𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Double-blind, placebo-controlled study ofL-acetylcarnitine for the treatment of hyperactive behavior in fragile X syndrome

✍ Scribed by Torrioli, M.G.; Vernacotola, S.; Mariotti, P.; Bianchi, E.; Calvani, M.; De Gaetano, A.; Chiurazzi, P.; Neri, G.


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
5 KB
Volume
87
Category
Article
ISSN
0148-7299
DOI
10.1002/(sici)1096-8628(19991203)87:4<366::aid-ajmg18>3.0.co;2-f

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Longitudinal course of behavioral and em
✍ Einfeld, Stewart; Tonge, Bruce; Turner, Gillian πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 33 KB πŸ‘ 1 views

We describe a follow-up of a study of behavior and emotional problems in a cohort of young people with Fragile X syndrome over 7 years. The study demonstrates that there is substantial persistence of the overall level of behavior and emotional problems. However, there are changes in certain types of

Frontal-subcortical hypofunction in the
✍ Hjalgrim, Helle; Jacobsen, Torsten B.; NοΏ½rgaard, Karin; Lou, Hans C.; BrοΏ½ndum-Ni πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 10 KB πŸ‘ 2 views

Fragile X syndrome (FRAXA) is the most common form of inherited mental retardation. The syndrome is caused by a CGG-expansion mutation in the gene FMR-1, located at Xq27.3. The morphologic anomalies in this syndrome can be subtle: elongated face, large ears, and macro-orchidism. More striking is the

Dental maturity is advanced in fragile X
✍ Kotilainen, J.; Pirinen, S. πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 13 KB πŸ‘ 2 views

Fragile X (FraX) syndrome is the most common cause of inherited mental retardation. The FraX gene (FMR1) has been cloned, and the mutation causing the disease is now known. We estimated the effect of FraX on dental development in 28 affected boys (aged 4.9-17.6 years) and three carrier girls (aged 5