Literature DB >> 13326036

Congenital methemoglobinemia in the newborn period.

M S DINE.   

Abstract

Entities:  

Keywords:  INFANT, NEWBORN/diseases; METHEMOGLOBINEMIA/in infant and child

Mesh：

Year:  1956        PMID： 13326036     DOI： 10.1001/archpedi.1956.02060030017005

Source DB:  PubMed          Journal:  AMA J Dis Child        ISSN： 0096-6916


× No keyword cloud information.
  4 in total

1.  Discussion on some clinical, genetic and biochemical aspects of metabolic disorders of the nervous system: metabolic disease of the nervous system: clinical aspects.

Authors:  W B MATTHEWS
Journal:  Proc R Soc Med       Date:  1958-10

2.  Methemoglobinemia in infancy; two case reports, one of the congenital and one of the acquired variety of methemoglobinemia.

Authors:  J G ARMSTRONG; J B McKENDRY; K W SLEMON
Journal:  Can Med Assoc J       Date:  1958-09-01       Impact factor: 8.262

3.  Automated determination of red cell methaemoglobin reductase activity by a continuous-flow system for screening hereditary methaemoglobinaemia.

Authors:  K Tanishima; N Fukuda; M Takeshita; Y Takizawa; T Kitamura; Y Yoneyama
Journal:  J Clin Pathol       Date:  1979-06       Impact factor: 3.411

4.  Alteration of NADH-diaphorase and cytochrome b5 reductase activities of erythrocytes, platelets, and leucocytes in hereditary methaemoglobinaemia with and without mental retardation.

Authors:  M Takeshita; T Matsuki; K Tanishima; T Yubisui; Y Yoneyama; K Kurata; N Hara; T Igarashi
Journal:  J Med Genet       Date:  1982-06       Impact factor: 6.318
  4 in total

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