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Journal Abstract Search

288 related items for PubMed ID: 27460399

  • 1. Cord blood transplantation in a young child with pyruvate kinase deficiency.
    Akiyoshi K, Sekiguchi K, Okamoto T, Suenobu S, Izumi T.
    Pediatr Int; 2016 Jul; 58(7):634-6. PubMed ID: 27460399
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  • 2. Mitral Valve Replacement With Cardiopulmonary Bypass in a Patient With Pyruvate Kinase Deficiency.
    Basantwani S, Govardhane B, Shinde S, Tendolkar B.
    J Cardiothorac Vasc Anesth; 2017 Feb; 31(1):262-265. PubMed ID: 27498259
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  • 5. Molecular and clinical heterogeneity in pyruvate kinase deficiency in India.
    Warang P, Kedar P, Ghosh K, Colah R.
    Blood Cells Mol Dis; 2013 Oct; 51(3):133-7. PubMed ID: 23770304
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  • 7. Tanaka KR, Valentine WN, Miwa S. Pyruvate kinase (PK) deficiency hereditary nonspherocytic hemolytic anemia. Blood. 1962;19(3):267-295.
    Blood; 2016 May 26; 127(21):2505. PubMed ID: 27231390
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  • 9. The pyruvate kinase (PK) to hexokinase enzyme activity ratio and erythrocyte PK protein level in the diagnosis and phenotype of PK deficiency.
    Al-Samkari H, Addonizio K, Glader B, Morton DH, Chonat S, Thompson AA, Kuo KHM, Ravindranath Y, Wang H, Rothman JA, Kwiatkowski JL, Kung C, Kosinski PA, Al-Sayegh H, London WB, Grace RF.
    Br J Haematol; 2021 Mar 26; 192(6):1092-1096. PubMed ID: 32463523
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  • 11. Red blood cell PK deficiency: An update of PK-LR gene mutation database.
    Canu G, De Bonis M, Minucci A, Capoluongo E.
    Blood Cells Mol Dis; 2016 Mar 26; 57():100-9. PubMed ID: 26832193
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  • 12. A case of hereditary spherocytosis misdiagnosed as pyruvate kinase deficient hemolytic anemia.
    Vercellati C, Marcello AP, Fermo E, Barcellini W, Zanella A, Bianchi P.
    Clin Lab; 2013 Mar 26; 59(3-4):421-4. PubMed ID: 23724634
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  • 13. Management of pyruvate kinase deficiency in children and adults.
    Grace RF, Barcellini W.
    Blood; 2020 Sep 10; 136(11):1241-1249. PubMed ID: 32702739
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  • 15. Development of an Automated Enzymatic Method to Quantify Pyruvate Kinase in Red Blood Cells.
    Lu J, Grenache DG.
    J Appl Lab Med; 2020 Jan 01; 5(1):54-61. PubMed ID: 32445340
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  • 16. Chronic haemolytic anaemia because of pyruvate kinase (PK) deficiency in a child heterozygous for haemoglobin S and no clinical features of sickle cell disease.
    Manco L, Vagace JM, Relvas L, Rebelo U, Bento C, Villegas A, Letícia Ribeiro M.
    Eur J Haematol; 2010 Jan 01; 84(1):89-90. PubMed ID: 19758413
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  • 17. Hemolytic anemia associated with a novel heterozygote mutation 1183A in the PK-LR gene (PK- Jordan).
    Karadsheh NS, Gelbart T, Naffa RG.
    Int J Lab Hematol; 2014 Aug 01; 36(4):e66-8. PubMed ID: 24330591
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  • 19. Screening of hereditary spherocytosis and pyruvate kinase deficiency by automated blood count using erythrocytic and reticulocytic parameters.
    Bobée V, Daliphard S, Schrapp A, Lahary A.
    Int J Lab Hematol; 2018 Dec 01; 40(6):697-703. PubMed ID: 30184319
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