Winchester B - Search Results

1

Saposins A, B, C, and D in plasma of patients with lysosomal storage disorders.

Chang MH, Bindloss CA, Grabowski GA, Qi X, Winchester B, Hopwood JJ, Meikle PJ. Chang MH, et al. Among authors: winchester b. Clin Chem. 2000 Feb;46(2):167-74. Clin Chem. 2000. PMID: 10657372

2

Transport, enzymatic activity, and stability of mutant sulfamidase (SGSH) identified in patients with mucopolysaccharidosis type III A.

Muschol N, Storch S, Ballhausen D, Beesley C, Westermann JC, Gal A, Ullrich K, Hopwood JJ, Winchester B, Braulke T. Muschol N, et al. Among authors: winchester b. Hum Mutat. 2004 Jun;23(6):559-66. doi: 10.1002/humu.20037. Hum Mutat. 2004. PMID: 15146460

3

Are there useful biochemical markers of disease activity in lysosomal storage diseases?

Winchester B. Winchester B. J Inherit Metab Dis. 2001;24 Suppl 2:52-6; discussion 45-6. doi: 10.1023/a:1012415706901. J Inherit Metab Dis. 2001. PMID: 11758679 Review.

4

Identification and characterization of 13 new mutations in mucopolysaccharidosis type I patients.

Matte U, Yogalingam G, Brooks D, Leistner S, Schwartz I, Lima L, Norato DY, Brum JM, Beesley C, Winchester B, Giugliani R, Hopwood JJ. Matte U, et al. Among authors: winchester b. Mol Genet Metab. 2003 Jan;78(1):37-43. doi: 10.1016/s1096-7192(02)00200-7. Mol Genet Metab. 2003. PMID: 12559846

5

Lysosomal membrane proteins.

Winchester BG. Winchester BG. Eur J Paediatr Neurol. 2001;5 Suppl A:11-9. doi: 10.1053/ejpn.2000.0428. Eur J Paediatr Neurol. 2001. PMID: 11588980 Review.

6

The molecular basis of lysosomal storage diseases and their treatment.

Winchester B, Vellodi A, Young E. Winchester B, et al. Biochem Soc Trans. 2000 Feb;28(2):150-4. doi: 10.1042/bst0280150. Biochem Soc Trans. 2000. PMID: 10816117 Review.

7

Identification of alpha(1)-antitrypsin variants in plasma with the use of proteomic technology.

Mills K, Mills PB, Clayton PT, Johnson AW, Whitehouse DB, Winchester BG. Mills K, et al. Among authors: winchester bg. Clin Chem. 2001 Nov;47(11):2012-22. Clin Chem. 2001. PMID: 11673370

8

Prenatal diagnosis of lysosomal storage diseases.

Lake BD, Young EP, Winchester BG. Lake BD, et al. Among authors: winchester bg. Brain Pathol. 1998 Jan;8(1):133-49. doi: 10.1111/j.1750-3639.1998.tb00141.x. Brain Pathol. 1998. PMID: 9458172 Free PMC article.

9

Clinical utility gene card for: Fabry disease.

Gal A, Beck M, Winchester B. Gal A, et al. Among authors: winchester b. Eur J Hum Genet. 2012 Feb;20(2). doi: 10.1038/ejhg.2011.178. Epub 2011 Sep 21. Eur J Hum Genet. 2012. PMID: 21934708 Free PMC article. No abstract available.

10

Toward a consensus in the laboratory diagnostics of Fabry disease - recommendations of a European expert group.

Gal A, Hughes DA, Winchester B. Gal A, et al. Among authors: winchester b. J Inherit Metab Dis. 2011 Apr;34(2):509-14. doi: 10.1007/s10545-010-9261-9. Epub 2011 Jan 13. J Inherit Metab Dis. 2011. PMID: 21229318 Free PMC article. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

226 results

Search Page

Filters