✦ LIBER ✦

COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome

✍ Scribed by Vandana Shashi; Timothy D. Howard; Matcheri S. Keshavan; Jessica Kaczorowski; Margaret N. Berry; Kelly Schoch; Edward J. Spence; Thomas R. Kwapil

Book ID: 116850115
Publisher: Elsevier Science
Year: 2010
Tongue: English
Weight: 141 KB
Volume: 178
Category: Article
ISSN: 0165-1781
DOI: 10.1016/j.psychres.2010.04.048

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Visuospatial and Numerical Cognitive Def

Visuospatial and Numerical Cognitive Deficits in Children with Chromosome 22Q11.2 Deletion Syndrome

✍ Tony J. Simon; Carrie E. Bearden; Donna McDonald Mc-Ginn; Elaine Zackai 📂 Article 📅 2005 🏛 Masson, Italy (now Elsevier Masson) 🌐 English ⚖ 163 KB

Cognitive correlates of a functional COM

Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome

✍ V Shashi; MS Keshavan; TD Howard; MN Berry; MJ Basehore; E Lewandowski; TR Kwapi 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 109 KB

Disabilities and cognition in children a

Disabilities and cognition in children and adolescents with 22q11 deletion syndrome

✍ S Óskarsdóttir; M Belfrage; E Sandstedt; G Viggedal; P Uvebrant 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 1008 KB

COMT genotype predicts longitudinal cogn

COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome

✍ Gothelf, Doron; Eliez, Stephan; Thompson, Tracy; Hinard, Christine; Penniman, La 📂 Article 📅 2005 🏛 Nature Publishing Group 🌐 English ⚖ 118 KB

Overlapping numerical cognition impairme

Overlapping numerical cognition impairments in children with chromosome 22q11.2 deletion or Turner syndromes

✍ T.J. Simon; Y. Takarae; T. DeBoer; D.M. McDonald-McGinn; E.H. Zackai; J.L. Ross 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 403 KB

Cognitive and behavior profile of presch

Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion

✍ Gerdes, Marsha; Solot, Cynthia; Wang, Paul P.; Moss, Edward; LaRossa, Don; Randa 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 19 KB 👁 2 views

A microscopic deletion of chromosome 22q11.2 has been identified in most patients with the DiGeorge, velocardiofacial syndrome, conotruncal anomaly face syndrome, and in some patients with isolated conotruncal cardiac anomalies. This study presents the neurodevelopmental outcome, including cognitive