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2 Am J Hematol
1 Blood
12 Hemoglobin
4 Int J Hematol
1 N Engl J Med
1 Pediatr Rev
1 Transplant Proc

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    Am J Hematol

  1. GALADANCI N, Abdullahi SU, Vance LD, Tabari AM, et al
    Feasibility Trial for Primary Stroke Prevention in Children with Sickle Cell Anemia in Nigeria (SPIN Trial).
    Am J Hematol. 2017 Apr 25. doi: 10.1002/ajh.24770.
    PubMed     Text format     Abstract available

  2. RAVINDRAN A, Sankaran J, Jacob EK, Kreuter JD, et al
    High prevalence of monoclonal gammopathy among patients with warm autoimmune hemolytic anemia.
    Am J Hematol. 2017 Apr 24. doi: 10.1002/ajh.24765.
    PubMed     Text format    


  3. WANG CY, Core AB, Canali S, Zumbrennen-Bullough KB, et al
    Smad1/5 is required for erythropoietin-mediated suppression of hepcidin in mice.
    Blood. 2017 Apr 24. pii: blood-2016-12-759423. doi: 10.1182/blood-2016-12-759423
    PubMed     Text format     Abstract available


  4. KURTOGLU A, Karakus V, Erkal O, Kurtoglu E, et al
    beta-Thalassemia gene mutations in Antalya, Turkey: results from a single centre study.
    Hemoglobin. 2016;40:392-395.
    PubMed     Text format     Abstract available

  5. CHAN NC, Lau KM, Cheng KC, Chan NP, et al
    A Multi-locus Approach to Characterization of Major Quantitative Trait Loci Influencing Hb F Regulation in Chinese beta-thalassemia Carriers.
    Hemoglobin. 2016;40:400-404.
    PubMed     Text format     Abstract available

  6. ZHAO L, Qing J, Liang Y, Chen Z, et al
    A novel compound heterozygosity in Southern China: IVS-II-5 (G > C) and IVS-II-672 (A > C).
    Hemoglobin. 2016;40:428-430.
    PubMed     Text format     Abstract available

  7. PULE GD, Ngo Bitoungui VJ, Chetcha Chemegni B, Kengne AP, et al
    Studies of novel variants associated with Hb F in Sardinians and Tanzanians in sickle cell disease patients from Cameroon.
    Hemoglobin. 2016;40:377-380.
    PubMed     Text format     Abstract available

  8. MEJRI A, Mansri M, Hadj Fredj S, Ouali F, et al
    First description of the rs45496295 polymorphism of the C/EBPE gene in beta-thalassemia intermedia patients.
    Hemoglobin. 2016;40:411-416.
    PubMed     Text format     Abstract available

  9. BHATTACHARYYA KK, Chatterjee T, Mondal UB
    A comprehensive screening program for beta-thalassemia and other hemoglobinopathies in the Hooghly District of West Bengal, India, dealing with 21 137 cases.
    Hemoglobin. 2016;40:396-399.
    PubMed     Text format     Abstract available

  10. JIANG H, Yan JM, Zhou JY, Li DZ, et al
    Hb Alesha [beta67(E11)Val-->Met (GTG>ATG); HBB: c.202G > A] Found in a Chinese Girl.
    Hemoglobin. 2016;40:420-421.
    PubMed     Text format     Abstract available

  11. LAI Y, Chen Y, Chen B, Zheng H, et al
    Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang beta-Thalassemia Intermedia Patients.
    Hemoglobin. 2016;40:405-410.
    PubMed     Text format     Abstract available

  12. MAINOU M, Kotsiafti A, Klonizakis P, Soulountsi V, et al
    A Case of Fatal Agranulocytosis That Developed in a Patient with beta-Thalassemia Major Treated with Deferiprone.
    Hemoglobin. 2016;40:435-437.
    PubMed     Text format     Abstract available

  13. GORELLO P, Arcioni F, Palmieri A, Barbanera Y, et al
    The Molecular Spectrum of beta- and alpha-Thalassemia Mutations in Non-Endemic Umbria, Central Italy.
    Hemoglobin. 2016;40:371-376.
    PubMed     Text format     Abstract available

  14. LEE HH, Mak AS, Kou KO, Poon CF, et al
    An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Kruppel-like Factor 1 mutations.
    Hemoglobin. 2016;40:431-434.
    PubMed     Text format     Abstract available

  15. GARCIA-MORIN M, Lopez-Sanguos C, Vazquez P, Alvarez T, et al
    Lactate Dehydrogenase: A Marker of the Severity of Vaso-Occlusive Crisis in Children with Sickle Cell Disease Presenting at the Emergency Department.
    Hemoglobin. 2016;40:388-391.
    PubMed     Text format     Abstract available

    Int J Hematol

  16. IKI S, Ohgi K, Suzuki K
    Eculizumab treatment improved renal hemosiderosis in a patient with paroxysmal nocturnal hemoglobinuria.
    Int J Hematol. 2017;105:231-232.
    PubMed     Text format    

  17. ZAHRAN AM, Saad K, Elsayh KI, Alblihed MA, et al
    Characterization of circulating CD4+ CD8+ double positive and CD4- CD8- double negative T-lymphocyte in children with beta-thalassemia major.
    Int J Hematol. 2017;105:265-271.
    PubMed     Text format     Abstract available

  18. KOMATSU N, Kirito K, Shimoda K, Ishikawa T, et al
    Assessing the safety and efficacy of ruxolitinib in a multicenter, open-label study in Japanese patients with myelofibrosis.
    Int J Hematol. 2017;105:309-317.
    PubMed     Text format     Abstract available

  19. ABAZA Y, Yin CC, Bueso-Ramos CE, Wang SA, et al
    Primary autoimmune myelofibrosis: a case report and review of the literature.
    Int J Hematol. 2017;105:536-539.
    PubMed     Text format     Abstract available

    N Engl J Med

  20. LAVERY K, Gilden DJ, Saint S, Judson MA, et al
    A Bare-Bones Approach.
    N Engl J Med. 2017;376:1371-1376.
    PubMed     Text format    

    Pediatr Rev

  21. POMMERT L, Friedman H, Wathen D, Saini S, et al
    Case 3: Acute Jaundice in a 16-year-old Boy.
    Pediatr Rev. 2016;37:542-545.
    PubMed     Text format    

    Transplant Proc

  22. YAMAZAKI K, Sakai K, Ohashi Y, Nihei H, et al
    Similar Anemic Control Between Chronic Kidney Diseases in Patients With and Without Transplantation on Entry to Dialysis.
    Transplant Proc. 2017;49:57-60.
    PubMed     Text format     Abstract available

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