glutamine and Scoliosis

glutamine has been researched along with Scoliosis in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Traboulsi, EI	1
Baránková, L; Horácek, O; Hühne, K; Mazanec, R; Mikesová, E; Rautenstrauss, B; Seeman, P; Vyhnálek, M	1

Other Studies

2 other study(ies) available for glutamine and Scoliosis

Article	Year
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

Article

Year

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