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Wyniki wyszukiwania dla: rare genetic disease
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Shape Optimisation of Kaplan Turbine Blades Using Genetic Algorithms
PublikacjaThis monograph is a comprehensive guide to a method of blade profile optimisation for Kaplan-type turbines. This method is based on modelling the interaction between rotor and stator blades. Additionally, the shape of the draft tube is investigated. The influence of the periodic boundary condition vs. full geometry is also discussed. Evolutionary algorithms (EA) are used as an optimisation method together with artificial neural...
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Grid Implementation of a Parallel Multiobjective Genetic Algorithm for Optimized Allocation of Chlorination Stations in Drinking Water Distribution Systems: Chojnice Case Study
PublikacjaSolving multiobjective optimization problems requires suitable algorithms to find a satisfactory approximation of a globally optimal Pareto front. Furthermore, it is a computationally demanding task. In this paper, the grid implementation of a distributed multiobjective genetic algorithm is presented. The distributed version of the algorithm is based on the island algorithm with forgetting island elitism used instead of a genetic...
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Evaluation of the anti-tyrosinase activity of extracts and rare flavonoids from Scleranthus perennis L.
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Distribution and mobility of rare earth elements (Sc,Y) in selected types of soils (Poland)
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Myeloperoxidase Modulates Inflammation in Generalized Pustular Psoriasis and Additional Rare Pustular Skin Diseases
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Enhanced acceptor concentration, proton conductivity, and hydration in multicomponent rare‐earth ortho‐niobates
PublikacjaThe structural properties of (La0.2Nd0.2Sm0.2Gd0.2Eu0.2)1−xCaxNbO4−δ (x = 0–0.05) series have been studied by X-ray powder diffraction at room temperature. The thermal properties were investigated using thermogravimetry, from which the concentration of proton defects was determined. Additionally, dilatometry studies were carried out, from which the thermal expansion coefficients and the phase transition temperature between low-...
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Cognitive decline in Huntington's disease expansion gene carriers
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The Impact of Huntington Disease on Family Carers: a Literature Overview
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EDITORIALHypertension and cardiovascular disease: Is arterial stiffness the heart of the matter?
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Plasma Lipid Composition and Risk of Developing Cardiovascular Disease
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Tackling age-related disease: time for a step forward
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Pet Ownership and the Risk of Arterial Hypertension and Cardiovascular Disease
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The Global Burden of Disease Study 2015 and Blood Pressure
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Managing comorbid cardiovascular disease and sleep apnea with pharmacotherapy
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Estimation of Oxidative Stress Markers in Chronic Kidney Disease
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Exhaled nitric oxide in pediatric patients with respiratory disease
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Selected biologic markers of inflammation and activity of Crohn’s disease
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Female Fabry disease patients and X-chromosome inactivation
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Elite athletes with COVID-19 — Predictors of the course of disease
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An Overview of Several Inhibitors for Alzheimer’s Disease: Characterization and Failure
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Acceptance of the disease and sexual functions of patients with heart failure
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B35 The Significance The Level Of Mitochondrial Dna In Huntington's Disease
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Genetic determinants of plasma ACE and renin activity in young normotensive twins
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Optimization of a three-bed adsorption chiller by genetic algorithms and neural networks
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Association between susceptibility to photodynamic oxidation and the genetic background of Staphylococcus aureus
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A multilocus genetic risk score is associated with arterial stiffness in hypertensive patients
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Genetic variation in IL-10 influences the progression of hepatitis B infection
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Finding Temperature Distribution at Heat Recovery Unit Using Genetic Algorithms
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The role of genetic factors and monocyte-to-osteoclast differentiation in the pathogenesis of Charcot neuroarthropathy
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A genetic algorithm application for automatic layout design of modular residential homes
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DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE
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Professional activity, gender and disease-related emotions: The impact on parents' experiences in caring for children with phenylketonuria
PublikacjaIntroduction: Clinical management of rare diseases often fails to acknowledge the challenges faced by caregivers.Whilst management of phenylketonuria (PKU) may not be considered as dire as other conditions, most studiesprimarily concentrate on clinical issues, dietary adherence, or the quality of life of the PKU patients, leavingcaregivers in the background. The aim of the study was to evaluate the psychosocial...
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Animal Genetic Resources an international journal
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Plant Genetic Resources-Characterization and Utilization
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GENETIC SOCIAL AND GENERAL PSYCHOLOGY MONOGRAPHS
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Journal of Genetic Syndromes & Gene Therapy
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The Awareness of Rare Diseases Among Medical Students and Practicing Physicians in the Republic of Kazakhstan. An Exploratory Study
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Coexistence of HFE and rare UGT1A1 genes mutations in patients with iron overload related liver injury
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Influence of plasmon resonance on the luminescence of titanium dioxide thin films doped with rare earth ions
PublikacjaIn this work the study of the optical properties of europium doped titanium dioxide thin films (TiO2:Eu) enhanced by gold plasmonic nanostructures are presented. Plasmonic platforms were manufactured by thermal annealing of thin film of Au, deposited on a Corning glass substrate. As a result of thermal treatment, gold spherical nanostructures with average dimensions of 50 nm were obtained. Luminescent TiO2:Eu film was deposited...
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Risk factors for chronic kidney disease do not influence the serum levels of asymmetric dimethylarginine in HIV-1-infected patients without significant renal disease
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Design, synthesis and biological evaluation of novel N-phosphorylated and O-phosphorylated tacrine derivatives as potential drugs against Alzheimer’s disease
PublikacjaIn this work, we designed, synthesised and biologically investigated a novel series of 14N- and O-phosphorylated tacrine derivatives as potential anti-Alzheimer’s disease agents. In the reaction of 9-chlorotacrine and corresponding diamines/aminoalkylalcohol we obtained diamino and aminoalkylhydroxy tacrine derivatives. Next, the compounds were acid to give final products 6–13 and 16–21 that were characterised by 1H, 13 C, 31P...
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Visual control improves the accuracy of hand positioning in Huntington’s disease
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Definitions of health and disease among physicians and Społem PSS employees
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Family caregivers’ experiences with healthcare services: a case of Huntington disease
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Caring for patients with Huntington disease – A survey of caregivers’ experiences and views
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Are advanced glycation end-products specific biomarkers for Alzheimer's disease?
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Hypertension and coronary artery disease: Mechanistic insights and therapeutic challenges
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Population pharmacokinetics of hydroxyurea for children and adolescents with sickle cell disease
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Vitamin D receptor gene polymorphisms in Alzheimer's disease patients
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Parkinson’s disease: Etiopathogenesis, molecular basis and potential treatment opportunities
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