aineenvaihduntahäiriöt

name

• aineenvaihduntahäiriöt

Works about aineenvaihduntahäiriöt

• Adipose tissue metabolism in acquired obesity
• Aineenvaihdunta tasapainoon, terveys kuntoon
• Aineenvaihduntataudit : oireista diagnoosiin
• Androgen secretion and cardiovascular risk factors in women with and without PCOS :
• Arginiini ja terveys
• Arginin och hälsa
• Biochemical changes in inborn and acquired errors of metabolism
• Body composition and molecular reflections of obesity-related cardio-metabolic disorders :
• Combination antiretroviral therapy -associated lipodystrophy : insights into pathogenesis and treatment
• Cross-sectional associations and effect of a lifestyle intervention
• Cutaneous porphyrias : clinical and histopathological study
• Determinants of cognitive impairment in old age and their genetic architecture
• Diet, body adiposity and cardiometabolic risk in a population sample of primary school children
• Effects of lifestyle counselling on cardiometabolic risk factors :
• Endogenous sex hormones and lipoproteins in healthy men and in men with coronary heart disease
• Fatty acids, fibre, carotenoids and tocopherols in relation to glucose metabolism in subjects at high risk for type 2 diabetes : a cross-sectional analysis
• Genetic causes of mitochondrial complex I deficiency in children
• Glucose metabolism in preclinical type 1 diabetes
• Gut microbiota and metabolic disorders
• Haem arginate : a new haem compound for acute porphyrias
• Hyperandrogenism, menstrual irregularities and polycystic ovary syndrome :
• Laboratory diagnostics of dyslipidemia : from cholesterol to apolipoproteins
• Lipidiaineenvaihdunnan häiriöt : kliininen merkitys & hoito
• Lipidiaineenvaihdunnan häiriöt, kliininen merkitys ja hoito
• Lipotoxicity in obesity and coronary artery disease : studies by PET, CT and MR
• Mechanism and effects of mitochondrial DNA instability and copy number manipulation
• Metabolic and genetic determinants of HDL in families with low HDL cholesterol and premature coronary heart disease
• Metabolinen oireyhtymä Suomessa : Metabolic syndrome in Finland
• Mitochondrial helicase Twinkle in mtDNA copy number regulation and a late-onset disease model
• Modelling metabolic disorders : multiplexin collagens in bone remodelling, and lipid and energy metabolism
• Molecular and cell phenotype changes in mitochondrial diseases
• Molecular genetics of acute intermittent porphyria in Finland
• Molecular genetics of variegate porphyria in Finland
• Mulibrey nanism : clinical characteristics and pathophysiologic features of growth restriction, insulin resistance and tumour development
• Nuclear receptors as molecular machines : mechanistic investigations on DNA-, ligand- and coactivator-nuclear receptor interactions
• Population attributable fraction (PAF) in epidemiologic follow-up studies
• Reuma ja kihti
• Searching for genes predisposing to common dyslipidemias
• Sokerinhimo kuriin : helppo ja tehokas ohjelma sokerista luopumiseen - makeudesta tinkimättä
• Suomalainen lääkärikeskus : 1
• Toimintakyky : arviointi ja kliininen käyttö
• Vastasyntyneiden harvinaisten aineenvaihduntatautien seulonta