Gordon BA - Search Results

1

Rupar CA, Gillett J, Gordon BA, Ramsay DA, Johnson JL, Garrett RM, Rajagopalan KV, Jung JH, Bacheyie GS, Sellers AR. Rupar CA, et al. Among authors: gordon ba. Neuropediatrics. 1996 Dec;27(6):299-304. doi: 10.1055/s-2007-973798. Neuropediatrics. 1996. PMID: 9050047

2

Medium-chain acyl-CoA dehydrogenase deficiency is not a cause of previously diagnosed Reye syndrome.

Rupar CA, Frewen TW, Gordon BA. Rupar CA, et al. Among authors: gordon ba. J Inherit Metab Dis. 1995;18(3):365-6. doi: 10.1007/BF00710436. J Inherit Metab Dis. 1995. PMID: 7474911 No abstract available.

3

Retrospective diagnosis of medium chain acyl-CoA dehydrogenase deficiency.

Christodoulou J, Clarke JT, Rupar CA, Gordon BA, Kelly DP. Christodoulou J, et al. Among authors: gordon ba. J Paediatr Child Health. 1993 Jun;29(3):237-8. doi: 10.1111/j.1440-1754.1993.tb00496.x. J Paediatr Child Health. 1993. PMID: 8518011

4

Aspartylglucosaminuria in a Canadian family.

Gordon BA, Rupar CA, Rip JW, Haust MD, Coulter-Mackie MB, Scott E, Hinton GG. Gordon BA, et al. Clin Invest Med. 1998 Jun;21(3):114-23. Clin Invest Med. 1998. PMID: 9627765

5

Purification and structure of human liver aspartylglucosaminidase.

Rip JW, Coulter-Mackie MB, Rupar CA, Gordon BA. Rip JW, et al. Among authors: gordon ba. Biochem J. 1992 Dec 15;288 ( Pt 3)(Pt 3):1005-10. doi: 10.1042/bj2881005. Biochem J. 1992. PMID: 1281977 Free PMC article.

6

Use of a genetic variant to study the hexose transport properties of human skin fibroblasts.

Mesmer OT, Gordon BA, Rupar CA, Lo TC. Mesmer OT, et al. Among authors: gordon ba. Biochem J. 1990 Feb 1;265(3):823-9. doi: 10.1042/bj2650823. Biochem J. 1990. PMID: 2306216 Free PMC article.

7

Heteroallelic missense mutations of the galactosamine-6-sulfate sulfatase (GALNS) gene in a mild form of Morquio disease (MPS IVA).

Cole DE, Fukuda S, Gordon BA, Rip JW, LeCouteur AN, Rupar CA, Tomatsu S, Ogawa T, Sukegawa K, Orii T. Cole DE, et al. Among authors: gordon ba. Am J Med Genet. 1996 Jun 28;63(4):558-65. doi: 10.1002/(SICI)1096-8628(19960628)63:4<558::AID-AJMG9>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8826435

8

Fucosidosis with dystonia.

Gordon BA, Gordon KE, Seo HC, Yang M, DiCioccio RA, O'Brien JS. Gordon BA, et al. Among authors: gordon ke. Neuropediatrics. 1995 Dec;26(6):325-7. doi: 10.1055/s-2007-979784. Neuropediatrics. 1995. PMID: 8719750

9

Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH)-syndrome. Ultrastructural changes of mitochondria in cultured dermal fibroblasts of three patients.

Haust MD, Dewar RA, Gatfield DP, Gordon BA. Haust MD, et al. Among authors: gordon ba. Pathol Res Pract. 1996 Mar;192(3):271-80. doi: 10.1016/S0344-0338(96)80230-5. Pathol Res Pract. 1996. PMID: 8739474

10

A simple spectrophotometric enzyme assay with absolute specificity for arylsulfatase A.

Rip JW, Gordon BA. Rip JW, et al. Among authors: gordon ba. Clin Biochem. 1998 Feb;31(1):29-31. doi: 10.1016/s0009-9120(97)00142-2. Clin Biochem. 1998. PMID: 9559221 No abstract available.

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