dr. azlin binti ithnin

pensyarah perubatan du56 (tg)

jabatan patologi

No. rasmi:
UKM : 03 8921 5555



   Biografi/ Biography :


  • 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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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.