Search results for "dominant"

showing 10 items of 231 documents

Non-invasive Spatial Mapping of Frequencies in Atrial Fibrillation: Correlation With Contact Mapping

2021

[EN] Introduction: Regional differences in activation rates may contribute to the electrical substrates that maintain atrial fibrillation (AF), and estimating them non-invasively may help guide ablation or select anti-arrhythmic medications. We tested whether non-invasive assessment of regional AF rate accurately represents intracardiac recordings. Methods: In 47 patients with AF (27 persistent, age 63 +/- 13 years) we performed 57-lead non-invasive Electrocardiographic Imaging (ECGI) in AF, simultaneously with 64-pole intracardiac signals of both atria. ECGI was reconstructed by Tikhonov regularization. We constructed personalized 3D AF rate distribution maps by Dominant Frequency (DF) ana…

medicine.medical_specialtyPhysiologymedicine.medical_treatmentDriverBasket mapping030204 cardiovascular system & hematologyIntracardiac injectionlcsh:PhysiologyCorrelationTECNOLOGIA ELECTRONICA03 medical and health sciences0302 clinical medicineInternal medicinePhysiology (medical)medicineOriginal ResearchImatges tridimensionals en medicinalcsh:QP1-981Dominant frequencybusiness.industryNon invasiveSpatial mappingElectrocardiographic imagingAtrial fibrillationDominant frequencyAblationmedicine.diseaseAtrial fibrillationElectrocardiographic imagingNon-invasive mappingCardiologyEnginyeria biomèdicabusiness030217 neurology & neurosurgery
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Changes in the Spectral Characteristics of Ventricular Fibrillation in Lesions Produced by Radiofrequency Ablation. An Experimental Study

2008

INTRODUCTION AND OBJECTIVES Although electro- physiological databases contain information about changes in the time domain in lesions produced by radiofrequency ablation, very few data on changes in the frequency domain are available. The aim of this study was to investigate changes in the spectral characteristics of ventricular fibrillation in zones with radiofrequency lesions. METHODS Recordings of ventricular fibrillation were obtained in 11 isolated perfused rabbit heart preparations using a multiple epicardial electrode located on the left ventricular free wall. Spectral parameters derived by Fourier analysis before and after the creation of transmural radiofrequency lesions were compa…

medicine.medical_specialtyRadiofrequency ablationHeart VentriclesIn Vitro TechniquesStandard deviationlaw.inventionLesionNuclear magnetic resonancelawInternal medicineAnimalsMedicinebusiness.industrySpectral densityGeneral MedicineDominant frequencymedicine.diseaseMean frequencyFrequency domainVentricular FibrillationVentricular fibrillationCatheter AblationCardiologyRabbitsmedicine.symptombusinessRevista Española de Cardiología (English Edition)
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Critical role of cardiac magnetic resonance in the diagnosis of left-dominant arrhythmogenic cardiomyopathy: A paradigmatic case in a recreational mi…

2021

medicine.medical_specialtySports cardiologyCardiac magnetic resonancebusiness.industryCardiomyopathyCase Reportmedicine.diseaseDefibrillatorInternal medicineDiagnosisCardiologyMedicineCardiology and Cardiovascular MedicinebusinessCardiac magnetic resonanceLEFT DOMINANTArrhythmiaHeartRhythm Case Reports
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Expression of differentiation antigens and growth-related genes in normal kidney, autosomal dominant polycystic kidney disease, and renal cell carcin…

1992

Cellular differentiation and mRNA levels of genes involved in kidney growth were investigated in normal kidney cells, cyst-lining epithelial cells of polycystic kidney disease, and renal carcinoma cells (RCC). All cells comparatively studied exhibited an antigenic phenotype of proximal tubular cells as shown by the expression of a panel of brush border membrane enzymes and kidney-associated cell surface antigens. The epithelial developmental antigen Exo-1 was expressed in 50% to 80% of cyst-lining epithelia in polycystic kidney tissue and in 20% to 30% of polycystic kidney cells cultured in vitro. Normal kidney cells and RCC were negative under identical culture conditions. The expression o…

medicine.medical_specialtyTGF alphaCellular differentiationAutosomal dominant polycystic kidney diseaseGene ExpressionBiologyKidneyEpitheliumProto-Oncogene Proteins c-mycGrowth factor receptorEpidermal growth factorInternal medicinemedicinePolycystic kidney diseaseHumansRNA MessengerGrowth SubstancesCarcinoma Renal CellCells CulturedKidneyurogenital systemAntibodies MonoclonalTransforming Growth Factor alphamedicine.diseasePolycystic Kidney Autosomal DominantAntigens DifferentiationImmunohistochemistryKidney NeoplasmsErbB ReceptorsEndocrinologymedicine.anatomical_structureGenesNephrologyAntigens SurfaceCancer researchTransforming growth factorAmerican journal of kidney diseases : the official journal of the National Kidney Foundation
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Dominant frequency and complexity of electrical reentrant activation during ventricular fibrillation with releasing of NO after acute local stretchin…

2013

medicine.medical_specialtybusiness.industryRabbit heartCardiac arrhythmiaDominant frequencymedicine.diseaseReentrancyInternal medicineVentricular fibrillationCardiologymedicineMyocyteCardiology and Cardiovascular MedicinebusinessPerfusionInotropic agentEuropean Heart Journal
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Mutations in the NKX2.5 Gene and the PAX8 Promoter in a Girl with Thyroid Dysgenesis

2011

Screening of the known candidate genes involved in thyroid organogenesis has revealed mutations in a small subset of patients with congenital hypothyroidism due to thyroid dysgenesis (TD).We studied a girl with TD who had mutations in two transcription factors involved in thyroid development.Sequencing analysis of candidate genes involved in thyroid gland development revealed a new paternally inherited heterozygous mutation in the NKX2.5 gene (S265R) and a new maternally inherited heterozygous mutation in the PAX8 promoter region (-456CT). Both parents and a brother, who was also heterozygous for both mutations, were phenotypically normal. Immunofluorescence microscopy showed a correct nucl…

medicine.medical_specialtyendocrine systemendocrine system diseasesEndocrinology Diabetes and Metabolismmedicine.medical_treatmentClinical BiochemistryBiologyGene mutationDominant-Negative Mutationmedicine.disease_causeBiochemistryThyroid dysgenesisPAX8 Transcription FactorEndocrinologyInternal medicinemedicineCongenital HypothyroidismHumansPaired Box Transcription FactorsPromoter Regions GeneticGeneticsHomeodomain ProteinsMutationBiochemistry (medical)ThyroidJCEM Online: Brief Reportsmedicine.diseaseCongenital hypothyroidismmedicine.anatomical_structureEndocrinologyMutationThyroid DysgenesisCancer researchHomeobox Protein Nkx-2.5ThyroglobulinFemalePAX8Transcription Factors
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Analysis of inter-atrium differences in paroxysmal and persistent atrial fibrillation using principal component analysis

2007

The pathophysiological mechanisms of atrial fibrillation (AF) are not entirely clear yet, and there is no full explanation for the development and evolution of the arrhythmia. The goal of this study is to find inter-atrium differences in electrophysiological behavior between persistent and paroxysmal AF. The database analyzed contains intra-cardiac records from 14 patients with paroxysmal AF and 10 with persistent AF. Dominant frequency and sample entropy measurements showed that in the paroxysmal group there was a left-to-right gradient. These differences were enhanced after the extraction of the main components with principal component analysis. These findings may be interpreted as a poss…

medicine.medical_specialtymedicine.diagnostic_testbusiness.industryLeft atriumAtrial fibrillationDominant frequencymedicine.diseaseSample entropymedicine.anatomical_structureAnesthesiaInternal medicinePersistent atrial fibrillationPrincipal component analysiscardiovascular systemmedicineCardiologybusinessElectrocardiographyParoxysmal AF2007 Computers in Cardiology
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Does δ-sarcoglycan-associated autosomal-dominant cardiomyopathy exist?

2009

In this study we clinically and genetically characterize a consanguineous family with a homozygous novel missense mutation in the delta-sarcoglycan gene and a second delta-sarcoglycan mutation that has previously been reported to cause severe autosomal-dominant dilated cardiomyopathy. We identified a novel missense mutation in exon 6 (p.A131P) of the delta-sarcoglycan gene, which in a homozygous state leads to the clinical picture of a limb girdle muscular dystrophy. In four heterozygous carriers for the mutation, aged 3-64 years, a second sequence variant in exon 6 (p.S151A) of the delta-sarcoglycan gene was detected on the other allele. This second missense change had previously been repo…

musculoskeletal diseasesAdultCardiomyopathy DilatedMalemedicine.medical_specialtyAdolescentBiopsyDNA Mutational AnalysisCardiomyopathyMutation MissenseCompound heterozygosityArticleExonConsanguinityElectrocardiographyYoung AdultInternal medicineSarcoglycansGeneticsMedicineMissense mutationHumansMuscular dystrophyChildGenetics (clinical)Genes DominantGeneticsFamily Healthbusiness.industryMusclesMyocardiumDilated cardiomyopathyMiddle Agedmedicine.diseasePedigreeEndocrinologyEchocardiographyChild PreschoolMutation (genetic algorithm)FemalebusinessLimb-girdle muscular dystrophy
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Factors Enabling and Hindering Value Co-Creation in Continuous Service Development: A Systematic Literature Review

2022

This paper presents a systematic literature review (SLR) investigating the factors that enable and hinder value co-creation in organizations’ continuous service development processes. Employing the lens of service-dominant (S-D) logic, we classify the identified factors into three interrelated dimensions: institutions, resources, and service exchange. Our systematic findings may inform organizations’ efforts to support the emergence of positive rather than negative value outcomes when implementing continuous practices in their service development. In addition, we outline avenues for further research in this emerging topic area. peerReviewed

palvelutDigital and Cybernized Services and Digitalization of Servicescontinuous practicesdevopsarvonluontisystematic literature revieworganisaatiotcontinuous service developmentservice-dominant logicdigitalisaatiosystemaattiset kirjallisuuskatsauksetvalue co-creationProceedings of the Annual Hawaii International Conference on System Sciences
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Value Co-Destruction: A Conceptual Review and Future Research Agenda

2023

The service-dominant (S-D) logic lens for understanding value co-creation and customers’ interactive roles in the service exchange has emerged as a focal theme of interest among service academics and practitioners. While recent investigations have also focused on the process of value co-destruction—that is, how potential negative outcomes occur—the concept and its distinction from value co-creation remain unclear. This conceptual review synthesizes the concept of value co-destruction and proposes a framework consisting of two interrelated dimensions—actor–actor interaction and individual actor —and their components at three temporal points of the service encounter. We distinguish value co-…

palvelutOrganizational Behavior and Human Resource ManagementSociology and Political Sciencearvojohtaminenservice-dominant logicasiakaslähtöisyysvalue co-destructionarvot (käsitykset)arvo (ominaisuudet)asiakkaatliiketoimintaarvokasvatusconceptual reviewco-creationservice actorInformation SystemsJournal of Service Research
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