Page last updated: 2024-10-27

gaboxadol and Rett Syndrome

gaboxadol has been researched along with Rett Syndrome in 2 studies

gaboxadol: GABA agonist; inhibitor of GABA uptake systems; structure

Rett Syndrome: An inherited neurological developmental disorder that is associated with X-LINKED INHERITANCE and may be lethal in utero to hemizygous males. The affected female is normal until the age of 6-25 months when progressive loss of voluntary control of hand movements and communication skills; ATAXIA; SEIZURES; autistic behavior; intermittent HYPERVENTILATION; and HYPERAMMONEMIA appear. (From Menkes, Textbook of Child Neurology, 5th ed, p199)

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
Zhong, W2
Cui, N2
Jin, X1
Oginsky, MF1
Wu, Y2
Zhang, S1
Bondy, B1
Johnson, CM2
Jiang, C2
Xing, H1

Other Studies

2 other studies available for gaboxadol and Rett Syndrome

ArticleYear
Methyl CpG Binding Protein 2 Gene Disruption Augments Tonic Currents of γ-Aminobutyric Acid Receptors in Locus Coeruleus Neurons: IMPACT ON NEURONAL EXCITABILITY AND BREATHING.
    The Journal of biological chemistry, 2015, Jul-24, Volume: 290, Issue:30

    Topics: Animals; Bicuculline; GABA Agonists; GABAergic Neurons; Humans; Isoxazoles; Locus Coeruleus; Methyl-

2015
Effects of chronic exposure to low dose THIP on brainstem neuronal excitability in mouse models of Rett syndrome: Evidence from symptomatic females.
    Neuropharmacology, 2017, Volume: 116

    Topics: Animals; Brain Stem; Disease Models, Animal; Dose-Response Relationship, Drug; Double-Blind Method;

2017