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30.12.2018

1 Am J Hematol
1 Am J Kidney Dis
1 Am J Obstet Gynecol
2 Exp Hematol
15 Hemoglobin
1 J Pediatr
1 J Pediatr Hematol Oncol
1 N Engl J Med
2 PLoS One
1 Transplant Proc


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


    Am J Hematol

  1. SHET AS, Mendelsohn L, Harper J, Ostrowski D, et al
    Voxelotor Treatment of a Patient With Sickle Cell Disease and Very Severe Anemia.
    Am J Hematol. 2018 Dec 27. doi: 10.1002/ajh.25389.
    PubMed     Text format    


    Am J Kidney Dis

  2. MC CAUSLAND FR, Claggett B, Burdmann EA, Chertow GM, et al
    Treatment of Anemia With Darbepoetin Prior to Dialysis Initiation and Clinical Outcomes: Analyses From the Trial to Reduce Cardiovascular Events With Aranesp Therapy (TREAT).
    Am J Kidney Dis. 2018 Dec 19. pii: S0272-6386(18)31087.
    PubMed     Text format     Abstract available


    Am J Obstet Gynecol

  3. SULTAN P, Bampoe S, Shah R, Guo N, et al
    Oral versus intravenous iron therapy for postpartum anemia: A systematic review and meta-analysis.
    Am J Obstet Gynecol. 2018 Dec 19. pii: S0002-9378(18)32226.
    PubMed     Text format     Abstract available


    Exp Hematol

  4. DIGHE NM, Tan KW, Tan LG, Shaw SSW, et al
    A comparison of intrauterine hemopoietic cell transplantation and lentiviral gene transfer for the correction of severe beta-thalassemia in a HbbTh3/+ murine model.
    Exp Hematol. 2018;62:45-55.
    PubMed     Text format     Abstract available

  5. HOLLINGER MK, Giudice V, Cummings NA, Rivell G, et al
    PD-1 deficiency augments bone marrow failure in a minor-histocompatibility antigen mismatch lymphocyte infusion model.
    Exp Hematol. 2018;62:17-23.
    PubMed     Text format     Abstract available


    Hemoglobin

  6. THEODORIDOU S, Teli A, Yfanti E, Vyzantiadis TA, et al
    Compound Heterozygosity for Hb Adana (HBA2: c.179G>A) and the -alpha(3.7)/alphaalpha Thalassemia Deletion in Greece: Clinical Phenotype and Genetic Counseling.
    Hemoglobin. 2018;42:129-131.
    PubMed     Text format     Abstract available

  7. ARDUINI GAO, Trovo de Marqui AB
    Prevalence and Characteristics of Priapism in Sickle Cell Disease.
    Hemoglobin. 2018;42:73-77.
    PubMed     Text format     Abstract available

  8. NICKARIA S, Haghpanah S, Ramzi M, Karimi M, et al
    Relationship of the Interaction Between Two Quantitative Trait Loci with gamma-Globin Expression in beta-Thalassemia Intermedia Patients.
    Hemoglobin. 2018;42:108-112.
    PubMed     Text format     Abstract available

  9. DANA M, Fibach E
    Fetal Hemoglobin in the Maternal Circulation - Contribution of Fetal Red Blood Cells.
    Hemoglobin. 2018;42:138-140.
    PubMed     Text format     Abstract available

  10. TANG HS, Wang DG, Huang LY, Li DZ, et al
    delta-Thalassemia with Complete Absence of Hb A2 in a Chinese Family.
    Hemoglobin. 2018;42:135-137.
    PubMed     Text format     Abstract available

  11. SUN M, Lou J, Zhao Y, Liu Y, et al
    Molecular and Hematological Characterization of Two Novel delta-Globin Gene Mutations Found in Chinese Individuals.
    Hemoglobin. 2018;42:132-134.
    PubMed     Text format     Abstract available

  12. ZHAO P, Weng R, Wu H
    Molecular Spectrum of alpha- and beta-Thalassemia Mutations in a Large Ethnic Hakka Population in Southern China.
    Hemoglobin. 2018;42:117-121.
    PubMed     Text format     Abstract available

  13. GRIMHOLT RM, Vestli A, Urdal P, Bechensteen AG, et al
    Hb Oslo [beta42(CD1)Phe-->Ile; HBB: c.127T>A]: A Novel Unstable Hemoglobin Variant Found in a Norwegian Patient.
    Hemoglobin. 2018;42:78-83.
    PubMed     Text format     Abstract available

  14. GRIMHOLT RM, Harteveld CL, Arkesteijn SGJ, Fjeld B, et al
    Characterization of Two Deep Intronic Variants on the beta-Globin Gene with Inconsistent Interpretations of Clinical Significance.
    Hemoglobin. 2018;42:126-128.
    PubMed     Text format     Abstract available

  15. JHA AN, Mishra H, Verma HK, Pandey I, et al
    Compound Heterozygosity of beta-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India.
    Hemoglobin. 2018;42:84-90.
    PubMed     Text format     Abstract available

  16. KHAN NM, Rehman SU, Shakeel M, Khan S, et al
    Molecular Characterization of beta-Thalassemia Mutations Via the Amplification Refractory Mutation System-Polymerase Chain Reaction Method at the North Waziristan Agency, Pakistan.
    Hemoglobin. 2018;42:91-95.
    PubMed     Text format     Abstract available

  17. BELHAJ NEFISSI R, Doggui R, Ouali F, Messaoud T, et al
    Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia.
    Hemoglobin. 2018;42:96-102.
    PubMed     Text format     Abstract available

  18. LISTI F, Sclafani S, Agrigento V, Barone R, et al
    Study on the Role of Polymorphisms of the SOX-6 and MYB Genes and Fetal Hemoglobin Levels in Sicilian Patients with beta-Thalassemia and Sickle Cell Disease.
    Hemoglobin. 2018;42:103-107.
    PubMed     Text format     Abstract available

  19. BAYHAN T, Unal S, Konuskan B, Erdem O, et al
    Assessment of Peripheral Neuropathy in Patients with beta-Thalassemia via Electrophysiological Study: Reevaluation in the Era of Iron Chelators.
    Hemoglobin. 2018;42:113-116.
    PubMed     Text format     Abstract available

  20. VAN DE WATER N, Tan T, Crowley M, Kerr R, et al
    Novel alpha-Globin Splice Site Mutation (HBA2: c.96-5C>A) in Combination with Three-Gene Deletion Hb H Disease.
    Hemoglobin. 2018;42:122-125.
    PubMed     Text format     Abstract available


    J Pediatr

  21. BARFFOUR MA, Hinnouho GM, Kounnavong S, Wessells KR, et al
    Effects of Daily Zinc, Daily Multiple Micronutrient Powder, or Therapeutic Zinc Supplementation for Diarrhea Prevention on Physical Growth, Anemia, and Micronutrient Status in Rural Laotian Children: A Randomized Controlled Trial.
    J Pediatr. 2018 Dec 21. pii: S0022-3476(18)31610.
    PubMed     Text format     Abstract available


    J Pediatr Hematol Oncol

  22. BURGER NCM, van Wijk R, Bresters D, Schell EA, et al
    A Novel Mutation of Glucose Phosphate Isomerase (GPI) Causing Severe Neonatal Anemia Due to GPI Deficiency.
    J Pediatr Hematol Oncol. 2018 Dec 21. doi: 10.1097/MPH.0000000000001393.
    PubMed     Text format     Abstract available


    N Engl J Med

  23. HIDER RC, Hoffbrand AV
    The Role of Deferiprone in Iron Chelation.
    N Engl J Med. 2018;379:2140-2150.
    PubMed     Text format    


    PLoS One

  24. TOPTAN T, Brusadelli MG, Turpin B, Witte DP, et al
    Limited detection of human polyomaviruses in Fanconi anemia related squamous cell carcinoma.
    PLoS One. 2018;13:e0209235.
    PubMed     Text format     Abstract available

  25. YOUNG N, Taegtmeyer M, Aol G, Bigogo GM, et al
    Integrated point-of-care testing (POCT) of HIV, syphilis, malaria and anaemia in antenatal clinics in western Kenya: A longitudinal implementation study.
    PLoS One. 2018;13:e0198784.
    PubMed     Text format     Abstract available


    Transplant Proc

  26. ZHANG Y, Zhou S, Hu JM, Chen H, et al
    Preliminary Study of Bone Marrow-Derived Mesenchymal Stem Cells Pretreatment With Erythropoietin in Preventing Acute Rejection After Rat Renal Transplantation.
    Transplant Proc. 2018;50:3873-3880.
    PubMed     Text format     Abstract available


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