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Items: 1 to 20 of 112

1.

Cerebral and cerebellar MRI volumes in Williams syndrome.

Osório A, Soares JM, Prieto MF, Vasconcelos C, Fernandes C, Sousa S, Carracedo A, Gonçalves OF, Sampaio A.

Res Dev Disabil. 2014 Apr;35(4):922-8. doi: 10.1016/j.ridd.2013.12.014. Epub 2014 Feb 14.

PMID:
24529862
2.

3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry.

Chiang MC, Reiss AL, Lee AD, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Toga AW, Thompson PM.

Neuroimage. 2007 Jul 15;36(4):1096-109. Epub 2007 Apr 20.

3.

Regional brain differences in cortical thickness, surface area and subcortical volume in individuals with Williams syndrome.

Meda SA, Pryweller JR, Thornton-Wells TA.

PLoS One. 2012;7(2):e31913. doi: 10.1371/journal.pone.0031913. Epub 2012 Feb 15. Erratum in: PLoS One. 2012;7(5): doi/10.1371/annotation/e4ec835e-932f-4956-b9fd-7113eee67347.

4.

Cerebellar vermis abnormalities and cognitive functions in individuals with Williams syndrome.

Menghini D, Di Paola M, Murri R, Costanzo F, Caltagirone C, Vicari S, Petrosini L.

Res Dev Disabil. 2013 Jul;34(7):2118-26. doi: 10.1016/j.ridd.2013.03.026. Epub 2013 Apr 30.

PMID:
23643765
5.

Quantitative analysis of gray and white matter in Williams syndrome.

Faria AV, Landau B, O'Hearn KM, Li X, Jiang H, Oishi K, Zhang J, Mori S.

Neuroreport. 2012 Mar 28;23(5):283-9. doi: 10.1097/WNR.0b013e3283505b62.

6.

Smaller grey matter volumes in the anterior cingulate cortex and greater cerebellar volumes in patients with long-term remission of Cushing's disease: a case-control study.

Andela CD, van der Werff SJ, Pannekoek JN, van den Berg SM, Meijer OC, van Buchem MA, Rombouts SA, van der Mast RC, Romijn JA, Tiemensma J, Biermasz NR, van der Wee NJ, Pereira AM.

Eur J Endocrinol. 2013 Oct 21;169(6):811-9. doi: 10.1530/EJE-13-0471. Print 2013 Dec.

7.

An experiment of nature: brain anatomy parallels cognition and behavior in Williams syndrome.

Reiss AL, Eckert MA, Rose FE, Karchemskiy A, Kesler S, Chang M, Reynolds MF, Kwon H, Galaburda A.

J Neurosci. 2004 May 26;24(21):5009-15.

8.

MRI amygdala volume in Williams Syndrome.

Capitão L, Sampaio A, Sampaio C, Vasconcelos C, Férnandez M, Garayzábal E, Shenton ME, Gonçalves OF.

Res Dev Disabil. 2011 Nov-Dec;32(6):2767-72. doi: 10.1016/j.ridd.2011.05.033. Epub 2011 Jul 12.

PMID:
21752593
9.

Abnormal cortical complexity and thickness profiles mapped in Williams syndrome.

Thompson PM, Lee AD, Dutton RA, Geaga JA, Hayashi KM, Eckert MA, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Toga AW, Reiss AL.

J Neurosci. 2005 Apr 20;25(16):4146-58.

10.

Relationship between brain abnormalities and cognitive profile in Williams syndrome.

Menghini D, Di Paola M, Federico F, Vicari S, Petrosini L, Caltagirone C, Bozzali M.

Behav Genet. 2011 May;41(3):394-402. doi: 10.1007/s10519-010-9419-0. Epub 2010 Dec 10.

PMID:
21153484
11.

MRI assessment of superior temporal gyrus in Williams syndrome.

Sampaio A, Sousa N, Férnandez M, Vasconcelos C, Shenton ME, Gonçalves OF.

Cogn Behav Neurol. 2008 Sep;21(3):150-6. doi: 10.1097/WNN.0b013e31817720e4.

12.

Preliminary evidence of abnormal white matter related to the fusiform gyrus in Williams syndrome: a diffusion tensor imaging tractography study.

Haas BW, Hoeft F, Barnea-Goraly N, Golarai G, Bellugi U, Reiss AL.

Genes Brain Behav. 2012 Feb;11(1):62-8. doi: 10.1111/j.1601-183X.2011.00733.x. Epub 2011 Oct 19.

13.

Association between cerebral shape and social use of language in Williams syndrome.

Gothelf D, Searcy YM, Reilly J, Lai PT, Lanre-Amos T, Mills D, Korenberg JR, Galaburda A, Bellugi U, Reiss AL.

Am J Med Genet A. 2008 Nov 1;146A(21):2753-61. doi: 10.1002/ajmg.a.32507.

14.

Patterns of magnetic resonance imaging abnormalities in symptomatic patients with Krabbe disease correspond to phenotype.

Abdelhalim AN, Alberico RA, Barczykowski AL, Duffner PK.

Pediatr Neurol. 2014 Feb;50(2):127-34. doi: 10.1016/j.pediatrneurol.2013.10.001. Epub 2013 Oct 11.

PMID:
24262341
15.

Brain structural differences associated with the behavioural phenotype in children with Williams syndrome.

Campbell LE, Daly E, Toal F, Stevens A, Azuma R, Karmiloff-Smith A, Murphy DG, Murphy KC.

Brain Res. 2009 Mar 3;1258:96-107. doi: 10.1016/j.brainres.2008.11.101. Epub 2008 Dec 11.

PMID:
19118537
16.

Dissociations of cerebral cortex, subcortical and cerebral white matter volumes in autistic boys.

Herbert MR, Ziegler DA, Deutsch CK, O'Brien LM, Lange N, Bakardjiev A, Hodgson J, Adrien KT, Steele S, Makris N, Kennedy D, Harris GJ, Caviness VS Jr.

Brain. 2003 May;126(Pt 5):1182-92.

17.

cerebellar atrophy after moderate-to-severe pediatric traumatic brain injury.

Spanos GK, Wilde EA, Bigler ED, Cleavinger HB, Fearing MA, Levin HS, Li X, Hunter JV.

AJNR Am J Neuroradiol. 2007 Mar;28(3):537-42.

18.

In vivo evidence of cerebellar atrophy and cerebral white matter loss in Huntington disease.

Fennema-Notestine C, Archibald SL, Jacobson MW, Corey-Bloom J, Paulsen JS, Peavy GM, Gamst AC, Hamilton JM, Salmon DP, Jernigan TL.

Neurology. 2004 Sep 28;63(6):989-95.

PMID:
15452288
19.

Antidepressant treatment normalizes white matter volume in patients with major depression.

Zeng LL, Liu L, Liu Y, Shen H, Li Y, Hu D.

PLoS One. 2012;7(8):e44248. doi: 10.1371/journal.pone.0044248. Epub 2012 Aug 30.

20.

MRI neuroanatomy in young girls with autism: a preliminary study.

Bloss CS, Courchesne E.

J Am Acad Child Adolesc Psychiatry. 2007 Apr;46(4):515-23.

PMID:
17420687
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