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.
   

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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.
   

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   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.
   

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   Blood

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

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   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.
   

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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.
   

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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.
   

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   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.
   

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   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.
   

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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.
    

    Lys; HBB: c.22G>A] and Hb H Disease.&body=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. https://www.ncbi.nlm.nih.gov/m/pubmed/36691989" ALT="Email" TITLE="Email"> --> >> Share

    
    
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.
    

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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.
    

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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.
    

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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.
    

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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.
    

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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.
    

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    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.
    

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