Kimonis V - Search Results

1

Nutritional phases in Prader-Willi syndrome.

Miller JL, Lynn CH, Driscoll DC, Goldstone AP, Gold JA, Kimonis V, Dykens E, Butler MG, Shuster JJ, Driscoll DJ. Miller JL, et al. Among authors: kimonis v. Am J Med Genet A. 2011 May;155A(5):1040-9. doi: 10.1002/ajmg.a.33951. Epub 2011 Apr 4. Am J Med Genet A. 2011. PMID: 21465655 Free PMC article.

2

Genetics of craniosynostosis.

Kimonis V, Gold JA, Hoffman TL, Panchal J, Boyadjiev SA. Kimonis V, et al. Semin Pediatr Neurol. 2007 Sep;14(3):150-61. doi: 10.1016/j.spen.2007.08.008. Semin Pediatr Neurol. 2007. PMID: 17980312 Review.

3

Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome.

Su H, Fan W, Coskun PE, Vesa J, Gold JA, Jiang YH, Potluri P, Procaccio V, Acab A, Weiss JH, Wallace DC, Kimonis VE. Su H, et al. Among authors: kimonis ve. Neurosci Lett. 2011 Jan 7;487(2):129-33. doi: 10.1016/j.neulet.2009.06.079. Epub 2009 Jun 27. Neurosci Lett. 2011. PMID: 19563863 Free PMC article.

4

Is gestation in Prader-Willi syndrome affected by the genetic subtype?

Butler MG, Sturich J, Myers SE, Gold JA, Kimonis V, Driscoll DJ. Butler MG, et al. Among authors: kimonis v. J Assist Reprod Genet. 2009 Aug;26(8):461-6. doi: 10.1007/s10815-009-9341-7. Epub 2009 Sep 17. J Assist Reprod Genet. 2009. PMID: 19760168 Free PMC article.

5

Growth standards of infants with Prader-Willi syndrome.

Butler MG, Sturich J, Lee J, Myers SE, Whitman BY, Gold JA, Kimonis V, Scheimann A, Terrazas N, Driscoll DJ. Butler MG, et al. Among authors: kimonis v. Pediatrics. 2011 Apr;127(4):687-95. doi: 10.1542/peds.2010-2736. Epub 2011 Mar 14. Pediatrics. 2011. PMID: 21402637 Free PMC article.

6

Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome.

Henkhaus RS, Kim SJ, Kimonis VE, Gold JA, Dykens EM, Driscoll DJ, Butler MG. Henkhaus RS, et al. Genet Test Mol Biomarkers. 2012 Mar;16(3):178-86. doi: 10.1089/gtmb.2011.0115. Epub 2011 Oct 6. Genet Test Mol Biomarkers. 2012. PMID: 21977908 Free PMC article.

7

Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology.

Gold JA, Ruth C, Osann K, Flodman P, McManus B, Lee HS, Donkervoort S, Khare M, Roof E, Dykens E, Miller JL, Driscoll DJ, Butler MG, Heinemann J, Cassidy S, Kimonis VE. Gold JA, et al. Genet Med. 2014 Feb;16(2):164-9. doi: 10.1038/gim.2013.97. Epub 2013 Aug 8. Genet Med. 2014. PMID: 23928912 Free PMC article.

8

Differential gene expression reveals mitochondrial dysfunction in an imprinting center deletion mouse model of Prader-Willi syndrome.

Yazdi PG, Su H, Ghimbovschi S, Fan W, Coskun PE, Nalbandian A, Knoblach S, Resnick JL, Hoffman E, Wallace DC, Kimonis VE. Yazdi PG, et al. Clin Transl Sci. 2013 Oct;6(5):347-55. doi: 10.1111/cts.12083. Epub 2013 Jul 29. Clin Transl Sci. 2013. PMID: 24127921 Free PMC article.

9

Effect of genetic subtypes and growth hormone treatment on bone mineral density in Prader-Willi syndrome.

Khare M, Gold JA, Wencel M, Billimek J, Surampalli A, Duarte B, Pontello A, Galassetti P, Cassidy S, Kimonis VE. Khare M, et al. J Pediatr Endocrinol Metab. 2014 May;27(5-6):511-8. doi: 10.1515/jpem-2013-0180. J Pediatr Endocrinol Metab. 2014. PMID: 24515997

10

Growth charts for non-growth hormone treated Prader-Willi syndrome.

Butler MG, Lee J, Manzardo AM, Gold JA, Miller JL, Kimonis V, Driscoll DJ. Butler MG, et al. Among authors: kimonis v. Pediatrics. 2015 Jan;135(1):e126-35. doi: 10.1542/peds.2014-1711. Epub 2014 Dec 8. Pediatrics. 2015. PMID: 25489013 Free PMC article.

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