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

Results: 10

FMR1 premutation and full mutation molecular mechanisms related to autism.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 3, p. 211, doi. 10.1007/s11689-011-9084-5

By:

Hagerman, Randi;
Au, Jacky;
Hagerman, Paul

Publication type:

Article

Language and sociability: insights from Williams syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 3, p. 185, doi. 10.1007/s11689-011-9086-3

By:

Fishman, Inna;
Yam, Anna;
Bellugi, Ursula;
Mills, Debra

Publication type:

Article

Treatment effects of stimulant medication in young boys with fragile X syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 3, p. 175, doi. 10.1007/s11689-011-9085-4

By:

Roberts, Jane;
Miranda, Margot;
Boccia, Maria;
Janes, Heather;
Tonnsen, Bridgette;
Hatton, Deborah

Publication type:

Article

The neurobiology of mouse models syntenic to human chromosome 15q.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 3, p. 270, doi. 10.1007/s11689-011-9088-1

By:

Takumi, Toru

Publication type:

Article

Targeted treatments for fragile X syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 3, p. 193, doi. 10.1007/s11689-011-9074-7

By:

Berry-Kravis, Elizabeth;
Knox, Andrew;
Hervey, Crystal

Publication type:

Article

Role of MeCP2, DNA methylation, and HDACs in regulating synapse function.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 3, p. 250, doi. 10.1007/s11689-011-9078-3

By:

Kavalali, Ege;
Nelson, Erika;
Monteggia, Lisa

Publication type:

Article

DNA methylation, the early-life social environment and behavioral disorders.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 3, p. 238, doi. 10.1007/s11689-011-9079-2

By:

Szyf, Moshe

Publication type:

Article

A new synaptic player leading to autism risk: Met receptor tyrosine kinase.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 3, p. 282, doi. 10.1007/s11689-011-9081-8

By:

Judson, Matthew;
Eagleson, Kathie;
Levitt, Pat

Publication type:

Article

Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum Disorders.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 3, p. 257, doi. 10.1007/s11689-011-9087-2

By:

De Rubeis, Silvia;
Bagni, Claudia

Publication type:

Article

Prader-Willi syndrome and autism spectrum disorders: an evolving story.

Published in:

Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 3, p. 225, doi. 10.1007/s11689-011-9092-5

By:

Dykens, Elisabeth;
Lee, Evon;
Roof, Elizabeth

Publication type:

Article