Search results for "types"

showing 10 items of 956 documents

Impact of clinical phenotypes on management and outcomes in European atrial fibrillation patients: a report from the ESC-EHRA EURObservational Resear…

2021

Abstract Background Epidemiological studies in atrial fibrillation (AF) illustrate that clinical complexity increase the risk of major adverse outcomes. We aimed to describe European AF patients’ clinical phenotypes and analyse the differential clinical course. Methods We performed a hierarchical cluster analysis based on Ward’s Method and Squared Euclidean Distance using 22 clinical binary variables, identifying the optimal number of clusters. We investigated differences in clinical management, use of healthcare resources and outcomes in a cohort of European AF patients from a Europe-wide observational registry. Results A total of 9363 were available for this analysis. We identified three …

RegistrieResearch Reportmedicine.medical_specialtyMajor adverse outcomeCardiovascular risk factorsCluster analysisRisk FactorsInternal medicineClinical phenotypeAtrial FibrillationEpidemiologyHumansMedicineRegistriesCluster analysiAtrial fibrillation; Clinical management; Clinical phenotypes; Cluster analysis; Major adverse outcomes; Humans; Phenotype; Registries; Research Report; Risk Factors; Atrial FibrillationClinical managementbusiness.industryProportional hazards modelRisk FactorHazard ratioRAtrial fibrillationClinical phenotypesMajor adverse outcomesGeneral Medicinemedicine.diseaseAtrial fibrillationConfidence intervalPhenotypeCohortMedicineObservational studybusinessResearch ArticleHumanBMC Medicine
researchProduct

Understanding Factors Associated With Psychomotor Subtypes of Delirium in Older Inpatients With Dementia

2020

Objectives Few studies have analyzed factors associated with delirium subtypes. In this study, we investigate factors associated with subtypes of delirium only in patients with dementia to provide insights on the possible prevention and treatments. Design This is a cross-sectional study nested in the "Delirium Day" study, a nationwide Italian point-prevalence study. Setting and participants Older patients admitted to 205 acute and 92 rehabilitation hospital wards. Measures Delirium was evaluated with the 4-AT and the motor subtypes with the Delirium Motor Subtype Scale. Dementia was defined by the presence of a documented diagnosis in the medical records and/or prescription of acetylcholine…

Rehabilitation hospitalmedicine.medical_specialtyUrinary systemSocio-culturaledementia; elderly; Motor subtypes of delirium; Aged; Cross-Sectional Studies; Humans; Inpatients; Italy; Delirium; Dementiaelderly03 medical and health sciences0302 clinical medicineInternal medicinemental disordersmedicineDementiaMotor subtypes of delirium dementia elderlyHumansdementia elderly Motor subtypes of delirium030212 general & internal medicineLS4_4Medical prescriptionGeneral NursingAgedPsychomotor learningInpatientsbusiness.industryHealth PolicyMedical recordMotor subtypes of deliriumMemantineDeliriumGeneral Medicinemedicine.diseasedementia; elderly; Motor subtypes of deliriumSettore MED/26 - NEUROLOGIACross-Sectional StudiesItalyDeliriumDementiaGeriatrics and Gerontologymedicine.symptombusiness030217 neurology & neurosurgerymedicine.drug
researchProduct

Pre-invasion history and demography shape the genetic variation in the insecticide resistance-related acetylcholinesterase 2 gene in the invasive Col…

2012

Abstract Background Invasive pest species offers a unique opportunity to study the effects of genetic architecture, demography and selection on patterns of genetic variability. Invasive Colorado potato beetle (Leptinotarsa decemlineata) populations have experienced a rapid range expansion and intense selection by insecticides. By comparing native and invasive beetle populations, we studied the origins of organophosphate (OP) resistance-associated mutations in the acetylcholinesterase 2 (AChE2) gene, and the role of selection and demography on its genetic variability. Results Analysis of three Mexican, two US and five European populations yielded a total of 49 haplotypes. Contrary to the exp…

Resistenssin evoluutio0106 biological sciencesInsecticidesDNA Mutational AnalysisGenes Insect01 natural sciencesInsecticide ResistanceJuvenile hormone esteraseDiapause protein 1Genetics0303 health sciencesbiologytulokaslajitMajor geneOrganophosphatesJuveniilihormoniesteraasiColeopteraTuholaistorjunta-aineresistenssiAcetylcholinesteraseInvaasiobiologiaAsetyylikoliiniesteraasiResearch ArticlePesticide resistanceEvolutionPesticide resistanceLocus (genetics)valinta03 medical and health sciencesGenetic variationQH359-425AnimalsGenetic variabilityDiapaussiproteiini 1SelectionEcology Evolution Behavior and SystematicsSolanum tuberosum030304 developmental biologyGenetic diversityInvasive speciesColorado potato beetleGenetic VariationResistance evolutionbiology.organism_classification010602 entomologyGenetics PopulationPopulation bottleneckHaplotypesInvasiolajiMutationIntroduced SpeciesInvasion biologyDemographyBMC Evolutionary Biology
researchProduct

Mutation Analysis Identifies GUCY2D as the Major Gene Responsible for Autosomal Dominant Progressive Cone Degeneration

2008

PURPOSE. Heterozygous mutations in the GUCY2D gene, which encodes the membrane-bound retinal guanylyl cyclase-1 protein (RetGC-1), have been shown to cause autosomal dominant inherited cone degeneration and cone–rod degeneration (adCD, adCRD). The present study was a comprehensive screening of the GUCY2D gene in 27 adCD and adCRD unrelated families of these rare disorders. METHODS. Mutation analysis was performed by direct sequencing as well as PCR and subsequent restriction length polymorphism analysis (PCR/RFLP). Haplotype analysis was performed in selected patients by using microsatellite markers. RESULTS. GUCY2D gene mutations were identified in 11 (40%) of 27 patients, and all mutation…

Retinal degenerationMaleDNA Mutational AnalysisReceptors Cell SurfaceBiologyPolymerase Chain ReactionArticlemedicineElectroretinographyMissense mutationHumansGenetic Predisposition to DiseaseCodonGeneGeneticsHaplotypeRetinal DegenerationDNAmedicine.diseasePrognosisRod Cell Outer SegmentMajor geneMolecular biologyPedigreeHaplotypesGuanylate CyclaseMutationMutation testingDisease ProgressionGUCY2DFemaleRestriction fragment length polymorphism
researchProduct

Predominio del genotipo G9 de rotavirus en Valencia y Castellón entre 2005 y 2007

2010

Resumen: Introducción: Las infecciones por rotavirus son la causa más frecuente de gastroenteritis aguda en la infancia. Existen disponibles vacunas para su prevención, pero su uso todavía es limitado y estos virus continúan infectando a la población infantil, principalmente en los meses fríos del año. Objetivos: Caracterizar los genotipos G (VP7) y P (VP4) de rotavirus detectados en niños con gastroenteritis aguda y determinar la prevalencia de las cepas de rotavirus con genotipo G9 en 3 departamentos de Salud Pública de la Comunidad Valenciana. Pacientes y métodos: Se estudiaron de forma prospectiva 541 muestras de heces de niños con gastroenteritis desde octubre de 2005 a septiembre de 2…

RotavirusRotavirusPediatrics Perinatology and Child HealthGenotypesmedicineBiologymedicine.disease_causeHumanitiesPediatricsRJ1-570GastroenteritisAnales de Pediatría
researchProduct

Small-diameter titanium Grade IV and titanium-zirconium implants in edentulous mandibles: three-year results from a double-blind, randomized controll…

2015

OBJECTIVE: The aim of this study was to compare crestal bone-level changes, soft tissue parameters and implant success and survival between small-diameter implants made of titanium/zirconium (TiZr) alloy or of Grade IV titanium (Ti) in edentulous mandibles restored with removable overdentures. MATERIALS AND METHODS: This was a randomized, controlled, double-blind, split-mouth multicenter clinical trial. Patients with edentulous mandibles received two Straumann bone-level implants (diameter 3.3 mm), one of Ti Grade IV (control) and one of TiZr (test), in the interforaminal region. Implants were loaded after 6-8 weeks and removable Locator-retained overdentures were placed within 2 weeks of l…

RoxolidMaleSmall diameterSLActive surfaceDentistrychemistry.chemical_elementMandibleCONVENTIONAL COMPLETE DENTURESlaw.inventionDouble blindRETROSPECTIVE EVALUATION IMPLANTDouble-Blind MethodRandomized controlled triallawMARGINAL BONE LOSSHumansJaw EdentulousMedicineMANDIBULAR 2-IMPLANT OVERDENTURES610 Medicine & healthAgedDental ImplantsTitaniumPATIENT SATISFACTIONTitanium/zirconiumSTRESS-DISTRIBUTIONbusiness.industryDental Implantation Endosseoustechnology industry and agricultureWITHIN-SUBJECT COMPARISONSSoft tissueDIFFERENT LOADING PROTOCOLSDenture Overlayequipment and suppliesTitanium zirconiumddc:617.6Treatment OutcomeDental Prosthesis DesignchemistryImplant typesedentulousFemaleZirconiumImplantFINITE-ELEMENT-ANALYSISOral SurgerybusinessDental AlloysTitaniumClinical Oral Implants Research
researchProduct

Pleistocene allopatric differentiation followed by recent range expansion explains the distribution and molecular diversity of two congeneric crustac…

2021

AbstractPleistocene glaciations had a tremendous impact on the biota across the Palaearctic, resulting in strong phylogeographic signals of range contraction and rapid postglacial recolonization of the deglaciated areas. Here, we explore the diversity patterns and history of two sibling species of passively dispersing taxa typical of temporary ponds, fairy shrimps (Anostraca). We combine mitochondrial (COI) and nuclear (ITS2 and 18S) markers to conduct a range-wide phylogeographic study including 56 populations of Branchinecta ferox and Branchinecta orientalis in the Palaearctic. Specifically, we investigate whether their largely overlapping ranges in Europe resulted from allopatric differe…

SCALE DISPERSALPleistoceneRange (biology)LARGE BRANCHIOPODS CRUSTACEASciencePopulation DynamicsSettore BIO/05 - ZoologiaAllopatric speciationGENETIC CONSEQUENCESDNA MitochondrialArticleEvolution MolecularANOSTRACAN FAUNAAnimalsGlacial periodPondsEcosystemPhylogenyFAIRY SHRIMPStochastic ProcessesBranchiopodaScience & TechnologyMultidisciplinaryModels GeneticbiologyEcologyGenetic DriftQRGenetic VariationBranchinectaBiodiversityBAYESIAN PHYLOGENETIC INFERENCEFRESH-WATER INVERTEBRATESbiology.organism_classificationBRINE SHRIMPSPhylogeneticsMultidisciplinary SciencesGenetic divergencePhylogeographyPhylogeographyHaplotypesBiogeographyScience & Technology - Other TopicsMEDITERRANEAN BASINPASSIVE DISPERSALBiological dispersalMedicineAnostracaScientific Reports
researchProduct

Mitochondrial genetic haplogroups and incident obesity: a longitudinal cohort study.

2018

Background/Objectives: A small number of case-control studies have suggested that mitochondrial haplogroups could be associated with obesity. We examined whether obesity risk was influenced by mitochondrial haplogroup in a large North American cohort across an 8-year period. We conducted a longitudinal cohort study including individuals from the Osteoarthritis Initiative. Subjects/Methods: Mitochondrial haplogroups were determined by sequencing and PCR-RFLP techniques using this nomenclature: HV, JT, KU, IWX, and super HV/others. The strength of the association between mitochondrial haplogroups and incident obesity was quantified with hazard ratios (HRs), adjusted for potential confounders …

SELECTIONMale0301 basic medicinePopulationBFMedicine (miscellaneous)DNA MitochondrialHaplogroupCohort Studies03 medical and health sciencesHumansMedicineObesityeducationAgedRISKeducation.field_of_studyNutrition and Dieteticsbusiness.industryHaplotypeHazard ratioConfoundingMiddle AgedUnited StatesMedicine (miscellaneous); Nutrition and DieteticsPHYSICAL-ACTIVITY030104 developmental biologyHaplotypesCohortFemalebusinessCohort studyDemographyHuman mitochondrial DNA haplogroup
researchProduct

Polymorphisms of beta-lactoglobulin promoter region in three Sicilian goat breeds

2012

Several beta-lactoglobulin (BLG) polymorphisms have been described within the proximal promoter region and coding region of the caprine gene, although no genetic variants affecting the protein amino acid composition and/or expression level have been characterized so far. Binding sites for several transcription factors (TFs) are present in the BLG promoter region. The aims of this work were to sequence the full-length promoter region of three Sicilian goat breeds in order to identify polymorphisms, analyze the identified haplotypes, search for differences between breeds for the presence of polymorphisms in this gene region, search for putative TFs binding sites, and check if polymorphisms la…

SICILIAN GOATMolecular Sequence DataSNPSingle-nucleotide polymorphismLactoglobulinsBiologyPolymerase Chain ReactionPolymorphism Single NucleotideSettore AGR/17 - Zootecnica Generale E Miglioramento GeneticoSpecies SpecificityBETA LACTOGLOBULIN GENEGene expressionGeneticsAnimalsCluster AnalysisCoding regionBinding sitePromoter Regions GeneticSicilyMolecular BiologyGeneTranscription factorGeneticsBase SequenceModels GeneticGoatsHaplotypeGenetic VariationPromoterSequence Analysis DNAGeneral MedicineMilk ProteinsMolecular biologyNFI Transcription FactorsTRANSCRIPTION FACTORSBeta-lactoglobulin Polymorphisms Promoter Sicilian goatsHAPLOTYPES
researchProduct

Serotypes, antibiotic resistance, and class 1 integrons in Salmonella isolates from paediatric cases of enteritis in Tehran, Iran.

2011

Salmonella serotypes antibiotic resistance class 1 integrons IranSettore MED/07 - Microbiologia E Microbiologia ClinicaSettore MED/42 - Igiene Generale E Applicata
researchProduct