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 *

128 related articles for article (PubMed ID: 4390269)

  • 1. Heterogeneity of the enzymatic defect in congenital methemoglobinemia.
    Bloom GE; Zarkowsky HS
    N Engl J Med; 1969 Oct; 281(17):919-22. PubMed ID: 4390269
    [No Abstract]   [Full Text] [Related]  

  • 2. Is it bad to be blue?
    Jaffe ER
    N Engl J Med; 1969 Oct; 281(17):957-8. PubMed ID: 4312802
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

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

  • 5. Inherited methemoglobinemia (enzyme deficiencies).
    Waller HD
    Humangenetik; 1970; 9(3):217-8. PubMed ID: 4393777
    [No Abstract]   [Full Text] [Related]  

  • 6. Congenital methemoglobinemia due to DPNH-methemoglobin reductase deficiency: another inherited defect of red blood cell metabolism found in Thailand.
    Panich V; Na-Nakorn S; Kruatrachue M
    J Med Assoc Thai; 1970 May; 53(5):322-36. PubMed ID: 5505653
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. Congenital methemoglobinemia methemoglobin reductase deficiency.
    Koepke JA
    Ann Clin Lab Sci (1971); 1971; 1(3):222-6. PubMed ID: 5154970
    [No Abstract]   [Full Text] [Related]  

  • 9. Electrophoretic study of glutathione reductase in human erythrocytes and leucocytes.
    Kaplan JC; Beutler E
    Nature; 1968 Jan; 217(5125):256-8. PubMed ID: 4384274
    [No Abstract]   [Full Text] [Related]  

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

  • 11. Activity of NADH- and NADPH-dependent methemoglobin reductases in erythrocytes from fetal to adult age. A parallel assessment.
    Vetrella M; Astedt B; Barthelmai W; Neuvians D
    Klin Wochenschr; 1971 Sep; 49(17):972-7. PubMed ID: 4398423
    [No Abstract]   [Full Text] [Related]  

  • 12. [Congenital methemoglobulinemia of recessive type caused by DPNH-methemoglobin reductase deficiency. Description of a family].
    Fabris C; Norelli MT; Ciriotti G; Perfetto V; Franceschini P
    Minerva Pediatr; 1971 Oct; 23(42):1743-52. PubMed ID: 5132353
    [No Abstract]   [Full Text] [Related]  

  • 13. Methemoglobin reductase (cytochrome b5 reductase) deficiency in congenital methemoglobinemia.
    Kitao T; Sugita Y; Yoneyama Y; Hattori K
    Blood; 1974 Dec; 44(6):879-84. PubMed ID: 4138943
    [No Abstract]   [Full Text] [Related]  

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

  • 15. 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]  

  • 16. [Case of hereditary enzymopenic methemoglobinemia].
    German SV; Napalkova NN; Kolokol'nikova OA
    Klin Med (Mosk); 1997; 75(10):71-3. PubMed ID: 9490348
    [No Abstract]   [Full Text] [Related]  

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

  • 18. Methemoglobinemia--sleuthing for a new cause.
    Charache S
    N Engl J Med; 1986 Mar; 314(12):776-8. PubMed ID: 3951508
    [No Abstract]   [Full Text] [Related]  

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

  • 20. Biochemical and functional properties of methemoglobin diaphorase in congenital methemoglobinemia.
    Bianchi-Scarra G; Ajmar F; Bruzzone G; Gaetani GF
    Haematologica; 1976 Sep; 61(3):261-8. PubMed ID: 828121
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.