arginine and Scoliosis

arginine has been researched along with Scoliosis in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's3 (60.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
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, K1
Ignatius, J; Kääriäinen, H; Körkkö, J; Löppönen, T; Lundan, T; Seppänen, U1
Traboulsi, EI1
Baránková, L; Horácek, O; Hühne, K; Mazanec, R; Mikesová, E; Rautenstrauss, B; Seeman, P; Vyhnálek, M1
Avery, N; Crean, JK; Duance, VC; Eisenstein, SM; Menage, J; Roberts, S; Sims, TJ; Smith, S1

Reviews

1 review(s) available for arginine and Scoliosis

ArticleYear
Childhood-onset osteoarthritis, tall stature, and sensorineural hearing loss associated with Arg75-Cys mutation in procollagen type II gene (COL2A1).
    Arthritis and rheumatism, 2004, Dec-15, Volume: 51, Issue:6

    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

Other Studies

4 other study(ies) available for arginine and Scoliosis

ArticleYear
Pentosidine concentration is associated with degenerative lumbar scoliosis in older women: preliminary results.
    European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society, 2018, Volume: 27, Issue:3

    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.
    Transactions of the American Ophthalmological Society, 2004, Volume: 102

    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.
    Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:11

    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.
    Spine, 1998, Dec-01, Volume: 23, Issue:23

    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