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Similar articles for PubMed (Select 21952424)

1.

Prader-Willi syndrome.

Cassidy SB, Schwartz S, Miller JL, Driscoll DJ.

Genet Med. 2011 Sep 26. [Epub ahead of print]

PMID:
21952424
2.

Prader-Willi syndrome.

Cassidy SB, Schwartz S, Miller JL, Driscoll DJ.

Genet Med. 2012 Jan;14(1):10-26. doi: 10.1038/gim.0b013e31822bead0. Epub 2011 Sep 26. Review.

PMID:
22237428
3.

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
4.

Prader-Willi Syndrome.

Driscoll DJ, Miller JL, Schwartz S, Cassidy SB.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2015.
1998 Oct 06 [updated 2014 Jan 23].

5.

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
6.

Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

Butler MG.

Curr Genomics. 2011 May;12(3):204-15. doi: 10.2174/138920211795677877.

7.

Systematic review of the clinical and genetic aspects of Prader-Willi syndrome.

Jin DK.

Korean J Pediatr. 2011 Feb;54(2):55-63. doi: 10.3345/kjp.2011.54.2.55. Epub 2011 Feb 28.

8.

Prader-Willi syndrome.

Cassidy SB.

J Med Genet. 1997 Nov;34(11):917-23. Review.

9.

Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.

Angulo MA, Butler MG, Cataletto ME.

J Endocrinol Invest. 2015 Jun 11. [Epub ahead of print]

PMID:
26062517
10.

Prader-Willi syndrome.

Cassidy SB, Driscoll DJ.

Eur J Hum Genet. 2009 Jan;17(1):3-13. doi: 10.1038/ejhg.2008.165. Epub 2008 Sep 10.

11.

Molecular diagnosis of Prader-Willi syndrome.

Pangkanon S.

J Med Assoc Thai. 2003 Aug;86 Suppl 3:S510-6.

PMID:
14700141
12.

Prader-Willi syndrome with a long-contiguous stretch of homozygosity not covering the critical region.

Yingjun X, Yi Z, Jianzhu W, Yunxia S, Yongzhen C, Liangying Z, Xiangyi J, Qun F.

J Child Neurol. 2015 Mar;30(3):371-7. doi: 10.1177/0883073814535492. Epub 2014 May 22.

PMID:
24859787
13.

[Prader Willi syndrome patients: study of 77 patients].

Poyatos D, Camprubí C, Gabau E, Nosas R, Villatoro S, Coll MD, Guitart M.

Med Clin (Barc). 2009 Nov 7;133(17):649-56. doi: 10.1016/j.medcli.2009.04.051. Epub 2009 Sep 13. Spanish.

PMID:
19748638
14.

[Prader-Willi syndrome].

Beccaria L, Bosio L, Benzi F, Bregani P, Achutegui I, Chiumello G, Livieri C, Trifirò G, de Toni T, Iughetti L, Ragusa L, Salvatoni A, Tonini G, Corrias A, Crinò A.

Ann Ist Super Sanita. 1999;35(2):221-32. Review. Italian.

PMID:
10645655
16.

The genetic basis for Prader-Willi syndrome: the importance of imprinted genes.

Brøndum-Nielsen K.

Acta Paediatr Suppl. 1997 Nov;423:55-7.

PMID:
9401540
17.

Neonatal presentation of Prader Willi sindrome. Personal records.

Maggio MC, Corsello M, Piccione M, Piro E, Giuffrè M, Liotta A.

Minerva Pediatr. 2007 Dec;59(6):817-23.

PMID:
17978792
18.
19.

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
20.

Genetic imprinting: the paradigm of Prader-Willi and Angelman syndromes.

Gurrieri F, Accadia M.

Endocr Dev. 2009;14:20-8. doi: 10.1159/000207473. Epub 2009 Feb 27. Review.

PMID:
19293572
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