Penerbitan Lain-lain

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. 

nadiah binti sulaiman;ruszymah binti haji idrus;mohd ramzisham bin abdul rahman;hafiza binti alauddin;raja zahratul azma raja sabudin;mohd fauzi bin mh busra;muhammad da`in bin yazid.  (2022).  characterisation of blood outgrowth endothelial cells (boecs) for human saphenous veins (hsv) re-endothelialisation optimisation.  -

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. 

siti nurrazan z, azma rz, alauddin h, noraesah m.  (2022).  molecular genetics of alpha thalassaemia in south-east asia a narrative review.  - 24th medical & health research week, faculty of medicine ukm.  1. 

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. 

siti nurrazan z, azma rz, alauddin h, noraesah m.  (2022).  molecular genetics of alpha thalassaemia in south-east asia: a narrative review.  - the 19th annual scientific meeting malaysian society of haematology.  0. 

joclyn priscilla jipun, alia suzana asri, farah azima abdul muttlib, wan ahmad syukri wan abdul aziz, rinie awai albert, muhammad ziqrill mohd zapri, norunaluwar jalil, hafiza alauddin, raja zahratul azma raja sabudin.  (2021).  molecular characterisation of thalassaemia and haemoglobinopathies amomg orang asli proto malay communities in peninsular malaysia.  - 1. 

hari priya raghyan, raja zahratul azma, hafiza alauddin, reena rahayu md zin, sivakumar palaniappan, nor rafeah tumian.  (2021).  a case of primary bone marrow lymphoma with secondary cns involvement.  - national pathology conference 2021.  45. 

norafiza mohd yasin, haifa hanani mohamad zaki, faidatul syazlin abdul hamid, syahzuwan hassan, raja zahratul azma raja sabudin, hafiza alauddin,norunaluwar jalil, ezalia esa.  (2021).  genomic landscape of hbe/beta thalassaemia in malaysian population.  - national pathology conference 2021.  47. 

alia suzana asri, hafiza alauddin, raja zahratul azma, rinie awai @ albert, norunaluwar jalil, norlida mohamad tahir.  (2021).  characterization of haemoglobin malay phenotypes in tertiary hospital.  - the 18th annual scientific meeting malaysian society of haematology.  1. 

zetti zainol rashid, hafiza alauddin, asrul abdul wahab.  (2021).  kissing fever, year 2 sem 1 (pbl package).  - 1-28. 

alia suzana asri, raja zahratul azma, norlida mt, sharifah ms, m. hafiz, hafizah hashim, norunaluwar jalil, hafiza alauddin..  (2020).  homozygous and compound heterozygous hb malay - a case series.  - 17th malaysian society of haematology scientific meeting - personalised haematology: now and the future.  72. 

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. 

faridah hanim zan, raja zahratul azma, hafiza alauddin, sharifah azura salle, loh c.khai.  (2020).  human parvovirus b19 and ebv co-infection in hbe/beta thalassemia child associated with bone marrow necrosis and trilineage dysplasia.  - 17th malaysian society of haematology scientific meeting - personalised haematology: now and the future.  1-2. 

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. 

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. 

noor zetti zainol rashid, hafiza alauddin.  (2020).  kissing fever: blood & lymph (pbl package).  - 1-26. 

wong ying ying, hafiza alauddin,raja zahratul azma1,norunaluwar jalil, noraesah mahmud, ainoon othman.  (2019).  molecular characterization of alpha thalassaemia among secondary school students in klang valley.  - 16th msh annual scientific meeting: targeting haematology towards excellence.  122. 

hafiza alauddin.  (2019).  challenges in diagnosis of alpha and beta thalassaemia.  - molecular workshop in advanced diagnosis of thalassemia 2019.  1-15. 

nor syazana jamali, raja zahratul azma, hafiza alauddin, azlin ithnin, nor rafeah tumian, norunaluwar jalil, rinie awai, siti hawa, salwati shuib..  (2019).  bcr-abl1 mutation testing to predict response to tyrosine kinase inhibitors in patients with chronic myeloid leukemia.  -

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. 

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.  -

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. 

wee s y, azma r z, hafiza a, norunaluwar j, malisa my, qistina wn, ainoon o.  (2018).  sickle cell case series.  - global globin 2020 challenge conferences precision medicine in thalassemia and published in asian journal of medicine and biomedicine unisza. 

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..  -

hatta rm, azma rz, hafiza a, norunaluwar j, rafeah t, ainoon o.  (2018).  compound heterozygous hb adana with one gene deletion alpha thalassaemia in pregnancy.  - 15th annual scientific meeting malaysian society of haematology. 

wong yy, azma rz, norunaluwar j, lau dsc, hafiza a..  (2018).  hb siriraj causing severe thalassaemia intermedia in compound heterozygote state.  - 15th annual scientific meeting malaysian society of haematology. 

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. 

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. 

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. 

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 j, hafiza a, azlin i, azma rz, malisa my, illaina hikmah i, nurul izzah ar, and ainoon o.  (2017).  g6pd enzyme activity in normal neonates by mindray g6pd test kit on mindray bs-480.  - indian ocean rim 2017, laboratory haematology congress. 

salwati shuib, rz azma, hafiza alauddin, norafiza mohd yasin, julia mohd idris, chia wk.  (2017).  two novel translocations in a complex karyotype of a patient with acute myeloid leukaemia transformed from myelodysplastic syndrome.  - malaysian society of haematology 14th annual scientific meeting. 

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. 

tze sean khoo, wui chuen chia, s fadilah s. abdul wahid, noor farisah a razak, hafiza alauddin, raja zahratul azma raja sabudin, ainoon othman, roshida hassan, noor hamidah hussin.  (2017).  determination of a robust paired-end sequence assembler for short tandem repeat (str) sequences: a simulation-guided approach.  - international conference in medicine icim 2017. 

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. 

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. 

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. 

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. 

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. 

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, 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. 

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. 

assoc prof dr noor zetti zainol rashid, ap dr hafiza alauddin, ap dr salasawati hussin, ap dr azian abd latiff.  (2016).  pakej pbl `kissing fever`.  -

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. 

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. 

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. 

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. 

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. 

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. 

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. 

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. 

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. 

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. 

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. 

nh hamidah, nr farisah, rz azma, o ainoon, a hafiza, saw fadillah.  (2014).  str analysis for chimerism status of allogeneic peripheral blood stem cell transplantation.  - 2014 international congress of pathology & laboratory medicine (icpalm) & 48th malaysia-singapore congress of medicine. malaysian j pathol. 

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. 

siti sarah mustapa, nurismah md isa, hafiza alauddin, reena md zin, nor aini umar, baizurah m hussain, siti aishah abdul wahab, khalidah mazlan bador.  (2013).  lambda light chain myeloma with co-migrating paraprotein at beta region of agarose gel electrophoresis: a case report.  - malaysian association of clinical biochemists 23rd conference. 

y.l. tang, azma rz, c.f. leong, c.h. ko, hafiza a., w.k. chia, sharifah na, c.l. wong.  (2013).  double philadephia chromosome positive b acute lymphoblastic leukaemia seen in an elderly.  - 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 alpha-thalassaemia: a case report.  - international conference on medical & health sciences. 

khamisah mg, azma rz, suria aa, hafiza a, leong cf, farisah nr, hidayati ns, malisa my, zarina al, hamidah a, loh ck, ainoon o.  (2013).  detection of homozygous haemoglobin constant spring by capillary electrophoresis method.  - 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. 

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. 

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. 

suziana mn, hafiza a, azma rz, fadhilah saw, rafeah t, cheah wk, salwati s, sharifah a, hamidah nh.  (2013).  burkitt lymphoma with additional isochromosome 1q in an adult hiv-positive patient.  - xth 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. 

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. 

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, 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. 

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. 

dr noor zetti zainol rashid, dr hafiza alauddin, a. p. dr salasawati hussin, a. p. dr azian abd latiff.  (2011).  kissing fever.  -

assoc prof dr norazlina mohamed, dr israa maatop sulaiman, dr hafiza allauddin, dr christopher ho chee kong.  (2009).  oh no!! not again.. i wet my pants..  -