Johnson A - Search Results

1

Validity of the in vitro fertilisation league tables: influence of patients' characteristics.

Johnson A, El-Toukhy T, Sunkara SK, Khairy M, Coomarasamy A, Ross C, Bora S, Khalaf Y, Braude P. Johnson A, et al. BJOG. 2007 Dec;114(12):1569-74. doi: 10.1111/j.1471-0528.2007.01539.x. BJOG. 2007. PMID: 17995498

2

Randomised controlled trials in perinatal medicine: 3. Identifying and measuring endpoints in randomised controlled trials.

Johnson A. Johnson A. Br J Obstet Gynaecol. 1997 Jul;104(7):768-71. doi: 10.1111/j.1471-0528.1997.tb12017.x. Br J Obstet Gynaecol. 1997. PMID: 9236638 No abstract available.

3

A case of the carbohydrate-deficient glycoprotein syndrome type 1 (CDGS type 1) with normal phosphomannomutase activity.

Charlwood J, Clayton P, Johnson A, Keir G, Mian N, Winchester B. Charlwood J, et al. Among authors: johnson a. J Inherit Metab Dis. 1997 Nov;20(6):817-26. doi: 10.1023/a:1005380003902. J Inherit Metab Dis. 1997. PMID: 9427152

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

Diagnosis of respiratory chain defects using 1H n.m.r. spectroscopy in vitro.

Rafter JE, Chalmers RA, Johnson A, Iles RA. Rafter JE, et al. Among authors: johnson a. Biochem Soc Trans. 1990 Aug;18(4):551-2. doi: 10.1042/bst0180551. Biochem Soc Trans. 1990. PMID: 2177408 No abstract available.

6

The mitochondrial trifunctional protein: centre of a beta-oxidation metabolon?

Eaton S, Bursby T, Middleton B, Pourfarzam M, Mills K, Johnson AW, Bartlett K. Eaton S, et al. Among authors: johnson aw. Biochem Soc Trans. 2000 Feb;28(2):177-82. doi: 10.1042/bst0280177. Biochem Soc Trans. 2000. PMID: 10816122 Review.

7

Renal tubular dysfunction in multiple acyl-CoA dehydrogenase deficiency.

Morris AA, Olpin SE, Van't Hoff WG, Johnson AW, Leonard JV. Morris AA, et al. Among authors: johnson aw. J Inherit Metab Dis. 1997 Aug;20(4):604-5. doi: 10.1023/a:1005371428912. J Inherit Metab Dis. 1997. PMID: 9266400 No abstract available.

8

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

9

The efficacy of very long-chain fatty acid analysis in the diagnosis of peroxisomal disorders: an audit report.

Harkness RA, Lynes GW, Johnson AW. Harkness RA, et al. Among authors: johnson aw. J Inherit Metab Dis. 1992;15(2):287-8. doi: 10.1007/BF01799648. J Inherit Metab Dis. 1992. PMID: 1528000 No abstract available.

10

GM1-gangliosidosis in a cross-bred dog confirmed by detection of GM1-ganglioside using electrospray ionisation-tandem mass spectrometry.

Whitfield P, Johnson AW, Dunn KA, Delauche AJ, Winchester BG, Franklin RJ. Whitfield P, et al. Among authors: johnson aw. Acta Neuropathol. 2000 Oct;100(4):409-14. doi: 10.1007/s004010000187. Acta Neuropathol. 2000. PMID: 10985700

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