Page last updated: 2024-08-26

taraxerol and Rett Syndrome

taraxerol has been researched along with Rett Syndrome in 1 studies

*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) [MeSH]

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (100.00)2.80

Authors

AuthorsStudies
Asaro, F; Cortesi, A; Gardossi, L; Kašpar, J; Pezzella, C; Roggero, OM; Spennato, M; Tongiorgi, E; Varriale, S1

Other Studies

1 other study(ies) available for taraxerol and Rett Syndrome

ArticleYear
Neuroprotective Properties of Cardoon Leaves Extracts against Neurodevelopmental Deficits in an In Vitro Model of Rett Syndrome Depend on the Extraction Method and Harvest Time.
    Molecules (Basel, Switzerland), 2022, Dec-10, Volume: 27, Issue:24

    Topics: Cynara; Plant Extracts; Rett Syndrome; Squalene

2022