Apolipoprotein E and neurocognitive outcome from coronary artery surgery von Robson, M J A, Alston, R P, Andrews, P J D, Wenham, P R, Souter, M J, Deary, I J

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Plasma lactate dehydrogenase: a marker of disease activity in cryptogenic fibrosing alveolitis and extrinsic allergic alveolitis? von Matusiewicz, SP, Williamson, IJ, Sime, PJ, Brown, PH, Wenham, PR, Crompton, GK, Greening, AP

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Apolipoprotein E genotyping by one-stage PCR von Wenham, PhilipR, Price, WilliamH, Blundell, Gillian

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CSF spectrophotometry in the diagnosis of subarachnoid haemorrhage [Letters to JCP] von Beetham, R, Fahie-Wilson, M N, Holbrook, I, Thomas, P, Ward, A M, Watson, I D, Wenham, P R, White, P A E

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Detecting familial defective apolipoprotein B-100: three molecular scanning methods compared von Henderson, Bryony G, Wenham, Philip R, Ashby, J. Peter, Blundell, Gillian

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Familial ligand-defective apolipoprotein B-100: detection, biochemical features and haplotype analysis of the R3531C mutation in the UK von Wenham, Philip R, Henderson, Bryony G, Penney, Michael D, Ashby, J.Peter, Rae, Peter W.H, Walker, Simon W

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DNA-Based Techniques in Clinical Biochemistry: A Beginner's Guide to Theory and Practice von Wenham, Philip R

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Apolipoprotein E Phenotyping: A Word of Caution von Wenham, Philip R, Sedky, Alyaa, Spooner, Richard J

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Clinical follow-up of high mid-trimester maternal serum intact human chorionic gonadotrophin concentrations in singleton pregnancies von Blundell, Gillian, Ashby, J. Peter, Martin, Cameron, Shearing, Catherine H., Langdale-Brown, Barbara, Keeling, Jean, Ellis, Patricia M., Shade, Mary, Chambers, Sarah E., Wenham, Philip R.

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Familial Defective Apolipoprotein B-100: A Study of Patients from Lipid Clinics in Scotland and Wales von Wenham, Philip R, Bloomfield, Peter, Blundell, Gillian, Penney, Michael D, Rae, Peter W H, Walker, Simon W

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Simplified Detection of a Mutation Causing Familial Hypercholesterolaemia Throughout Britain: Evidence for an Origin in a Common Distant Ancestor von Wenham, Philip R, Haddad, Lema, Panarelli, Maurizio, Ashby, J Peter, Day, Ian N M, Giles, Paul D, Humphries, Steve E, Penney, Michael D, Rae, Peter W H, Walker, Simon W

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Salivary Immunoglobulin a in Irritable Bowel Syndrome: No Correlation with Anxiety von Fowlie, S, Eastwood, M A, Wenham, P R

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Genetic markers of familial coronary heart disease von Price, W.H., Morris, S.W., Kitchin, A.H., Wenham, P.R., Mckenzie, P.R.S., Donald, P.M.

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Physical properties of γ-glutamyltransferase in human serum von Wenham, Philip R., Horn, David B., Smith, Alistair F.

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Hypercholesterolaemia presenting in a patient with familial defective apolipoprotein B-100 and hypothyroidism von WENHAM, P. R, GILES, P. D, ASHBY, J. P

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DNA RESTRICTION FRAGMENT LENGTH POLYMORPHISMS AS MARKERS OF FAMILIAL CORONARY HEART DISEASE von Price, W.H., Kitchin, A.H., Burgon, P.R.S., Morris, S.W., Wenham, P.R., Donald, P.M.

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Rare apolipoprotein E variant identified in a patient with Type III hyperlipidaemia von Wenham, Philip R., McDowell, Ian F.W., Hodges, Vivien M., McEneny, Jane, O'Kane, Maurice J., Jeremy, R., Davies, H., Paul Nicholls, D., Trimble, Elisabeth R., Blundell, Gillian

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gamma-Glutamyl transferase isoenzymes in human bile von Wenham, P R, Price, C P, Sammons, H G

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A Short Review of Techniques for the Localisation of γ-Glutamyl Transferase Isoenzymes after Electrophoresis von Wenham, P. R., Price, C. P., Sammons, H. G.

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DNA restriction fragment length polymorphisms as markers of familial coronary heart disease von PRICE, W. H, MORRIS, S. W, KITCHIN, A. H, WEDNHAM, P. R, BURGON, PR. S, DONALD, P. M

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