✦ LIBER ✦

Sleep and EEG features in genetic models of Down syndrome

✍ Scribed by Damien Colas; Janice S. Valletta; Ryoko Takimoto-Kimura; Seiji Nishino; Nobuhiro Fujiki; William C. Mobley; Emmanuel Mignot

Book ID: 113812175
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 567 KB
Volume: 30
Category: Article
ISSN: 0969-9961
DOI: 10.1016/j.nbd.2007.07.014

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Early Clinical and EEG Features of Infan

Early Clinical and EEG Features of Infantile Spasms in Down Syndrome

✍ M. L. Silva; C. Cieuta; R. Guerrini; P. Plouin; M. O. Livet; O. Dulac 📂 Article 📅 1996 🏛 Wiley (Blackwell Publishing) 🌐 English ⚖ 520 KB

THE EEG AND INCIDENCE OF EPILEPSY IN DOW

THE EEG AND INCIDENCE OF EPILEPSY IN DOWN'S SYNDROME

✍ SHEILA R. TANGYE 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 119 KB

Parental report of sleep problems in Dow

Parental report of sleep problems in Down syndrome

✍ J. H. Breslin; J. O. Edgin; R. R. Bootzin; J. L. Goodwin; L. Nadel 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 196 KB

Sleep and circadian abnormalities in pat

Sleep and circadian abnormalities in patients with cirrhosis: features of delayed sleep phase syndrome?

✍ Sara Montagnese; Benita Middleton; Ali R. Mani; Debra J. Skene; Marsha Y. Morgan 📂 Article 📅 2009 🏛 Springer 🌐 English ⚖ 320 KB

The genetics of sleep disorders in human

The genetics of sleep disorders in humans: Narcolepsy, restless legs syndrome, and obstructive sleep apnea syndrome

✍ Emrah Caylak 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 165 KB 👁 2 views

Genetic mechanisms involved in the pheno

Genetic mechanisms involved in the phenotype of Down syndrome

✍ Patterson, David 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 161 KB

## Abstract Down syndrome (DS) is the most common genetic cause of significant intellectual disability in the human population, occurring in roughly 1 in 700 live births. The ultimate cause of DS is trisomy of all or part of the set of genes located on chromosome 21. How this trisomy leads to the p