glycocyamine has been researched along with Muscle Disorders in 8 studies
glycocyamine: RN given refers to parent cpd; structure
guanidinoacetate : A monocarboxylic acid anion that is the conjugate base of guanidinoacetic acid, obtained by deprotonation of the carboxy group.
guanidinoacetic acid : The N-amidino derivative of glycine.
Excerpt | Relevance | Reference |
---|---|---|
"Treatment with creatine monohydrate (100-800 mg/kg/day) resulted in almost complete restoration of brain creatine levels and significant improvement of myopathy." | 1.42 | Arginine:glycine amidinotransferase (AGAT) deficiency: Clinical features and long term outcomes in 16 patients diagnosed worldwide. ( Apatean, D; Battini, R; DeBrosse, S; Dessoffy, K; Dowling, MD; Edvardson, S; Eichler, F; Johnston, K; Koeller, DM; Nouioua, S; Stockler-Ipsiroglu, S; Tazir, M; Verma, A; Wierenga, AM; Wierenga, KJ; Wong, LJ; Zhang, V, 2015) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (37.50) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 3 (37.50) | 24.3611 |
2020's | 2 (25.00) | 2.80 |
Authors | Studies |
---|---|
Balestrino, M | 1 |
Adriano, E | 1 |
Neu, A | 1 |
Hornig, S | 1 |
Sasani, A | 1 |
Isbrandt, D | 1 |
Gerloff, C | 1 |
Tsikas, D | 1 |
Schwedhelm, E | 1 |
Choe, CU | 1 |
Córdova-Noboa, HA | 2 |
Oviedo-Rondón, EO | 2 |
Sarsour, AH | 2 |
Barnes, J | 2 |
Sapcota, D | 1 |
López, D | 1 |
Gross, L | 1 |
Rademacher-Heilshorn, M | 2 |
Braun, U | 2 |
Ferzola, P | 1 |
Stockler-Ipsiroglu, S | 1 |
Apatean, D | 1 |
Battini, R | 1 |
DeBrosse, S | 1 |
Dessoffy, K | 1 |
Edvardson, S | 1 |
Eichler, F | 1 |
Johnston, K | 1 |
Koeller, DM | 1 |
Nouioua, S | 1 |
Tazir, M | 1 |
Verma, A | 1 |
Dowling, MD | 1 |
Wierenga, KJ | 1 |
Wierenga, AM | 1 |
Zhang, V | 1 |
Wong, LJ | 1 |
CUMINGS, JN | 1 |
ALDES, JH | 1 |
Afting, EG | 1 |
Bernhardt, W | 1 |
Janzen, RW | 1 |
Röthig, HJ | 1 |
8 other studies available for glycocyamine and Muscle Disorders
Article | Year |
---|---|
Presence of guanidinoacetate may compensate creatine absence and account for less statin-induced muscle damage in GAMT-deficient compared to AGAT-deficient mice.
Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Animals; Creatine; Developmental Disabili | 2020 |
Creatine, guanidinoacetate and homoarginine in statin-induced myopathy.
Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Animals; Creatine; Developmental Disabili | 2020 |
Effect of guanidinoacetic acid supplementation on live performance, meat quality, pectoral myopathies and blood parameters of male broilers fed corn-based diets with or without poultry by-products.
Topics: Animal Feed; Animal Nutritional Physiological Phenomena; Animals; Blood Chemical Analysis; Chickens; | 2018 |
Performance, meat quality, and pectoral myopathies of broilers fed either corn or sorghum based diets supplemented with guanidinoacetic acid.
Topics: Animal Feed; Animal Nutritional Physiological Phenomena; Animals; Chickens; Diet; Dietary Supplement | 2018 |
Arginine:glycine amidinotransferase (AGAT) deficiency: Clinical features and long term outcomes in 16 patients diagnosed worldwide.
Topics: Adolescent; Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Crea | 2015 |
Creatine and guanidoacetic acid metabolism in muscle disease.
Topics: Acetates; Blood; Creatine; Disease; Glycine; Muscles; Muscular Diseases; Urine | 1953 |
Glycocyamine betaine as an adjunct in the treatment of neuromuscular disease patients.
Topics: Amidines; Betaine; Choline; Disease; Glycine; Humans; Muscles; Muscular Diseases; Neuromuscular Dise | 1957 |
Quantitative importance of non-skeletal-muscle N tau-methylhistidine and creatine in human urine.
Topics: Creatine; Creatinine; Glycine; Histidine; Humans; Male; Methylhistidines; Middle Aged; Muscles; Musc | 1981 |