Detalhe da pesquisa
1.
Multiplex STR panel for assessment of chimerism following hematopoietic stem cell transplantation (HSCT).
Ann Hematol
; 98(5): 1279-1291, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30783731
2.
A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-Thalassemia.
Hemoglobin
; 42(4): 247-251, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-30623696
3.
Molecular Characterisation of α- and ß-Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia.
Ann Hum Genet
; 81(5): 205-212, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28620953
4.
Importance of extended blood group genotyping in multiply transfused patients.
Transfus Apher Sci
; 56(3): 410-416, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28438419
5.
Glucose-6-phosphate dehydrogenase (G6PD)-deficient infants: Enzyme activity and gene variants as risk factors for phototherapy in the first week of life.
J Paediatr Child Health
; 53(7): 705-710, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28376293
6.
Increased basal oxidation of peroxiredoxin 2 and limited peroxiredoxin recycling in glucose-6-phosphate dehydrogenase-deficient erythrocytes from newborn infants.
FASEB J
; 28(7): 3205-10, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24636884
7.
Hb lepore/ß0-thalassaemia with α+-thalassaemia interactions, a potential diagnostic pitfall.
Malays J Pathol
; 37(3): 287-92, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26712677
8.
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.
Hemoglobin
; 38(4): 277-81, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24829075
9.
Risk factors associated with unconjugated neonatal hyperbilirubinemia in Malaysian neonates.
J Trop Pediatr
; 59(4): 280-5, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23640907
10.
Population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review.
Front Genet
; 14: 1098828, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37388931
11.
Prevalence and molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Senoi Malaysian Orang Asli population.
PLoS One
; 18(12): e0294891, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38085718
12.
Ex vivo expanded SSEA-4+ human limbal stromal cells are multipotent and do not express other embryonic stem cell markers.
Mol Vis
; 18: 1289-300, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22665977
13.
Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.
Malays J Pathol
; 34(1): 57-62, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22870600
14.
Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia: Insights on Pathophysiology, Diagnosis, and Gene Variants in Disease Heterogeneity.
Front Pediatr
; 10: 875877, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35685917
15.
Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia.
Pediatr Int
; 51(4): 488-93, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19674361
16.
Evaluation of Glucose-6-Phosphate Dehydrogenase stability in stored blood samples.
EXCLI J
; 15: 155-62, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27103895
17.
Immature reticulocyte fraction is an early predictor of bone marrow recovery post chemotherapy in patients with acute leukemia.
Saudi Med J
; 35(4): 346-9, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24749130
18.
Genotyping of OATP2 Variants in a Group of Malaysian Neonates Using High-Resolution Melting Analysis.
Biores Open Access
; 1(2): 92-6, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23514972
19.
Immunophenotyping analysis of lymph node biopsies by flow cytometry.
Saudi Med J
; 33(10): 1131-3, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23047221