Literature DB >> 5438972

[Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies].

H G Terheggen, A Schwenk, A Lowenthal, M van Sande, J P Colombo.   

Abstract

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Year:  1970        PMID： 5438972

Source DB:  PubMed          Journal:  Z Kinderheilkd        ISSN： 0044-2917


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  6 in total

1.  Unsuccessful trial of gene replacement in arginase deficiency.

Authors:  H G Terheggen; A Lowenthal; F Lavinha; J P Colombo; S Rogers
Journal:  Z Kinderheilkd       Date:  1975

2.  Human hyperargininemia: a mutation not expressed in skin fibroblasts?

Authors:  A F Van Elsen; J G Leroy
Journal:  Am J Hum Genet       Date:  1977-07       Impact factor: 11.025

3.  [Developing mechanism of the adverse effects of L-asparaginase and their control].

Authors:  J Kodama; K Higashino; S Kobayashi; K Izumi; M Satani
Journal:  Blut       Date:  1974-01

4.  Amino acids in CSF and plasma in hyperammonaemic coma due to arginase1 deficiency.

Authors:  S Scholl-Bürgi; S Baumgartner Sigl; J Häberle; E Haberlandt; K Rostásy; C Ertl; U Eichinger-Öttl; P Heinz-Erian; D Karall
Journal:  J Inherit Metab Dis       Date:  2008-12-06       Impact factor: 4.982

Review 5.  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

6.  Differential expression of multiple forms of arginase in cultured cells.

Authors:  E B Spector; R M Kern; D F Haggerty; S D Cederbaum
Journal:  Mol Cell Biochem       Date:  1985-02       Impact factor: 3.396
  6 in total

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