(Q52009075)

English

Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH)-syndrome. Ultrastructural changes of mitochondria in cultured dermal fibroblasts of three patients.

scientific article published in March 1996

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scholarly article

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/8739474

Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH)-syndrome. Ultrastructural changes of mitochondria in cultured dermal fibroblasts of three patients. (English)

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/8739474

author name string

Haust MD

1

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/8739474

Dewar RA

2

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/8739474

Gatfield DP

3

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/8739474

Gordon BA

4

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/8739474

publication date

1 March 1996

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/8739474

Pathology, Research and Practice

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/8739474

192

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/8739474

3

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/8739474

271-280

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/8739474

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

1 reference

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7 January 2021

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Hyperornithinemia, Hyperammonemia, and Homocitrullinuria Associated with Decreased Carbamyl Phosphate Synthetase I Activity

1 reference

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7 January 2021

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Ultrastructure of hepatic mitochondria in a child with hyperornithinemia, hyperammonemia, and homocitrullinuria

1 reference

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7 January 2021

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Biochemical analysis of decreased ornithine transport activity in the liver mitochondria from patients with hyperornithinemia, hyperammonemia and homocitrullinuria

1 reference

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7 January 2021

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The mechanism of hyperammonaemia and hyperornithinaemia in the syndrome of hyperornithinaemia, hyperammonaemia with homocitrullinuria

1 reference

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7 January 2021

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Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: neurologic, ophthalmologic, and neuropsychologic examination of six patients.

1 reference

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Clinical, biochemical and ultrastructural study on the pathogenesis of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

1 reference

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Hyperornithinemia, hyperammonemia, and homocitrullinuria: case report and biochemical study

1 reference

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Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria)

1 reference

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7 January 2021

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Hyperornithinemia, hyperammonemia and homocitrullinuria--a case report and study of ornithine metabolism using in vivo deuterium labelling

1 reference

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7 January 2021

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Ornithine loading did not prevent induced hyperammonemia in a patient with hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

1 reference

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Abnormal urinary excretion of polyamines in HHH syndrome (hyperornithinemia associated with hyperammonemia and homocitrullinuria)

1 reference

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7 January 2021

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Episodic hyperammonemia in adult siblings with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0344-0338%2896%2980230-5

7 January 2021

based on heuristic

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Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome: low creatine excretion and effect of citrulline, arginine, or ornithine supplement

1 reference

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7 January 2021

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Proceedings: Hepatic ultrastructure in a child with carbamyl phosphate synthetase deficiency, hyperornithinaemia, hyperammonaemia, and homocitrullinuria

1 reference

https://api.crossref.org/works/10.1016%2FS0344-0338%2896%2980230-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0344-0338%2896%2980230-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0344-0338%2896%2980230-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Reduced ornithine catabolism in cultured fibroblasts and phytohaemagglutinin-stimulated lymphocytes from a patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria

1 reference

https://api.crossref.org/works/10.1016%2FS0344-0338%2896%2980230-5

7 January 2021

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Myogenic foam cells in explants of fatty dots and streaks from rabbit aorta. Morphological studies

1 reference

https://api.crossref.org/works/10.1016%2FS0344-0338%2896%2980230-5

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1016%2FS0344-0338%2896%2980230-5

7 January 2021

based on heuristic

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Menstrual cycle and gonadal steroid effects on symptomatic hyperammonaemia of urea-cycle-based and idiopathic aetiologies

1 reference

https://api.crossref.org/works/10.1016%2FS0344-0338%2896%2980230-5

7 January 2021

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Effect of ammonium chloride on homocitrulline and homoarginine synthesis from lysine

1 reference

https://api.crossref.org/works/10.1016%2FS0344-0338%2896%2980230-5

7 January 2021

based on heuristic

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Identifiers

10.1016/S0344-0338(96)80230-5

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/8739474

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/8739474

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