Ann Hematol

1. MA X, Zuo Y, Xu Z, Zhang Y, et al
   Comparable clinical outcomes of haploidentical hematopoietic stem cell transplantation in patients with hepatitis-associated aplastic anemia and non-hepatitis-associated aplastic anemia.
   Ann Hematol. 2022 Jun 23. pii: 10.1007/s00277-022-04885.
   

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2. HAN B, Kim HJ, Yhim HY, Oh D, et al
   Sequential eradication of Helicobacter pylori as a treatment for immune thrombocytopenia in patients with moderate thrombocytopenia: a multicenter prospective randomized phase 3 study.
   Ann Hematol. 2022;101:1435-1445.
   

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3. JUNG EH, Park JH, Hwan Kim K, Kim JS, et al
   Characteristics of Sweet syndrome in patients with or without malignancy.
   Ann Hematol. 2022;101:1499-1508.
   

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4. ROPERO P, Gonzalez Fernandez FA, Nieto JM, Recasens V, et al
   Does size matter? Two new deletions in the HBB gene cause beta(0)-thalassemia.
   Ann Hematol. 2022;101:1465-1471.
   

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5. WU X, Cheng L, Liu X, Sun Y, et al
   Clinical characteristics and outcomes of 100 adult patients with pure red cell aplasia.
   Ann Hematol. 2022;101:1493-1498.
   

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6. PATSOURAKOS D, Aggeli C, Gatzoulis KA, Delicou S, et al
   Left atrial deformation indices in beta-thalassemia major patients.
   Ann Hematol. 2022;101:1473-1483.
   

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7. ADAM AS, Cotton F, Cantinieaux B, Benyaich S, et al
   Screening for hereditary spherocytosis in daily practice: what is the best algorithm using erythrocyte and reticulocyte parameters?
   Ann Hematol. 2022;101:1485-1491.
   

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8. COSTANTINI S, Meloni A, Spasiano A, Cinque P, et al
   The unexpected impact of cabozantinib on red blood cells consumption in patients with transfusion-dependent thalassemia.
   Ann Hematol. 2022;101:1621-1623.
   

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   BMC Pediatr

9. DISSANAYAKE R, Samarasinghe N, Waidyanatha S, Pathirana S, et al
   Assessment of iron overload in a cohort of Sri Lankan patients with transfusion dependent beta thalassaemia and its correlation with pathogenic variants in HBB, HFE, SLC40A1, and TFR2 genes.
   BMC Pediatr. 2022;22:344.
   

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   Haematologica

10. DONG P, Chen L, Wu H, Huo J, et al
    Impaired immunosuppressive role of myeloid-derived suppressor cells in acquired aplastic anemia.
    Haematologica. 2022 Jun 23. doi: 10.3324/haematol.2021.280292.
    

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    J Clin Invest

11. LIN Q, Wu L, Chatla S, Chowdhury FA, et al
    Hematopoietic stem cell regeneration through paracrine regulation of the Wnt5a/Prox1 signaling axis.
    J Clin Invest. 2022;132.
    

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    J Pediatr

12. SOLEVAG AL, Andresen JH, Saugstad OD
    50 Years Ago in TheJournalofPediatrics: Iron Supplementation in Infants Born at Term.
    J Pediatr. 2022;245:110.
    

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13. MANTADAKIS E
    Serum Ferritin Threshold for Iron Deficiency Screening in One-Year-Old Children.
    J Pediatr. 2022;245:12-14.
    

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14. MUKHTAROVA N, Ha B, Diamond CA, Plumb AJ, et al
    Serum Ferritin Threshold for Iron Deficiency Screening in One-Year-Old Children.
    J Pediatr. 2022;245:217-221.
    

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    J Pediatr Hematol Oncol

15. EL-BESHLAWY A, Abdel-Azim K, Abdel-Salam A, Gebril NA, et al
    Clinical Characteristics, Molecular Background, and Survival of Egyptian Patients With Gaucher Disease Over a 20-Year Follow-up.
    J Pediatr Hematol Oncol. 2022;44:243-248.
    

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16. GALADANCI NA, Sohail M, Akinyelure OP, Kanter J, et al
    Treatment-related Correlates of Growth in Children With Sickle Cell Disease in the DISPLACE Cohort.
    J Pediatr Hematol Oncol. 2022;44:249-254.
    

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17. DOSHI BS, Kamdar A, Lambert MP, Obstfeld AE, et al
    Hemolysis After Medication Exposure in Pediatric Patients With G6PD Deficiency.
    J Pediatr Hematol Oncol. 2022;44:261-263.
    

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18. BOSCH A, Watad S, Willmott S, McKinnon NK, et al
    Identifying and Treating Severe Bone Marrow Necrosis and Fat Embolism Syndrome in Pediatric Patients With Sickle Cell Disease: A Case Report.
    J Pediatr Hematol Oncol. 2022;44:e884-e887.
    

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19. CALHOUN C, Luo L, Baumann AA, Bauer A, et al
    Transition for Adolescents and Young Adults With Sickle Cell Disease in a US Midwest Urban Center: A Multilevel Perspective on Barriers, Facilitators, and Future Directions.
    J Pediatr Hematol Oncol. 2022;44:e872-e880.
    

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20. TAS N, Gokceoglu AU, Yayla BCC, Ozcan A, et al
    Hemophagocytic Lymphohistiocytosis Associated With Hemolytic Uremic Syndrome in a Child: A Case Report and Systematic Literature Review.
    J Pediatr Hematol Oncol. 2022;44:e905-e910.
    

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    J Trop Pediatr

21. BOONRUSMEE S, Thongkhao A, Wongchanchailert M, Mo-Suwan L, et al
    Coexisting Iron Deficiency Anemia and Thalassemia Traits in Infants: Implication for an Anemia Screening Program.
    J Trop Pediatr. 2022;68.
    

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    JAMA

22. OSHIMA T, Kinjo K, Kinjo M
    Chronic Abdominal Pain and Anemia in a 59-Year-Old Man.
    JAMA. 2022 Jun 24. pii: 2793812. doi: 10.1001/jama.2022.9194.
    

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    Kidney Int

23. BATTE A, Menon S, Ssenkusu JM, Kiguli S, et al
    Neutrophil gelatinase-associated lipocalin is elevated in children with acute kidney injury and sickle cell anemia, and predicts mortality.
    Kidney Int. 2022 Jun 16. pii: S0085-2538(22)00453.
    

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    Lancet

24. KATTAMIS A, Kwiatkowski JL, Aydinok Y
    Thalassaemia.
    Lancet. 2022;399:2310-2324.
    

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    PLoS One

25. SILVA-PINTO AC, Costa FF, Gualandro SFM, Fonseca PBB, et al
    Economic burden of sickle cell disease in Brazil.
    PLoS One. 2022;17:e0269703.
    

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26. DEVALARAJA-NARASHIMHA K, Huang C, Cao M, Chen YP, et al
    Pharmacokinetics and pharmacodynamics of pozelimab alone or in combination with cemdisiran in non-human primates.
    PLoS One. 2022;17:e0269749.
    

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