Cooper A - 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: cooper a. J Inherit Metab Dis. 1999 Jun;22(5):638-48. doi: 10.1023/a:1005525931994. J Inherit Metab Dis. 1999. PMID: 10399096

2

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: cooper a. J Inherit Metab Dis. 1993;16(6):1024-33. doi: 10.1007/BF00711520. J Inherit Metab Dis. 1993. PMID: 8127052

3

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: cooper a. 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.

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: cooper a. 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

First-trimester diagnosis of Hunter syndrome: very low iduronate sulphatase activity in chorionic villi from a heterozygous female fetus.

Cooper A, Thornley M, Wraith JE. Cooper A, et al. Prenat Diagn. 1991 Sep;11(9):731-5. doi: 10.1002/pd.1970110911. Prenat Diagn. 1991. PMID: 1820774

6

beta-mannosidase deficiency in a female infant with epileptic encephalopathy.

Cooper A, Wraith JE, Savage WJ, Thornley M, Noronha MJ. Cooper A, et al. J Inherit Metab Dis. 1991;14(1):18-22. doi: 10.1007/BF01804383. J Inherit Metab Dis. 1991. PMID: 1861456

7

The clinical phenotype of two patients with a complete deletion of the iduronate-2-sulphatase gene (mucopolysaccharidosis II--Hunter syndrome).

Wraith JE, Cooper A, Thornley M, Wilson PJ, Nelson PV, Morris CP, Hopwood JJ. Wraith JE, et al. Among authors: cooper a. Hum Genet. 1991 Jun;87(2):205-6. doi: 10.1007/BF00204183. Hum Genet. 1991. PMID: 1906048

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: cooper a. 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

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: cooper a. 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.

10

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

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