Homocysteine and cardiovascular disease
An elevated level of total homocysteine (tHcy) in blood, denoted hyperhomocysteinemia, is
emerging as a prevalent and strong risk factor for atherosclerotic vascular disease in the …
emerging as a prevalent and strong risk factor for atherosclerotic vascular disease in the …
Hyperhomocysteinemia, atherosclerosis and thrombosis
M Cattaneo - Thrombosis and haemostasis, 1999 - thieme-connect.com
High plasma levels of homocysteine are the results of the interplay between congenital and
environmental factors. In the last two decades, a growing amount of interest has focused on …
environmental factors. In the last two decades, a growing amount of interest has focused on …
Plasma homocysteine as a risk factor for vascular disease: the European Concerted Action Project
IM Graham, LE Daly, HM Refsum, K Robinson… - Jama, 1997 - jamanetwork.com
Context.—Elevated plasma homocysteine is a known risk factor for atherosclerotic vascular
disease, but the strength of the relationship and the interaction of plasma homocysteine with …
disease, but the strength of the relationship and the interaction of plasma homocysteine with …
Roles of homocysteine in cell metabolism: old and new functions
MÁ Medina, JL Urdiales… - European journal of …, 2001 - Wiley Online Library
Mild hyperhomocysteinemia has been suggested as a new, independent risk factor for
cardiovascular disease. This fact has produced a new, increased interest in the study of …
cardiovascular disease. This fact has produced a new, increased interest in the study of …
[PDF][PDF] Plasma homocysteine and cardiovascular disease
PM Ueland, H Refsum, L Brattstrom - … disease, hemostasis, and …, 1992 - bevital.no
Homocysteine is a sulfur amino acid with a free sulfhydryl group (Fig. 1). It was first
discovered by du Vigneaud in 1932 as a product of demethylation of methionine (1). The …
discovered by du Vigneaud in 1932 as a product of demethylation of methionine (1). The …
Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC)
DS Rosenblatt, AL Aspler, MI Shevell… - Journal of inherited …, 1997 - Springer
The clbC form of methylmalonic acidaemia is a rare and poorly understood condition which
results from impaired biosynthesis of methylcobalamin and adenosylcobalamin. The …
results from impaired biosynthesis of methylcobalamin and adenosylcobalamin. The …
Neurologic presentations of nutritional deficiencies
N Kumar - Neurologic clinics, 2010 - neurologic.theclinics.com
Optimal functioning of the central and peripheral nervous system is dependent on a constant
supply of appropriate nutrients. Neurologic signs occur late in malnutrition. Deficiency …
supply of appropriate nutrients. Neurologic signs occur late in malnutrition. Deficiency …
Nutritional neuropathies
N Kumar - Neurologic Clinics, 2007 - neurologic.theclinics.com
Optimal functioning of the central and peripheral nervous system is dependent on a constant
supply of appropriate nutrients. Estimates provided by the United Nations Food and …
supply of appropriate nutrients. Estimates provided by the United Nations Food and …
Metabolic derangement of methionine and folate metabolism in mice deficient in methionine synthase reductase
CL Elmore, X Wu, D Leclerc, ED Watson… - Molecular genetics and …, 2007 - Elsevier
Hyperhomocyst (e) inemia is a metabolic derangement that is linked to the distribution of
folate pools, which provide one-carbon units for biosynthesis of purines and thymidylate and …
folate pools, which provide one-carbon units for biosynthesis of purines and thymidylate and …
Genetic defects of folate and cobalamin metabolism
B Fowler - European journal of pediatrics, 1998 - Springer
Deficient activity of an enzyme can result from a defect in the conversion of the vitamin to a
co-enzyme as well from an abnormal apo-enzyme or disturbed binding of co-enzyme to …
co-enzyme as well from an abnormal apo-enzyme or disturbed binding of co-enzyme to …