Gold JA - Search Results

1

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

2

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: gold ja. 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.

3

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: gold ja. 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.

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. Among authors: gold ja. 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

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: gold ja. 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.

6

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.

7

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: gold ja. Pediatrics. 2015 Jan;135(1):e126-35. doi: 10.1542/peds.2014-1711. Epub 2014 Dec 8. Pediatrics. 2015. PMID: 25489013 Free PMC article.

8

Growth Charts for Prader-Willi Syndrome During Growth Hormone Treatment.

Butler MG, Lee J, Cox DM, Manzardo AM, Gold JA, Miller JL, Roof E, Dykens E, Kimonis V, Driscoll DJ. Butler MG, et al. Among authors: gold ja. Clin Pediatr (Phila). 2016 Sep;55(10):957-74. doi: 10.1177/0009922815617973. Epub 2016 Feb 3. Clin Pediatr (Phila). 2016. PMID: 26842920 Free PMC article.

9

A novel mutation of orthodenticle homeobox 2 contributing to a case of otocephaly initially diagnosed by prenatal ultrasound in the first trimester.

Jones M, Chung J, Kimonis V, Gold JA. Jones M, et al. Among authors: gold ja. Clin Dysmorphol. 2017 Apr;26(2):98-100. doi: 10.1097/MCD.0000000000000145. Clin Dysmorphol. 2017. PMID: 27442045 No abstract available.

10

Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(15;19)(q12;p13.3).

Dang V, Surampalli A, Manzardo AM, Youn S, Butler MG, Gold JA, Kimonis VE. Dang V, et al. Among authors: gold ja. Cytogenet Genome Res. 2016;150(1):29-34. doi: 10.1159/000452611. Epub 2016 Nov 29. Cytogenet Genome Res. 2016. PMID: 27894106 Free PMC article.

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