Besley GT - Search Results

1

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: besley gt. 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.

2

Retrovirally mediated correction of bone marrow-derived mesenchymal stem cells from patients with mucopolysaccharidosis type I.

Baxter MA, Wynn RF, Deakin JA, Bellantuono I, Edington KG, Cooper A, Besley GT, Church HJ, Wraith JE, Carr TF, Fairbairn LJ. Baxter MA, et al. Among authors: besley gt. Blood. 2002 Mar 1;99(5):1857-9. doi: 10.1182/blood.v99.5.1857. Blood. 2002. PMID: 11861306 Free article.

3

Towards gene therapy of Hurler syndrome.

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: besley gt. Cas Lek Cesk. 1997 Jan 8;136(1):27-31. Cas Lek Cesk. 1997. PMID: 9127508

4

Common MCAD mutation in a healthy parent of two affected siblings.

Heptinstall LE, Till J, Wraith JE, Besley GT. Heptinstall LE, et al. Among authors: besley gt. J Inherit Metab Dis. 1995;18(5):638-9. doi: 10.1007/BF02436011. J Inherit Metab Dis. 1995. PMID: 8598647 No abstract available.

5

Trifunctional protein deficiency: three families with significant maternal hepatic dysfunction in pregnancy not associated with E474Q mutation.

Chakrapani A, Olpin S, Cleary M, Walter JH, Wraith JE, Besley GT. Chakrapani A, et al. Among authors: besley gt. J Inherit Metab Dis. 2000 Dec;23(8):826-34. doi: 10.1023/a:1026712719416. J Inherit Metab Dis. 2000. PMID: 11196108

6

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: besley gt. 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.

7

Generalised uridine diphosphate galactose-4-epimerase deficiency.

Walter JH, Roberts RE, Besley GT, Wraith JE, Cleary MA, Holton JB, MacFaul R. Walter JH, et al. Among authors: besley gt. Arch Dis Child. 1999 Apr;80(4):374-6. doi: 10.1136/adc.80.4.374. Arch Dis Child. 1999. PMID: 10086948 Free PMC article.

8

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: besley gt. J Inherit Metab Dis. 2002 Oct;25(6):491-500. doi: 10.1023/a:1021259403196. J Inherit Metab Dis. 2002. PMID: 12555942

9

Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene.

Jansen GA, Ofman R, Ferdinandusse S, Ijlst L, Muijsers AO, Skjeldal OH, Stokke O, Jakobs C, Besley GT, Wraith JE, Wanders RJ. Jansen GA, et al. Among authors: besley gt. Nat Genet. 1997 Oct;17(2):190-3. doi: 10.1038/ng1097-190. Nat Genet. 1997. PMID: 9326940

10

First trimester diagnosis of inherited metabolic disease: experience in the UK.

Besley GT, Young EP, Fensom AH, Cooper A. Besley GT, et al. J Inherit Metab Dis. 1991;14(2):128-33. doi: 10.1007/BF01800583. J Inherit Metab Dis. 1991. PMID: 1886402

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