Literature DB >> 6015896

Arginosuccine aciduria.

B Levin.   

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Year:  1967        PMID： 6015896

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN： 0002-922X


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  6 in total

1.  Hyperammonemia through deficiency of ornithine carbamyl transferase.

Authors:  J P Farriaux; J L Dhondt; L Cathelineau; J Ratel; G Fontaine
Journal:  Z Kinderheilkd       Date:  1974

2.  Screening tests for argininosuccinic aciduria, orotic aciduria, and other inherited enzyme deficiencies using dried blood specimens.

Authors:  W H Murphey; L Patchen; R Guthrie
Journal:  Biochem Genet       Date:  1972-02       Impact factor: 1.890

3.  Sibs with mental and physical retardation and trichorrhexis nodosa with abnormal amino acid composition of the hair.

Authors:  R J Pollitt; F A Jenner; M Davies
Journal:  Arch Dis Child       Date:  1968-04       Impact factor: 3.791

4.  Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child.

Authors:  B Levin; J M Abraham; V G Oberholzer; E A Burgess
Journal:  Arch Dis Child       Date:  1969-04       Impact factor: 3.791

5.  Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase.

Authors:  B Levin; R H Dobbs; E A Burgess; T Palmer
Journal:  Arch Dis Child       Date:  1969-04       Impact factor: 3.791

6.  Neonatal argininosuccinic aciduria with normal brain and kidney but absent liver argininosuccinate lyase activity.

Authors:  N R Glick; P J Snodgrass; I A Schafer
Journal:  Am J Hum Genet       Date:  1976-01       Impact factor: 11.025
  6 in total

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