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Journal Abstract Search

106 related items for PubMed ID: 14080259

  • 21. Diaphroase activity and variants in normal adults and newborns.
    Eng LI, Loo M, Fah FK.
    Br J Haematol; 1972 Oct; 23(4):419-25. PubMed ID: 5084807
    [No Abstract] [Full Text] [Related]

  • 22. The enzymic defect of hereditary methemoglobinemia: diaphorase.
    SCOTT EM, GRIFFITH IV.
    Biochim Biophys Acta; 1959 Aug; 34():584-6. PubMed ID: 14444208
    [No Abstract] [Full Text] [Related]

  • 23. [Hereditary methemoglobinemia with mental retardation. Study of 3 further cases].
    Heusden A, Willems C, Lambotte C, Hainaut H, Chapelle P, Malchair R.
    Arch Fr Pediatr; 1971 Aug; 28(6):631-45. PubMed ID: 5114945
    [No Abstract] [Full Text] [Related]

  • 24. [The enzyme defect in recessive congenital methemoglobinemia with encephalopathy. A new defective variant of NADH-diaphorase (Beni-Messous variant)].
    Kaplan JC, Leroux A, Bakouri S, Grangaud JP, Benabadji M.
    Nouv Rev Fr Hematol; 1974 Aug; 14(6):755-70. PubMed ID: 4282504
    [No Abstract] [Full Text] [Related]

  • 25. Mental retardation in methemoglobinemia due to diaphorase deficiency.
    Fialkow PJ, Browder JA, Sparkes RS, Motulsky AG.
    N Engl J Med; 1965 Oct 14; 273(16):840-5. PubMed ID: 4378489
    [No Abstract] [Full Text] [Related]

  • 26. Hereditary methaemoglobinaemia due to enzyme deficiency: a case report and study of a Chatham Island family.
    Watt MW, Taylor IM.
    N Z Med J; 1973 Oct 24; 78(501):354-5. PubMed ID: 4519433
    [No Abstract] [Full Text] [Related]

  • 27. [A family with congenital methemoglobinemia due to diaphorase deficiency].
    Frick PG, Bachmann F, Schmid JR.
    Acta Haematol; 1965 Oct 24; 34(4):215-27. PubMed ID: 4955559
    [No Abstract] [Full Text] [Related]

  • 28. [Congenital methemoglobinemia caused by the NADH-diaphorase deficiency].
    Stanulović M, Mijatović B, Marković O.
    Med Pregl; 1971 Oct 24; 24(9):463-7. PubMed ID: 4333391
    [No Abstract] [Full Text] [Related]

  • 29. [Congenital methemoglobinemia due to NADH (DPNH) dependent methemoglobin reductase deficiency].
    Orsini A, Vovan L, Brusquet Y, Gabriel B, Sebag F, Galtier M.
    Mars Med; 1972 Oct 24; 109(4):279-81. PubMed ID: 5070403
    [No Abstract] [Full Text] [Related]

  • 30. [A case of recessive congenital methemoglobinemia].
    LUCET P, JARLIER H, NOUAILLE J.
    Arch Fr Pediatr; 1963 Apr 24; 20():496-502. PubMed ID: 13931447
    [No Abstract] [Full Text] [Related]

  • 31. Diaphorase deficiency methaemoglobinaemia mimicking cardiac disease in pregnancy.
    Vassallo L, Cauchi M.
    J Obstet Gynaecol Br Commonw; 1970 Feb 24; 77(2):178-9. PubMed ID: 5419883
    [No Abstract] [Full Text] [Related]

  • 32. [CONGENITAL METHEMOGLOBINEMIA OF THE RECESSIVE TYPE DUE TO DIAPHORASE DEFICIT WITH OLIGOPHRENIA].
    RONCONI G, FERRACIN G.
    Riv Clin Pediatr; 1964 Sep 24; 74():152-9. PubMed ID: 14316460
    [No Abstract] [Full Text] [Related]

  • 33. [CONGENITAL METHEMOGLOBINEMIA AND ITS SIGNIFICANCE IN THE DIFFERENTIAL DIAGNOSIS OF CYANOSIS].
    BOLT W, ZERLETT G, RITZL F.
    Dtsch Med Wochenschr; 1963 Nov 15; 88():2247-50. PubMed ID: 14111916
    [No Abstract] [Full Text] [Related]

  • 34. [Familial NADH diaphorase deficiency].
    Vergnes H, Gherardi M, Bernadet P, Biermé R.
    Nouv Rev Fr Hematol; 1972 Nov 15; 12(4):560-3. PubMed ID: 4344374
    [No Abstract] [Full Text] [Related]

  • 35. [Familial methemoglobinemia due to diaphorase deficiency: a 3d Swiss line].
    Marti HR, Dorta T, Deubelbeiss KA.
    Schweiz Med Wochenschr; 1966 Mar 19; 96(11):355-7. PubMed ID: 5987762
    [No Abstract] [Full Text] [Related]

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  • 38. Purification of diphosphopyridine nucleotide diaphorase from methemoglobinemic erythrocytes.
    SCOTT EM.
    Biochem Biophys Res Commun; 1962 Sep 25; 9():59-62. PubMed ID: 13992522
    [No Abstract] [Full Text] [Related]

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