Zobrazeno 1 - 10
of 93
pro vyhledávání: '"R. Valve"'
Publikováno v:
The American Journal of Clinical Nutrition. 73:31-35
Background The affinity of intestinal fatty acid binding protein (FABP) for fatty acids is regulated by the polymorphism at codon 54 of the FABP2 gene (alanine-to-threonine shift). We found earlier that the threonine-encoding allele (Thr54) is associ
Publikováno v:
International Journal of Obesity. 24:514-519
OBJECTIVE: To investigate the independent and combined effects of the Trp64Arg polymorphism of the β3-adrenergic receptor (β3AR) gene and the (−3826) A→G polymorphism of the uncoupling protein 1 (UCP1) gene on body weight change in type 2 diabe
Autor:
P.B. García Jurado, E. Roldán Romero, M.E. Pérez Montilla, R. Valverde Moyano, I.M. Bravo Rey, F. Delgado Acosta, F.A. Bravo-Rodríguez
Publikováno v:
Neurología, Vol 36, Iss 8, Pp 589-596 (2021)
Resumen: Introducción: La transformación hemorrágica es una complicación importante del ictus isquémico agudo (IIA). El propósito del trabajo es analizar el impacto clínico y los factores predictores de las hemorragias intracraneales (HIC) tra
Externí odkaz:
https://doaj.org/article/c4f6d8ce71264d8cbcfe075d97423a68
Autor:
P.B. García Jurado, E. Roldán Romero, M.E. Pérez Montilla, R. Valverde Moyano, I.M. Bravo Rey, F. Delgado Acosta, F.A. Bravo-Rodríguez
Publikováno v:
Neurología (English Edition), Vol 36, Iss 8, Pp 589-596 (2021)
Introduction: Haemorrhagic transformation is a major complication of acute ischaemic stroke (AIS). We sought to determine the predictors and clinical impact of intracranial haemorrhage (ICH) after revascularisation therapy. Methods: We conducted a re
Externí odkaz:
https://doaj.org/article/57e34c59de8d4af8b53dd7cce7dd5d4b
Autor:
A, Vilppula, P, Collin, M, Mäki, R, Valve, M, Luostarinen, I, Krekelä, H, Patrikainen, K, Kaukinen, L, Luostarinen
Publikováno v:
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver. 40(10)
Up to 1% of the population suffer from coeliac disease. Data on the prevalence in elderly people is scant. We hypothesized that they would over time have developed obvious symptoms. Clinically silent or undiagnosed disease would thus be relatively un
Akademický článek
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Publikováno v:
European journal of clinical investigation. 31(4)
Insulin resistance in the most common familial dyslipidemia, familial combined hyperlipidemia (FCHL), could be due to variations in the hormone sensitive lipase (HSL) gene.The coding region of the HSL gene was screened with the single strand conforma
Autor:
J, Pihlajamäki, R, Miettinen, R, Valve, L, Karjalainen, L, Mykkänen, J, Kuusisto, S, Deeb, J, Auwerx, M, Laakso
Publikováno v:
Atherosclerosis. 151(2)
Dyslipidemias and insulin resistance often present simultaneously, as in familial combined hyperlipidemia (FCHL), and therefore may have a common genetic background. In our previous study the Pro12A1a substitution of peroxisome proliferator receptor
Autor:
L, Niskanen, M K, Karvonen, R, Valve, M, Koulu, U, Pesonen, M, Mercuri, R, Rauramaa, J, Töyry, M, Laakso, M I, Uusitupa
Publikováno v:
The Journal of clinical endocrinology and metabolism. 85(6)
We have recently demonstrated that subjects having Pro7 in the signal peptide ofneuropeptide Y (NPY) have higher serum cholesterol and apolipoprotein B levels than individuals with wild-type (Leu7Leu7) signal peptide sequence. We investigated the ass
Publikováno v:
Clinical pharmacology and therapeutics. 66(3)
Objective To determine whether there are any changes in the fatty acid composition of serum triglycerides, cholesterol esters, and phospholipids induced by administration of orlistat three times a day compared with placebo as combined with a low-fat