Literature DB >> 5861763

[Argininuria, convulsions and oligophrenia; a new inborn error of metabolism?].

A Peralta Serrano.   

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Year:  1965        PMID： 5861763

Source DB:  PubMed          Journal:  Rev Clin Esp        ISSN： 0014-2565            Impact factor:   1.556


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  4 in total

1.  Familial hyperargininaemia.

Authors:  H G Terheggen; A Lowenthal; F Lavinha; J P Colombo
Journal:  Arch Dis Child       Date:  1975-01       Impact factor: 3.791

2.  A new case of arginase deficiency in a Spanish male.

Authors:  A Jordá; V Rubio; M Portolés; J Vilas; J García-Piño
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

3.  Treatment of hyperargininaemia due to arginase deficiency with a chemically defined diet.

Authors:  S D Cederbaum; S J Moedjono; K N Shaw; M Carter; E Naylor; M Walzer
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

Review 4.  The human arginases and arginase deficiency.

Authors:  R Iyer; C P Jenkinson; J G Vockley; R M Kern; W W Grody; S Cederbaum
Journal:  J Inherit Metab Dis       Date:  1998       Impact factor: 4.982
  4 in total

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