Kimonis VE - Search Results

1

Genetic Subtype-Phenotype Analysis of Growth Hormone Treatment on Psychiatric Behavior in Prader-Willi Syndrome.

Montes AS, Osann KE, Gold JA, Tamura RN, Driscoll DJ, Butler MG, Kimonis VE. Montes AS, et al. Among authors: kimonis ve. Genes (Basel). 2020 Oct 23;11(11):1250. doi: 10.3390/genes11111250. Genes (Basel). 2020. PMID: 33114160 Free PMC article.

2

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. 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.

3

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. Pediatrics. 2011 Apr;127(4):687-95. doi: 10.1542/peds.2010-2736. Epub 2011 Mar 14. Pediatrics. 2011. PMID: 21402637 Free PMC article.

4

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. 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.

5

Radiological features of Paget disease of bone associated with VCP myopathy.

Farpour F, Tehranzadeh J, Donkervoort S, Smith C, Martin B, Vanjara P, Osann K, Kimonis VE. Farpour F, et al. Among authors: kimonis ve. Skeletal Radiol. 2012 Mar;41(3):329-37. doi: 10.1007/s00256-011-1193-4. Epub 2011 Jun 4. Skeletal Radiol. 2012. PMID: 21643886

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. Among authors: kimonis ve. 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

Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia.

Mehta SG, Khare M, Ramani R, Watts GD, Simon M, Osann KE, Donkervoort S, Dec E, Nalbandian A, Platt J, Pasquali M, Wang A, Mozaffar T, Smith CD, Kimonis VE. Mehta SG, et al. Among authors: kimonis ve. Clin Genet. 2013 May;83(5):422-31. doi: 10.1111/cge.12000. Epub 2012 Oct 4. Clin Genet. 2013. PMID: 22909335 Free PMC article.

8

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. Among authors: kimonis ve. 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.

9

Familial incidence and associated symptoms in a population of individuals with nonsyndromic craniosynostosis.

Greenwood J, Flodman P, Osann K, Boyadjiev SA, Kimonis V. Greenwood J, et al. Genet Med. 2014 Apr;16(4):302-10. doi: 10.1038/gim.2013.134. Epub 2013 Sep 26. Genet Med. 2014. PMID: 24071792 Free PMC article.

10

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. Among authors: kimonis ve. 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.

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