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Journal Abstract Search

170 related items for PubMed ID: 8890572

  • 1. [Gene diagnosis of hemolytic anemia].
    Miyazaki S.
    Nihon Rinsho; 1996 Sep; 54(9):2416-22. PubMed ID: 8890572
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  • 5. [Reduced deformability of erythrocytes as a common denominator of hemolytic anemias].
    Tillmann W.
    Wien Med Wochenschr; 1986 Sep; 136 Spec No():14-6. PubMed ID: 3548086
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  • 6. Editorial: the haemolytic anaemias--a brief review of recent advances.
    Dacie JV.
    Semin Hematol; 1969 Apr; 6(2):109-15. PubMed ID: 4888953
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  • 7. [The appearance of a PNH clone during enzymopenic hemolytic anemia].
    Gori E, Tata F, Zanna M.
    Clin Ter; 1992 Apr; 140(4):395-6. PubMed ID: 1587123
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  • 8. Differential diagnosis of hereditary hemolytic disorders.
    Jaffe ER.
    Med Times; 1972 Mar; 100(3):254-72. PubMed ID: 4559277
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  • 9. Laboratory Approach to Hemolytic Anemia.
    Jamwal M, Sharma P, Das R.
    Indian J Pediatr; 2020 Jan; 87(1):66-74. PubMed ID: 31823208
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  • 10. Confounding factors in the diagnosis and clinical course of rare congenital hemolytic anemias.
    Fattizzo B, Giannotta JA, Cecchi N, Barcellini W.
    Orphanet J Rare Dis; 2021 Oct 09; 16(1):415. PubMed ID: 34627331
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  • 11. Anemia in the newborn period.
    Lubin B, Vichinsky E.
    Pediatr Ann; 1979 Jul 09; 8(7):416-34. PubMed ID: 471553
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  • 12. 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
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  • 13. Congenital Hemolytic Anemia.
    Haley K.
    Med Clin North Am; 2017 Mar 24; 101(2):361-374. PubMed ID: 28189176
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  • 14. [Hereditary enzyme defects of erythrocytes: glucose-6-phosphate dehydrogenase deficiency and pyruvate kinase deficiency].
    Sedano II, Röthlisberger B, Huber AR.
    Ther Umsch; 2006 Jan 24; 63(1):47-56. PubMed ID: 16450734
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  • 15. Acquired hemolytic anemia with features simulating hereditary spherocytosis and paroxysmal nocturnal hemoglobinuria in the same patient.
    Mohler DN.
    Trans Am Clin Climatol Assoc; 1972 Jan 24; 83():177-85. PubMed ID: 5040114
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  • 16. Looking for red cell enzyme deficiencies in hemolytic anemias.
    Chapman RG.
    Am J Med Technol; 1971 Nov 24; 37(11):423-7. PubMed ID: 5154328
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  • 17. [Hereditary hemolytic anemias. (A review)].
    Reimer EE.
    Wien Med Wochenschr; 1972 May 06; 122(19):267-71. PubMed ID: 4558766
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