Prediction of sifnificant neonatal jaundice in babies with ABO incompatibility by cord blood tests

by Azma RZ, Farisyah SMZ, Nurasyikin Y, Noria M
Published 2011

Effect of higher centrifugation speed and shortened centrifugation time on prothrombin and activated thromboplastin time

by Azlin I, Hafiza A, Azma RZ, Aidifitrina RK, Hamidah NH
Published 2011

Minimal residual disease status in childhood acute lymphoblastic leukaemias by flow cytometry and their clinical and haematological features

by Azma RZ, Zarina AL, Hamidah A, Cheong SK, Jamal R, Hamidah NH
Published 2010

Early lineage switch from T-acute lymphoblastic leukaemia to common B-all.

by Hafiza, A, Azura, AH, Azma, RZ, Azlin, I, Zarina, AL, Hamidah, NH
Published 2011

The Msi2 protein expression positive correlation with favorable cytogenetics findings in AML

by Bakheet, Omayma Saad Eldeen, Nurasyikin Y, Azma RZ, Suria Abdul Aziz, Chandramaya S, Noraidah Masir
Published 2017

Short tandem repeat (STR) analysis of chimerism in allogeneic peripheral blood stem cell transplant in UKMMC Kuala Lumpur

by Hamidah, NH, Farisah, NR, Hidayati, NS, Aidilfitrina, KR, Azma, RZ, Fadillah, SAW, Ainoon, O
Published 2011

Impact of CD34+ stem cell dose on engraftment period in allogeneic peripheral blood stem cell transplanted patients

by Suria Abdul Aziz, Hazlina Diyana B, Zed Zakari AH, Nurasyikin Y, Yousuf R, Azma RZ
Published 2021

Idiopathic hypereosinophilic syndrome with unusual presentation : two case reports and review of literature

by Suria Abdul Aziz, Hafizah H, Nurasyikin Yusof, Azlin Ithnin, Yousuf R, Azma RZ, Hamidah NH
Published 2018

Infantile acute megakaryoblastic leukaemia with T(1:22) in a non-down syndrome child.

by Nurasyikin Y, shenaz SK, Suria AAA, Azma RZ, zarina AL, Hamidah A, Salwati S, Zubaidah Z, Aminah NH
Published 2012

Detection of partial G6PD deficiency using OSMMR2000-D kit with Hb normalization.

by Azma RZ, Siti Zubaidah M, Azlin I, Hafiza A, Nurasyikin Y, Nor Hidayati S, Noor Farisah AR, Noor Hamidah H, Ainoon O
Published 2014

Co-inheritance of compound heterozygous Hb constant spring and a single -α 3.7 gene deletion with heterozygous δβ thalassaemia: A diagnostic challenge

by Azma R.Z., Othman A., Azman N., Alauddin H., Ithnin A., Yusof N., Razak N.F., Sardi N.H., Hussin N.H.
Published 2017

The HbA2 levels in normal, B-thalassaemia and haemoglobin E heterozygotes and haemoglobin E (HbE) level in HbE heterozygotes by capillary electrophoresis system

by Hafiza A, Azma RZ, Chong MKT, Irwan MA, Yeoh Z-N, Lailyvia MI, Nur Rabiatuladawiah MR, Aidilfitrina M, Malissa Y, Azlin I, Hamidah NH
Published 2011

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

by Alauddin H., Jaapar N.-A., Azma R.Z., Ithnin A., Razak N.-F.A., Loh C.-K., Alias H., Abdul-Latiff Z., Othman A
Published 2018