Search
ID

Ita Margaretha Nainggolan

Senior Research Fellow

Qualification:

  • S.Si. (Padjajaran University)
  • M.Biomed (University of Indonesia)
  • Doctor in Biomedical Science (University of Indonesia)

Publications

  1. A rare case of Hb H disease caused by compound heterozygous for α thalassemia and Hb Quong Sze in Chinese Indonesian proband: A case Report. Bali Med J. 2019;2:333-336. doi:10.15562/bmj.v8i2.1411
  2. Molecular Mechanism of Severe Clinical Manifestation of α-Thalassemia Due to Hb Adana Mutation. ESH International Conference - Erythropoiesis Control and Ineffective Erythropoiesis : from bench to bedside. 2019 (Poster)
  1. Polymorphism and expression of Multidrug Resistant-1 C3435T In Indonesian Temporal Lobe Resistant Epilepsy. The 12th Asian & Oceanian Epilepsy Congress (AOEC). 2018.
  2. Potensi Penggunaan Materi Genetik Fetus pada Sirkulasi Maternal untuk Diagnosis Prenatal Noninvasif Penyakit Genetik. Warmadewa Medical Journal. 2017;1(1): 1-9. doi: http://dx.doi.org/10.22225/wmj.1.1.4.1-9
  3. Detection of Papua New Guinea Thalassemia Alpha Mutation in Gayo, Sumba, Ternate, and Timika Populations. Makara J. Sci. 18/2 (2014), 47-51 doi: 10.7454/mss.v18i2.3138
  4. Interaction of Hb adana (HBA2: c.179G>A) with deletional and nondeletional alpha(+)-thalassemia mutations: diverse hematological and clinical features.
    Hemoglobin. 2013;37(3):297-305. doi: 10.3109/03630269.2013.775149. Epub 2013 Apr 25.
    PubMed
  5. Thalassemia Alfa Mayor dengan Mutasi Non-Delesi Heterozigot Ganda. Sari Pediatri. 2006;8(3):244-250.
  1. The Role of Complete Blood Count in the Diagnosis of Hemoglobin E in Pseudo High Level of Hemoglobin A2. Open Journal of Hematology. 2015;6-5
  2. Frequency of thalassemia carrier and Hb variant and the quality of stored donor blood. Medical Journal of Indonesia. 2014; 23(4): 209-12. doi: https://doi.org/10.13181/mji.v23i4.766
  3. Severe alpha-thalassemia intermedia due to a compound heterozygosity for the highly unstable Hb Adana (HBA2: c.179G>A) and a novel codon 24 (HBA2: c.75T>A) mutation.
    Hemoglobin. 2014;38(2):149-51. doi: 10.3109/03630269.2013.863206. Epub 2013 Dec 18.
    PubMed
  1. Hydrops fetalis associated with homozygosity for Hb Adana [alpha59(E8)Gly-->Asp (alpha2)].
    Hemoglobin. 2010;34(4):394-401. doi: 10.3109/03630269.2010.493405.
    PubMed
  1. Alpha thalassaemia in Indonesia: phenotypes and molecular defects.
    Adv Exp Med Biol. 2003;531:47-56.
    PubMed
  2. The hemoglobin O mutation in Indonesia: distribution and phenotypic expression.
    J Hum Genet. 2001;46(9):499-505.
    PubMed

Publications

  1. Challenges in Thalassemia Carrier Detection in a Low Resource Setting Area of Eastern Indonesia: the Use of Erythrocyte Indices.
    Mediterr J Hematol Infect Dis. 2021 Jan 1;13(1):e2021003. doi: 10.4084/MJHID.2021.003. eCollection 2021.
    PubMed
  2. Severe alpha-thalassemia intermedia due to a compound heterozygosity for the highly unstable Hb Adana (HBA2: c.179G>A) and a novel codon 24 (HBA2: c.75T>A) mutation.
    Hemoglobin. 2014;38(2):149-51. doi: 10.3109/03630269.2013.863206. Epub 2013 Dec 18.
    PubMed
  3. Interaction of Hb adana (HBA2: c.179G>A) with deletional and nondeletional alpha(+)-thalassemia mutations: diverse hematological and clinical features.
    Hemoglobin. 2013;37(3):297-305. doi: 10.3109/03630269.2013.775149. Epub 2013 Apr 25.
    PubMed
  4. Hydrops fetalis associated with homozygosity for Hb Adana [alpha59(E8)Gly-->Asp (alpha2)].
    Hemoglobin. 2010;34(4):394-401. doi: 10.3109/03630269.2010.493405.
    PubMed
  5. Alpha thalassaemia in Indonesia: phenotypes and molecular defects.
    Adv Exp Med Biol. 2003;531:47-56.
    PubMed
  6. The hemoglobin O mutation in Indonesia: distribution and phenotypic expression.
    J Hum Genet. 2001;46(9):499-505.
    PubMed