Compounds > arginine

arginine and Rett Syndrome

arginine has been researched along with Rett Syndrome in 6 studies

Research

Studies (6)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (33.33)	29.6817
2010's	4 (66.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bao, X; Downs, J; Leonard, H; Williams, S; Wong, K	1
Sheen, V; Torres, AR; Valencia, IM	1
Ballatore, C; Bennaceur-Griscelli, A; Bienvenu, T; Billuart, P; Chang, Q; Dahan, M; Delépine, C; Duboin, A; Herault, Y; Meziane, H; Nectoux, J; Opitz, M; Saillour, Y; Smith, AB; Williams, EC	1
Bebbington, A; Downs, J; Foley, KR; Girdler, S; Jacoby, P; Kaufmann, WE; Leonard, H	1
Kyllerman, M; Lundvall, M; Samuelsson, L	1
Barlow, PN; Bird, AP; Dryden, DT; Free, A; Smith, BO; Wakefield, RI	1

Other Studies

6 other study(ies) available for arginine and Rett Syndrome

Article	Year
Using a large international sample to investigate epilepsy in Rett syndrome. Developmental medicine and child neurology, 2013, Volume: 55, Issue:6 Topics: Adolescent; Adult; Age Factors; Age of Onset; Anticonvulsants; Arginine; Child; Child, Preschool; Cysteine; Epilepsy; Female; Gene Deletion; Genotype; Humans; Infant; Internationality; Methionine; Methyl-CpG-Binding Protein 2; Middle Aged; Mutation; Odds Ratio; Phenotype; Polymorphism, Single Nucleotide; Rett Syndrome; Sampling Studies; Severity of Illness Index; Threonine	2013
Atypical features in MECP2 P152R-associated Rett syndrome. Pediatric neurology, 2013, Volume: 49, Issue:2 Topics: Arginine; Child; Female; Genotype; Humans; Methyl-CpG-Binding Protein 2; Phenotype; Proline; Rett Syndrome	2013
Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes. Human molecular genetics, 2016, Jan-01, Volume: 25, Issue:1 Topics: Acetylation; Animals; Arginine; Astrocytes; Cell Line; Cells, Cultured; Epothilones; Histone Deacetylase 6; Histone Deacetylases; Humans; Male; Methyl-CpG-Binding Protein 2; Mice; Mice, Inbred C57BL; Microtubules; Pluripotent Stem Cells; Rett Syndrome; Transport Vesicles; Tubulin; Tubulin Modulators	2016
Change in gross motor abilities of girls and women with rett syndrome over a 3- to 4-year period. Journal of child neurology, 2011, Volume: 26, Issue:10 Topics: Adolescent; Adult; Age Factors; Arginine; Australia; Disease Progression; Female; Humans; Linear Models; Longitudinal Studies; Methyl-CpG-Binding Protein 2; Motor Skills; Movement Disorders; Mutation; Retrospective Studies; Rett Syndrome; Young Adult	2011
Male Rett phenotypes in T158M and R294X MeCP2-mutations. Neuropediatrics, 2006, Volume: 37, Issue:5 Topics: Arginine; Child, Preschool; DNA Mutational Analysis; Humans; Infant; Male; Methionine; Methyl-CpG-Binding Protein 2; Mutation; Rett Syndrome; Siblings; Tyrosine	2006
DNA recognition by the methyl-CpG binding domain of MeCP2. The Journal of biological chemistry, 2001, Feb-02, Volume: 276, Issue:5 Topics: Alanine; Amino Acid Substitution; Arginine; Aspartic Acid; Chromosomal Proteins, Non-Histone; CpG Islands; DNA; DNA-Binding Proteins; Electrophoresis; Glycine; Humans; Methyl-CpG-Binding Protein 2; Mutagenesis, Site-Directed; Mutation, Missense; Proline; Protein Conformation; Protein Structure, Tertiary; Repressor Proteins; Rett Syndrome	2001