Literature DB >> 13716368

Recent developments in inborn errors of metabolism.

D Y HSIA.   

Abstract

Entities:  

Keywords:  METABOLIC DISEASES

Mesh:

Year:  1960        PMID: 13716368      PMCID: PMC1373530          DOI: 10.2105/ajph.50.11.1653

Source DB:  PubMed          Journal:  Am J Public Health Nations Health        ISSN: 0002-9572


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  8 in total

1.  The heterozygous carrier in galactosaemia.

Authors:  D Y HSIA; I HUANG; S G DRISCOLL
Journal:  Nature       Date:  1958-11-15       Impact factor: 49.962

2.  Enzymic evidence of a galactosemic trait in parents of galactosemic children.

Authors:  H N KIRKMAN; E BYNUM
Journal:  Ann Hum Genet       Date:  1959-04       Impact factor: 1.670

3.  Galactosemia, a congenital defect in a nucleotide transferase.

Authors:  H M KALCKAR; E P ANDERSON; K J ISSELBACHER
Journal:  Biochim Biophys Acta       Date:  1956-04

4.  On the nature of enzymatic defect in phenylpyruvic oligophrenia.

Authors:  C MITOMA; R M AULD; S UDENFRIEND
Journal:  Proc Soc Exp Biol Med       Date:  1957-04

5.  A one-year, controlled study of the effect of low-phenylalanine diet on phenylketonuria.

Authors:  D Y HSIA; W E KNOX; K V QUINN; R S PAINE
Journal:  Pediatrics       Date:  1958-02       Impact factor: 7.124

6.  Detection by phenylalanine tolerance tests of heterozygous carriers of phenylketonuria.

Authors:  K W DRISCOLL; D Y HSIA; W E KNOX; W TROLL
Journal:  Nature       Date:  1956-12-01       Impact factor: 49.962

7.  Some disturbances of erythrocyte metabolism in galactosaemia.

Authors:  V SCHWARZ; L GOLBERG; G M KOMROWER; A HOLZEL
Journal:  Biochem J       Date:  1956-01       Impact factor: 3.857

8.  Influence of phenylalanine intake on phenylketonuria.

Authors:  H BICKEL; J GERRARD; E M HICKMANS
Journal:  Lancet       Date:  1953-10-17       Impact factor: 79.321

  8 in total

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