Literature DB >> 4747314

Renal function studies and kidney pyruvate carboxylase in subacute necrotizing encephalomyelopathy (Leigh's syndrome).

A B Gruskin, M S Patel, M Linshaw, R Ettenger, D Huff, W Grover.   

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Year:  1973        PMID： 4747314     DOI： 10.1203/00006450-197310000-00007

Source DB:  PubMed          Journal:  Pediatr Res        ISSN： 0031-3998            Impact factor:   3.756


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  6 in total

1.  Congenital lactic acidosis due to pyruvate carboxylase deficiency: absence of an inhibitor of TPP-ATP phosphoryl transferase.

Authors:  K Tada; G Takada; K Omura; Y Itokawa
Journal:  Eur J Pediatr       Date:  1978-01-17       Impact factor: 3.183

2.  Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy.

Authors:  S Miyabayashi; T Ito; K Narisawa; K Iinuma; K Tada
Journal:  Eur J Pediatr       Date:  1985-03       Impact factor: 3.183

3.  Neonatal pyruvate carboxylase deficiency with renal tubular acidosis and cystinuria.

Authors:  J Oizumi; K N Shaw; T A Giudici; M Carter; G N Donnell; W G Ng
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

4.  Is pyruvate carboxylase involved in the renal tubular reabsorption of bicarbonate?

Authors:  N R Buist
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982

Review 5.  Renal involvement in mitochondrial cytopathies.

Authors:  P Niaudet; A Rötig
Journal:  Pediatr Nephrol       Date:  1996-06       Impact factor: 3.714

6.  Evidence for two genetic complementation groups in pyruvate carboxylase-deficient human fibroblast cell lines.

Authors:  G L Feldman; B Wolf
Journal:  Biochem Genet       Date:  1980-06       Impact factor: 1.890
  6 in total

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