creatine has been researched along with CBS Deficiency in 3 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Patients with homocystinuria due to remethylation defects have an isolated brain choline deficiency, probably secondary to depletion of labile methyl groups produced by the transmethylation pathway." | 7.74 | Reduced brain choline in homocystinuria due to remethylation defects. ( Blom, HJ; Boulanger, Y; Debray, FG; Decarie, JC; Jakobs, C; Khiat, A; Lambert, M; Levy, E; Lortie, A; Mitchell, GA; Orquin, J; Ramos, F; Roy, MS; Struys, E; Verhoeven, NM, 2008) |
| " Individuals with combined methylmalonic aciduria and homocystinuria have a functional impairment of the creatine synthetic pathway probably secondary to a relative depletion of labile methyl groups." | 7.73 | Creatine metabolism in combined methylmalonic aciduria and homocystinuria. ( Beaudet, AL; Bodamer, OA; Bottiglieri, T; O'Brien, WE; Sahoo, T; Scaglia, F; Stöckler-Ipsiroglu, S; Wagner, C, 2005) |
| "Patients with homocystinuria due to remethylation defects have an isolated brain choline deficiency, probably secondary to depletion of labile methyl groups produced by the transmethylation pathway." | 3.74 | Reduced brain choline in homocystinuria due to remethylation defects. ( Blom, HJ; Boulanger, Y; Debray, FG; Decarie, JC; Jakobs, C; Khiat, A; Lambert, M; Levy, E; Lortie, A; Mitchell, GA; Orquin, J; Ramos, F; Roy, MS; Struys, E; Verhoeven, NM, 2008) |
| " Individuals with combined methylmalonic aciduria and homocystinuria have a functional impairment of the creatine synthetic pathway probably secondary to a relative depletion of labile methyl groups." | 3.73 | Creatine metabolism in combined methylmalonic aciduria and homocystinuria. ( Beaudet, AL; Bodamer, OA; Bottiglieri, T; O'Brien, WE; Sahoo, T; Scaglia, F; Stöckler-Ipsiroglu, S; Wagner, C, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Debray, FG | 1 |
| Boulanger, Y | 1 |
| Khiat, A | 1 |
| Decarie, JC | 1 |
| Orquin, J | 1 |
| Roy, MS | 1 |
| Lortie, A | 1 |
| Ramos, F | 1 |
| Verhoeven, NM | 1 |
| Struys, E | 1 |
| Blom, HJ | 1 |
| Jakobs, C | 1 |
| Levy, E | 1 |
| Mitchell, GA | 1 |
| Lambert, M | 1 |
| Younessi, D | 1 |
| Moseley, K | 1 |
| Yano, S | 1 |
| Bodamer, OA | 1 |
| Sahoo, T | 1 |
| Beaudet, AL | 1 |
| O'Brien, WE | 1 |
| Bottiglieri, T | 1 |
| Stöckler-Ipsiroglu, S | 1 |
| Wagner, C | 1 |
| Scaglia, F | 1 |
3 other studies available for creatine and CBS Deficiency
| Article | Year |
|---|---|
Reduced brain choline in homocystinuria due to remethylation defects.
Topics: Adolescent; Adult; Aspartic Acid; Brain; Brain Chemistry; Child; Child, Preschool; Choline; Choline | 2008 |
Creatine metabolism in combined methylmalonic aciduria and homocystinuria disease revisited.
Topics: Amino Acid Metabolism, Inborn Errors; Creatine; Homocystinuria; Humans; Methylmalonic Acid | 2009 |
Creatine metabolism in combined methylmalonic aciduria and homocystinuria.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Creatine; Female; Glycine; Hom | 2005 |