Penerbitan SCOPUS/ERA

shiang yui wee, siti shahrum muhamed said, raja zahratul azma raja sabudin, hafiza alauddin, azlin ithnin.  (2020).  microcytic to hypochromic ratio as a discriminant index of thalassaemia trait in subjects with hypochromic anaemia.  - malaysian journal of pathology.  195-201. 

nur zainura mohamad, norunaluwar jalil, loh c-khai, zarina abdul latiff, hafiza alauddin & raja zahratul azma.  (2019).  a rare ivs-i-2 (t>c) hbb gene mutation diagnosed in a child with anemia.  - hemoglobin.  357. 

qhasmira abu hazir, norunaluwar jalil, raja zahratul azma raja sabudin, hafiza alauddin, nurasyikin yusof & nor rafeah tumian.  (2019).  a fast-moving hemoglobin, hb j-bangkok: a case study from a single referral center in malaysia.  - hemoglobin.  358. 

ahmed maseh haidary, raja zahratul azma, azlin ithnin, hafiza alauddin, nor rafeah tumian, azmi mohd tamil, noor farisah a razak, siti hawa abu amis, nozi mat zin, salwati shuib.  (2019).  fish versus real-time quantitative pcr for monitoring of minimal residual disease in chronic myeloid leukaemia patients on tyrosine kinase inhibitor therapy.  - malaysian journal of pathology.  149-160. 

lailatul hadziyah mohd pauzy, norunaluwar jalil, raja zahratul azma raja sabudin & hafiza alauddin.  (2019).  case series of ivs-ii-666 (c>t) (hbb: c.316-185c>t) polymorphism: experience from a single referral center in malaysia.  - hemoglobin.  356. 

wui chuen chia, tze sean khoo, s fadilah s. abdul wahid, noor farisah abdul razak, hafiza alauddin, raja zahratul azma raja sabudin, ainoon othman, roshida hassan, noor hamidah hussin.  (2019).  multiplex str panel for assessment of chimerism following hematopoietic stem cell transplantation (hsct)..  - annals of hematology.  1279-1291. 

jalil norunaluwar, raja zahratul azma, hafiza alauddin, azlin ithnin, zarina abdul latiff, hamidah alias, nor rafeah tumian, malisa mohd yusoff, syahzuwan hassan & ainoon othman.  (2019).  application of molecular diagnostics in detection of b-thalassemia and hemoglobin variants at hospital canselor tuanku muhriz ukm, kuala lumpur, malaysia.  - hemoglobin.  351. 

jalil norunaluwar, raja zahratul azma raja sabudin, alauddin hafiza, ithnin azlin, hussin badrulzaman, carmene kah-mei, abu bakar sanada & othman ainoon.  (2019).  hplc tosoh hlc 723 g8 analyzer performance in detection of b thalassemia and hb e traits.  - hemoglobin international journal for hemoglobin research.  355. 

raja zahratul azma raja sabudin, alina md fauzi, darnina abdul jalil, azlin ithnin, hafiza alauddin, cheah fook-choe, najiah-ajlaa ayub, moh yusuf malisa, jalil norunaluwar & othman ainoon.  (2019).  updates on laboratory tests for diagnosis of glucose-6-phosphate dehydrogenase deficiency in malaysia.  - hemoglobin.  312. 

hafiza alauddin, khairina kamarudin, tang yee loong, raja zahratul azma, azlin ithnin, norunaluwar jalil, noor-farisah razak, danny koh-xuan-rong, endom ismail, loh c-khai, zarina abdul latiff, hamidah alias & ainoon othman..  (2018).  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 a thalassemia.  - hemoglobin. 

hamidah alias, woon lee yong, farah azima abdul muttlib, ho wai koo, c-khai loh, sie chong doris lau, hafiza alauddin and raja zahratul azma.  (2018).  acquired thrombotic thrombocytopenia purpura associated with severe adamts13 deficiency in a 3-year-old boy: a case report and review of the literature.  - journal of medical case reports. 

s.a.a. razak, n.a.a. murad, f. masra, d.l.s. chong, n. abdullah, n. jalil, h. alauddin, r.z.a.r. sabudin, a. ithnin, l.c. khai, n.a. aziz, z. muda, h. ibrahim and z.a. latiff.  (2018).  genetic modifiers of fetal haemoglobin (hbf) and phenotypic severity in beta thalassemia patients.  - current molecular medicine. 

hafiza alauddin, mustafa langa, malisa mohd yusoff, raja zahratul azma raja sabudin, azlin ithnin, noor farisah abdul razak, nor hidayati sardi, noor hamidah hussin.  (2017).  detection of a-thalassaemia in neonates on cord blood and dried blood spot samples by capillary electrophoresis.  - malaysian journal of pathology.  17-23. 

norunaluwar jalil, raja zahratul azma, emida mohamed, azlin ithnin, hafiza alauddin, siti noor baya, ainoon othman.  (2016).  evaluation of glucose-6-phosphate dehydrogenase stability in stored blood samples.  - excli journal.  155-162. 

azlin ithnin, jubaidah paraja, raja zahratul azma, hafiza alauddin, cheah foo choe, noor farisah abdul razak, siti hawa abu amis, siti noor baya mohd noor, ainoon othman.  (2015).  neonatal jaundice in g6pd-deficient females and the association with commonly occurring genetic mutations using single-nucleotide polymorphism detection via real-time pcr.  - malaysian journal of pathology.  198. 

nurasyikin yusuf, caroline ho siew ling, hafiza alauddin, suria abdul aziz m, indhira subiah & raja zahratul azma.  (2015).  assessment of iron deficiency in the paediatric age group: the clinical utility of reticulocyte haemoglobin equivalent (retic-he).  - the malaysian journal of pathology.  199. 

hafiza alauddin, suziana mohamad nasir, madzlifah ahadon, raja zahratul azma raja sabudin, azlin ithnin, noor hamidah hussin, hamidah alias, loh c-khai, zarina abdul latiff, nor azian abdul murad, ai.  (2015).  hb lepore/b thalassaemia with a+- thalassaemia interactions, a potential diagnostic pitfall.  - malaysian journal of pathology.  287-292. 

mustafa langa, hafiza alauddin, malisa mohd yusoff, raja zahratul azma, azlin ithnin, farisah nr, nor hidayati sardi, noor hamidah hussein.  (2015).  screening of a-thalassaemia in newborns by capillary electrophoresis system on fresh and dried cord blood samples.  - malaysian journal of pathology.  197. 

nor khairina mohamed kamaruddin, caroline ho siew ling, faridah ahmad maulana, raja zahratul azma, azlin ithnin, hafiza alauddin, noor farisah abdul razak, nor hidayati sardi, rafeah tumian, ainoon ot.  (2015).  concomitant hbh-pakse with jak2v617f mutation: case report.  - the malaysian journal of pathology.  196. 

j norunaluwar, rz azma, i azlin, a hafiza, sn baya, m emida, o ainoon.  (2014).  evaluation of glucose-6-phosphate dehydrogenase stability in stored edta blood samples.  - malaysian journal of pathology.  112-113. 

raja zahratul azma, ainoon othman, hafiza alauddin, azlin ithnin, noor farisah abdul razak, nor hidayati sardi, noor hamidah hussin.  (2014).  molecular characteristic of alpha thalassaemia among patients diagnosed in ukm medical centre.  - malaysian journal of pathology.  36(1):27-32. 

zainal n.z., alauddin h., ahmad s., hussin n.h..  (2014).  ?-thalassemia with haemoglobin adana mutation: prenatal diagnosis.  - malaysian journal of pathology.  207-211. 

hafiza alauddin, noor-adilah jaapar, raja z azma, azlin ithnin, noor-farisah a razak, c-khai loh, hamidah alias, zarina abdul-latiff, ainoon othman.  (2014).  a case series alpha-thalassaemia intermedia due to compound heterozygosity for hb adana with other alpha-thalassaemias in malay families..  - hemoglobin.  277 - 281. 

raja-zahratul a. raja sabudin, ainoon othman, khalid-awad e. ahmed-mohamed, azlin ithnin, hafiza alauddin, hamidah alias, zarina abdul-latif, srijit das, fadhilah s. abdul-wahid, noor h. hussin.  (2014).  immature reticulocyte fraction is an early predictor of bone marrow recovery post chemotherapy in patients with acute leukemia.  - saudi medical journal.  35(4):346-349. 

z norsafina, rz azma, i azlin, y nurasyikin, a hafiza, o nurasyikin, n rus mazeni.  (2014).  diagnostic performance of reticulocyte haemoglobin equivalent (ret-he) in detecting iron deficiency anaemia in haemodialysis patient.  - malaysian journal of pathology.  113. 

nh hamidah, ar munirah, a hafiza, ar farisah, a shuhaila, mn norzilawati, my jamil, o ainoon.  (2014).  prenatal diagnosis of aneuploidies in amniotic fluid by multiple ligation-dependent probe amplification (mlpa) analysis.  - malaysian journal of pathology.  163-168. 

nur zaireena zainal, hafiza alauddin, suhaila ahmad, noor hamidah hussin.  (2014).  a-thalassemia with haemoglobin adana mutation:prenatal diagnosis.  - malaysian journal of pathology.  207-211. 

m. siti sarah, u. nor aini, m.i. nurismah, a . hafiza, m. khalidah, a .b. mokhtar, s. das.  (2014).  lambda light chain myeloma with co-migrating paraprotein at beta region on agarose gel electrophoresis: a case report.  - clinica terapeutica.  165(1):35-39. 

raja-zahratul a raja-sabudin, azura a hamid, nurasyikin yusof, hafiza alauddin, sivagengei kulaveerasingam, norzi m zin, siti-aishah m ali, rohaizak muhammad, srijit das, ainoon othman, noor h hussin.  (2012).  immunophenotyping analysis of lymph node biopsies by flow cytometry.  - saudi medical journal.  33(10):1131-3. 

adilah nj, azma rz, suria aa, azlin i, hafiza a, hamidah nh,salwati s, chia wk, rafeah t, zubaidah z, sharifah na.  (2012).  a rare t (9; 12; 22) (q34; q23; q11) translocation in a patient with typical chronic myeloid leukemia: a case report.  - malaysian journal of pathology.  34(2):203. 

hafiza a, jaapar na, azma rz, azlin i, hamidah nh, ainoon o.  (2012).  a case series of hb adanainteraction with beta thalassaemia.  - malaysian journal of pathology.  34(2):198. 

hafiza alauddin, malisa mohd yusoff, , rd aidifitrina khirotdin, azlin ithnin , raja zahratul azma , matthew chong kwok thong,irwan mohamad ali, noor hamidah hussin.  (2012).  hba2 levels in normal, beta-thalassaemia and haemoglobin e carriers by capillary electrophoresis.  - malaysian journal of pathology.  34(2) : 161-164. 

raja zahratul azma, ainoon othman, norazlina azman, hafiza alauddin, azlin ithnin, nurasyikin yusof, noor farisah razak, nor hidayati sardi, noor hamidah hussin.  (2012).  co-inheritance of compound heterozyqous hb constant spring and a single -a3.7 gene deletion with heterozyqous db thalassaemia: a diagnostic challenge.  - malaysian journal of pathology.  34(1):57-62. 

azlin i, nurasyikin y, norazlina a, hafi za a, azma rz, cheong sk, hamidah nh.  (2011).  pure erythroid leukaemia in a four year old child: a diagnostic dilemma.  - malaysian journal of pathology.  33(2):136. 

hafiza alauddin, noor hamidah hussin, noor farisah a razak, azlin ithnin and ainoon othman.  (2010).  a family study of hbs in a malay family by molecular analysis.  - malaysian journal of pathology.  32(2):137-141.