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Journal Abstract Search

109 related items for PubMed ID: 4286791

  • 21. [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]

  • 22. [Enterogenons methemoglobinemia caused by heterozygotic deficiency of erythrocytic NADH-methemoglobin reductase].
    Schmidt K, Faber K, Heni F.
    Blut; 1974 Jul 19; 29(1):43-9. PubMed ID: 4367854
    [No Abstract] [Full Text] [Related]

  • 23.
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  • 24. NADH diaphorase: an inherited variant associated with normal methemoglobin reduction.
    Detter JC, Anderson JE, Giblett ER.
    Am J Hum Genet; 1970 Jan 19; 22(1):100-4. PubMed ID: 5411644
    [No Abstract] [Full Text] [Related]

  • 25. Studies on methemoglobin reductase. I. Comparative studies of diaphorases from normal and methemoglobinemic erythrocytes.
    Kuma F, Ishizawa S, Hirayama K, Nakajima H.
    J Biol Chem; 1972 Jan 25; 247(2):550-5. PubMed ID: 4400377
    [No Abstract] [Full Text] [Related]

  • 26. [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 30; 59(5):626-30. PubMed ID: 6882561
    [Abstract] [Full Text] [Related]

  • 27. The effect of primaquine and acetylphenylhydrazine on the enzymatic and nonenzymatic oxidation of reduced pyridine nucleotides.
    Shrago E.
    J Lab Clin Med; 1966 Jul 30; 68(1):1-11. PubMed ID: 4380287
    [No Abstract] [Full Text] [Related]

  • 28. Congenital methemoglobinemia: the result of age-dependent decay of methemoglobin reductase.
    Feig SA, Nathan DG, Gerald PS, Zarkowski HS.
    Blood; 1972 Mar 30; 39(3):407-14. PubMed ID: 4400622
    [No Abstract] [Full Text] [Related]

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  • 31. [A family with congenital methemoglobinemia due to diaphorase deficiency].
    Frick PG, Bachmann F, Schmid JR.
    Acta Haematol; 1965 Oct 30; 34(4):215-27. PubMed ID: 4955559
    [No Abstract] [Full Text] [Related]

  • 32. [Hereditary methemoglobinemic cyanosis].
    Păsculescu G.
    Med Interna (Bucur); 1972 Apr 30; 24(4):413-21. PubMed ID: 5027787
    [No Abstract] [Full Text] [Related]

  • 33. [Erythrocyte DPNH-dependent diaphorases in viro-microbial infections of the respiratory system in infants].
    Bărbuţă R, Grigoraş O, Dragomir C, Grădinaru E.
    Rev Med Chir Soc Med Nat Iasi; 1977 Apr 30; 81(2):201-6. PubMed ID: 905676
    [No Abstract] [Full Text] [Related]

  • 34. Leukocyte diaphorase deficiency in congenital methemoglobinemia: a valuable prognostic indicator.
    Lawson DL, Miale TD, Harvey JL, Bucciarelli RL, Nelson LS.
    Biol Neonate; 1977 Apr 30; 32(3-4):193-6. PubMed ID: 603804
    [No Abstract] [Full Text] [Related]

  • 35. Congenital methemoglobinemia due to diaphorase deficiency.
    Ozsoylu S.
    Acta Haematol; 1972 Apr 30; 47(3):175-81. PubMed ID: 4624255
    [No Abstract] [Full Text] [Related]

  • 36. [Genetic injuries in 2 families with congenital methemoglobinemia caused by diaphorase I deficiency].
    Pedrinazzi RC, Della Cella G, Famularo L, Cerruti Mainardi P, Borrone C.
    Minerva Pediatr; 1969 May 05; 21(18):800-4. PubMed ID: 5404915
    [No Abstract] [Full Text] [Related]

  • 37. [A case of methemoglobinemia M. Preliminary note].
    Kissin C, Collombel C, Baltassat P, Freycon F, Cotte J.
    Nouv Rev Fr Hematol; 1971 May 05; 11(1):17-23. PubMed ID: 4252102
    [No Abstract] [Full Text] [Related]

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  • 39. [DEFICIENCY OF DIAPHORASE ACTIVITY IN THE NEWBORN INFANT].
    MININNI G.
    Riv Clin Pediatr; 1963 May 05; 71():284-9. PubMed ID: 14080259
    [No Abstract] [Full Text] [Related]

  • 40. DIAPHORASE I, CATALASE AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE ACTIVITY IN THE ERYTHROCYTES OF AGED SUBJECTS.
    BERTOLINI AM, QUARTODIPALO FM, GASTALDI L.
    Gerontologia; 1963 May 05; 10():167-73. PubMed ID: 14304812
    [No Abstract] [Full Text] [Related]

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