Creatine corrects muscle 31P spectrum in gyrate atrophy with hyperornithinaemia. (Q54276250)

27 May 2018

title

Creatine corrects muscle 31P spectrum in gyrate atrophy with hyperornithinaemia. (English)

1 reference

27 May 2018

author name string

Heinänen K

1

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27 May 2018

Näntö-Salonen K

2

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27 May 2018

Komu M

3

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27 May 2018

Erkintalo M

4

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27 May 2018

Alanen A

5

1 reference

27 May 2018

Heinonen OJ

6

1 reference

27 May 2018

Pulkki K

7

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27 May 2018

Nikoskelainen E

8

1 reference

27 May 2018

Sipilä I

9

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27 May 2018

Simell O

10

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27 May 2018

publication date

1 December 1999

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27 May 2018

European Journal of Clinical Investigation

published in

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27 May 2018

volume

29

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27 May 2018

issue

12

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27 May 2018

page(s)

1060-1065

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27 May 2018

Raised plasma-ornithine and gyrate atrophy of the choroid and retina.

cites work

1 reference

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L-Ornithine-ketoacid-transaminase deficiency in cultured fibroblasts of a patient with hyperornithinaemia and gyrate atrophy of the choroid and retina

21 January 2018

1 reference

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Skeletal muscle of patients with gyrate atrophy of the choroid and retina and hyperornithinaemia in ultralow-field magnetic resonance imaging and computed tomography.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2362.1999.00569.X

Inhibition of arginine-glycine amidinotransferase by ornithine. A possible mechanism for the muscular and chorioretinal atrophies in gyrate atrophy of the choroid and retina with hyperornithinemia

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2362.1999.00569.X

Creatine supplementation in health and disease. Effects of chronic creatine ingestion in vivo: down-regulation of the expression of creatine transporter isoforms in skeletal muscle.

21 January 2018

1 reference

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Creatine deficiency in the brain: a new, treatable inborn error of metabolism

21 January 2018

1 reference

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Creatine replacement therapy in guanidinoacetate methyltransferase deficiency, a novel inborn error of metabolism.

21 January 2018

1 reference

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Guanidinoacetate methyltransferase deficiency: new clinical features.

21 January 2018

1 reference

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Mitochondrial regulation of phosphocreatine/inorganic phosphate ratios in exercising human muscle: a gated 31P NMR study

21 January 2018

1 reference

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Control of energetic processes in contracting human skeletal muscle

21 January 2018

1 reference

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Mammalian skeletal muscle fibers distinguished by contents of phosphocreatine, ATP, and Pi.

21 January 2018

1 reference

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Reduced brain creatine in gyrate atrophy of the choroid and retina with hyperornithinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2362.1999.00569.X

Extracellular creatine regulates creatine transport in rat and human muscle cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2362.1999.00569.X

Creatine transport in cultured cells of rat and mouse brain.

21 January 2018

1 reference

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10.1046/J.1365-2362.1999.00569.X

21 January 2018

Identifiers

DOI

1 reference

27 May 2018

release_ri6qymrbo5atvpqb25izk7wov4

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ri6qymrbo5atvpqb25izk7wov4

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

10583455

1 reference

27 May 2018