arginine and Amyotonia Congenita

arginine has been researched along with Amyotonia Congenita in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (75.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cassol, G; de Carvalho Gonçalves, M; de Zorzi, VN; Della-Pace, ID; Farinha, JB; Fighera, MR; Furian, AF; Godinho, DB; Oliveira, MS; Royes, LFF1
Bailey, TL; O'Connor, TR; Richard, S; Thandapani, P1
Souayah, N; Tick Chong, PS1
Inoue, R; Kakimoto, Y; Kanazawa, A; Miyake, M; Sato, M1

Reviews

2 review(s) available for arginine and Amyotonia Congenita

ArticleYear
Potential therapeutic implications of ergogenic compounds on pathophysiology induced by traumatic brain injury: A narrative review.
    Life sciences, 2019, Sep-15, Volume: 233

    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.
    Molecular cell, 2013, Jun-06, Volume: 50, Issue:5

    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

Other Studies

2 other study(ies) available for arginine and Amyotonia Congenita

ArticleYear
Asymmetric phenotype associated with rare myelin protein zero mutation.
    Journal of clinical neuromuscular disease, 2010, Volume: 11, Issue:3

    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.
    Metabolism: clinical and experimental, 1979, Volume: 28, Issue:8

    Topics: Adolescent; Adult; Amino Acids; Arginine; Child; Histidine; Humans; Methylhistidines; Middle Aged; Motor Neurons; Muscular Diseases; Muscular Dystrophies; Neuromuscular Diseases

1979