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13 in total

1. A new patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria treated early with low protein diet.

Authors: L R Gjessing; H A Lunde; T Undrum; H Broch; A Alme; S O Lie
Journal: J Inherit Metab Dis Date: 1986 Impact factor: 4.982

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

Authors: I Inoue; M Koura; T Saheki; K Kayanuma; M Uono; M Nakajima; K Takeshita; R Koike; T Yuasa; T Miyatake
Journal: J Inherit Metab Dis Date: 1987 Impact factor: 4.982

3. Liver pathology in transient neonatal hyperammonemia.

Authors: A Zimmermann; C Bachmann; I Högger; J Gehler; A Mielfried; E Mönch; H Peters
Journal: Virchows Arch A Pathol Anat Histopathol Date: 1983

4. Studies on the pathway from ornithine to proline in cultured skin fibroblasts with reference to the defect in hyperornithinaemia with hyperammonaemia and homocitrullinuria.

Authors: R G Gray; S E Hill; R J Pollitt
Journal: J Inherit Metab Dis Date: 1983 Impact factor: 4.982

5. Comparison of ornithine metabolism in hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome, lysinuric protein intolerance and gyrate atrophy fibroblasts.

Authors: J Botschner; D W Smith; O Simell; C R Scriver
Journal: J Inherit Metab Dis Date: 1989 Impact factor: 4.982

10. Gyrate atrophy of the choroid and retina with hyperornithinemia. Deficient formation of guanidinoacetic acid from arginine.

Authors: I Sipilä; O Simell; P Arjomaa
Journal: J Clin Invest Date: 1980-10 Impact factor: 14.808

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

1. A new patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria treated early with low protein diet.

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

3. Liver pathology in transient neonatal hyperammonemia.

4. Studies on the pathway from ornithine to proline in cultured skin fibroblasts with reference to the defect in hyperornithinaemia with hyperammonaemia and homocitrullinuria.

5. Comparison of ornithine metabolism in hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome, lysinuric protein intolerance and gyrate atrophy fibroblasts.

6. The pH of mitochondria of fibroblasts from a hyperornithinaemia, hyperammonaemia, homocitrullinuria-syndrome patient.

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

Review 8. The biochemical basis of mitochondrial diseases.

9. Ultrastructural changes in fibroblast mitochondria of a patient with HHH-syndrome.

10. Gyrate atrophy of the choroid and retina with hyperornithinemia. Deficient formation of guanidinoacetic acid from arginine.