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Journal Abstract Search

109 related items for PubMed ID: 4286791

  • 1. Erythrocyte DPNH dependent diaphorase levels in infants.
    Bartos HR, Desforges JF.
    Pediatrics; 1966 Jun; 37(6):991-3. PubMed ID: 4286791
    [No Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. [DECREASE OF METHEMOGLOBIN REDUCTIONS DIAPHORASE ACTIVITY AND FLAVINS IN ERYTHROCYTES OF YOUNG INFANTS].
    BETKE K, KLEIHAUER E, GAERTNER C, SCHIEBE G.
    Arch Kinderheilkd; 1964 Feb; 170():66-76. PubMed ID: 14163932
    [No Abstract] [Full Text] [Related]

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

  • 6. [Activity of NADH-dependent diaphorase in newborn infants and infants].
    Pantlitschko M, Weippl G, Kröger W.
    Wien Klin Wochenschr; 1970 Feb 13; 82(7):123-4. PubMed ID: 5513207
    [No Abstract] [Full Text] [Related]

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  • 9. Hereditary methemoglobinemia due to DPNH-methemoglobin reductase deficiency: report of a family.
    Angelopoulos B, Karalis D, Tsoukantas A, Eleftheriadou A.
    Acta Haematol; 1967 Feb 13; 37(5):284-93. PubMed ID: 4292867
    [No Abstract] [Full Text] [Related]

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  • 11. Deficient activity of DPNH-dependent methemoglobin diaphorase in cord blood erythrocytes.
    ROSS JD.
    Blood; 1963 Jan 13; 21():51-62. PubMed ID: 13975106
    [No Abstract] [Full Text] [Related]

  • 12. [Diminished activity of DPN dependent methemoglobinreductase in erythrocytes of newborn infants as cause of decreased methemoglobin reduction].
    Gärtner C.
    Z Kinderheilkd; 1966 Jan 13; 96(2):163-71. PubMed ID: 4293066
    [No Abstract] [Full Text] [Related]

  • 13. The diaphorase bands of human erythrocytes.
    Hegesh E, Calmanovici N, Lupo M, Bochkowsky R.
    J Lab Clin Med; 1971 May 13; 77(5):859-66. PubMed ID: 4104240
    [No Abstract] [Full Text] [Related]

  • 14. [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 May 13; 28(6):631-45. PubMed ID: 5114945
    [No Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. DPNH-methemoglobin reductase deficiency and hereditary methemoglobinemia.
    Jaffe ER, Hsieh HS.
    Semin Hematol; 1971 Oct 25; 8(4):417-37. PubMed ID: 4333562
    [No Abstract] [Full Text] [Related]

  • 17. NAD(P) glycohydrolase deficiency in human erythrocytes and alteration of cytosol NADH-methemoglobin diaphorase by membrane NAD-glycohydrolase activity.
    Frischer H, Nelson R, Noyes C, Carson PE, Bowman JE, Rieckmann KH, Ajmar F.
    Proc Natl Acad Sci U S A; 1973 Aug 25; 70(8):2406-10. PubMed ID: 4365376
    [Abstract] [Full Text] [Related]

  • 18. A comparison of two methods of determining DPNH-methemoglobin reductase.
    Scott EM.
    Clin Chim Acta; 1969 Mar 25; 23(3):495-8. PubMed ID: 4307481
    [No Abstract] [Full Text] [Related]

  • 19. [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 Mar 25; 14(6):755-70. PubMed ID: 4282504
    [No Abstract] [Full Text] [Related]

  • 20. [A NEW CASE OF RECESSIVE CONGENITAL METHEMOGLOBINEMIA LINKED WITH A DIAPHORASE I DEFICIENCY].
    HARTLEYB H, FISCHER D, HEIDT P, LOHR GW, LAUSECKER C.
    Arch Fr Pediatr; 1964 Dec 25; 21():1197-204. PubMed ID: 14248326
    [No Abstract] [Full Text] [Related]

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