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 *

159 related articles for article (PubMed ID: 7757371)

  • 1. [Familial case of methemoglobinemia associated with glucose-4-phosphate dehydrogenase deficiency].
    Askerova TA; Kichibekov BR; Panakhova KhG
    Klin Lab Diagn; 1995; (1):51-3. PubMed ID: 7757371
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Detection of combined forms of hemoglobino- and enzymopathies in newborns].
    Askerova TA; Movsum-zade KM; Kichibekov BR
    Vopr Med Khim; 1993; 39(6):51-4. PubMed ID: 8303876
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Unstable variant of NADH methemoglobin reductase in Puerto Ricans with hereditary methemoglobinemia.
    Schwartz JM; Paress PS; Ross JM; DiPillo F; Rizek R
    J Clin Invest; 1972 Jun; 51(6):1594-601. PubMed ID: 4336945
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Heterozygous NADH-methemoglobin reductase defect with methemoglobinemia in an infant (author's transl)].
    Witt I; Gunkel J; Seibert G; Wehinger H; Schuchmann L; Künzer W
    Z Kinderheilkd; 1973 Nov; 115(4):273-81. PubMed ID: 4149782
    [No Abstract]   [Full Text] [Related]  

  • 5. [Enterogenons methemoglobinemia caused by heterozygotic deficiency of erythrocytic NADH-methemoglobin reductase].
    Schmidt K; Faber K; Heni F
    Blut; 1974 Jul; 29(1):43-9. PubMed ID: 4367854
    [No Abstract]   [Full Text] [Related]  

  • 6. Clinical problem-solving. Why "why" matters.
    Janssen WJ; Dhaliwal G; Collard HR; Saint S
    N Engl J Med; 2004 Dec; 351(23):2429-34. PubMed ID: 15575060
    [No Abstract]   [Full Text] [Related]  

  • 7. Congenital methemoglobinemia due to hemoglobin M.
    Ozsoylu S
    Acta Haematol; 1972; 47(4):225-32. PubMed ID: 4625305
    [No Abstract]   [Full Text] [Related]  

  • 8. [Methemoglobinemia and acidosis during the first week of life].
    Buonocore G; Cantarini A; De Biase L; Bagnoli F; Casadei AM; Melideo F
    Boll Soc Ital Biol Sper; 1983 May; 59(5):626-30. PubMed ID: 6882561
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The reduction of methemoglobin in erythrocytes of a patient with congenital methemoglobinemia, subjects with erythrocyte glucose-6-phosphate dehydrogenase deficiency, and normal individuals.
    JAFFE ER
    Blood; 1963 May; 21():561-72. PubMed ID: 13964447
    [No Abstract]   [Full Text] [Related]  

  • 10. Acquired methemoglobinemia: a retrospective series of 138 cases at 2 teaching hospitals.
    Ash-Bernal R; Wise R; Wright SM
    Medicine (Baltimore); 2004 Sep; 83(5):265-273. PubMed ID: 15342970
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital methemoglobinemia: the result of age-dependent decay of methemoglobin reductase.
    Feig SA; Nathan DG; Gerald PS; Zarkowski HS
    Blood; 1972 Mar; 39(3):407-14. PubMed ID: 4400622
    [No Abstract]   [Full Text] [Related]  

  • 12. [Beta-thalassemia and glucose-6-phosphate dehydrogenase deficiency].
    Troitskaia OV; Ermil'chenko GV; Levitskaia SV; Varzieva LK
    Klin Lab Diagn; 1996; (6):17-24. PubMed ID: 9044721
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analyis of met-form haemoglobins in human erythrocytes of normal adults and of a patient with hereditary methaemoglobinaemia due to deficiency of NADH-cytochrome b5 reductase.
    Tomoda A; Imoto M; Hirano M; Yoneyama Y
    Biochem J; 1979 Aug; 181(2):505-7. PubMed ID: 496898
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Electrophoretic and functional variants of NADH-methemoglobin reductase in hereditary methemoglobinemia.
    Hsieh HS; Jaffé ER
    J Clin Invest; 1971 Jan; 50(1):196-202. PubMed ID: 5543874
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Polyacrylamide gel isoelectric focusing for the study of erythrocyte methemoglobin reductase].
    Kazanets EG; Zakharova FA; Levina AA; Andreeva AP; Tokarev IuN
    Probl Gematol Pereliv Krovi; 1982 Nov; 27(11):56-8. PubMed ID: 7156081
    [No Abstract]   [Full Text] [Related]  

  • 16. Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian families.
    Kedar PS; Colah RB; Ghosh K; Mohanty D
    Haematologia (Budap); 2002; 32(4):543-9. PubMed ID: 12803131
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Recessive hereditary methemoglobinemia: two novel mutations in the NADH-cytochrome b5 reductase gene.
    Fermo E; Bianchi P; Vercellati C; Marcello AP; Garatti M; Marangoni O; Barcellini W; Zanella A
    Blood Cells Mol Dis; 2008; 41(1):50-5. PubMed ID: 18343696
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Why "why" matters.
    Grimsley EW
    N Engl J Med; 2005 Mar; 352(12):1270-1; author reply 1270-1. PubMed ID: 15788511
    [No Abstract]   [Full Text] [Related]  

  • 19. Screening for glucose-6-phosphate dehydrogenase deficiency.
    Beutler E
    Isr J Med Sci; 1973; 9(9):1350-2. PubMed ID: 4775115
    [No Abstract]   [Full Text] [Related]  

  • 20. Red cell enzymes.
    Prchal JT; Gregg XT
    Hematology Am Soc Hematol Educ Program; 2005; ():19-23. PubMed ID: 16304354
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.