Hatton CE - 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: hatton ce. 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

Uptake of alpha-(L)-iduronidase produced by retrovirally transduced fibroblasts into neuronal and glial cells in vitro.

Stewart K, Brown OA, Morelli AE, Fairbairn LJ, Lashford LS, Cooper A, Hatton CE, Dexter TM, Castro MG, Lowenstein PR. Stewart K, et al. Among authors: hatton ce. Gene Ther. 1997 Jan;4(1):63-75. doi: 10.1038/sj.gt.3300364. Gene Ther. 1997. PMID: 9068797

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

4

Accelerated telomere shortening in young recipients of allogeneic bone-marrow transplants.

Wynn RF, Cross MA, Hatton C, Will AM, Lashford LS, Dexter TM, Testa NG. Wynn RF, et al. Lancet. 1998 Jan 17;351(9097):178-81. doi: 10.1016/S0140-6736(97)08256-1. Lancet. 1998. PMID: 9449873

5

Bone marrow transplantation in the treatment of alpha-mannosidosis.

Will A, Cooper A, Hatton C, Sardharwalla IB, Evans DI, Stevens RF. Will A, et al. Arch Dis Child. 1987 Oct;62(10):1044-9. doi: 10.1136/adc.62.10.1044. Arch Dis Child. 1987. PMID: 3314721 Free PMC article.

6

Mutation analysis in 46 British and Irish patients with Gaucher's disease.

Hatton CE, Cooper A, Whitehouse C, Wraith JE. Hatton CE, et al. Arch Dis Child. 1997 Jul;77(1):17-22. doi: 10.1136/adc.77.1.17. Arch Dis Child. 1997. PMID: 9279145 Free PMC article.

7

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: hatton ce. 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.

8

Alpha- and beta-mannosidoses.

Cooper A, Hatton CE, Thornley M, Sardharwalla IB. Cooper A, et al. Among authors: hatton ce. J Inherit Metab Dis. 1990;13(4):538-48. doi: 10.1007/BF01799511. J Inherit Metab Dis. 1990. PMID: 2122120

9

Human beta-mannosidase deficiency: biochemical findings in plasma, fibroblasts, white cells and urine.

Cooper A, Hatton C, Thornley M, Sardharwalla IB. Cooper A, et al. J Inherit Metab Dis. 1988;11(1):17-29. doi: 10.1007/BF01800054. J Inherit Metab Dis. 1988. PMID: 3128685

10

Detection of Fabry's disease carriers by enzyme assay of hair roots.

Hatton CE, Cooper A, Sardharwalla IB. Hatton CE, et al. J Inherit Metab Dis. 1989;12 Suppl 2:369-71. doi: 10.1007/BF03335425. J Inherit Metab Dis. 1989. PMID: 2556612 No abstract available.

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