle cell disease.

Al Salem AH, Qaisaruddin S, Nasserullah Z, Al Dabbous I, Abu Srair H, Al Jam'a A. Al Salem AH, et al. Among authors: nasserullah z. Pediatr Surg Int. 1996 Dec;11(1):26-8. doi: 10.1007/BF00174580. Epub 2013 Sep 21. Pediatr Surg Int. 1996. PMID: 24057466

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