Literature DB >> 3088322

Pyruvate carboxylase deficiency in twins.

M A Pollock, M Cumberbatch, M J Bennett, R G Gray, M Brand, K Hyland, P J Congdon, T Pitts-Tucker, S Gray.   

Abstract

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Year:  1986        PMID： 3088322     DOI： 10.1007/bf01813898

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  4 in total

1.  Pyruvate carboxylase deficiency and lactic acidosis in a retarded child without Leigh's disease.

Authors:  B M Atkin; N R Buist; M F Utter; A B Leiter; B Q Banker
Journal:  Pediatr Res       Date:  1979-02       Impact factor: 3.756

2.  Acute neonatal citrullinaemia.

Authors:  M J Bennett; P R Dear; J M McGinlay; R G Gray
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

3.  Secondary citrullinemia with hyperammonemia in four neonatal cases of pyruvate carboxylase deficiency.

Authors:  F X Coude; H Ogier; C Marsac; A Munnich; C Charpentier; J M Saudubray
Journal:  Pediatrics       Date:  1981-12       Impact factor: 7.124

4.  Organic acids in urine of patients with congenital lactic acidoses: an aid to differential diagnosis.

Authors:  R A Chalmers
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982
  4 in total

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