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 *

130 related articles for article (PubMed ID: 826072)

  • 21. [Congenital enzymopenic methemoglobinemia and its pharmacogenetic aspects].
    Stanulović M; Gebauter E; Popović K; Velisavljev M
    Bilt Hematol Transfuz; 1977; 5(3-4):75-80. PubMed ID: 615613
    [TBL] [Abstract][Full Text] [Related]  

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

  • 23. Enzymopenic methaemoglobinaemia and spastic diplegia in an Italian-Yugoslavian child.
    Agar NS; Irvine S; Davis JR; Harley JD
    Med J Aust; 1972 Aug; 2(8):429-30. PubMed ID: 5086303
    [No Abstract]   [Full Text] [Related]  

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

  • 25. Demonstration of an enzyme variant in a case of congenital methaemoglobinaemia.
    West CA; Gomperts BD; Huehns ER; Kessel I; Ashby JR
    Br Med J; 1967 Oct; 4(5573):212-4. PubMed ID: 6061565
    [No Abstract]   [Full Text] [Related]  

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

  • 27. Heterogeneity of hereditary methaemoglobinaemia: a study of 4 Cuban families with NADH-Methaemoglobin reductase deficiency including a new variant (Santiago de Cuba variant).
    González R; Estrada M; Wade M; de la Torre E; Svarch E; Fernández O; Ortiz R; Guzmán E; Colombo B
    Scand J Haematol; 1978 May; 20(5):385-93. PubMed ID: 663552
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: first report of two cases.
    Junien C; Leroux A; Lostanlen D; Reghis A; Boue J; Nicolas H; Boue A; Kaplan JC
    Prenat Diagn; 1981 Jan; 1(1):17-24. PubMed ID: 7346809
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [High altitude methaemoglobinaemia. Methaemoglobin and NADH diaphorase ].
    Arnaud J; Gutiérrez N; Quilici JC; Vergnes H
    Sangre (Barc); 1982; 27(2):150-5. PubMed ID: 6896934
    [No Abstract]   [Full Text] [Related]  

  • 30. [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]  

  • 31. 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]  

  • 32. Associated red cell enzyme deficiencies and their significance in a case of congenital enzymopenic methemoglobinemia.
    Das Gupta A; Vaidya MS; Bapat JP; Pavri RS; Baxi AJ; Advani SH
    Acta Haematol; 1980; 64(5):285-8. PubMed ID: 6779487
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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; 78(501):354-5. PubMed ID: 4519433
    [No Abstract]   [Full Text] [Related]  

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

  • 35. 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]  

  • 36. Recessive congenital methaemoglobinaemia: functional characterization of the novel D239G mutation in the NADH-binding lobe of cytochrome b5 reductase.
    Percy MJ; Crowley LJ; Davis CA; McMullin MF; Savage G; Hughes J; McMahon C; Quinn RJ; Smith O; Barber MJ; Lappin TR
    Br J Haematol; 2005 Jun; 129(6):847-53. PubMed ID: 15953014
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Congenital enzymopenic methaemoglobinaemia.
    Kueh YK; Chio LF; Guan R
    Ann Acad Med Singap; 1986 Apr; 15(2):250-4. PubMed ID: 3752898
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Cyanosis in children caused by inherited methemoglobinemia due to deficiency of NADH-dependent methemoglobin reductase in erythrocytes].
    Jabłońska-Skwiecińska E; Wierzbicka M; Kubicka K
    Pediatr Pol; 1989 Jan; 64(1):53-9. PubMed ID: 2812907
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Hereditary methemoglobinemic cyanosis due to diaphorase deficiency in three successive generations.
    Ozsoylu S
    Acta Haematol; 1967; 37(5):276-83. PubMed ID: 4963515
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.