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Results: 1 to 20 of 120

Similar articles for PubMed (Select 23967326)

1.

Psychiatric illness and intellectual disability in the Prader-Willi syndrome with different molecular defects--a meta analysis.

Yang L, Zhan GD, Ding JJ, Wang HJ, Ma D, Huang GY, Zhou WH.

PLoS One. 2013 Aug 14;8(8):e72640. doi: 10.1371/journal.pone.0072640. eCollection 2013.

2.

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
3.

Highest accuracy of combined consensus clinical criteria and SNRPN gene molecular markers in diagnosis of Prader-Willi syndrome in Thai patients.

Promkan M, Teingtat S, Stheinkijkarnchai A, Wasant P, Patmasiriwat P.

Clin Chem Lab Med. 2007;45(8):972-80.

PMID:
17867985
4.

Psychiatric illness in a cohort of adults with Prader-Willi syndrome.

Sinnema M, Boer H, Collin P, Maaskant MA, van Roozendaal KE, Schrander-Stumpel CT, Curfs LM.

Res Dev Disabil. 2011 Sep-Oct;32(5):1729-35. doi: 10.1016/j.ridd.2011.02.027. Epub 2011 Mar 31.

PMID:
21454045
5.

Autism spectrum disorders and hyperactive/impulsive behaviors in Japanese patients with Prader-Willi syndrome: a comparison between maternal uniparental disomy and deletion cases.

Ogata H, Ihara H, Murakami N, Gito M, Kido Y, Nagai T.

Am J Med Genet A. 2014 Sep;164A(9):2180-6. doi: 10.1002/ajmg.a.36615. Epub 2014 May 21.

6.

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
7.

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
8.

The phenomenology and diagnosis of psychiatric illness in people with Prader-Willi syndrome.

Soni S, Whittington J, Holland AJ, Webb T, Maina EN, Boer H, Clarke D.

Psychol Med. 2008 Oct;38(10):1505-14. doi: 10.1017/S0033291707002504. Epub 2008 Jan 4.

PMID:
18177526
9.

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.

10.

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
11.

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.

12.

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
13.

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
14.

Genetic studies of Prader-Willi patients provide evidence for conservation of genomic architecture in proximal chromosome 15q.

Hou A, Lin SP, Ho SY, Chen CF, Lin HY, Chen YJ, Huang CY, Chiu HC, Chuang CK, Chen KS.

Ann Hum Genet. 2011 Mar;75(2):211-21. doi: 10.1111/j.1469-1809.2010.00633.x. Epub 2010 Dec 27.

PMID:
21198515
15.

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
16.

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
17.

De novo interstitial duplication of 15q11.2-q13.1 with complex maternal uniparental trisomy for the 15q11-q13 region in a patient with Prader-Willi syndrome.

Burrage LC, Person RE, Flores A, Villanos MT, Bi W, Wiszniewska J, Bacino CA.

Am J Med Genet A. 2012 Oct;158A(10):2557-63. doi: 10.1002/ajmg.a.35549. Epub 2012 Aug 17.

PMID:
22903639
18.

The proportion of uniparental disomy is increased in Prader-Willi syndrome due to an advanced maternal childbearing age in Korea.

Cho SY, Ki CS, Sohn YB, Maeng SH, Jung YJ, Kim SJ, Jin DK.

J Hum Genet. 2013 Mar;58(3):150-4. doi: 10.1038/jhg.2012.148. Epub 2013 Jan 10.

PMID:
23303386
19.

Combined cytogenetic and molecular analyses for the diagnosis of Prader-Willi/Angelman syndromes.

Borelina D, Engel N, Esperante S, Ferreiro V, Ferrer M, Torrado M, Goldschmidt E, Francipane L, Szijan I.

J Biochem Mol Biol. 2004 Sep 30;37(5):522-6.

20.

A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes.

Driscoll DJ, Waters MF, Williams CA, Zori RT, Glenn CC, Avidano KM, Nicholls RD.

Genomics. 1992 Aug;13(4):917-24.

PMID:
1505981
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