glutamine and Child Development Deviations

glutamine has been researched along with Child Development Deviations in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bakkers, JPW; Bakkers, MJG; Bhogal, AA; Black, GCM; Dansen, TB; Duran, KJ; Houwen, RHJ; Jans, JJM; Klomp, DWJ; Kroes, HY; Pouwels, PJW; Prinsen, HCMT; Ramos, RJJ; Rehmann, H; Rumping, L; Savelberg, SMC; Schellekens, PAW; Taylor, RL; Tessadori, F; van der Knaap, MS; van Haaften, G; van Hasselt, PM; Verhoeven-Duif, NM; Vringer, E; Wijnen, JP; Zwartkruis, FJT1
Brand-Arzamendi, K; Dobritzsch, D; Dolzhenko, E; Drögemöller, BI; Eberle, MA; Geraghty, MT; Hayward, B; Jones, MJ; Karbassi, F; Kobor, MS; Koster, J; Kumari, D; Leen, R; Li, M; MacIsaac, J; McDonald, C; Meijer, J; Nguyen, C; Pouladi, MA; Rajan-Babu, IS; Richmond, PA; Ross, CJ; Santra, S; Scherer, SW; Sim, B; Tarailo-Graovac, M; Trost, B; Tseng, LA; Turkenburg, M; Usdin, K; van Karnebeek, CDM; van Kuilenburg, ABP; van Vugt, JJFA; van Weeghel, M; Veldink, JH; Walia, JS; Wanders, RJA; Wang, Y; Wasserman, WW; Waterham, HR; Wen, XY; Wright, GEB; Xu, X; Yuen, RKC; Zhang, J1

Other Studies

2 other study(ies) available for glutamine and Child Development Deviations

ArticleYear
GLS hyperactivity causes glutamate excess, infantile cataract and profound developmental delay.
    Human molecular genetics, 2019, 01-01, Volume: 28, Issue:1

    Topics: Adolescent; Animals; Brain; Cataract; Child, Preschool; Developmental Disabilities; Disease Models, Animal; Female; Fibroblasts; Gain of Function Mutation; Glutamate-Ammonia Ligase; Glutamic Acid; Glutaminase; Glutamine; HEK293 Cells; Humans; Male; Oxidative Stress; Reactive Oxygen Species; Zebrafish

2019
Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in
    The New England journal of medicine, 2019, 04-11, Volume: 380, Issue:15

    Topics: Amino Acid Metabolism, Inborn Errors; Ataxia; Atrophy; Cerebellum; Child, Preschool; Developmental Disabilities; Female; Genotype; Glutaminase; Glutamine; Humans; Male; Microsatellite Repeats; Mutation; Phenotype; Polymerase Chain Reaction; Whole Genome Sequencing

2019