Works matching IS 18661947 AND DT 2011 AND VI 3 AND IP 1

Results: 9

Developmental malformation of the corpus callosum: a review of typical callosal development and examples of developmental disorders with callosal involvement.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 3, doi. 10.1007/s11689-010-9059-y

By:

Paul, Lynn

Publication type:

Article

Electrophysiological study of local/global processing in Williams syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 28, doi. 10.1007/s11689-010-9064-1

By:

Key, Alexandra;
Dykens, Elisabeth

Publication type:

Article

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 39, doi. 10.1007/s11689-010-9065-0

By:

Peter, Beate;
Raskind, Wendy;
Matsushita, Mark;
Lisowski, Mark;
Vu, Tiffany;
Berninger, Virginia;
Wijsman, Ellen;
Brkanac, Zoran

Publication type:

Article

Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 57, doi. 10.1007/s11689-010-9067-y

By:

Cordeiro, Lisa;
Ballinger, Elizabeth;
Hagerman, Randi;
Hessl, David

Publication type:

Article

Angelman syndrome: advancing the research frontier of neurodevelopmental disorders.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 50, doi. 10.1007/s11689-010-9066-z

By:

Philpot, Benjamin;
Thompson, Coral;
Franco, Lisa;
Williams, Charles

Publication type:

Article

How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome?

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 68, doi. 10.1007/s11689-010-9069-9

By:

Beaton, Elliott;
Simon, Tony

Publication type:

Article

Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 76, doi. 10.1007/s11689-010-9070-3

By:

Stoddard, Joel;
Beckett, Laurel;
Simon, Tony

Publication type:

Article

List of reviewers for 2010.

Published in:: Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 2, doi. 10.1007/s11689-011-9073-8
Publication type:: Article

Cover art description.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 1, doi. 10.1007/s11689-011-9075-6

By:

Piven, Joseph

Publication type:

Article