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Journal Abstract Search

247 related items for PubMed ID: 5114945

  • 1. [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; 28(6):631-45. PubMed ID: 5114945
    [No Abstract] [Full Text] [Related]

  • 2. [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; 14(6):755-70. PubMed ID: 4282504
    [No Abstract] [Full Text] [Related]

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

  • 4. 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]

  • 5. [Congenital enzymatic methemoglobinemia. Apropos of a heterozygous form in a newborn child].
    Schneegans E, Hasselmann JL, Lutz D, Guillemette J.
    Ann Pediatr (Paris); 1971 Dec 14; 18(12):771-6. PubMed ID: 5151280
    [No Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. [On a new case of congenital methemoglobinemia caused by deficiency of diaphorease with grave cerebropathy].
    Ronconi G, Ferracin G.
    Fracastoro; 1968 Oct 14; 61(2):121-8. PubMed ID: 5704045
    [No Abstract] [Full Text] [Related]

  • 8. Congenital methemoglobinemia due to diaphorase deficiency.
    Ozsoylu S.
    Acta Haematol; 1972 Oct 14; 47(3):175-81. PubMed ID: 4624255
    [No Abstract] [Full Text] [Related]

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  • 10. [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 19; 115(4):273-81. PubMed ID: 4149782
    [No Abstract] [Full Text] [Related]

  • 11. [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 Nov 19; 109(4):279-81. PubMed ID: 5070403
    [No Abstract] [Full Text] [Related]

  • 12. An enzyme variation in a case of congenital methemoglobinemia.
    Gotlieb A, Nordan UZ, Hegesh E.
    Isr J Med Sci; 1973 Jul 19; 9(7):909-13. PubMed ID: 4354625
    [No Abstract] [Full Text] [Related]

  • 13. [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]

  • 14. [Hereditary methemoglobinemic cyanosis].
    Păsculescu G.
    Med Interna (Bucur); 1972 Apr 19; 24(4):413-21. PubMed ID: 5027787
    [No Abstract] [Full Text] [Related]

  • 15. [Hereditary methemoglobinemia with mental and growth retardation found in a Japanese boy. With special reference to xylitol, sorbitol metabolism and methemoglobin reduction in the erythrocyte].
    Nishina T, Miwa S, Hara N, Asakura T.
    Nihon Ketsueki Gakkai Zasshi; 1970 Aug 19; 33(4):455-61. PubMed ID: 5534618
    [No Abstract] [Full Text] [Related]

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  • 18. DPNH-methemoglobin reductase deficiency and hereditary methemoglobinemia.
    Jaffe ER, Hsieh HS.
    Semin Hematol; 1971 Oct 19; 8(4):417-37. PubMed ID: 4333562
    [No Abstract] [Full Text] [Related]

  • 19. [A case of methemoglobinemia M. Preliminary note].
    Kissin C, Collombel C, Baltassat P, Freycon F, Cotte J.
    Nouv Rev Fr Hematol; 1971 Oct 19; 11(1):17-23. PubMed ID: 4252102
    [No Abstract] [Full Text] [Related]

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