aida nurul hanim rahman , alina md fauzi, raja zahratul azma raja sabudin, azlin ithnin, ainoon binti othman, cheah fook choe, wan ahmad shukri aziz.  (2023).  evaluation of carestart s1 analyzer biosensor quantitative assay of g6pd activity and establishment of reference range for point of care testing in diagnosis of g6pd deficiency..  - malaysian journal of pathology.  540. 

mohamed afiq hidayat zailani, raja zahratul azma raja sabudin, azlin ithnin, hafiza alauddin, muhammad ziqrill mohd zapri, muhammad dinie afif jamaludin, najiah ajlaa ayub, siti aishah sulaiman, ainoon othman.  (2023).  small device, big impact: point-of-care testing for glucose-6-phosphate dehyrogenase (g6pd) deficiency in six proto malay orang asli settlements.  - malaysian journal of pathology.  529-530. 

aida nurul hanim, raja zahratul azma raja sabudin, alina md fauzi, azlin ithnin & ainoon binti othman.  (2023).  evaluation of carestarttm si analyzer biosensor quantitative assay of rbc g6pd enzyme and establishment of reference range for poct in diagnosing of g6pd def.  - 20th annual scientific meeting malaysian society of haematology.  1. 

cheah fook choe, ainoon othman, azlin ithnin, raja zahratul azma raja sabudin, norunaluwar jalil, goon jo aan, tan jen kit, armindo salvador.  (2023).  characterization of the biochemical and enzymatic properties of two novel g6pd mutations..  - .  1-7. 

mohamed afiq hidayat zailani, raja zahratul azma raja sabudin, azlin ithnin, hafiza alauddin, muhammad ziqrill mohd zapri, muhammad dinie afif jamaludin, siti aishah sulaiman, ainoon othman.  (2023).  small device, big impact: point-of-care testing for glucose-6-phosphate dehyrogenase (g6pd) deficiency in six proto malay orang asli settlements.  - international congress of pathology and laboratory medicine (icpalm) 2023.  1. 

izzatul aliaa badaruddin, dian nasriana nasuruddin, azlin ithnin, nurasyikin yusof, munirah md mansor.  (2023).  a case of paraproteinaemia with systemic amyloidosis: a progression or merely a coincidence?.  - journal of clinical and health sciences.  52-56. 

alia suzana asri, azlin ithnin, hafiza alauddin, nor rafeah tumian, siti mariam yusuf, norunaluwar jalil, salwati shuib, raja zahratul azma.  (2023).  concomitant bcr-abl and jak2 v617f in a patient with myeloproliferative neoplasm: a case report..  - medicine & health.  233-240. 

t. s. lim, w. nyunt, k. then, s. cheong, k. then, g. ooi, v. govindasamy, m. mohd idris, s. azura, n. abdullah, m. muhd zakaria, a. h. chang, a. ithnin , s. s. abdul wahid.  (2023).  locally manufactured autologous cd19 chimeric antigen receptor-t (car-t) cells for phase ii prospective clinical trial for relapsed/refractory b-acute lymphoblastic leukaemia in malaysia.  - cytotherapy.  S225-S226. 

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. 

s fadilah abdul wahid1, wint wint thu nyunt2, timothy lim2, mohd razif mohd idris1, muhd zanapiah muhd zakaria1,3, alex chang h s4, wan fariza wan jamaludin1, loh c-khai5, hamidah alias5, suria abd aziz6, azlin ithnin7, seery zaliza azura1, noraimy abdu.  (2022).  autologous cd19 chimeric antigen receptor-t therapy for relapsed/ refractory b-acute lymphoblastic leukaemia patients- a phase ii clinical trial in malaysia.  - 19th malaysian society haematology scientific meeting 2022.  50. 

qhasmira abu hazir, raja zahratul azma raja sabudin, azlin ithnin, nor rafeah tumian, salwati shuib.  (2022).  cytogenetics findings and its correlation with overall survival (os) and event free survival (efs) in patients with aml.  - the 19th annual scientific meeting malaysian society of haematology.  1. 

lailatul hadziyah binti mohd pauzy, raja zahratul azma, azlin ithnin, rinie albert, hafiza alauddin.  (2022).  molecular landscape of cases with borderline hba2 levels in hctm.  - the 19th annual scientific meeting malaysian society of haematology.  0. 

mohd fikri mustapa, raja zahratul azma, azlin ithnin, salwati shuib, thatcheiany kumariah.  (2022).  significance of aberrant expression of myeloid marker in correlation of cytogenetic abnormality in patient with b-all.  - the 19th annual scientific meeting malaysian society of haematology.  1. 

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. 

mohamed afiq hidayat zailani, raja zahratulazma raja sabudin, azlin ithnin, hafiza alauddin, siti aishah sulaiman, endom ismail, ainoon othman.  (2022).  genetic variants of g6pd deficiency in southeast asian countries and future directions of genomic medicine..  - the 19th annual scientific meeting malaysian society of haematology.  1. 

azlin ithnin, tan toh leong.  (2022).  post sepsis food for thought.  - the health newspaper.  26. 

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. 

mohamed afiq hidayat zailani, raja zahratul azma raja sabudin, hafiza alauddin, azlin ithnin, siti aishah sulaiman, endom ismail, ainoon othman.  (2022).  point-of-care genetic testing for glucose-6-phosphate dehydrogenase (g6pd) deficiency as a novel molecular diagnostic approach: challenges and opportunities.  - medical genetics conference kuala lumpur 2022: the future is now.  1. 

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. 

azlin binti ithnin, tan toh leong.  (2021).  severe covid-19 leads to sepsis!.  - the health.  23. 

ahmad zulhimi, raja zahratul azma, ziqrill zapri, norunaluwar jalil, azlin ithnin.  (2021).  calreticulin mutations in myeloproliferative neoplasms patients diagnosed in ukm medical centre.  - the 18th annual scientific meeting malaysian society of haematology.  1. 

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. 

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. 

tan toh leong, azlin ithnin.  (2021).  covid-19 yang teruk penyebab sepsis.  - penerbit: myhealth malaysia.  18-19. 

aida nurul hanim abd rahman, azlin ithnin, tang yee loong, farah azima abdul muttlib.  (2021).  rare translocation t(3;21)(q26.2;q22) in primary myelofibrosis with blast transformation: a case report.  - 18th annual scientific meeting of malaysian society of haematology; shifting paradigms, changing practices.  1. 

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. 

aliff saifuddin mohd shukri, nor rafeah tumian, nurasyikin yusof, azlin ithnin, petrick periyasamy, najma kori, noorzilawati sahak.  (2021).  comparison of coagulation parameters between covid-19 patients with and without pneumonia in a single tertiary hospital in kuala lumpur, malaysia.  - 18th malaysian society of haematology annual scientific meeting.  1-7. 

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. 

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. 

m fikri, a zulhilmi, a hafiza, i azlin, j norunaluwar, r z azma.  (2020).  myeloproliferative neoplasm with cml features but positive calreticulin (calr) - a case report.  - 17th malaysian society of haematology scientific meeting. personalised haematology. now and the future.  67. 

wee sy, hafiza a, azma rz, norunaluwar j, azlin i, malisa my, qistina wn, ainoon o.  (2020).  detection of haemoglobin s using multiplex ligation-dependent probe amplification and flow-through hybridization techniques: experience in a tertiary hospital.  - medicine & health.  106-118. 

alia suzana asri, azlin ithnin, hafiza alauddin, nor rafeah tumian, siti mariam yusuf, nozi mat zin, norunaluwar jalil, aizuddin al banna ramlee, salwati shuib, raja zahratul azma.  (2020).  concomitant bcrabl and jak2 v617f mutation in a patient with myeloproliferative neoplasm - a case report.  - 17th malaysian society of haematology scientific meeting - personalised haematology: new & the future.  67. 

dewi nurmaya spree, raja zahratul azma, suria abdul aziz, s fadilah s abdul wahid , azlin ithnin.  (2020).  pre infusion cd34 peripheral blood stem cell enumeration as a predictor of haematopoetic engraftment and chimera status in allogeneic stem cell transplantation.  - 17th malaysian society of haematology scientific meeting - personalised haematology: now and the future.  75. 

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. 

farah-azima am, maizatul-husna mr, norunaluwar j, hafiza a, azlin i, norafiza my, yuslina my, ermi-neiza ms, shahzuwan h, faidatul-syazlin ah, ezalia e, azma rz and ainoon o.  (2020).  multiplex ligation-dependent probe amplification (mlpa) assay: its application in characterising unsolved alpha globin gene rearrangements.  - 17th annual scientific meeting, malaysian society of haematology.  67. 

mohd khairul mohd kamil, rozita mohd, rizna abdul cader, azlin ithnin, shamsul azhar mohd shah.  (2019).  regulatory t cells (cd4+cd25+foxp3+) in lupus nephritis.  - international journal of research in medical sciences.  . 

mohd nur aizat bin mohd yasim, azlin binti ithnin, raja zahratul azma raja sabudin, cheah fook choe.  (2019).  evaluation of the performance of a point-of-care diagnostic test for g6pd deficiency in newborn infants with hyperbilirubinaemia.  - .  . 

nor syazana jamali, raja zahratul azma, hafiza alauddin, azlin ithnin, nor rafeah tumian, norunaluwar jalil, rinie awai, siti hawa, salwati shuib.  (2019).  bcrabl1 mutation testing in a patient with treatment failure in cml.  - the 16th annual scientific meeting, msh.  121-122. 

dr. mohd nur aizat bin mohd yasim, dr. azlin binti ithnin, prof. dr. zahratul azma, prof. dr. cheah fook choe.  (2019).  evaluation of the performance of a point-of-care diagnostic test for g6pd deficiency in newborn infants with hyperbilirubinemia.  - the 26th regional congress of the perinatal society of malaysia.  77. 

mardziah m, salwati s, azlin i, hafiza a, noor farisah ar, noraesah m, tumian nr, wong cl, azma rz.  (2019).  detection of bcr-abl t315i mutation in imatinib resistant chronic myeloid leukemia patients.  - medicine & health.  145-156. 

tan toh leong, azlin binti ithnin.  (2019).  sepsis neutropenik mimpi ngeri pesakit.  - al-siha.  15. 

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 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. 

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. 

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.  . 

suria aa, hafizah h, nurasyikin y, azlin i, yousuf r, azma rz, hamidah nh.  (2018).  idiopathic hypereosinophilic syndrome with unusual presentation: two case reports and review of literature.  - medicine and health.  208-216. 

nik nurhanan nik mansor, tan toh leong, nurul saadah ahmad, dian nasriana nasuruddin, azlin ithnin, ida zarina zaini, eka safitri, dedi futra, lee yook heng & nurul izzaty hassan.  (2018).  an amperometric biosensor for the determination of bacterial sepsis biomarker, secretory phospholipase group 2-iia using a tri-enzyme system.  - the 8th international conference on sensors 2018 (asiasense 2018).  . 

raja zahratul azma raja sabudin;shuhaila bt. ahmad;endom bt. ismail;zarina binti abdul latiff;siti hawa binti abu amis;hamidah binti alias;azlin binti ithnin;noor farisah binti a razak;hafiza binti alauddin;norunaluwar binti jalil;nor rafeah binti tumian;.  (2018).  molecular characterization of unknown alpha and beta globin gene rearrangements..  - .  . 

zarina binti abdul latiff;a. rahman bin a. jamal;hamidah binti alias;azlin binti ithnin;hafiza binti alauddin;nor azian binti abdul murad;raja zahratul azma raja sabudin;doris lau sie chong.  (2018).  genetic modifiers of hbf and phenotypic severity in malaysian beta-thalassaemia patients.  - .  . 

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.  . 

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. 

nor syazana j, nr tumian, azlin i, suria aa.  (2018).  therapy related acute promyelocytic leukaemia :a case report.  - 15th msh annual scientific meeting.  . 

alina mf, norunaluwar j, azma rz, azlin i, cheah fc, noor-farisah ar, siti-hawa aa, noor-fadzilah zulkifli and ainoon o.  (2018).  simultaneous detection of g6pd mutations by flow-through hybridization - a potential tool for genetic screening of newborn.  - 15th annual scientific meeting malaysian society of haematology, 2018.  . 

azma rz, hafiza a, azlin i, norunaluwar j, maizatul-husna ma, joanna skk1, farah-hazirah sa, nurul-najiehah nm, najatul-adawiyah k, farah-azima am, ainoon o..  (2018).  a comparative study of red blood cell parameters of alpha and beta thalassaemia patients diagnosed in a university hospital in cheras, malaysia.  - arc journal of haematology.  . 

mohd khairul mohd kamil, rozita mohd, rizna abdul cader, azlin ithin, shamsul azhar.  (2018).  percentage of regulatory t cells (cd4+cd25+foxp3+) in lupus nephritis.  - 34th annual congress of malaysian society of nephrology.  . 

ahmed maseh, azma rz, azlin i, hafiza a, tumian nr, azmi mtamil, noor farisah ar siti hawa, mz nozi and salwati shuib.  (2018).  fluorescence in situ hybridization (fish) versus real time quantitative polymerase chain reaction (qrt-pcr) for monitoring minimal residual disease (mrd) in chronic myeloid leukaemia (cml) patients on.  - 15th annual scientific meeting malaysian society of haematology.  . 

norunaluwar jalil, raja zahratul azma, hafiza alauddin, azlin ithnin, zarina abdul latiff, hamidah alias, nor rafeah tumian, noor farisah a. razak, malisa mohd yusoff and ainoon othman.  (2018).  detection of beta-globin gene deletions in high hbf level patients using multiplex ligation-dependent probe amplification (mlpa).  - 29th mimls national scientific conference.  . 

salwati shuib, siti fairuz abdul rashid, julia mohd idris, siti mariam yusuf, chia wai kit, rafeah tumian, azlin ithnin, hafiza alauddin, raja zahratul azma raja sabudin.  (2018).  the importance of interphase fluorescence in situ hybridisation (ifish) in the detection of chromosomal abnormalities in patients with acute lymphoblastic leukemia.  - 15th msh annual scientific meeting.  . 

salwati shuib, hamidah alias, rafeah tumian, azlin ithnin, hafizah alauddin, raja zahratul azma raja sabudin, siti fairuz abdul rashid.  (2018).  application of interphase fluorescence in situ hybridisation (ifish) for the detection of chromosome abnormalities in acute lymphoblastic luekaemia.  - simposium kebangsaan penyelidikan perubatan dan kesihatan& minggu penyelidikan ke-20.  . 

alina mf, azma rz, hafiza a, norunaluwar j, azlin i, zarina al, loh c-k, malisa my, ainoon o.  (2018).  co-inheritance of haemoglobin e with rare beta-thalassaemia cd 35 (c-a)- the other end of the spectrum of compound heterozygous hbe/ beta-thalassaemia.  - the belt and road conference on thalassaemia.  . 

darnina aj, azlin i, azma rz, alina mf, mimi-azura a, cheah fc, nazarudin s, najiah-ajlaa a, malisa my, norunaluwar j and ainoon o..  (2018).  point-of-care quantitative measure of g6pd enzyme activity.  - global globin 2020 challenge conferences precision medicine in thalassemia.  . 

fook-choe cheah, fei-liang wong, azlin ithnin and ainoon othman.  (2018).  association between udp-glucuronosyltransferase 1a1 (ugt1a1) gene polymorphism, (c.-3279t>g) and phototherapy among glucose-6-phosphate dehydrogenase (g6pd)-deficient neonates.  - biomedical journal of scientific and technical research.  1-3. 

siti aisyah abdul razak, nor azian abdul murad, doris lau sie chong, farin masra, raja zahratul azma raja sabudin, hafiza alauddin, azlin ithnin, hamidah alias, zarina abdul latif, rahman jamal.  (2017).  genetic modifiers of hbf and phenotypic severity among malaysian beta-thalassemia patients.  - global globin 2020 challenge (gg2020) conference.  . 

toh leong tan, lee yook heng, hui-min neoh, gan kok beng, ida zarina zaini, dian nasriana nasuruddin, khaizurin tajul arifin, azlin ithnin, nurul izzaty hassan, nurul saadah, nik nurhanan nik mansor,.  (2017).  pay it forward: sepsis no more.  - .  . 

najiah a, darnina aj, azma rz, azlin i, hafiza a, cheah fc, malisa my, saidatul aa, wan ahmad shukri waa lim ls and ainoon o..  (2017).  evaluation of quantitative point of care test: g6pd activity in normal subjects using carestarttm biosensor1kit.  - 10th malaysia-indonesia-brunei medical sciences conference 2017.  . 

syirah nmt, ida mi, suria aa, azma rz, azlin i, rahimah a, norunaluwar j, hamidah a, zarina al, loh ck, hafiza a..  (2017).  alpha-globin gene triplication in beta thalassaemia patients at htcm, ukmmc.  - 14th annual scientific meeting, malaysian society of haematology.  . 

norunaluwar j, azma rz, hafiza a, azlin i, zarina al, hamidah a, nor-rafeah t, endom i, danny-koh xr, noor-farisah ar, malisa my, rahimah a, and ainoon o.  (2017).  detection of beta thalassaemia mutations by multiplex amplification refractory system and gap-pcr.  - global globin 2020 challenge conference 2017.  . 

rahayu draman, darnina abdul jalil, rafeah tumian, tang yee loong, azlin ithnin.  (2017).  pure erythroid leukemia in a retroviral positive patient.  - 14th malaysian society of haematology annual scientific meeting.  . 

siti aishah abdul razak, nor azian abdul murad, doris lau sie chong, farin masra, raja zahratul azma, hafiza alauddin, azlin ithnin, hamidah alias, zarina abdul latiff, rahman jamal.  (2017).  detection of genetic modifiers of hbf among malaysian beta-thalassemia patients.  - malaysian society of haematology 14th annual scientific meeting.  . 

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. 

nor syazana, norunaluwar j, azma rz, hafiza a, azlin i, noor farisah ar, siti hawa, malisa my, zarina al, hamidah a, loh ck, azian m, ainoon o.  (2017).  concomitant inheritance of alpha-thalassaemia in beta thalassaemia major: a case report.  - global globin 2020 challence conference 2017.  . 

norunaluwar j, azma rz, hafiza a, azlin i, badrulzaman h, carmene c, sanada ab and ainoon o.  (2017).  determination of hba2 level among beta-thalassaemia and haemoglobin-e traits by ion exchange hplc tosoh hlc-723 g8 analyzer.  - 14th annual scientific meeting, malaysian society of haematology.  . 

norunaluwar j, azlin i, azma rz, hafiza a, malisa my, illaina hikmah i, nurul izzah ar, and ainoon o.  (2017).  evaluation of g6pd enzyme activity in neonates by mindray g6pd test kit on mindray bs-480.  - 14th annual scientific meeting malaysian society of haematology.  . 

darnina abd jalil, azlin ithnin, raja zahratul azma, mimi azura aziz, cheah foo choe, nazarudin safian, najiah ajlaa ayub, malisa mohd yusoff, and ainoon othman..  (2017).  evaluaton of poct (point of care testing); carestart biosensor; single kit and carestart biosensor 1; combo kit vs the standard reference method (osmmr2000d) in the quantification of g6pd enzyme level.  - 14th annual scientific meeting, malaysian society of haematology.  . 

farah azima am, maizatul-husna mr, azma rz, hafiza a, azlin i, zarina al, hamidah a, noor-farisah ar, shuhaila a and ainoon o.  (2017).  the use of multiplex ligation-dependent probe amplification (mlpa) assay in detecting alpha thalassaemia gene abnormalities: comparison with multiplex pcr.  - 14th malaysian society of haematology annual scientific meeting.  . 

najiah aa, darnina aj, azma rz, azlin i, lim ls, hafiza a, malisa my, saidatul aa, wan ahmad shukri waa and ainoon o..  (2017).  near patient testing of g6pd enzyme activity by carestart tm biosensor 1 kit.  - 3rd msmlt national scientific conference.  . 

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. 

norunaluwar j, azma rz, hafiza a, azlin i, khairiliah ak, rusilawaty a, emida m, zarina al, hamidah a, rafeah t, farisah nar, malisa my, rahimah a, azian nam and ainoon o.  (2016).  detection of beta thalassaemia alleles: multiplex amplification refractory mutation system versus flow through hybridization kit.  - the 13th msh annual scientific meeting malaysian society of haematology.  . 

azlin i, azma rz, cheah fc, jubaidah p, nurulfatihah s, emida m, farisah nr, siti hawa aa, hafiza a, ainoon o.  (2016).  neonatal jaundice in g6pd-deficient females and the association with commonly occurring genetic mutations using single-nucleotide polymorphism detection via real-time pcr.  - the 13th msh annual scientific meeting malaysian society of haematology.  . 

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. 

joanna skk, farah hazirah sa, nurul najiehah nm, najatul adawiyah k, muhammad zm, norunaluwar j, maizatul husna ma, hafiza a, azlin i, raja zahratul azma rs.  (2016).  a comparative study of haematological parameters of alpha and beta thalassaemia patients diagnosed in ukm med centre.  - the 8th medical undergraduates annual scientific research meeting.  . 

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. 

faa muttlib, i azlin, ck loh, s salwati, nh hamidah.  (2016).  a child with pancytopenia - a diagnostic dilemma.  - 13th msh annual scientific meeting malaysian society of haematology.  . 

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, 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. 

raja-zahratul azma, khamisah m-gaus, suria a-aziz, hafiza alauddin, azlin ithnin, noor-farisah razak, nor-hidayati sardi, malisa mohd-yusoff, zarina a-latiff, hamidah alias, endom ismail, danny koh-xuan-rong and ainoon othman.  (2016).  detection of homozygous haemoglobin constant spring by capillary electrophoresis method..  - arc journal of hematology.  28-32. 

m faridah, o raudhawati, a rahimah, rz azma, i azlin, nh hamidah, s norhidayati, a hafiza.  (2016).  haemoglobin paksé or haemoglobin constant spring?.  - 13th msh annual scientific meeting malaysian society of haematology.  . 

mardziah m, salwati s, azlin i, hafiza a, farisah nr, noraesah m, siti hawa aa, aizuddin ab, tumian nr, wong cl, azma rz.  (2016).  detection of t315i mutated bcr-abl in imatinib mesylate resistance chronic myeloid leukemia patients diagnosed in ukmmc.  - the 13th msh annual scientific meeting malaysian society of haematology.  . 

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. 

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. 

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. 

toh leong tan, dian nasriana, azlin ithnin, neoh hui-min.  (2015).  a pilot prospective study for the use of secretory phospholipase a2 group iia and cd64 in distinguishing bacterial infections and sepsis in adult who presented in emergency department of teaching hosp.  - regional congress of molecular medicine 2015, malaysia.  . 

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. 

farisah nr, siti hawa aa, hidayati ns, norunaluwar j, aizuddin b, hamidah nh, azlin i, hafiza a, rafeah t, fadilah saw, azma rz.  (2015).  quantification of bcr-abl transcripts in chronic myeloid leukemia (cml) patients by real-time quantitative polymerase chain reaction.  - minggu penyelidikan perubatan dan kesihatan ke 17.  . 

norunaluwar j, khairiliah ausikhin k, rusilawaty a, azma rz, emida m, hafiza a, azlin i, zarina al, hamidah a, rafeah t,noor farisah ar, malisa my, ainoon o.  (2015).  molecular analysis of beta-globin gene mutations in ukmmc using multiplex amplification refractory mutation system and flow-through hybridization kit: a comparison of two methods.  - 2015 annual scientific meeting of the college of pathologists, academy of medicine malaysia & 40th anniversary celebration of the pathology advocates at berjaya times square hotel kuala lumpur.  . 

siti hawa aa, farisah nr, hidayati ns, jubaida paraja md, nurulfatihah s, nur asma m, norunaluwar j, aizuddin ab, cheah fc, hafiza a, azma rz, azlin i.  (2015).  detection of g6pd variants among malaysian newborns with g6pd abnormalities in ukmmc by molecular testing.  - minggu penyelidikan perubatan dan kesihatan kali ke17.  . 

ahmad nasiruddin mustafa, raja zahratul azma, raudhawati osman, wan hayati mohd yaakob, azlin ithnin, hafiza alauddin, nurasyikin yusuf, afifah hassan.  (2015).  influence of multiple, regular plateletpheresis donations on immature platelet fraction and platelet count.  - 2015 annual scientific meeting of the college of pathologists, academy of medicine malaysia & 40th anniversary celebration of the pathology advocates at berjaya times square hotel kuala lumpur.  . 

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.  (2015).  concomitant hbh-paksé with jak2v617f mutation : case report.  - 2015 annual scientific meeting, 40th anniversary celebration of pathology advocates.  . 

tan toh leong, ida zarina, neoh hui-min, nidzwani mahdi, fadzlon yatim, dian nasriana, azlin ithnin and ramliza ramli.  (2015).  distinguishing bacterial and non-bacterial sepsis by using secretory phospholipase a2 group iia level and c-reactive protein in emergency department - a prospective study.  - international congress of the malaysian society for microbiology 2015 (icmsm 2015).  . 

tl tan, dn nasuruddin, a ithnin, h neoh.  (2015).  a pilot study for the usage of secretory phospholipase a2 group iia and cd64 levels in distinguishing bacterial infections and sepsis in adults presented to the emergency department of a teaching hosp.  - 6th regional conference on molecular medicine (rcmm) in conjunction with the 2nd national conference for cancer research.  . 

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. 

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. 

caroline h, azma rz, hafiza a, azlin i, noorhidayati s, zarina al, hamidah a.  (2014).  a case report: non-deletional hbh-hb quong sze disease.  - international congress of pathology & laboratory medicine (icpalm) & 48th malaysia-singapore congress of medicine.  . 

z norsafina, rz azma, i azlin, y nurasyikin, a hafiza, o nurasyikin, n rus mazeni.  (2014).  diagnostik performance of reticulocyte haemoglobin equivalent (ret-he) in detecting iron deficiency anaemia in haemodialysis patient.  - 2014 international congress of pathology & laboratory medicine (icpalm) & 48th malaysia-singapore congress of medicine.  . 

m ahmad nasirudin, y nurasyikin, rz azma, i azlin, wk loh, za zainura anita, z mohd yazid.  (2014).  bone marrow necrosis in cml patient receiving imatinib treatment.  - 2014 international congress of pathology & laboratory medicine (icpalm) & 48th malaysia-singapore congress of medicine.  . 

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 fc, peskin av, wong fl, ithnin a, othman a, winterbourn cc.  (2014).  increased basal oxidation of peroxiredoxin 2 and limited peroxiredoxin recycling in glucose-6-phosphate dehydrogenase-deficient erythrocytes from newborn infants.  - world biomedical frontiers - anemia 2014.  . 

raja-zahratul azma raja-sabudin, suziana m nor, azlin ithnin, hafiza alauddin, rafeah tumian, chia wai kit, salwati shuib.  (2014).  burkitt lymphoma with additional isochromosome 1q in an adult hiv-positive patient.  - case reports in clinical pathology.  1(2):5-11. 

fook-choe cheah, alexander v peskin, fei-liang wong, azlin ithnin, ainoon othman, cristine c.  (2014).  increased erythrocyte peroxiredoxin ii oxidation and diminished recovery after oxidant exposure in newborn infants with glucose-6-phosphate dehydrogenase deficiency.  - pediatric academic societies and asian society for pediatric research joint meeting.  . 

nozi mat zin, wan ahmad shukri wan abdul aziz, najiah ajla ayub, nurul anisyah nuroddin, ilaina hikmah ismail, azlin ithnin, raja zahratul azma raja sabudin.  (2014).  evaluation of alternative dried reagents for cd4 and cd8 t-cell lymphocyte enumeration using flow cytometry system.  - the xith malaysian national haematology scientific meeting 2014.  . 

caroline h, azlin i, azma rz, indhira s, ehram j, soo min l.  (2014).  a case of hairy cell leukaemia presenting as a third malignancy.  - the xith malaysian national haematology scientific meeting 2014.  . 

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. 

j norunaluwar, rz azma, i azlin, a hafiza, sn baya, m emida, o ainoon.  (2014).  rbc g6pd activity measurement - a comparison between whole blood edta sample and dried blood spot.  - 2014 international congress of pathology & laboratory medicine (icpalm) & 48th malaysia-singapore congress of medicine.  . 

azma rz, siti zubaidah m, azlin i, hafiza a, nurasyikin y, nor hidayati s, noor farisah ar, noor hamidah h, ainoon o.  (2014).  detection of partial g6pd deficiency using osmmr2000-d kit with hb normalization.  - medicine and health.  11-21. 

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. 

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. 

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. 

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. 

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. 

azma rz, endom i, danny kxr, zafirah j, zafirah z, azlah kamilah a, hanisah s, aizat naeeim n, hafiza a, azlin i, hamidah nh, ainoon o.  (2013).  interaction of haemoglobin e and haemoglobin constant spring in a jahut family.  - international conference on medical and health sciences.  . 

yuslina my, azlin i, raudhawati o, nurul azwa md, ainoon o.  (2013).  clinical utility of a thalassaemia immunochromatographic (ic) strip test in the detection of a thalassaemia.  - the xth malaysian national haematology scientific meeting.  . 

hafiza a, tang yl, azma rz, azlin i, loh ck, hamidah a, zarina al, ainoon o.  (2013).  a severe a-thalassaemia due to compound heterozygosity for rare codon 59 (ggc>gac) with ivs i nt i (g/a) mutations in a2-gene.  - international conference on medical and health sciences.  . 

adilah nj, azlin i, hidayati ns, azma rz, shareena i.  (2013).  evaluation of glucose-6-phosphate dehydrogenase stability in stored blood samples.  - the xth malaysian national haematology scientific meeting.  . 

madzlifah a, suziana mn, azma rz, hafiza a, azlin i, farisah nr, malisa my, hidayati ns, loh ck, hamidah a, zarina al, hamidah nh, ainoon o.  (2013).  co-inheritance of compound heterozygous hb lepore and beta-thalassaemia with single gene deletion a-thalassaemia (-a3.7 type): a case report.  - international conference on medical and health sciences.  . 

omayma sa, azma rz, suria aa, azlin i, nurasyikin y, loh ck, zarina al and hamidah a.  (2013).  secondary sea-blue histiocytosis in a patient with hbe-beta thalassemia major.  - xth malaysian national haematology scientific meeting.  . 

madzlifah a, suziana mn, azma rz, hafiza a, azlin i, farisah nr, malisa my, hidayati ns, loh ck, hamidah a, zarina al, hamidah nh, ainoon o.  (2013).  co-inheritance of compound heterozygous hb lepore and beta-thalassaemia with single gene deletion alpha-thalassaemia: a case report.  - international conference on medical & health sciences.  . 

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. 

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. 

f -c cheah, f-l wong, s -k chow, a ithnin, a othman.  (2012).  mutations in the g6pd and ugt1a1 genes associated with significant hyperbilirubinaemia in asian newborn infants.  - the 4th congress of the european academy of paediatric societies.  . 

raja z. azma, noor a. jaapar, hafiza alauddin, suria a. aziz, azlin ithnin, noor h. hussin chia w. kit, rafeah tumian, zubaidah zakaria, sharifah n. akmal, salwati shuib.  (2012).  a rare t (9; 12; 22) (q34; q23; q11) translocation in a patient with typical chronic myeloid leukemia: a case report.  - journal of hematological malignancies.  2(4): 17-21. 

soon-ken chow, fwi-liang wong, azlin ithnin, fook-choe cheah.  (2012).  comparison of the fluorescent spot test and enzyme assay in the detection of glucose-6-phosphate dehydrogenase deficiency in infants with hyperbilirubinaemia.  - 19th annual congress of the perinatal society of malaysia.  . 

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. 

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. 

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. 

azlin i, hafiza a, azma rz, aidifitrina rk, hamidah nh.  (2011).  effect of higher centrifugarion speed and shortened centrifugation time on prothrombin and activated thromboplastin time.  - medicine & health.  68-72. 

hafiza a, azma rz, chong mkt, irwan ma, yeoh z-n, lailyvia mi, nur rabiatuladawiyah mr, aidilfitrina m, malissa y, azlin i, hamidah nh.  (2011).  the hba2 levels in normal, b -thalassaemia and haemoglobin e heterozygotes and haemoglobin e (hbe) level in hbe heterozygotes by capillary electrophoresis system.  - medicine and health.  302. 

azlin i, saifeldenn he, khalid aa, farisyah mz, hafiza a, azma rz, noraidah m, tumian nr, hamidah nh..  (2011).  three unusual cases of granulocytic sarcoma from a single institution.  - the ixth malaysian national haematology scientific meeting.  . 

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. 

rz azma, m zubaidah, i azlin, a hafiza, ns hidayati, nr farisah, nh hamidah, o ainoon..  (2011).  detection of partial g6pd deficiency using osmmr-d with hb normalization.  - 9th malaysian national haematology scientific meeting.  . 

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 a, azura ah, azma rz, azlin i, zarina al, hamidah nh.  (2011).  early lineage switch from t-acute lymphoblastic leukaemia to common b-all.  - medicine & health.  131-138. 

hamidah nh, suzana z, azma rz, azlin i, hafiza a, mohd ariff mh,raudhawati o.  (2011).  analysis of immature platelet fraction in dengue infection.  - the ixth malaysian national haematology scientific meeting.  . 

azlin i, aidifitrina rk, azma rz, hafiza a, jessie cs , ling kl, anisah m, ahmad shukri wa, sivagengei k, hamidah nh.  (2011).  performance evaluation of sta-r® evolution at ukm medical centre.  - the ixth malaysian national haematology scientific meeting.  . 

hafiza a, malissa y, aidifitrina m, azlin i, azma rz and hamidah nh.  (2011).  the hba2 levels in normal, ?-thalassaemia and haemoglobin e heterozygotes in by capillary electrphoresis..  - the ixth malaysian national haematology scientific meeting.  . 

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. 

azlin i, leong cf, nh hamidah, sharifah na, isa mr, rohaizak m.  (2010).  primary thyroid lymphoma: two different presentations of a rare disease.  - medicine & health.  114-119. 

azlin i, rz azma, nurasyikin y, rk aidifitrina, nh hamidah.  (2010).  centrifugation time: effect on prtothrombin and activated thromboplastin time.  - the first asean federation of haematology and the viiith malaysian national haematology scientific meeting.  . 

munirah ri, sum sh, azlin i, maisarah j, anisah m, hamidah nh.  (2010).  evaluation of a haematology counter: the abx pentra dx 120.  - first asean federation of hematology & viiith malaysian society of hematology scientific meeting.  . 

hafizah h, zarina al, hamidah a, azlin i, ainoon o, hamidah n h.  (2010).  alpha thalassaemia mutation, haemaglobin adana (a2 cd59[g>a]) with congenital dyserythropoietic anaemia- a rare presentation.  - first asean federation of hematology & viiith malaysian society of hematology scientific meeting.  . 

rz azma, i azlin, h hamenuddin, na hadi, ktwong, in syazana, am asmaliza, o ainoon, nh hamidah.  (2010).  prevalence of iron deficiency anaemia and thalassaemia among medical students of universiti kebangsaan malaysia (ukm).  - the first asean federation of haematology and the v111th malaysian national haematology scientific meeting.  . 

azlin i, wong fl, ezham m, ainoon o, rohana j.  (2009).  prevalence of udp-glucurunosyl transferase 1a1 mutations in malay neonates with severe jaundice.  - pembentangan poster di pathology update 2009 in conjunction with xxv waspalm world congress, sydney convention and exhibition centre, australia.  . 

dr azlin ithnin, dr tan geok chin, prof dr kamsiah jaarin, prof. madya dr faridah mohd nor, dr hamat hamdi che hassan.  (2009).  walking in pain.  - .  . 

ainoon o, muhamad ezham az, fei liang wong, norulanwar, rohana j, azlin i & hamidah nh.  (2009).  taqman mgb snps genotyping assay of malay g6pd variants for detection of female heterozygotes- a potential useful screening method.  - randomised controlled tri.  . 

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. 

azlin, leong cf, hamidah nh, swaminathan m, sharifah na.  (2007).  primary thyroid lymphoma: a report of two cases.  - the malaysian journal of pathology - 24th world congress of pathology and laboratory medicine.  .