Wraith JE - Search Results

1

Long-term follow-up following bone marrow transplantation for Hunter disease.

Vellodi A, Young E, Cooper A, Lidchi V, Winchester B, Wraith JE. Vellodi A, et al. Among authors: wraith je. J Inherit Metab Dis. 1999 Jun;22(5):638-48. doi: 10.1023/a:1005525931994. J Inherit Metab Dis. 1999. PMID: 10399096

2

Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres.

Vellodi A, Young EP, Cooper A, Wraith JE, Winchester B, Meaney C, Ramaswami U, Will A. Vellodi A, et al. Among authors: wraith je. Arch Dis Child. 1997 Feb;76(2):92-9. doi: 10.1136/adc.76.2.92. Arch Dis Child. 1997. PMID: 9068295 Free PMC article.

3

Long-term clinical progress in bone marrow transplanted mucopolysaccharidosis type I patients with a defined genotype.

Hopwood JJ, Vellodi A, Scott HS, Morris CP, Litjens T, Clements PR, Brooks DA, Cooper A, Wraith JE. Hopwood JJ, et al. Among authors: wraith je. J Inherit Metab Dis. 1993;16(6):1024-33. doi: 10.1007/BF00711520. J Inherit Metab Dis. 1993. PMID: 8127052

4

Mutation analysis in 57 unrelated patients with MPS II (Hunter's disease).

Vafiadaki E, Cooper A, Heptinstall LE, Hatton CE, Thornley M, Wraith JE. Vafiadaki E, et al. Among authors: wraith je. Arch Dis Child. 1998 Sep;79(3):237-41. doi: 10.1136/adc.79.3.237. Arch Dis Child. 1998. PMID: 9875019 Free PMC article.

5

Juvenile Sandhoff disease--nine new cases and a review of the literature.

Hendriksz CJ, Corry PC, Wraith JE, Besley GT, Cooper A, Ferrie CD. Hendriksz CJ, et al. Among authors: wraith je. J Inherit Metab Dis. 2004;27(2):241-9. doi: 10.1023/B:BOLI.0000028777.38551.5a. J Inherit Metab Dis. 2004. PMID: 15159655 Review.

6

Mortality and cause of death in mucopolysaccharidosis type II-a historical review based on data from the Hunter Outcome Survey (HOS).

Jones SA, Almássy Z, Beck M, Burt K, Clarke JT, Giugliani R, Hendriksz C, Kroepfl T, Lavery L, Lin SP, Malm G, Ramaswami U, Tincheva R, Wraith JE; HOS Investigators. Jones SA, et al. Among authors: wraith je. J Inherit Metab Dis. 2009 Aug;32(4):534-43. doi: 10.1007/s10545-009-1119-7. Epub 2009 Jul 14. J Inherit Metab Dis. 2009. PMID: 19597960

7

Treatment of infantile Pompe disease with alglucosidase alpha: the UK experience.

Chakrapani A, Vellodi A, Robinson P, Jones S, Wraith JE. Chakrapani A, et al. Among authors: wraith je. J Inherit Metab Dis. 2010 Dec;33(6):747-50. doi: 10.1007/s10545-010-9206-3. Epub 2010 Sep 24. J Inherit Metab Dis. 2010. PMID: 20865334

8

Long-term in vitro correction of alpha-L-iduronidase deficiency (Hurler syndrome) in human bone marrow.

Fairbairn LJ, Lashford LS, Spooncer E, McDermott RH, Lebens G, Arrand JE, Arrand JR, Bellantuono I, Holt R, Hatton CE, Cooper A, Besley GT, Wraith JE, Anson DS, Hopwood JJ, Dexter TM. Fairbairn LJ, et al. Among authors: wraith je. Proc Natl Acad Sci U S A. 1996 Mar 5;93(5):2025-30. doi: 10.1073/pnas.93.5.2025. Proc Natl Acad Sci U S A. 1996. PMID: 8700879 Free PMC article.

9

Niemann-Pick disease type C in adults.

Imrie J, Vijayaraghaven S, Whitehouse C, Harris S, Heptinstall L, Church H, Cooper A, Besley GT, Wraith JE. Imrie J, et al. Among authors: wraith je. J Inherit Metab Dis. 2002 Oct;25(6):491-500. doi: 10.1023/a:1021259403196. J Inherit Metab Dis. 2002. PMID: 12555942

10

Long-Term Cognitive and Functional Outcomes in Children with Mucopolysaccharidosis (MPS)-IH (Hurler Syndrome) Treated with Hematopoietic Cell Transplantation.

Kunin-Batson AS, Shapiro EG, Rudser KD, Lavery CA, Bjoraker KJ, Jones SA, Wynn RF, Vellodi A, Tolar J, Orchard PJ, Wraith JE. Kunin-Batson AS, et al. Among authors: wraith je. JIMD Rep. 2016;29:95-102. doi: 10.1007/8904_2015_521. Epub 2016 Jan 30. JIMD Rep. 2016. PMID: 26825088 Free PMC article.

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