These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

73 related articles for article (PubMed ID: 5711251)

  • 21. [Familial erythrocyte ATP: pyruvate phosphotransferase deficiency].
    Torliński L; Karoń H; Czech A; Michalewska D; Duczmal B
    Acta Haematol Pol; 1982; 13(3-4):157-63. PubMed ID: 7184297
    [No Abstract]   [Full Text] [Related]  

  • 22. Hereditary hemolytic disease.
    Morrison FS
    J Miss State Med Assoc; 1971 Mar; 12(3):101-5. PubMed ID: 5132287
    [No Abstract]   [Full Text] [Related]  

  • 23. [Hereditary hemolytic anemia in children].
    Spasibko AM; Tokarev IuN; Syr'eva TN; Bukhin AI
    Vopr Okhr Materin Det; 1976 Apr; 21(4):16-20. PubMed ID: 997338
    [No Abstract]   [Full Text] [Related]  

  • 24. [Hereditary anemia: genetic basis, clinical characteristics, diagnosis and treatment. WHO Workgroup].
    Bull World Health Organ; 1983; 61(2):179-98. PubMed ID: 6345012
    [No Abstract]   [Full Text] [Related]  

  • 25. [Familial hypochromic hypersideremic (sidero-achrestic) anemia].
    Berger H; Hochleitner M; Schumacher P; Huber H; Gabl F; Klima J
    Ann Paediatr; 1966; 206(2):97-119. PubMed ID: 5953113
    [No Abstract]   [Full Text] [Related]  

  • 26. [Hereditary hemolytic anemia].
    Johnsson R; Vuopio P
    Duodecim; 1981; 97(7):407-18. PubMed ID: 7274114
    [No Abstract]   [Full Text] [Related]  

  • 27. [Case of congenital ovalocytic hemolytic anemia].
    Dygin VP; Siubaeva NI
    Probl Gematol Pereliv Krovi; 1970 Mar; 15(3):58-9. PubMed ID: 5449829
    [No Abstract]   [Full Text] [Related]  

  • 28. Unstable hemoglobin as a cause of congenital hemolytic anemia.
    Singh R; Sudarsanam A
    Indian Pediatr; 1996 Jul; 33(7):587-9. PubMed ID: 8979570
    [No Abstract]   [Full Text] [Related]  

  • 29. Transfusion therapy in congenital hemolytic anemias.
    Sharon BI
    Hematol Oncol Clin North Am; 1994 Dec; 8(6):1053-86. PubMed ID: 7860437
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Hemoglobin Hammersmith [beta42 (CD1) Phe --> Ser] in a Brazilian girl with congenital Heinz body hemolytic anemia.
    Sonati MF; Kimura EM; Abreu CF; Oliveira DM; Pinheiro VR; Costa FF
    Pediatr Blood Cancer; 2006 Nov; 47(6):855-6; author reply 857-8. PubMed ID: 16619220
    [No Abstract]   [Full Text] [Related]  

  • 31. Hemoglobinopathies in childhood (a study of 51 cases).
    Giri DD; Patra SB; Patel RZ
    Indian J Pathol Microbiol; 1984 Apr; 27(2):81-9. PubMed ID: 6511037
    [No Abstract]   [Full Text] [Related]  

  • 32. Hemoglobin SE disease: a concise review.
    Masiello D; Heeney MM; Adewoye AH; Eung SH; Luo HY; Steinberg MH; Chui DH
    Am J Hematol; 2007 Jul; 82(7):643-9. PubMed ID: 17278112
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Diagnosis and gene analysis of congenital hemolytic anemia].
    Ideguchi H
    Rinsho Byori; 2006 Jun; 54(6):593-600. PubMed ID: 16872009
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Minkowski-Chauffard disease in 1 family].
    Atanasov K; Tashev V; Vakrilov V
    Vutr Boles; 1984; 23(6):106-8. PubMed ID: 6531863
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Congenital hemolytic anemias.
    Fernbach DJ
    Am J Med Technol; 1969 Apr; 35(4):209-18. PubMed ID: 5779414
    [No Abstract]   [Full Text] [Related]  

  • 36. Innovative parameters RET-Y, sTfR, and sTfR-F index in patients with microcytic, hypochromic anemia--their special value for hemoglobinopathies.
    Agorasti A; Trivellas T; Papadopoulos V; Konstantinidou D
    Lab Hematol; 2007; 13(2):63-8. PubMed ID: 17573284
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [S hemoglobin gene carrier born to a mother with microdrepanocytic disease. A rare occurrence of maternal survival and of the possibility of carrying a pregnancy to term].
    Ingiulla A; D'Asero G
    Riv Ostet Ginecol; 1968 May; 23(5):368-73. PubMed ID: 5748321
    [No Abstract]   [Full Text] [Related]  

  • 38. Hemolytic anaemia due to unstable hemoglobin arising from spontaneous mutation--a case report.
    Dash S; Menon S; Marwaha RK
    Indian J Pathol Microbiol; 2006 Apr; 49(2):269-70. PubMed ID: 16933736
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Minkowski-Chauffard disease. Apropos of a triple familial case].
    Giard P; Routier G; Lamoril JL
    J Sci Med Lille; 1969 Dec; 87(12):735-43. PubMed ID: 5403370
    [No Abstract]   [Full Text] [Related]  

  • 40. [Congenital dyserythropoiesis with erythroblastic polyploidy. Report of a variety found in Argentinian Mesopotamia (author's transl)].
    Accame EA; de Tezanos Pinto M
    Sangre (Barc); 1981; 26(5-A):545-55. PubMed ID: 7323912
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.