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Items: 1 to 20 of 116

1.

Is there a social module? Language, face processing, and theory of mind in individuals with williams syndrome.

Karmiloff-Smith A, Klima E, Bellugi U, Grant J, Baron-Cohen S.

J Cogn Neurosci. 1995 Spring;7(2):196-208. doi: 10.1162/jocn.1995.7.2.196.

PMID:
23961824
2.

Development itself is the key to understanding developmental disorders.

Karmiloff-Smith A.

Trends Cogn Sci. 1998 Oct 1;2(10):389-98.

PMID:
21227254
3.

Social-perceptual abilities in adolescents and adults with Williams syndrome.

Skwerer DP, Verbalis A, Schofield C, Faja S, Tager-Flusberg H.

Cogn Neuropsychol. 2006;23(2):338-49. doi: 10.1080/02643290542000076.

PMID:
21049334
4.

Nature and nurture: Williams syndrome across cultures.

Zitzer-Comfort C, Doyle T, Masataka N, Korenberg J, Bellugi U.

Dev Sci. 2007 Nov;10(6):755-62.

PMID:
17973792
5.

Language abilities in Williams syndrome: a critical review.

Brock J.

Dev Psychopathol. 2007 Winter;19(1):97-127.

PMID:
17241486
6.

Atypical epigenesis.

Karmiloff-Smith A.

Dev Sci. 2007 Jan;10(1):84-8. Review.

PMID:
17181704
7.

Anomalous sylvian fissure morphology in Williams syndrome.

Eckert MA, Galaburda AM, Karchemskiy A, Liang A, Thompson P, Dutton RA, Lee AD, Bellugi U, Korenberg JR, Mills D, Rose FE, Reiss AL.

Neuroimage. 2006 Oct 15;33(1):39-45. Epub 2006 Jul 28.

PMID:
16876437
8.

The tortuous route from genes to behavior: A neuroconstructivist approach.

Karmiloff-Smith A.

Cogn Affect Behav Neurosci. 2006 Mar;6(1):9-17. Review.

PMID:
16869225
9.

Prevalence of psychiatric disorders in 4 to 16-year-olds with Williams syndrome.

Leyfer OT, Woodruff-Borden J, Klein-Tasman BP, Fricke JS, Mervis CB.

Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):615-22.

10.

To modulate or not to modulate: differing results in uniquely shaped Williams syndrome brains.

Eckert MA, Tenforde A, Galaburda AM, Bellugi U, Korenberg JR, Mills D, Reiss AL.

Neuroimage. 2006 Sep;32(3):1001-7. Epub 2006 Jun 27.

PMID:
16806978
11.

Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour.

Meyer-Lindenberg A, Mervis CB, Berman KF.

Nat Rev Neurosci. 2006 May;7(5):380-93. Review.

PMID:
16760918
12.

Effects of visual experience on activity-dependent gene regulation in cortex.

Majdan M, Shatz CJ.

Nat Neurosci. 2006 May;9(5):650-9. Epub 2006 Apr 2.

PMID:
16582906
13.

Are numerical impairments syndrome specific? Evidence from Williams syndrome and Down's syndrome.

Paterson SJ, Girelli L, Butterworth B, Karmiloff-Smith A.

J Child Psychol Psychiatry. 2006 Feb;47(2):190-204.

PMID:
16423150
14.

Perceiving facial and vocal expressions of emotion in individuals with Williams syndrome.

Plesa-Skwerer D, Faja S, Schofield C, Verbalis A, Tager-Flusberg H.

Am J Ment Retard. 2006 Jan;111(1):15-26.

PMID:
16332153
15.

GTF2IRD1 in craniofacial development of humans and mice.

Tassabehji M, Hammond P, Karmiloff-Smith A, Thompson P, Thorgeirsson SS, Durkin ME, Popescu NC, Hutton T, Metcalfe K, Rucka A, Stewart H, Read AP, Maconochie M, Donnai D.

Science. 2005 Nov 18;310(5751):1184-7. Epub 2005 Nov 3.

16.

In-depth analysis of spatial cognition in Williams syndrome: A critical assessment of the role of the LIMK1 gene.

Gray V, Karmiloff-Smith A, Funnell E, Tassabehji M.

Neuropsychologia. 2006;44(5):679-85. Epub 2005 Oct 10.

PMID:
16216290
17.

Neural correlates of genetically abnormal social cognition in Williams syndrome.

Meyer-Lindenberg A, Hariri AR, Munoz KE, Mervis CB, Mattay VS, Morris CA, Berman KF.

Nat Neurosci. 2005 Aug;8(8):991-3. Epub 2005 Jul 10.

PMID:
16007084
18.

Is everybody always my friend? Perception of approachability in Williams syndrome.

Frigerio E, Burt DM, Gagliardi C, Cioffi G, Martelli S, Perrett DI, Borgatti R.

Neuropsychologia. 2006;44(2):254-9. Epub 2005 Jul 7.

PMID:
16005478
19.

Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome.

Meyer-Lindenberg A, Mervis CB, Sarpal D, Koch P, Steele S, Kohn P, Marenco S, Morris CA, Das S, Kippenhan S, Mattay VS, Weinberger DR, Berman KF.

J Clin Invest. 2005 Jul;115(7):1888-95. Epub 2005 Jun 9.

20.

Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval.

Zhao C, Avil├ęs C, Abel RA, Almli CR, McQuillen P, Pleasure SJ.

Development. 2005 Jun;132(12):2917-27.

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