Othman A - Search Results

1

Polymorphic sites in the African population detected by sequence analysis of the glucose-6-phosphate dehydrogenase gene outline the evolution of the variants A and A-.

Vulliamy TJ, Othman A, Town M, Nathwani A, Falusi AG, Mason PJ, Luzzatto L. Vulliamy TJ, et al. Among authors: othman a. Proc Natl Acad Sci U S A. 1991 Oct 1;88(19):8568-71. doi: 10.1073/pnas.88.19.8568. Proc Natl Acad Sci U S A. 1991. PMID: 1924316 Free PMC article.

2

Linkage disequilibrium of polymorphic sites in the G6PD gene in African populations and the origin of G6PD A-.

Vulliamy TJ, Othman A, Town M, Nathwani A, Falusi Y, Luzzatto L. Vulliamy TJ, et al. Among authors: othman a. Gene Geogr. 1991 Apr-Aug;5(1-2):13-21. Gene Geogr. 1991. PMID: 1687913

3

Glucose-6-phosphate dehydrogenase (G6PD)-deficient infants: Enzyme activity and gene variants as risk factors for phototherapy in the first week of life.

Wong FL, Ithnin A, Othman A, Cheah FC. Wong FL, et al. Among authors: othman a. J Paediatr Child Health. 2017 Jul;53(7):705-710. doi: 10.1111/jpc.13509. Epub 2017 Apr 4. J Paediatr Child Health. 2017. PMID: 28376293

4

Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia.

Boo NY, Wong FL, Wang MK, Othman A. Boo NY, et al. Among authors: othman a. Pediatr Int. 2009 Aug;51(4):488-93. doi: 10.1111/j.1442-200X.2008.02798.x. Pediatr Int. 2009. PMID: 19674361

5

Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.

Azma RZ, Othman A, Azman N, Alauddin H, Ithnin A, Yusof N, Razak NF, Sardi NH, Hussin NH. Azma RZ, et al. Among authors: othman a. Malays J Pathol. 2012 Jun;34(1):57-62. Malays J Pathol. 2012. PMID: 22870600 Free article.

6

Risk factors associated with unconjugated neonatal hyperbilirubinemia in Malaysian neonates.

Wong F, Boo N, Othman A. Wong F, et al. Among authors: othman a. J Trop Pediatr. 2013 Aug;59(4):280-5. doi: 10.1093/tropej/fmt023. Epub 2013 May 2. J Trop Pediatr. 2013. PMID: 23640907

7

Increased basal oxidation of peroxiredoxin 2 and limited peroxiredoxin recycling in glucose-6-phosphate dehydrogenase-deficient erythrocytes from newborn infants.

Cheah FC, Peskin AV, Wong FL, Ithnin A, Othman A, Winterbourn CC. Cheah FC, et al. Among authors: othman a. FASEB J. 2014 Jul;28(7):3205-10. doi: 10.1096/fj.14-250050. Epub 2014 Mar 17. FASEB J. 2014. PMID: 24636884

Erythrocytes require glucose-6-phosphate dehydrogenase (G6PD) to generate NADPH and protect themselves against hemolytic anemia induced by oxidative stress. Peroxiredoxin 2 (Prx2) is a major antioxidant enzyme that requires NADPH to recycle its oxidized (disulfide-bonded) …

Erythrocytes require glucose-6-phosphate dehydrogenase (G6PD) to generate NADPH and protect themselves against hemolytic anemia induced by o …

8

Immature reticulocyte fraction is an early predictor of bone marrow recovery post chemotherapy in patients with acute leukemia.

Raja-Sabudin RZ, Othman A, Ahmed-Mohamed KA, Ithnin A, Alauddin H, Alias H, Abdul-Latif Z, Das S, Abdul-Wahid FS, Hussin NH. Raja-Sabudin RZ, et al. Among authors: othman a. Saudi Med J. 2014 Apr;35(4):346-9. Saudi Med J. 2014. PMID: 24749130

9

A case series of α-thalassemia intermedia due to compound heterozygosity for Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] with other α-thalassemias in Malay families.

Alauddin H, Jaapar NA, Azma RZ, Ithnin A, Razak NF, Loh CK, Alias H, Abdul-Latiff Z, Othman A. Alauddin H, et al. Among authors: othman a. Hemoglobin. 2014;38(4):277-81. doi: 10.3109/03630269.2014.916720. Epub 2014 May 14. Hemoglobin. 2014. PMID: 24829075

10

Hb lepore/β0-thalassaemia with α+-thalassaemia interactions, a potential diagnostic pitfall.

Alauddin H, Mohamad Nasir S, Ahadon M, Raja Sabudin RZ, Ithnin A, Hussin NH, Alias H, Loh CK, Abdul Latiff Z, Abdul Murad NA, Othman A. Alauddin H, et al. Among authors: othman a. Malays J Pathol. 2015 Dec;37(3):287-92. Malays J Pathol. 2015. PMID: 26712677 Free article.

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