arginine has been researched along with Amyotonia Congenita in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 3 (75.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cassol, G; de Carvalho Gonçalves, M; de Zorzi, VN; Della-Pace, ID; Farinha, JB; Fighera, MR; Furian, AF; Godinho, DB; Oliveira, MS; Royes, LFF | 1 |
Bailey, TL; O'Connor, TR; Richard, S; Thandapani, P | 1 |
Souayah, N; Tick Chong, PS | 1 |
Inoue, R; Kakimoto, Y; Kanazawa, A; Miyake, M; Sato, M | 1 |
2 review(s) available for arginine and Amyotonia Congenita
Article | Year |
---|---|
Potential therapeutic implications of ergogenic compounds on pathophysiology induced by traumatic brain injury: A narrative review.
Topics: Animals; Arginine; Brain Injuries, Traumatic; Caffeine; Carnitine; Central Nervous System Stimulants; Cognitive Dysfunction; Creatine; Energy Metabolism; Epilepsy, Post-Traumatic; Glutamine; Humans; Mitochondria; Neuromuscular Diseases; Taurine | 2019 |
Defining the RGG/RG motif.
Topics: Alternative Splicing; Amino Acid Motifs; Amino Acid Sequence; Amyotrophic Lateral Sclerosis; Apoptosis; Arginine; DNA Damage; Fragile X Syndrome; Humans; Methylation; Molecular Sequence Data; Neoplasms; Neuromuscular Diseases; Protein Biosynthesis; Protein Interaction Domains and Motifs; Proteins | 2013 |
2 other study(ies) available for arginine and Amyotonia Congenita
Article | Year |
---|---|
Asymmetric phenotype associated with rare myelin protein zero mutation.
Topics: Adult; Aged; Arginine; Autoimmune Diseases of the Nervous System; Child, Preschool; Electromyography; Family Health; Foot Deformities; Functional Laterality; Histidine; Humans; Male; Muscle, Skeletal; Mutation; Myelin P0 Protein; Neural Conduction; Neuromuscular Diseases; Phenotype | 2010 |
Decrease of 3-methylhistidine and increase of NG,NG-dimethylarginine in the urine of patients with muscular dystrophy.
Topics: Adolescent; Adult; Amino Acids; Arginine; Child; Histidine; Humans; Methylhistidines; Middle Aged; Motor Neurons; Muscular Diseases; Muscular Dystrophies; Neuromuscular Diseases | 1979 |