Page last updated: 2024-11-04

rolipram and Rett Syndrome

rolipram 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)

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's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mironov, SL1
Skorova, EY1
Kügler, S1

Other Studies

1 other study available for rolipram and Rett Syndrome

ArticleYear
Epac-mediated cAMP-signalling in the mouse model of Rett Syndrome.
    Neuropharmacology, 2011, Volume: 60, Issue:6

    Topics: Animals; Biological Clocks; Brefeldin A; Cyclic AMP; Disease Models, Animal; Female; Guanine Nucleot

2011