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13.03.2023

2 Am J Hematol
1 Ann Hematol
1 Blood
3 Br J Haematol
1 Haematologica
8 Hemoglobin
1 PLoS One


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Single Articles


    Am J Hematol

  1. RAI P, Okhomina VI, Kang G, Martinez HR, et al
    Longitudinal effect of disease-modifying therapy on left ventricular diastolic function in children with sickle cell anemia.
    Am J Hematol. 2023 Mar 8. doi: 10.1002/ajh.26911.
    PubMed         Abstract available

  2. LANSER L, Plaikner M, Schroll A, Burkert FR, et al
    Tissue iron distribution in patients with anemia of inflammation: results of a pilot study.
    Am J Hematol. 2023 Mar 7. doi: 10.1002/ajh.26909.
    PubMed         Abstract available


    Ann Hematol

  3. AHMADI M, Beiranvand S, Poormansouri S, Matbouei M, et al
    Sense of coherence or self-efficacy as predictors of health-related quality of life in sickle cell disease patients.
    Ann Hematol. 2023;102:519-528.
    PubMed         Abstract available


    Blood

  4. FAKHOURI F, Schwotzer N, Fremeaux-Bacchi V
    How I diagnose and treat atypical hemolytic uremic syndrome.
    Blood. 2023;141:984-995.
    PubMed         Abstract available


    Br J Haematol

  5. TSITSIKAS DA, Rowe S, Bosch A, Hui C, et al
    Addition of plasma exchange to red cell exchange improves outcomes of fat embolism syndrome in sickle cell disease.
    Br J Haematol. 2023;200:e50-e52.
    PubMed        

  6. MCKEAGUE S, Peake N, Lovelock D, Chow J, et al
    Acquired HbH disease diagnosed by HbA1c capillary electrophoresis.
    Br J Haematol. 2023;200:687.
    PubMed        

  7. KOEHL B, Claude L, Reminy K, Tarer V, et al
    Erythrocyte type 1 equilibrative nucleoside transporter expression in sickle cell disease and sickle cell trait.
    Br J Haematol. 2023;200:812-820.
    PubMed         Abstract available


    Haematologica

  8. KOO J, Grom-Mansencal I, Howell JC, Rios JM, et al
    Gonadal function in pediatric Fanconi anemia patients treated with hematopoietic stem cell transplant.
    Haematologica. 2023 Mar 9. doi: 10.3324/haematol.2022.282094.
    PubMed         Abstract available


    Hemoglobin

  9. LONG J, Gong F, Sun L, Lai G, et al
    Identification of Three Families Carrying Hb Anti-Lepore Hong Kong Variant in Guangxi, China, and Analysis of Their Hematological Data.
    Hemoglobin. 2022;46:325-329.
    PubMed         Abstract available

  10. GUAN ZY, Zhong ZY, Xu ZB, Chen JH, et al
    A Case of Misdiagnosis Caused by the Coinheritance of Hb G-Siriraj [beta7(A4)Glu-->Lys; HBB: c.22G>A] and Hb H Disease.
    Hemoglobin. 2022;46:338-340.
    PubMed         Abstract available

  11. ASMARIAN N, Kamalipour A, Hosseini-Bensenjan M, Karimi M, et al
    Prediction of Heart and Liver Iron Overload in beta-Thalassemia Major Patients Using Machine Learning Methods.
    Hemoglobin. 2022;46:303-307.
    PubMed         Abstract available

  12. SUALI L, Mohammad Salih FA, Ibrahim MY, Jeffree MSB, et al
    Genotype-Phenotype Study of beta-Thalassemia Patients in Sabah.
    Hemoglobin. 2022;46:317-324.
    PubMed         Abstract available

  13. WU SM, Huang SR, Li C, Chen GL, et al
    Severe Hb H Disease Caused by Hb Zurich-Albisrieden (HBA1: c.178G>C): Another Case Report.
    Hemoglobin. 2022;46:341-343.
    PubMed         Abstract available

  14. ELEFTHERIOU A, Antoniou E, Darba J, Ascanio M, et al
    Estimating the Cost of Thalassemia Care across the World: A Thalassemia International Federation Model.
    Hemoglobin. 2022;46:308-311.
    PubMed         Abstract available

  15. GIAMBONA A, Leto F, Cassara F, Tartaglia V, et al
    Celocentesis for Early Prenatal Diagnosis in Couples at-Risk for beta-Thalassemia and Sicilian (deltabeta)(0)-Thalassemia.
    Hemoglobin. 2022;46:297-302.
    PubMed         Abstract available

  16. WEN YJ, Yu QX, Jiang F, Li DZ, et al
    Identification of a Novel Mutation in the 3' Untranslated Region of the beta-Globin Gene (HBB:c.*132C>G) in a Chinese Family.
    Hemoglobin. 2022;46:347-350.
    PubMed         Abstract available


    PLoS One

  17. CHUMCHUEN S, Sripichai O, Jearawiriyapaisarn N, Fucharoen S, et al
    Induction of fetal hemoglobin: Lentiviral shRNA knockdown of HBS1L in beta0-thalassemia/HbE erythroid cells.
    PLoS One. 2023;18:e0281059.
    PubMed         Abstract available


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