Literature DB >> 3123793

Abnormality of citrulline synthesis in liver mitochondria from patients with hyperornithinaemia, hyperammonaemia and homocitrullinuria.

I Inoue1, M Koura, T Saheki, K Kayanuma, M Uono, M Nakajima, K Takeshita, R Koike, T Yuasa, T Miyatake.   

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Year:  1987        PMID： 3123793     DOI： 10.1007/bf01800081

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


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  12 in total

1.  A spectrophotometric method for determination of urea.

Authors:  G CERIOTTI; L SPANDRIO
Journal:  Clin Chim Acta       Date:  1963-03       Impact factor: 3.786

2.  A COLORIMETRIC DETERMINATION OF OROTIC ACID.

Authors:  T ADACHI; A TANIMURA; M ASAHINA
Journal:  J Vitaminol (Kyoto)       Date:  1963-09-10

3.  Ornithinemia, hyperammonemia, and homocitrullinuria. A disease associated with mental retardation and possibly caused by defective mitochondrial transport.

Authors:  V Fell; R J Pollitt; G A Sampson; T Wright
Journal:  Am J Dis Child       Date:  1974-05

4.  Glucagon stimulation of citrulline formation in isolated hepatic mitochondria.

Authors:  R K Yamazaki; G S Graetz
Journal:  Arch Biochem Biophys       Date:  1977-01-15       Impact factor: 4.013

5.  Letter: Metabolic defect in hyperornithinaemia.

Authors:  V E Shih; R Mandell
Journal:  Lancet       Date:  1974-12-21       Impact factor: 79.321

6.  Decreased transport of ornithine across the inner mitochondrial membrane as a cause of hyperornithinaemia.

Authors:  F A Hommes; C K Ho; R A Roesel; M E Coryell; B A Gordon
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

7.  Regulation of urea synthesis. The effect of ammonia on the N-acetylglutamate content of isolated rat liver cells.

Authors:  H Zollner
Journal:  Biochim Biophys Acta       Date:  1981-08-17

8.  Defective ornithine metabolism in cultured skin fibroblasts from patients with the syndrome of hyperornithinemia, hyperammonemia and homocitrullinuria.

Authors:  V E Shih; R Mandell; A Herzfeld
Journal:  Clin Chim Acta       Date:  1982-02-05       Impact factor: 3.786

9.  Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.

Authors:  V E Shih; M L Efron; H W Moser
Journal:  Am J Dis Child       Date:  1969-01

10.  Qualitative and quantitative abnormalities of argininosuccinate synthetase in citrullinemia.

Authors:  T Saheki; A Ueda; M Hosoya; K Kusumi; S Takada; M Tsuda; T Katsunuma
Journal:  Clin Chim Acta       Date:  1981-02-05       Impact factor: 3.786
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  1 in total

1.  Multiple enzyme defects in mitochondria of a case with congenital lactic acidosis and hyperammonaemia.

Authors:  M Kobayashi; T Ichiki; N Sugiyama; T Sano; K Ban; T Tsuboi; H Inagaki; K Okajima; H Sobajima; S Suzuki
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982
  1 in total

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