Glycated haemoglobin (HbA1c) monitoring | The BMJ Skip to main content Intended for
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Copper is an essential cofactor for many enzymes, including cytochromes, but it is toxic in its
unbound form. The vast majority of serum copper is transported bound to ceruloplasmin; the …

Background Prescribing criteria have been suggested for proprotein convertase subtilisin
kexin‐9 (PCSK‐9) inhibitors but few studies exist of their real‐world effectiveness. Methods …

BACKGROUND: Copper is an essential nutrient but is toxic when the free form is in excess.
Wilson's disease (WD) is an autosomal recessive disorder of copper excess. Its diagnosis is …

The statistical procedure for discriminating between a Down syndrome or neural tube defect
(NTD) fetus and a normal fetus relies, to a great extent, on the reporting of maternal serum …

Genetic risk scores in lipid disorders : Current Opinion in Cardiology Genetic risk scores in lipid
disorders : Current Opinion in Cardiology Log in or Register Subscribe to journalSubscribe Get …

Background The burden of atherosclerosis has led to treatment prioritization on high-risk
individuals without established cardiovascular disease based on risk estimates. We …

Investigation of copper status can be a diagnostic challenge. The non-caeruloplasmin-
bound copper (NCC) has deficiencies; accordingly, the copper: caeruloplasmin ratio has …

Type V hyperlipidemia is distinguished by gross hypertriglyceridemia (1,770 mg/dl [20
mmol/L]) and the presence of high concentrations of chylomicrons, very-low density …

Objective To compare nine different algorithms for determining the necessity for drug
treatment of hyperlipidaemia in patients without cardiovascular disease. Design Risk-factor …