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1 Blood
3 Br J Haematol
2 Exp Hematol
6 Hemoglobin
3 PLoS One
2 Transfusion

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  1. FENAUX P, Kiladjian JJ, Platzbecker U
    Luspatercept for the treatment of anemia in myelodysplastic syndromes (MDS) and primary myelofibrosis (PMF).
    Blood. 2019 Jan 2. pii: blood-2018-11-876888. doi: 10.1182/blood-2018-11-876888.
    PubMed     Text format     Abstract available

    Br J Haematol

  2. VOGEL S, Thein SL
    Platelets at the crossroads of thrombosis, inflammation and haemolysis.
    Br J Haematol. 2018;180:761-767.
    PubMed     Text format     Abstract available

  3. RICCHI P, Meloni A, Spasiano A, Costantini S, et al
    The impact of liver steatosis on the ability of serum ferritin levels to be predictive of liver iron concentration in non-transfusion-dependent thalassaemia patients.
    Br J Haematol. 2018;180:721-726.
    PubMed     Text format     Abstract available

  4. JIANG Z, Luo HY, Farrell JJ, Zhang Z, et al
    A variant Sp1 (R218Q) transcription factor might enhance HbF expression in beta(0) -thalassaemia homozygotes.
    Br J Haematol. 2018;180:755-757.
    PubMed     Text format    

    Exp Hematol

  5. WILKINSON AC, Morita M, Nakauchi H, Yamazaki S, et al
    Branched-chain amino acid depletion conditions bone marrow for hematopoietic stem cell transplantation avoiding amino acid imbalance-associated toxicity.
    Exp Hematol. 2018 Apr 26. pii: S0301-472X(18)30173.
    PubMed     Text format     Abstract available

  6. LI Y, Liu D, Zhang X, Li Z, et al
    miR-326 regulates HbF synthesis by targeting EKLF in human erythroid cells.
    Exp Hematol. 2018;63:33-40.
    PubMed     Text format     Abstract available


  7. MOASSAS F, Alabloog A, Murad H
    Description of a Rare beta-Globin Gene Mutation: -86 (C>G) (HBB: c.-136C>G) Observed in a Syrian Family.
    Hemoglobin. 2018;42:203-205.
    PubMed     Text format     Abstract available

  8. CHOMEAN S, Pholyiam K, Thamwarokun A, Kaset C, et al
    Development of Visual Detection of alpha-Thalassemia-1 (the - -(SEA) Deletion) Using pH-Sensitive Loop-Mediated Isothermal Amplification.
    Hemoglobin. 2018;42:171-177.
    PubMed     Text format     Abstract available

  9. JIANG F, Qu YX, Chen GL, Li J, et al
    KFL1 Gene Variants in alpha-Thalassemia Individuals with Increased Fetal Hemoglobin in a Chinese Population.
    Hemoglobin. 2018;42:161-165.
    PubMed     Text format     Abstract available

  10. CHEN JK, Xin XQ, Huang JG
    A Novel beta-Thalassemia Mutation in a Chinese family: IVS-II-203-205 (TCT>CC) (HBB: c.315+203TCT>CC).
    Hemoglobin. 2018;42:159-160.
    PubMed     Text format     Abstract available

  11. BARBERO U, Fornari F, Guarguagli S, Gaglioti CM, et al
    Atrial fibrillation in beta-thalassemia Major Patients: Diagnosis, Management and Therapeutic Options.
    Hemoglobin. 2018;42:189-193.
    PubMed     Text format     Abstract available

  12. XU C, Liao B, Qi Y, Huangfu Z, et al
    Analysis of Gene Mutation Types of alpha- and beta-Thalassemia in Fuzhou, Fujian Province in China.
    Hemoglobin. 2018;42:143-147.
    PubMed     Text format     Abstract available

    PLoS One

  13. BEN HAMDA C, Sangeda R, Mwita L, Meintjes A, et al
    A common molecular signature of patients with sickle cell disease revealed by microarray meta-analysis and a genome-wide association study.
    PLoS One. 2018;13:e0199461.
    PubMed     Text format     Abstract available

  14. FISCHBEIN R, Nicholas L, Aultman J, Baughman K, et al
    Twin-twin transfusion syndrome screening and diagnosis in the United States: A triangulation design of patient experiences.
    PLoS One. 2018;13:e0200087.
    PubMed     Text format     Abstract available

  15. KAUR G, Helmer RA, Smith LA, Martinez-Zaguilan R, et al
    Alternative splicing of helicase-like transcription factor (Hltf): Intron retention-dependent activation of immune tolerance at the feto-maternal interface.
    PLoS One. 2018;13:e0200211.
    PubMed     Text format     Abstract available


  16. WIN N, Needs M, Thornton N, Webster R, et al
    Transfusions of least-incompatible blood with intravenous immunoglobulin plus steroids cover in two patients with rare antibody.
    Transfusion. 2018;58:1626-1630.
    PubMed     Text format     Abstract available

  17. CAMPBELL-LEE SA, Gvozdjan K, Choi KM, Chen YF, et al
    Red blood cell alloimmunization in sickle cell disease: assessment of transfusion protocols during two time periods.
    Transfusion. 2018;58:1588-1596.
    PubMed     Text format     Abstract available

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