Wraith JE - Search Results

1

Management of mucopolysaccharidosis type IH (Hurler's syndrome) presenting in infancy with severe dilated cardiomyopathy: a single institution's experience.

Wiseman DH, Mercer J, Tylee K, Malaiya N, Bonney DK, Jones SA, Wraith JE, Wynn RF. Wiseman DH, et al. Among authors: wraith je. J Inherit Metab Dis. 2013 Mar;36(2):263-70. doi: 10.1007/s10545-012-9500-3. Epub 2012 Jun 21. J Inherit Metab Dis. 2013. PMID: 22718273

2

Use of enzyme replacement therapy (Laronidase) before hematopoietic stem cell transplantation for mucopolysaccharidosis I: experience in 18 patients.

Wynn RF, Mercer J, Page J, Carr TF, Jones S, Wraith JE. Wynn RF, et al. Among authors: wraith je. J Pediatr. 2009 Jan;154(1):135-9. doi: 10.1016/j.jpeds.2008.07.004. J Pediatr. 2009. PMID: 19187736

3

Growth, final height and endocrine sequelae in a UK population of patients with Hurler syndrome (MPS1H).

Gardner CJ, Robinson N, Meadows T, Wynn R, Will A, Mercer J, Church HJ, Tylee K, Wraith JE, Clayton PE. Gardner CJ, et al. Among authors: wraith je. J Inherit Metab Dis. 2011 Apr;34(2):489-97. doi: 10.1007/s10545-010-9262-8. Epub 2011 Jan 21. J Inherit Metab Dis. 2011. PMID: 21253827

4

The craniocervical junction following successful haematopoietic stem cell transplantation for mucopolysaccharidosis type I H (Hurler syndrome).

Miebach E, Church H, Cooper A, Mercer J, Tylee K, Wynn RF, Wraith JE. Miebach E, et al. Among authors: wraith je. J Inherit Metab Dis. 2011 Jun;34(3):755-61. doi: 10.1007/s10545-011-9309-5. Epub 2011 Mar 17. J Inherit Metab Dis. 2011. PMID: 21416193

5

Hematopoietic stem cell and gene therapy corrects primary neuropathology and behavior in mucopolysaccharidosis IIIA mice.

Langford-Smith A, Wilkinson FL, Langford-Smith KJ, Holley RJ, Sergijenko A, Howe SJ, Bennett WR, Jones SA, Wraith J, Merry CL, Wynn RF, Bigger BW. Langford-Smith A, et al. Among authors: wraith j. Mol Ther. 2012 Aug;20(8):1610-21. doi: 10.1038/mt.2012.82. Epub 2012 May 1. Mol Ther. 2012. PMID: 22547151 Free PMC article.

6

Myeloid/Microglial driven autologous hematopoietic stem cell gene therapy corrects a neuronopathic lysosomal disease.

Sergijenko A, Langford-Smith A, Liao AY, Pickford CE, McDermott J, Nowinski G, Langford-Smith KJ, Merry CL, Jones SA, Wraith JE, Wynn RF, Wilkinson FL, Bigger BW. Sergijenko A, et al. Among authors: wraith je. Mol Ther. 2013 Oct;21(10):1938-49. doi: 10.1038/mt.2013.141. Epub 2013 Jun 7. Mol Ther. 2013. PMID: 23748415 Free PMC article.

7

Heparan sulfate inhibits hematopoietic stem and progenitor cell migration and engraftment in mucopolysaccharidosis I.

Watson HA, Holley RJ, Langford-Smith KJ, Wilkinson FL, van Kuppevelt TH, Wynn RF, Wraith JE, Merry CL, Bigger BW. Watson HA, et al. Among authors: wraith je. J Biol Chem. 2014 Dec 26;289(52):36194-203. doi: 10.1074/jbc.M114.599944. Epub 2014 Oct 30. J Biol Chem. 2014. PMID: 25359774 Free PMC article.

8

Haematopoietic Stem Cell Transplantation Arrests the Progression of Neurodegenerative Disease in Late-Onset Tay-Sachs Disease.

Stepien KM, Lum SH, Wraith JE, Hendriksz CJ, Church HJ, Priestman D, Platt FM, Jones S, Jovanovic A, Wynn R. Stepien KM, et al. Among authors: wraith je. JIMD Rep. 2018;41:17-23. doi: 10.1007/8904_2017_76. Epub 2017 Dec 7. JIMD Rep. 2018. PMID: 29214523 Free PMC article.

9

Enzyme replacement therapy for mucopolysaccharidosis VI: evaluation of long-term pulmonary function in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase.

Harmatz P, Yu ZF, Giugliani R, Schwartz IV, Guffon N, Teles EL, Miranda MC, Wraith JE, Beck M, Arash L, Scarpa M, Ketteridge D, Hopwood JJ, Plecko B, Steiner R, Whitley CB, Kaplan P, Swiedler SJ, Hardy K, Berger KI, Decker C. Harmatz P, et al. Among authors: wraith je. J Inherit Metab Dis. 2010 Feb;33(1):51-60. doi: 10.1007/s10545-009-9007-8. Epub 2010 Feb 6. J Inherit Metab Dis. 2010. PMID: 20140523 Free PMC article. Clinical Trial.

10

Enzyme replacement therapy with idursulfase in patients with mucopolysaccharidosis type II.

Wraith JE. Wraith JE. Acta Paediatr. 2008 Apr;97(457):76-8. doi: 10.1111/j.1651-2227.2008.00661.x. Acta Paediatr. 2008. PMID: 18339193 Review.

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