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07.11.2022

1 Am J Hematol
1 Ann Hematol
2 Blood
1 BMC Pediatr
1 Bone Marrow Transplant
3 Haematologica
9 Hemoglobin
1 J Pediatr Hematol Oncol
2 PLoS One


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Single Articles


    Am J Hematol

  1. ACHEBE MO, Mandell E, Jolley K, Park HS, et al
    Pagophagia and Restless Legs Syndrome are Highly Associated with Iron Deficiency and Should Be Included in Histories Evaluating Anemia.
    Am J Hematol. 2022 Nov 2. doi: 10.1002/ajh.26775.
    PubMed        


    Ann Hematol

  2. BANZIGER S, Weisshaar K, Arokoski R, Gerull S, et al
    Feasibility of electronic patient-reported outcome monitoring and self-management program in aplastic anemia and paroxysmal nocturnal hemoglobinuria-a pilot study (ePRO-AA-PNH).
    Ann Hematol. 2022 Nov 3. pii: 10.1007/s00277-022-05012.
    PubMed         Abstract available


    Blood

  3. ABDULLAHI S, Sunusi SM, Abba MS, Sani S, et al
    Hydroxyurea for Secondary Stroke Prevention in Children with Sickle Cell Anemia in Nigeria:a Randomized Controlled Trial.
    Blood. 2022 Nov 2. pii: 486968. doi: 10.1182/blood.2022016620.
    PubMed         Abstract available

  4. CARSON JL, Brittenham GM
    How I Treat Anemia with Red Blood Cell Transfusion and Iron.
    Blood. 2022 Oct 31. pii: 486955. doi: 10.1182/blood.2022018521.
    PubMed         Abstract available


    BMC Pediatr

  5. TSUGE M, Kodera A, Sumitomo H, Araki T, et al
    Neonatal hemochromatosis with epsilongammadeltabeta-thalassemia: a case report and analysis of serum iron regulators.
    BMC Pediatr. 2022;22:622.
    PubMed         Abstract available


    Bone Marrow Transplant

  6. SANTARONE S, Angelini S, Natale A, Vaddinelli D, et al
    Survival and late effects of hematopoietic cell transplantation in patients with thalassemia major.
    Bone Marrow Transplant. 2022;57:1689-1697.
    PubMed         Abstract available


    Haematologica

  7. AFZALI-HASHEMI L, Vaclavu L, Wood JC, Biemond BJ, et al
    Assessment of functional shunting in patients with sickle cell disease.
    Haematologica. 2022;107:2708-2719.
    PubMed         Abstract available

  8. LI X, Chatla S, Wilson AF, Wu L, et al
    Persistent DNA damage and oncogenic stress-induced Trem1 promotes leukemia in mice.
    Haematologica. 2022;107:2576-2588.
    PubMed         Abstract available

  9. ROSSATO P, Federti E, Matte A, Glantschnig H, et al
    Evidence of protective effects of recombinant ADAMTS13 in a humanized model of sickle cell disease.
    Haematologica. 2022;107:2650-2660.
    PubMed         Abstract available


    Hemoglobin

  10. ZHANG L, Bao LJ, Hong ZD, Yan MX, et al
    Dysregulated Serum Cytokine Production in Pediatric Patients with beta-Thalassemia Major.
    Hemoglobin. 2022;46:191-196.
    PubMed         Abstract available

  11. LIAO J, Li Q, Ling LQ, Liu CN, et al
    A Triple-Heterozygous beta-Thalassemia Patient Demonstrated an Unusual Electrophoresis Pattern Due to a Novel beta(0) Mutation [an IVS-II-654 (C>T) mutation with a Hb Zurich-Langstrasse (HBB: c.151A>T) mutation in cis].
    Hemoglobin. 2022;46:249-252.
    PubMed         Abstract available

  12. SEN A, Sen A, Dolai TK
    Diagnostic Dilemma of Hemoglobinopathies Using High Performance Liquid Chromatography Alone: A Case Report from a Resource-Constrained Setting.
    Hemoglobin. 2022;46:256-259.
    PubMed         Abstract available

  13. LIN XM, Jiang F, Li J, Li DZ, et al
    Dominantly Inherited beta-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the beta-Globin Gene: Hb Xiangyang (HBB: c.393delT).
    Hemoglobin. 2022;46:253-255.
    PubMed         Abstract available

  14. LOCKE M, Reddy PS, Badawy SM
    Adherence to Iron Chelation Therapy among Adults with Thalassemia: A Systematic Review.
    Hemoglobin. 2022;46:201-213.
    PubMed         Abstract available

  15. LAM TT, Nguyen DT, Le QT, Nguyen DA, et al
    Combined Gap-Polymerase Chain Reaction and Targeted Next-Generation Sequencing Improve alpha- and beta-Thalassemia Carrier Screening in Pregnant Women in Vietnam.
    Hemoglobin. 2022;46:233-239.
    PubMed         Abstract available

  16. FARMAKIS D, Angastiniotis M, El Ghoul MM, Cannon L, et al
    Thalassaemia Registries: A Call for Action. A Position Statement from the Thalassaemia International Federation.
    Hemoglobin. 2022;46:225-232.
    PubMed         Abstract available

  17. WARANG PP, Shinde NS, Umare VD, Deshmukh PV, et al
    Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell Disease.
    Hemoglobin. 2022;46:260-264.
    PubMed         Abstract available

  18. BAO XQ, Wang JC, Qin DQ, Yao CZ, et al
    A Novel 5 kb Deletion in the beta-Globin Gene Cluster Identified in a Chinese Patient.
    Hemoglobin. 2022;46:245-248.
    PubMed         Abstract available


    J Pediatr Hematol Oncol

  19. LEE AJ, Leonard A, Markham KB
    Fetal and Neonatal Reticulocyte Count Response to Intrauterine Transfusion for the Treatment of Red Blood Cell Alloimmunization.
    J Pediatr Hematol Oncol. 2022;44:e1046-e1049.
    PubMed         Abstract available


    PLoS One

  20. MUHAMMAD A, Saleem S, Ahmad D, Tariq E, et al
    Gutka consumption and dietary partialities explaining anemia in women of a coastal slum of Karachi, Pakistan: A mixed-method study.
    PLoS One. 2022;17:e0276893.
    PubMed         Abstract available

  21. VALLE J, Baker JR, Madrigal D, Ferrerosa J, et al
    Sickle cell disease among Latinx in California.
    PLoS One. 2022;17:e0276653.
    PubMed         Abstract available


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