Literature DB >> 14063066

HOMOCYSTINURIA.

R H JACKSON.   

Abstract

Mesh:

Year:  1963        PMID: 14063066      PMCID: PMC1873729     

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


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  8 in total

1.  Metabolic abnormalities detected in a survey of mentally backward individuals in Northern Ireland.

Authors:  N A CARSON; D W NEILL
Journal:  Arch Dis Child       Date:  1962-10       Impact factor: 3.791

2.  HOMOCYSTINURIA.

Authors:  G M KOMROWER; V K WILSON
Journal:  Proc R Soc Med       Date:  1963-11

3.  Idiopathic hyperglycinemia and hyperglycinuria: a new disorder of amino acid metabolism. I.

Authors:  B CHILDS; W L NYHAN; M BORDEN; L BARD; R E COOKE
Journal:  Pediatrics       Date:  1961-04       Impact factor: 7.124

4.  Studies in maple syrup urine disease.

Authors:  C E DENT; R G WESTALL
Journal:  Arch Dis Child       Date:  1961-06       Impact factor: 3.791

5.  Argininosuccinic aciduria. A new form of mental deficiency due to metabolic causes.

Authors:  C E DENT
Journal:  Proc R Soc Med       Date:  1959-10

6.  Maple syrup urine disease: branched-chain keto-aciduria.

Authors:  J DANCIS; M LEVITZ; R G WESTALL
Journal:  Pediatrics       Date:  1960-01       Impact factor: 7.124

7.  Cystathioniuria.

Authors:  H HARRIS; L S PENROSE; D H THOMAS
Journal:  Ann Hum Genet       Date:  1959-12       Impact factor: 1.670

8.  A disease, probably hereditary characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism.

Authors:  J D ALLAN; D C CUSWORTH; C E DENT; V K WILSON
Journal:  Lancet       Date:  1958-01-25       Impact factor: 79.321

  8 in total

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