arginine has been researched along with Scoliosis in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (20.00) | 18.2507 |
2000's | 3 (60.00) | 29.6817 |
2010's | 1 (20.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Abe, K; Aoki, Y; Eguchi, Y; Fujimoto, K; Furuya, T; Inage, K; Kanamoto, H; Koda, M; Norimoto, M; Ohtori, S; Orita, S; Suzuki, M; Takahashi, K; Toyoguchi, T; Umimura, T; Yamauchi, K | 1 |
Ignatius, J; Kääriäinen, H; Körkkö, J; Löppönen, T; Lundan, T; Seppänen, U | 1 |
Traboulsi, EI | 1 |
Baránková, L; Horácek, O; Hühne, K; Mazanec, R; Mikesová, E; Rautenstrauss, B; Seeman, P; Vyhnálek, M | 1 |
Avery, N; Crean, JK; Duance, VC; Eisenstein, SM; Menage, J; Roberts, S; Sims, TJ; Smith, S | 1 |
1 review(s) available for arginine and Scoliosis
Article | Year |
---|---|
Childhood-onset osteoarthritis, tall stature, and sensorineural hearing loss associated with Arg75-Cys mutation in procollagen type II gene (COL2A1).
Topics: Adult; Arginine; Arthritis, Juvenile; Body Height; Collagen Type II; Cysteine; Diagnosis, Differential; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Humans; Lumbar Vertebrae; Middle Aged; Mutation; Osteoarthritis; Scoliosis; Syndrome | 2004 |
4 other study(ies) available for arginine and Scoliosis
Article | Year |
---|---|
Pentosidine concentration is associated with degenerative lumbar scoliosis in older women: preliminary results.
Topics: Absorptiometry, Photon; Aged; Aged, 80 and over; Arginine; Biomarkers; Calcifediol; Calcitriol; Case-Control Studies; Female; Femur; Homocysteine; Humans; Kyphosis; Lordosis; Lumbar Vertebrae; Lysine; Middle Aged; Sarcopenia; Scoliosis; Spine | 2018 |
Congenital abnormalities of cranial nerve development: overview, molecular mechanisms, and further evidence of heterogeneity and complexity of syndromes with congenital limitation of eye movements.
Topics: Adenine; Adolescent; Adult; Amino Acid Substitution; Arginine; Child; Child, Preschool; Chromosome Mapping; Chromosomes, Human, Pair 11; Cranial Nerves; Female; Fibrosis; Genes, Recessive; Genetic Variation; Glutamine; Guanine; Humans; Kinesins; Male; Mobius Syndrome; Mutation; Nerve Tissue Proteins; Oculomotor Muscles; Ophthalmoplegia; Pedigree; Phenotype; Scoliosis; Syndrome | 2004 |
Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosis.
Topics: Adolescent; Arginine; Charcot-Marie-Tooth Disease; DNA Mutational Analysis; DNA-Binding Proteins; Female; Glutamine; Humans; Male; Mutation; Neural Conduction; Neurologic Examination; Peripheral Nerves; Radiography; Scoliosis; Trans-Activators; Transcriptional Regulator ERG | 2005 |
Changes in collagen cross-linking in degenerative disc disease and scoliosis.
Topics: Adolescent; Adult; Aged; Aging; Arginine; Child; Chromatography, High Pressure Liquid; Collagen; Cross-Linking Reagents; Dipeptides; Extracellular Matrix; Humans; Intervertebral Disc; Intervertebral Disc Displacement; Lumbar Vertebrae; Lysine; Middle Aged; Scoliosis | 1998 |