Search Results - "Wenham, P R"
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Apolipoprotein E and neurocognitive outcome from coronary artery surgery
Published in Journal of neurology, neurosurgery and psychiatry (01-05-2002)“…[...]using analysis of covariance, follow up cognitive score was the outcome variable, preoperative cognitive score was controlled by entering it as a…”
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2
Plasma lactate dehydrogenase: a marker of disease activity in cryptogenic fibrosing alveolitis and extrinsic allergic alveolitis?
Published in The European respiratory journal (01-10-1993)“…Total plasma lactate dehydrogenase (LDH) activity may be elevated in cryptogenic fibrosing alveolitis (CFA) and extrinsic allergic alveolitis (EAA), and may be…”
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3
Interference in spectrophotometric analysis of cerebrospinal fluid by haemolysis induced by transport through a pneumatic tube system
Published in Annals of clinical biochemistry (01-07-2001)“…The hypothesis that sending blood-stained cerebrospinal fluid (CSF) through a pneumatic tube causes in vitro haemolysis has been tested. Spectrophotometric…”
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CSF spectrophotometry in the diagnosis of subarachnoid haemorrhage [Letters to JCP]
Published in Journal of clinical pathology (01-06-2002)“…[...]we know that variously 10 000 × 106 erythrocytes/litre can be left for up to 30 minutes5 and 4000 × 106 erythrocytes/litre can be left for up to 24 hours6…”
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DNA-based techniques in clinical biochemistry: a beginner's guide to theory and practice
Published in Annals of clinical biochemistry (01-11-1992)Get more information
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Detecting familial defective apolipoprotein B-100: three molecular scanning methods compared
Published in Clinical chemistry (Baltimore, Md.) (01-09-1997)“…Familial defective apolipoprotein (apo) B-100 (FDB), a condition that may give rise to hypercholesterolemia, is caused by mutations around codon 3500 of the…”
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7
Apolipoprotein E genotyping by one-stage PCR
Published in The Lancet (British edition) (11-05-1991)Get more information
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Apolipoprotein E phenotyping: a word of caution
Published in Annals of clinical biochemistry (01-11-1991)“…Using two different techniques, phenotyping and genotyping, we have studied allelic variation at amino acids 112 and 158 of the apolipoprotein E gene locus in…”
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Familial ligand-defective apolipoprotein B-100: detection, biochemical features and haplotype analysis of the R3531C mutation in the UK
Published in Atherosclerosis (21-03-1997)“…Familial ligand-defective apolipoprotein (apo) B-100 (FDB) is an autosomal codominant disorder which may give rise to hypercholesterolaemia. It is caused by…”
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Clinical follow-up of high mid-trimester maternal serum intact human chorionic gonadotrophin concentrations in singleton pregnancies
Published in Prenatal diagnosis (01-03-1999)“…Mid‐trimester biochemical screening of 38143 pregnancies in south‐east Scotland revealed 127 cases (0·34 per cent) in which the maternal serum (MS) intact…”
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Salivary immunoglobulin A in irritable bowel syndrome: no correlation with anxiety
Published in Annals of clinical biochemistry (01-05-1993)Get more information
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Measurement of plasma phenytoin by EMIT in the Monarch centrifugal analyzer: studies on the elimination of within-rotor drift
Published in Clinical chemistry (Baltimore, Md.) (01-10-1988)“…We investigated the measurement of phenytoin in plasma by the EMIT method, in the Monarch centrifugal analyzer. When we used the standard protocol supplied by…”
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Multiple forms of gamma-glutamyltransferase: a clinical study
Published in Clinical chemistry (Baltimore, Md.) (01-04-1985)“…We have measured the amounts of different molecular forms of gamma-glutamyltransferase (EC 2.3.2.2), leucine aminopeptidase (EC 3.4.11.2), and alkaline…”
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Immunoturbidimetry of apolipoprotein A-II in a centrifugal analyzer
Published in Clinical chemistry (Baltimore, Md.) (01-07-1987)Get more information
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15
Familial defective apolipoprotein B-100: a study of patients from lipid clinics in Scotland and Wales
Published in Annals of clinical biochemistry (01-09-1996)“…Familial defective apolipoprotein (apo) B-100 (FDB) is an autosomal codominant disorder, which may be associated with hypercholesterolaemia. The defect is…”
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16
Two macromolecular complexes between alkaline phosphatase and immunoglobulin A in a patient's serum
Published in Clinical chemistry (Baltimore, Md.) (01-10-1983)“…We report the presence of two separate macromolecular complexes between an immunoglobulin and alkaline phosphatase (EC 3.1.3.1) in the serum of a patient with…”
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17
Simplified detection of a mutation causing familial hypercholesterolaemia throughout Britain: evidence for an origin in a common distant ancestor
Published in Annals of clinical biochemistry (01-03-1998)“…Familial hypercholesterolaemia (FH) is an inherited autosomal codominant disorder caused by many different mutations in the low-density lipoprotein receptor…”
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Rapid diagnosis of familial defective apolipoprotein B-100 by Amplification Refractory Mutation System
Published in Clinical chemistry (Baltimore, Md.) (01-11-1991)“…We report a method for the diagnosis of familial defective apolipoprotein (apo) B-100, using the Amplification Refractory Mutation System (ARMS) and either…”
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EMIT measurement of carbamazepine, phenobarbital, and theophylline in the "Monarch" centrifugal analyzer
Published in Clinical chemistry (Baltimore, Md.) (01-05-1989)Get more information
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20
The effect of testosterone replacement on plasma lipids and apolipoproteins
Published in European journal of clinical investigation (01-10-1989)“…Ten men with Klinefelter's syndrome were studied to assess the effect of testosterone replacement on plasma lipids and apolipoproteins. Measurements taken…”
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