Johnson AW - Search Results

1

Delta 4-3-oxosteroid 5 beta-reductase deficiency: failure of ursodeoxycholic acid treatment and response to chenodeoxycholic acid plus cholic acid.

Clayton PT, Mills KA, Johnson AW, Barabino A, Marazzi MG. Clayton PT, et al. Among authors: johnson aw. Gut. 1996 Apr;38(4):623-8. doi: 10.1136/gut.38.4.623. Gut. 1996. PMID: 8707100 Free PMC article.

2

Ataxia associated with increased plasma concentrations of pristanic acid, phytanic acid and C27 bile acids but normal fibroblast branched-chain fatty acid oxidation.

Clayton PT, Johnson AW, Mills KA, Lynes GW, Wilson J, Casteels M, Mannaerts G. Clayton PT, et al. Among authors: johnson aw. J Inherit Metab Dis. 1996;19(6):761-8. doi: 10.1007/BF01799170. J Inherit Metab Dis. 1996. PMID: 8982949

3

A method for the quantitation of conjugated bile acids in dried blood spots using electrospray ionization-mass spectrometry.

Mills KA, Mushtaq I, Johnson AW, Whitfield PD, Clayton PT. Mills KA, et al. Among authors: johnson aw. Pediatr Res. 1998 Mar;43(3):361-8. doi: 10.1203/00006450-199803000-00009. Pediatr Res. 1998. PMID: 9505275

4

The identification of unusual bile acid metabolites by tandem mass spectrometry: use of low-energy collision-induced dissociation to produce informative spectra.

Lemonde HA, Johnson AW, Clayton PT. Lemonde HA, et al. Among authors: johnson aw. Rapid Commun Mass Spectrom. 1999;13(12):1159-64. doi: 10.1002/(SICI)1097-0231(19990630)13:12<1159::AID-RCM636>3.0.CO;2-#. Rapid Commun Mass Spectrom. 1999. PMID: 10390861

5

Screening of newborn infants for cholestatic hepatobiliary disease with tandem mass spectrometry.

Mushtaq I, Logan S, Morris M, Johnson AW, Wade AM, Kelly D, Clayton PT. Mushtaq I, et al. Among authors: johnson aw. BMJ. 1999 Aug 21;319(7208):471-7. doi: 10.1136/bmj.319.7208.471. BMJ. 1999. PMID: 10454398 Free PMC article.

6

The use of automated electrospray ionization tandem MS for the diagnosis of inborn errors of metabolism from dried blood spots.

Johnson AW, Mills K, Clayton PT. Johnson AW, et al. Biochem Soc Trans. 1996 Aug;24(3):932-8. doi: 10.1042/bst0240932. Biochem Soc Trans. 1996. PMID: 8878877 No abstract available.

7

Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometry.

Clayton PT, Doig M, Ghafari S, Meaney C, Taylor C, Leonard JV, Morris M, Johnson AW. Clayton PT, et al. Among authors: johnson aw. Arch Dis Child. 1998 Aug;79(2):109-15. doi: 10.1136/adc.79.2.109. Arch Dis Child. 1998. PMID: 9797589 Free PMC article. Clinical Trial.

8

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: johnson aw. Clin Chem. 2001 Nov;47(11):2012-22. Clin Chem. 2001. PMID: 11673370

9

Analysis by matrix assisted laser desorption/ionisation-time of flight mass spectrometry of the post-translational modifications of alpha 1-antitrypsin isoforms separated by two-dimensional polyacrylamide gel electrophoresis.

Mills PB, Mills K, Johnson AW, Clayton PT, Winchester BG. Mills PB, et al. Among authors: johnson aw. Proteomics. 2001 Jun;1(6):778-86. doi: 10.1002/1615-9861(200106)1:6<778::AID-PROT778>3.0.CO;2-H. Proteomics. 2001. PMID: 11677785

10

The underglycosylation of plasma alpha 1-antitrypsin in congenital disorders of glycosylation type I is not random.

Mills K, Mills PB, Clayton PT, Mian N, Johnson AW, Winchester BG. Mills K, et al. Among authors: johnson aw. Glycobiology. 2003 Feb;13(2):73-85. doi: 10.1093/glycob/cwg026. Epub 2002 Dec 17. Glycobiology. 2003. PMID: 12626422

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