**Sumber data : e-REP.
   Tarikh kemaskini : 21-11-2018
dr. azlin binti ithnin

pensyarah perubatan du56 (tg)

jabatan patologi

No. rasmi:
UKM : 03 8921 5555



   Biografi/ Biography :
  • 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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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.  -

     

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

     

    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. 

     

    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.