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Results: 1 to 20 of 170

1.

Expressive and receptive language in Prader-Willi syndrome: report on genetic subtype differences.

Dimitropoulos A, Ferranti A, Lemler M.

J Commun Disord. 2013 Mar-Apr;46(2):193-201. doi: 10.1016/j.jcomdis.2012.12.001. Epub 2012 Dec 21.

PMID:
23295077
[PubMed - indexed for MEDLINE]
2.

Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype.

Milner KM, Craig EE, Thompson RJ, Veltman MW, Thomas NS, Roberts S, Bellamy M, Curran SR, Sporikou CM, Bolton PF.

J Child Psychol Psychiatry. 2005 Oct;46(10):1089-96.

PMID:
16178933
[PubMed - indexed for MEDLINE]
3.

Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome.

Bittel DC, Kibiryeva N, Butler MG.

Pediatrics. 2006 Oct;118(4):e1276-83. Epub 2006 Sep 18.

PMID:
16982806
[PubMed - indexed for MEDLINE]
Free Article
4.

Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes.

Roof E, Stone W, MacLean W, Feurer ID, Thompson T, Butler MG.

J Intellect Disabil Res. 2000 Feb;44 ( Pt 1):25-30.

PMID:
10711647
[PubMed - indexed for MEDLINE]
5.

Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome.

Whittington J, Holland A, Webb T, Butler J, Clarke D, Boer H.

J Intellect Disabil Res. 2004 Feb;48(Pt 2):172-87.

PMID:
14723659
[PubMed - indexed for MEDLINE]
6.

Genetic subtype differences in neural circuitry of food motivation in Prader-Willi syndrome.

Holsen LM, Zarcone JR, Chambers R, Butler MG, Bittel DC, Brooks WM, Thompson TI, Savage CR.

Int J Obes (Lond). 2009 Feb;33(2):273-83. doi: 10.1038/ijo.2008.255. Epub 2008 Dec 2.

PMID:
19048015
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Social responsiveness and competence in Prader-Willi syndrome: direct comparison to autism spectrum disorder.

Dimitropoulos A, Ho A, Feldman B.

J Autism Dev Disord. 2013 Jan;43(1):103-13. doi: 10.1007/s10803-012-1547-3.

PMID:
22576167
[PubMed - indexed for MEDLINE]
8.

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy.

Butler MG, Bittel DC, Kibiryeva N, Talebizadeh Z, Thompson T.

Pediatrics. 2004 Mar;113(3 Pt 1):565-73.

PMID:
14993551
[PubMed - indexed for MEDLINE]
9.

Clinical management of a child with Prader-Willi Syndrome from maternal uniparental disomy (UPD) genetic inheritance.

Bellon-Harn ML.

J Commun Disord. 2005 Nov-Dec;38(6):459-72. Epub 2005 Jun 24.

PMID:
15979635
[PubMed - indexed for MEDLINE]
10.

The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.

Gunay-Aygun M, Schwartz S, Heeger S, O'Riordan MA, Cassidy SB.

Pediatrics. 2001 Nov;108(5):E92.

PMID:
11694676
[PubMed - indexed for MEDLINE]
11.

Differences in behavioural phenotype between parental deletion and maternal uniparental disomy in Prader-Willi syndrome: an ERP study.

Stauder JE, Boer H, Gerits RH, Tummers A, Whittington J, Curfs LM.

Clin Neurophysiol. 2005 Jun;116(6):1464-70. Epub 2005 Apr 26.

PMID:
15978509
[PubMed - indexed for MEDLINE]
12.

Changing rates of genetic subtypes of Prader-Willi syndrome in the UK.

Whittington JE, Butler JV, Holland AJ.

Eur J Hum Genet. 2007 Jan;15(1):127-30. Epub 2006 Sep 6.

PMID:
16957680
[PubMed - indexed for MEDLINE]
Free Article
13.

Cognitive profile in a large French cohort of adults with Prader-Willi syndrome: differences between genotypes.

Copet P, Jauregi J, Laurier V, Ehlinger V, Arnaud C, Cobo AM, Molinas C, Tauber M, Thuilleaux D.

J Intellect Disabil Res. 2010 Mar;54(3):204-15. doi: 10.1111/j.1365-2788.2010.01251.x. Epub 2010 Feb 2.

PMID:
20136683
[PubMed - indexed for MEDLINE]
14.

Autistic-like symptomatology in Prader-Willi syndrome: a review of recent findings.

Dimitropoulos A, Schultz RT.

Curr Psychiatry Rep. 2007 Apr;9(2):159-64. Review.

PMID:
17389128
[PubMed - indexed for MEDLINE]
15.

Relationship between the IQ of people with Prader-Willi syndrome and that of their siblings: evidence for imprinted gene effects.

Whittington J, Holland A, Webb T.

J Intellect Disabil Res. 2009 May;53(5):411-8. doi: 10.1111/j.1365-2788.2009.01157.x. Epub 2009 Feb 4.

PMID:
19207281
[PubMed - indexed for MEDLINE]
16.

Prader-Willi syndrome--a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders.

Veltman MW, Thompson RJ, Roberts SE, Thomas NS, Whittington J, Bolton PF.

Eur Child Adolesc Psychiatry. 2004 Feb;13(1):42-50.

PMID:
14991431
[PubMed - indexed for MEDLINE]
17.

Different distribution of the genetic subtypes of the Prader-Willi syndrome in the elderly.

Sinnema M, van Roozendaal KE, Maaskant MA, Smeets HJ, Engelen JJ, Jonker-Houben N, Schrander-Stumpel CT, Curfs LM.

Eur J Hum Genet. 2010 Sep;18(9):993-8. doi: 10.1038/ejhg.2010.67. Epub 2010 May 12.

PMID:
20461108
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.

Bittel DC, Butler MG.

Expert Rev Mol Med. 2005 Jul 25;7(14):1-20. Review.

PMID:
16038620
[PubMed - indexed for MEDLINE]
19.

Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes.

Kim SJ, Miller JL, Kuipers PJ, German JR, Beaudet AL, Sahoo T, Driscoll DJ.

Eur J Hum Genet. 2012 Mar;20(3):283-90. doi: 10.1038/ejhg.2011.187. Epub 2011 Nov 2.

PMID:
22045295
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Behavior in Prader-Willi syndrome: relationship to genetic subtypes and age.

Dykens EM, Roof E.

J Child Psychol Psychiatry. 2008 Sep;49(9):1001-8. doi: 10.1111/j.1469-7610.2008.01913.x. Epub 2008 Jul 28.

PMID:
18665884
[PubMed - indexed for MEDLINE]

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