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Weekly publication summary


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1 Am J Hematol
1 Ann Hematol
1 Bone Marrow Transplant
9 Hemoglobin
1 N Engl J Med
2 Pediatrics
5 PLoS One

  Retrieve available abstracts of this week’s articles:
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Single Articles

    Am J Hematol

    Treating Sickle Cell Anemia: A New Era Dawns.
    Am J Hematol. 2020 Jan 10. doi: 10.1002/ajh.25724.
    PubMed     Text format    

    Ann Hematol

  2. EL-GAMAL RAE, Abdel-Messih IY, Habashy DM, Zaiema SEG, et al
    Erythroferrone, the new iron regulator: evaluation of its levels in Egyptian patients with beta thalassemia.
    Ann Hematol. 2020;99:31-39.
    PubMed     Text format     Abstract available

    Bone Marrow Transplant

  3. MA YR, Wang WJ, Cheng YF, Zhang YY, et al
    Impact of ABO incompatibility on outcomes after haploidentical hematopoietic stem cell transplantation for severe aplastic anemia.
    Bone Marrow Transplant. 2020 Jan 13. pii: 10.1038/s41409-020-0779.
    PubMed     Text format     Abstract available


  4. XIE XM, Liu YN, Li J, Jiang F, et al
    A Kruppel-Like Factor 1 Gene Mutation Ameliorates the Severity of beta-Thalassemia: A Case Report.
    Hemoglobin. 2019;43:137-139.
    PubMed     Text format     Abstract available

  5. SUN M, Lou J, Zhag Y, Fu Y, et al
    Polymorphisms of alpha-Globin Genes Compromise Polymerase Chain Reaction-Based alpha-Thalassemia Genotyping in Three Chinese Families.
    Hemoglobin. 2019;43:101-106.
    PubMed     Text format     Abstract available

  6. ADEKILE AD, Al-Sherida S, Marouf R, Mustafa N, et al
    The Sub-Phenotypes of Sickle Cell Disease in Kuwait.
    Hemoglobin. 2019;43:83-87.
    PubMed     Text format     Abstract available

  7. NGIM CF, Lee MY, Othman N, Lim SM, et al
    Prevalence and Risk Factors for Cardiac and Liver Iron Overload in Adults with Thalassemia in Malaysia.
    Hemoglobin. 2019;43:95-100.
    PubMed     Text format     Abstract available

  8. YANG K, Ren Q, Wu Y, Zhou Y, et al
    A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as beta-Thalassemia Intermedia Due to a KLF1 Gene Mutation.
    Hemoglobin. 2019;43:140-144.
    PubMed     Text format     Abstract available

  9. HEIREMAN L, Luyckx A, Schynkel K, Dheedene A, et al
    Detection of a Large Novel alpha-Thalassemia Deletion in an Autochthonous Belgian Family.
    Hemoglobin. 2019;43:112-115.
    PubMed     Text format     Abstract available

  10. ZHOU JY, Jiang F, Li J, Chen GL, et al
    Coinheritance of Hb City of Hope (HBB: c.208G>A) and beta-Thalassemia: Compromising the Molecular Diagnosis of the Codons 71/72 (+A) (HBB: c.216_217insA) Mutation by Reverse Dot-Blot Hybridization.
    Hemoglobin. 2019;43:145-147.
    PubMed     Text format     Abstract available

  11. JIT BP, Mohanty PK, Pradhan A, Purohit P, et al
    Erythrocyte cAMP in Determining Frequency of Acute Pain Episodes in Sickle Cell Disease Patients from Odisha State, India.
    Hemoglobin. 2019;43:88-94.
    PubMed     Text format     Abstract available

  12. MORADI K, Aznab M, Tahmasebi S, Dastafkan Z, et al
    The Spectrum of alpha-Thalassemia Mutations in the Lak Population of Iran.
    Hemoglobin. 2019;43:107-111.
    PubMed     Text format     Abstract available

    N Engl J Med

  13. JUUL SE, Comstock BA, Wadhawan R, Mayock DE, et al
    A Randomized Trial of Erythropoietin for Neuroprotection in Preterm Infants.
    N Engl J Med. 2020;382:233-243.
    PubMed     Text format     Abstract available


  14. NASTRO A, Rosenwasser N, Daniels SP, Magnani J, et al
    Scurvy Due to Selective Diet in a Seemingly Healthy 4-Year-Old Boy.
    Pediatrics. 2019 Aug 14. pii: peds.2018-2824. doi: 10.1542/peds.2018-2824.
    PubMed     Text format     Abstract available

  15. WARE RE, Odame I
    Newborn Screening With Sickle Cell Point of Care: A Valuable Resource in Low-Income Settings.
    Pediatrics. 2019 Sep 17. pii: peds.2019-1681. doi: 10.1542/peds.2019-1681.
    PubMed     Text format    

    PLoS One

  16. SOLANKI A, Rajendran A, Mohan S, Raj R, et al
    Mitochondrial DNA variations and mitochondrial dysfunction in Fanconi anemia.
    PLoS One. 2020;15:e0227603.
    PubMed     Text format     Abstract available

  17. ACCINELLI RA, Leon-Abarca JA
    Age and altitude of residence determine anemia prevalence in Peruvian 6 to 35 months old children.
    PLoS One. 2020;15:e0226846.
    PubMed     Text format     Abstract available

  18. ZHANG J, Jones SM, Lykotrafitis G, Andemariam B, et al
    Valsartan impedes epinephrine-induced ICAM-4 activation on normal, sickle cell trait and sickle cell disease red blood cells.
    PLoS One. 2019;14:e0216467.
    PubMed     Text format     Abstract available

  19. MASESE RV, Bulgin D, Douglas C, Shah N, et al
    Barriers and facilitators to care for individuals with sickle cell disease in central North Carolina: The emergency department providers' perspective.
    PLoS One. 2019;14:e0216414.
    PubMed     Text format     Abstract available

    Virulence gene profiles and phylogeny of Shiga toxin-positive Escherichia coli strains isolated from FDA regulated foods during 2010-2017.
    PLoS One. 2019;14:e0214620.
    PubMed     Text format     Abstract available

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