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Journal Abstract Search

337 related items for PubMed ID: 31823208

  • 21. [Probe test for the detection of hemoglobinopathies and enzyme defect anemias].
    Marti HR.
    Z Gesamte Inn Med; 1983 Feb 01; 38(3):65-6. PubMed ID: 6845778
    [Abstract] [Full Text] [Related]

  • 22. [Studies on erythrocyte metabolism in various hemolytic anemias: with special reference to pyruvate kinase deficiency].
    Miwa S, Nishina T, Kakehashi Y, Oyama H.
    Nihon Ketsueki Gakkai Zasshi; 1970 Oct 01; 33(5):501-18. PubMed ID: 4340177
    [No Abstract] [Full Text] [Related]

  • 23. Inherited erythrocyte metabolic and membrane disorders.
    Brewer GJ.
    Med Clin North Am; 1980 Jul 01; 64(4):579-96. PubMed ID: 6995724
    [Abstract] [Full Text] [Related]

  • 24. Enzymatic diagnosis in non-spherocytic hemolytic anemia.
    Hirono A, Forman L, Beutler E.
    Medicine (Baltimore); 1988 Mar 01; 67(2):110-7. PubMed ID: 3352512
    [Abstract] [Full Text] [Related]

  • 25. Clinical utility of targeted next-generation sequencing panel in routine diagnosis of hereditary hemolytic anemia: A national reference laboratory experience.
    Agarwal AM, McMurty V, Clayton AL, Bolia A, Reading NS, Mani C, Patel JL, Rets A.
    Eur J Haematol; 2023 Jun 01; 110(6):688-695. PubMed ID: 36825813
    [Abstract] [Full Text] [Related]

  • 26. Epidemiological Study of Hereditary Hemolytic Anemia in the Korean Pediatric Population during 1997-2016: a Nationwide Retrospective Cohort Study.
    Shim YJ, Jung HL, Shin HY, Kang HJ, Choi JY, Hah JO, Lee JM, Lim YT, Yang EJ, Baek HJ, Choi HS, Yoo KH, Park JE, Kim S, Kim JY, Park ES, Im HJ, Chueh HW, Kim SK, Lee JH, Yoo ES, Park HJ, Lee JA, Park M, Kang HS, Park JK, Lee NH, Park SK, Lee YH, Lee SW, Choi EJ, Kong SG, Red Blood Cell Disorder Working Party of the Korean Society of Hematology.
    J Korean Med Sci; 2020 Aug 24; 35(33):e279. PubMed ID: 32830468
    [Abstract] [Full Text] [Related]

  • 27. Glucose 6 Phosphate Isomerase Deficiency, a Rare Hemolytic Anemia Misdiagnosed as Hereditary Spherocytosis.
    Gruda Sussman R, Yan AP, Baker JM.
    J Pediatr Hematol Oncol; 2023 Jan 01; 45(1):41-43. PubMed ID: 36161881
    [Abstract] [Full Text] [Related]

  • 28. [THE SIGNIFICANCE OF QUANTITATIVE HAPTOGLOBIN DETERMINATION IN THE DIAGNOSIS OF HEMOLYTIC DISEASES].
    KLUTHE R, HEIMPEL H, SCHUBOTHE H.
    Dtsch Med Wochenschr; 1964 Apr 17; 89():785-9. PubMed ID: 14160344
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. [Modern diagnosis of hemolytic anemias].
    Pribilla W.
    Dtsch Med Wochenschr; 1966 Nov 04; 91(44):1978-82. PubMed ID: 5957740
    [No Abstract] [Full Text] [Related]

  • 31. Rare hereditary red blood cell enzymopathies associated with hemolytic anemia - pathophysiology, clinical aspects, and laboratory diagnosis.
    Koralkova P, van Solinge WW, van Wijk R.
    Int J Lab Hematol; 2014 Jun 04; 36(3):388-97. PubMed ID: 24750686
    [Abstract] [Full Text] [Related]

  • 32. [The clinical and laboratory characteristics of congenital pyruvate kinase deficiency].
    Song L, Li Y, Peng GX, Zhang L, Jing LP, Zhou K, Li Y, Ye L, Li JP, Fan HH, Zhao X, Yang WR, Yang Y, Zhao YP, Xiong YZ, Wu ZJ, Zhang FK.
    Zhonghua Nei Ke Za Zhi; 2018 Jul 01; 57(7):511-513. PubMed ID: 29996270
    [Abstract] [Full Text] [Related]

  • 33. Hereditary red cell membrane disorders and laboratory diagnostic testing.
    King MJ, Zanella A.
    Int J Lab Hematol; 2013 Jun 01; 35(3):237-43. PubMed ID: 23480868
    [Abstract] [Full Text] [Related]

  • 34. Concomitant Hereditary Spherocytosis and Pyruvate Kinase Deficiency in a Spanish Family with Chronic Hemolytic Anemia: Contribution of Laser Ektacytometry to Clinical Diagnosis.
    Vives Corrons JL, Krishnevskaya E, Montllor L, Leguizamon V, Garcia Bernal M.
    Cells; 2022 Mar 28; 11(7):. PubMed ID: 35406697
    [Abstract] [Full Text] [Related]

  • 35. Hereditary spherocytosis is associated with decreased pyruvate kinase activity due to impaired structural integrity of the red blood cell membrane.
    Andres O, Loewecke F, Morbach H, Kraus S, Einsele H, Eber S, Speer CP.
    Br J Haematol; 2019 Nov 28; 187(3):386-395. PubMed ID: 31273765
    [Abstract] [Full Text] [Related]

  • 36. [STUDY OF THE SURVIVAL OF ERYTHROCYTES WITH THE CR-51 METHOD].
    GIUSTINA G, FERRARIO G.
    Rass Clin Sci; 1963 Jun 28; 39():172-84. PubMed ID: 14044522
    [No Abstract] [Full Text] [Related]

  • 37. Hemolytic anemias due to erythrocyte enzyme deficiencies.
    Jacobasch G, Rapoport SM.
    Mol Aspects Med; 1996 Apr 28; 17(2):143-70. PubMed ID: 8813716
    [Abstract] [Full Text] [Related]

  • 38. An automated method of differential red blood cell classification with application to the diagnosis of anemia.
    Bacus JW, Weens JH.
    J Histochem Cytochem; 1977 Jul 28; 25(7):614-32. PubMed ID: 330716
    [Abstract] [Full Text] [Related]

  • 39. Newborn Screening for Hemoglobinopathies and Red Cell Enzymopathies in Tripura State: A Malaria-Endemic State in Northeast India.
    Upadhye D, Das RS, Ray J, Acharjee S, Ghosh K, Colah RB, Mukherjee MB.
    Hemoglobin; 2018 Jan 28; 42(1):43-46. PubMed ID: 29417859
    [Abstract] [Full Text] [Related]

  • 40. [Hereditary hemolytic anemias. (A review)].
    Reimer EE.
    Wien Med Wochenschr; 1972 May 06; 122(19):267-71. PubMed ID: 4558766
    [No Abstract] [Full Text] [Related]

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