ahmad zulhimi, raja zahratul azma, ziqrill izapri, norunaluwar jalil, azlin ithnin, rafeah tumian.  (2023).  calreticulin mutations in myeloproliferative neoplasms patients diagnosed in ukm medical centre.  - malaysian journal of medicine and health sciences.  48-54. 

mohamed afiq hidayat z, raja zahratul azma rs, darnina aj, azlin i, najiah-ajlaa a, hafiza a, norunaluwar j, alina mf, fook choe cheah, lee sim lim, nazarudin s, malisa moh y, ainoon o.  (2023).  evaluation of quantitative point-of-care test for measurement of glucose-6-phosphate dehydrogenase enzyme activity in malaysia.  - malaysian journal of pathology.  31-41. 

heng yang lee, azlin ithnin, raja zahratul azma, ainoon othman, armindo salvador, fook choe cheah.  (2022).  glucose-6-phosphate dehydrogenase deficiency and neonatal hyperbilirubinemia: insights on pathophysiology, diagnosis, and gene variants in disease heterogeneity.  - frontiers in pediatrics.  1-13. 

wan awatif wan mohd zohdi, ahmad zulhimi ismail, nurasyikin yusof, azlin ithnin, salwati shuib, noraidah masir, sivakumar palaniappan and nor rafeah tumian.  (2022).  rare but potentially fatal presentations of diffuse large b-cell lymphoma: leukemic phase or hemophagocytic syndrome in bone marrow.  - clinical pathology.  1-6. 

wing hang woo, azlin ithnin, mohd asyiq al-fard mohd raffali, mohamed faisal abd. hamid, s. fadilah abdul wahid and wan fariza wan jamaludin.  (2022).  recurrent pleural effusion in myeloma.  - oxford medical case reports.  318-321. 

toh leong tan, christabel wan-li kang, kai shen ooi, swee thian tan, nurul saadah ahmad, dian nasriana nasuruddin, azlin ithnin, khaizurin tajul arifin, yook heng lee, nurul izzaty hassan, kok beng gan, hui-min neoh.  (2021).  comparison of spla2-iia performance with high-sensitive crp, neutrophil percentage, pct and lactate to identify bacterial infection: a prospective study.  - scientific reports.  1-9. 

nor syazana jamali, raja zahratul azma raja sabudin, hafiza alauddin, azlin ithnin, nor rafeah tumian, norunaluwar jalil, rinie awai, siti hawa abu amis, salwati shuib.  (2021).  h396p mutation in chronic myeloid leukaemia patient on nilotinib - a case report.  - the malaysian journal of pathology.  63-68. 

dian nasriana nasuruddin, azlin ithnin, najwa hayati muzani, munirah md mansor.  (2021).  lambda light chain disease co-migrating in the beta region with normal renal profile.  - the malaysian journal of pathology.  153. 

ying ying wong, hafiza alauddin, raja zahratul azma raja sabudin , azlin ithnin , norunaluwar jalil , zarina abdul latiff , c-khai loh , hamidah alias , ainoon othman.  (2021).  siriraj i gy(aydb)0-thalassaemia causing severe thalassaemia intermedia in compound heterozygous state with ivs1-1(g-t) mutation.  - the malaysian journal of pathology.  95-100. 

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. 

m. f. alina, r. z. azma, j. norunaluwar, i. azlin, a. j. darnina, f. c. cheah, a. r. noor-farisah, a. a. siti-hawa, x. r. k.danny, noor-fadzilah zulkifli , o. ainoon.  (2020).  genotyping of malaysian g6pd-deficient neonates by reverse dot blot flow-through hybridisation..  - journal of human genetics.  263-270. 

woon lee yong, nurasyikin yusof, azlin ithnin , salwati shuib, rafeah tumian, rabeya yousuf, suria abdul aziz,.  (2020).  mixed phenotype acute leukaemia with t(9,22), bcr-abl1: a case report.  - malaysian journal of pathology.  469-476. 

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. 

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. 

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. 

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. 

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, 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.  . 

nor ainiza mansor, nurasyikin yusuf, yee-loong tang, azlin ithnin, raja zahratul azma, nor rafeah tumian and salwati shuib.  (2018).  myelodysplastic syndrome with fibrosis and complex karyotype arising in a patient with essential thrombocythaemia.  - malaysian journal of pathology.  191-197. 

fei-liang wong, azlin ithnin, ainoon othman, fook-choe cheah.  (2017).  glucose-6-phosphate dehydrogenase (g6pd)-deficient infants: enzyme activity and gene variants as risk factors for phototherapy in the first week of life..  - journal of paediatrics and child health.  705-710. 

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. 

toh leong tan, nurul saadah ahmad, dian nasriana nasuruddin, azlin ithnin , khaizurin tajul arifin, ida zarina zaini, wan zurinah wan ngah.  (2016).  cd64 and group ii secretory phospholipase a2 (spla2-iia) as biomarkers for distinguishing adult sepsis and bacterial infections in the emergency department.  - plos one.  e0152065. 

omayma saad eldeen bakheet, leong chooi fun, azlin ithnin, siti fadilah abdul wahid.  (2016).  igd-kappa multiple myeloma. case report and brief review of the literature.  - new zealand journal of medical laboratory science.  8-11. 

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. 

omayma saad eldeen bakheet, nurasyikin yusof, azma raja zahratul, azlin ithnin, suria abdul aziz, hamidah alias.  (2016).  secondary sea-blue histiocytosis in a patient with transfusion dependent hbe-beta thalassaemia and osteosarcoma.  - indian journal of hematology and blood transfusion.  s262-s266. 

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. 

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, ain.  (2015).  hb lepore/b0-thalassaemia with a+-thalassaemia interactions, a potential diagnostic pitfall.  - malaysian journal of pathology.  287-292. 

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. 

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. 

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. 

cheah, f.-c., peskin, a. v., wong, f.-l., ithnin, a., othman, a., winterbourn, c. c..  (2014).  increased basal oxidation of peroxiredoxin 2 and limited peroxiredoxin recycling in glucose-6-phosphate dehydrogenase-deficient erythrocytes from newborn infants.  - faseb journal.  3205-3210. 

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. 

m ahmad nasirudin, y nurasyikin, rz azma, i azlin, wk loh, za zainura anita, z mohd yazid.  (2014).  bone marrow necrosis in a chronic myeloid leukaemia patient receiving imatinib treatment.  - malaysian journal of pathology.  116-117. 

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. 

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. 

dian n nasuruddin, daphne dindu j, ng kk, ailah sariman, fong sh, r nor azura, azlin ithnin, hanita othman.  (2014).  a comparison between spot urine protein and 24-hour urine protein as biomarkers for the detection of urinary paraprotein in multiple myeloma.  - malaysian journal of pathology.  91. 

nh hamidah, m firdhaus, nurul azwa, i azlin, ms siti shahrum, a mimi azura, o raudhawati.  (2014).  immunophenotype and pml gene breakpoints in classical and variant acute promyelocytic leukaemia.  - malaysian journal of pathology.  109-110. 

cheah fc, wong fl, ithnin a, othman a.  (2013).  the genetics of g6pd deficiency and ugt1a1 mutation associated with jaundice in the early neonatal period.  - journal of paediatrics and child health.  83. 

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. 

r.z. azma, o. ainoon, i. azlin, h. hamenuddin, n.a. hadi, w.k. tatt, i.n. syazana, a.m. asmaliza,s. das, n.h. hamidah.  (2012).  prevalence of iron deficiency anaemia and thalassaemia trait among undergraduate medical students.  - la clinica terapeutica.  163(4):287-291. 

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. 

fc cheah, fl wong, sk chow, a ithnin, a othman.  (2012).  mutations in the g6pd and ugt1a1 genes associated with significant hyperbilirubinaemia in asian newborn infants.  - archives of disease in childhood.  A74. 

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. 

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. 

i azlin, fl wong, m ezham, a hafiza, o ainoon.  (2011).  prevalence of uridine glucuronosyl transferase 1a1 (ugt1a1) mutations in malay neonates in severe jaundice.  - malaysian journal of pathology.  33(2):95-100. 

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. 

s a w fadilah, m muhaya, i azlin.  (2007).  irreversible visual loss and optic nerve dysfunction associated with central retinal vein occlusion in waldenstrom macroglobulinemia.  - medical jounal of malaysia.  62(4):349-351.