creatine has been researched along with Gyrate Atrophy in 4 studies
Gyrate Atrophy: Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Eye fundus destruction and type II muscle fiber atrophy in gyrate atrophy of the choroid and retina with hyperornithinaemia (GA) may be mediated by elevated ornithine concentrations which strongly inhibit creatine biosynthesis." | 9.09 | Creatine corrects muscle 31P spectrum in gyrate atrophy with hyperornithinaemia. ( Alanen, A; Erkintalo, M; Heinänen, K; Heinonen, OJ; Komu, M; Näntö-Salonen, K; Nikoskelainen, E; Pulkki, K; Simell, O; Sipilä, I, 1999) |
| "Eye fundus destruction and type II muscle fiber atrophy in gyrate atrophy of the choroid and retina with hyperornithinaemia (GA) may be mediated by elevated ornithine concentrations which strongly inhibit creatine biosynthesis." | 5.09 | Creatine corrects muscle 31P spectrum in gyrate atrophy with hyperornithinaemia. ( Alanen, A; Erkintalo, M; Heinänen, K; Heinonen, OJ; Komu, M; Näntö-Salonen, K; Nikoskelainen, E; Pulkki, K; Simell, O; Sipilä, I, 1999) |
| "In gyrate atrophy of the choroid and retina with hyperornithinaemia (GA), a genetically determined deficiency of ornithine delta-aminotransferase activity leads to high ornithine concentrations in body fluids." | 5.09 | Central nervous system involvement in gyrate atrophy of the choroid and retina with hyperornithinaemia. ( Alanen, A; Erkintalo, M; Heinänen, K; Heinonen, OJ; Jääskeläinen, S; Lundbom, N; Näntö-Salonen, K; Simell, O; Valtonen, M, 1999) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Joncquel-Chevalier Curt, M | 1 |
| Voicu, PM | 1 |
| Fontaine, M | 1 |
| Dessein, AF | 1 |
| Porchet, N | 1 |
| Mention-Mulliez, K | 1 |
| Dobbelaere, D | 1 |
| Soto-Ares, G | 1 |
| Cheillan, D | 1 |
| Vamecq, J | 1 |
| Valayannopoulos, V | 1 |
| Boddaert, N | 1 |
| Mention, K | 1 |
| Touati, G | 1 |
| Barbier, V | 1 |
| Chabli, A | 1 |
| Sedel, F | 1 |
| Kaplan, J | 1 |
| Dufier, JL | 1 |
| Seidenwurm, D | 1 |
| Rabier, D | 1 |
| Saudubray, JM | 1 |
| de Lonlay, P | 1 |
| Heinänen, K | 2 |
| Näntö-Salonen, K | 2 |
| Komu, M | 1 |
| Erkintalo, M | 2 |
| Alanen, A | 2 |
| Heinonen, OJ | 2 |
| Pulkki, K | 1 |
| Nikoskelainen, E | 1 |
| Sipilä, I | 1 |
| Simell, O | 2 |
| Valtonen, M | 1 |
| Jääskeläinen, S | 1 |
| Lundbom, N | 1 |
1 review available for creatine and Gyrate Atrophy
| Article | Year |
|---|---|
Creatine biosynthesis and transport in health and disease.
Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Amino Acid Transport Systems, Basic; AMP- | 2015 |
2 trials available for creatine and Gyrate Atrophy
| Article | Year |
|---|---|
Creatine corrects muscle 31P spectrum in gyrate atrophy with hyperornithinaemia.
Topics: Adolescent; Adult; Child; Creatine; Dietary Supplements; Female; Glycine; Gyrate Atrophy; Humans; Ma | 1999 |
Central nervous system involvement in gyrate atrophy of the choroid and retina with hyperornithinaemia.
Topics: Adolescent; Adult; Aged; Brain; Central Nervous System; Child; Child, Preschool; Choroid; Creatine; | 1999 |
1 other study available for creatine and Gyrate Atrophy
| Article | Year |
|---|---|
Secondary creatine deficiency in ornithine delta-aminotransferase deficiency.
Topics: Adolescent; Adult; Aggression; Apraxias; Brain; Child; Creatine; Epilepsy; Female; Gyrate Atrophy; H | 2009 |