Am J Hematol

1. DI MODICA SM, Tanzi E, Olivari V, Lidonnici MR, et al
   Transferrin receptor 2 (Tfr2) genetic deletion makes transfusion-independent a murine model of transfusion-dependent beta-thalassemia.
   Am J Hematol. 2022;97:1324-1336.
   

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2. MKOMBACHEPA M, Khamis B, Rwegasira G, Urio F, et al
   High incidence of malaria in patients with sickle cell disease.
   Am J Hematol. 2022;97:E380-E381.
   

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3. GIBSON SJ, Kalfa TA, DeStefano CB
   Insane in the membrane: A case of hereditary spherocytic pyropoikilocytosis.
   Am J Hematol. 2022;97:1384-1385.
   

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4. LEWIS J, Greenway SC, Khan F, Singh G, et al
   Assessment of donor cell engraftment after hematopoietic stem cell transplantation for sickle cell disease: A review of current and future methods.
   Am J Hematol. 2022;97:1359-1371.
   

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   Ann Hematol

5. LIU XD, Yang K, Xiao J, Huang H, et al
   Whole exome sequencing identifies a novel SPTB frameshift mutation causing hereditary spherocytosis in the Chinese population.
   Ann Hematol. 2022;101:2355-2357.
   

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6. THEDSAWAD A, Wanachiwanawin W, Taka O, Hantaweepant C, et al
   Cut-off values for diagnosis of G6PD deficiency by flow cytometry in Thai population.
   Ann Hematol. 2022;101:2149-2157.
   

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7. ROTH A, Barcellini W, Tvedt THA, Miyakawa Y, et al
   Sutimlimab improves quality of life in patients with cold agglutinin disease: results of patient-reported outcomes from the CARDINAL study.
   Ann Hematol. 2022;101:2169-2177.
   

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   BMC Cancer

8. ZHU J, Lemaire P, Mathis S, Ronez E, et al
   Machine learning-based improvement of MDS-CBC score brings platelets into the limelight to optimize smear review in the hematology laboratory.
   BMC Cancer. 2022;22:972.
   

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   BMC Pediatr

9. QUARMYNE MO, Ross D, Sinha C, Bakshi N, et al
   Decision-making about gene therapy in transfusion dependent thalassemia.
   BMC Pediatr. 2022;22:536.
   

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10. WAGHMARE H, Mondal NA, Hossain B
    Nutritional policies and anaemia among under-five children in selected south Asian countries: 1950-2016.
    BMC Pediatr. 2022;22:540.
    

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    Br J Haematol

11. TANTRAVAHI SK, Huber BD, Vagher J, Maese L, et al
    Genome-wide uniparental disomy as a mechanism of immune escape in acquired aplastic anaemia.
    Br J Haematol. 2022;198:e78-e81.
    

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12. SONGDEJ D, Kadegasem P, Tangbubpha N, Sasanakul W, et al
    Whole-exome sequencing uncovered genetic diagnosis of severe inherited haemolytic anaemia: Correlation with clinical phenotypes.
    Br J Haematol. 2022;198:1051-1064.
    

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    Nephron

13. YILMAZ N, Yuksel S
    Hemolytic Uremic Syndrome Associated with Norovirus Gastroenteritis: Case Report and Literature Review.
    Nephron. 2022;146:489-493.
    

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    PLoS One

14. SPIRA JAO, Borges EL, Guedes ACM, Andrade PGR, et al
    Prevalence of people with sickle cell disease and leg ulcers in Brazil: Socioeconomic and clinical overview.
    PLoS One. 2022;17:e0274254.
    

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    Transfusion

15. HOPKINS CK, Townsend M, Vassallo RR
    Leukoreduction filters: Still stuck on sickle trait red cells.
    Transfusion. 2022;62:1683-1687.
    

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16. LAURIDSEN L, Campbell-Lee SA
    Doing more with less: Patient blood management meets sickle cell disease management.
    Transfusion. 2022;62:1688-1692.
    

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17. GEHRIE EA, Petran L, Young PP
    Sickle cell trait results in a high leukoreduction quality control failure rate for whole blood donations.
    Transfusion. 2022;62:1727-1730.
    

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18. JONES JM, Swett AD, Crowe EP, Lawrence C, et al
    Implementation of national blood conservation recommendations at an adult sickle cell center.
    Transfusion. 2022;62:1763-1771.
    

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