✦ LIBER ✦

Sleep phenotypes of intellectual disability: A polysomnographic evaluation in subjects with Down syndrome and Fragile-X syndrome

✍ Scribed by Silvia Miano; Oliviero Bruni; Maurizio Elia; Lidia Scifo; Arianna Smerieri; Alessia Trovato; Elisabetta Verrillo; Mario G. Terzano; Raffaele Ferri

Book ID: 119216915
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 116 KB
Volume: 119
Category: Article
ISSN: 1388-2457
DOI: 10.1016/j.clinph.2008.03.004

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Behavioral features of Williams Beuren s

Behavioral features of Williams Beuren syndrome compared to Fragile X syndrome and subjects with intellectual disability without defined etiology

✍ D. Pérez-García; R. Granero; F. Gallastegui; L.A. Pérez-Jurado; C. Brun-Gasca 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 133 KB

A solution to limitations of cognitive t

A solution to limitations of cognitive testing in children with intellectual disabilities: the case of fragile X syndrome

✍ David Hessl; Danh V. Nguyen; Cherie Green; Alyssa Chavez; Flora Tassone; Randi J 📂 Article 📅 2008 🏛 BioMed Central 🌐 English ⚖ 429 KB

Prevalence of fragile-X syndrome and FRA

Prevalence of fragile-X syndrome and FRAXE among children with intellectual disability in a Caribbean island, Guadeloupe, French West Indies

✍ A. Elbaz; J. Suédois; M. Duquesnoy; C. Beldjord; C. Berchel; G. Mérault 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 289 KB

A Longitudinal Comparison of Cognitive a

A Longitudinal Comparison of Cognitive and Adaptive Changes in Subjects with Down's Syndrome and an Intellectually Disabled Control Group

✍ J.M. Roeden; F.G. Zitman 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 896 KB

Concurrence of fragile X syndrome and 47

Concurrence of fragile X syndrome and 47, XYY in an individual with a Prader-Willi-like phenotype

✍ Stalker, Heather J. ;Keller, Kory L. ;Gray, Brian A. ;Zori, Roberto T. 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 114 KB 👁 3 views

Deletion of 8.5 Mb, including theFMR1 ge

Deletion of 8.5 Mb, including theFMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth

✍ Parvari, R.; Mumm, S.; Galil, A.; Manor, E.; Bar-David, Y.; Carmi, R. 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 29 KB 👁 2 views

A four-year-old boy with severe psychomotor retardation, facial appearance consistent with the fragile X syndrome, hypotonia, and overgrowth was found to have a deletion including the fragile X gene (FMR1). The breakpoints of the deletion were established between CDR1 and sWXD2905 (approximately 200