Literature DB >> 6061565

Demonstration of an enzyme variant in a case of congenital methaemoglobinaemia.

C A West, B D Gomperts, E R Huehns, I Kessel, J R Ashby.   

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Year:  1967        PMID: 6061565      PMCID: PMC1748606          DOI: 10.1136/bmj.4.5573.212

Source DB:  PubMed          Journal:  Br Med J        ISSN: 0007-1447


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  3 in total

1.  Erythrocyte metabolism. VI. Separation of erythrocyte enzymes from hemoglobin.

Authors:  M A HENNESSEY; A M WALTERSDORPH; F M HUENNEKENS; B W GABRIO
Journal:  J Clin Invest       Date:  1962-06       Impact factor: 14.808

2.  The relation of diaphorase of human erythrocytes to inheritance of methemoglobinemia.

Authors:  E M SCOTT
Journal:  J Clin Invest       Date:  1960-07       Impact factor: 14.808

3.  Mental retardation in methemoglobinemia due to diaphorase deficiency.

Authors:  P J Fialkow; J A Browder; R S Sparkes; A G Motulsky
Journal:  N Engl J Med       Date:  1965-10-14       Impact factor: 91.245

  3 in total
  11 in total

Review 1.  The genetics of metabolic disorders.

Authors:  D A Hopkinson
Journal:  Postgrad Med J       Date:  1972-04       Impact factor: 2.401

2.  [Enterogenons methemoglobinemia caused by heterozygotic deficiency of erythrocytic NADH-methemoglobin reductase].

Authors:  K Schmidt; K Faber; F Heni
Journal:  Blut       Date:  1974-07

3.  [Genetically determined variants of NADH-diaphorase].

Authors:  G Tariverdian; H Ritter; G G Wendt
Journal:  Humangenetik       Date:  1970

4.  Red blood cell NADH diaphorase in Italian populations.

Authors:  P Lucarelli; M Di Mino; E Carapella; R Agostino; R Palmarino
Journal:  Humangenetik       Date:  1972

5.  NADH diaphorase: an inherited variant associated with normal methemoglobin reduction.

Authors:  J C Detter; J E Anderson; E R Giblett
Journal:  Am J Hum Genet       Date:  1970-01       Impact factor: 11.025

6.  [Hb Tübingen. A new beta-chain variant (beta Tp 10-21) with increased spontaneous oxidation].

Authors:  E Kleihauer; H D Waller; H C Benöhr; E Kohne; P Gelinsky
Journal:  Klin Wochenschr       Date:  1971-06-01

7.  Hereditary methemoglobinemia associated with NADH diaphorase deficiency.

Authors:  H Ritter; K Schmidt; J Schmitt
Journal:  Humangenetik       Date:  1973

8.  Defective molecular variants of glucose-6-phosphate dehydrogenase and methaemoglobin reductase.

Authors:  J C Kaplan
Journal:  J Clin Pathol Suppl (R Coll Pathol)       Date:  1974

Review 9.  Enzyme assays in diseases of erythrocytes.

Authors:  T A Prankerd
Journal:  J Clin Pathol Suppl (Assoc Clin Pathol)       Date:  1970

Review 10.  Genetics and clinical enzymology.

Authors:  H Harris
Journal:  J Clin Pathol Suppl (Assoc Clin Pathol)       Date:  1970
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