Search results for "PPV"

showing 10 items of 17 documents

Pure Progressive Amnesia and the APPV717G Mutation

2009

We report an isolated, slowly progressive, pure amnestic phenotype in a 59-year-old member of a family affected by autosomal dominant familial Alzheimer disease. Early-onset Alzheimer disease in this family was associated with a V717G mutation in the amyloid precursor protein gene (APP). Subjective impairment of episodic memory began in our subject at the age of 44 years and subsequent, longitudinal neuropsychologic assessment confirmed progressive, severe, global impairment of memory functions over a period of 14 years with preservation of other cognitive domains. The mean annual hippocampal atrophy rate, determined by volumetric magnetic resonance imaging was intermediate between values p…

AdultMaleAgingPathologymedicine.medical_specialtyGlycineAmnesiaHippocampusAmyloid beta-Protein PrecursorAtrophyAlzheimer DiseasemedicineHumansDementiaMemory disorderEpisodic memoryAgedSettore M-PSI/02 - Psicobiologia E Psicologia FisiologicaCognitive disorderValineMiddle Agedmedicine.diseaseAPPV717G mutation.PedigreePsychiatry and Mental healthClinical PsychologyPhenotypeMutationDisease ProgressionPure progressive amnesiaFemaleAmnesiaAtrophyGeriatrics and Gerontologymedicine.symptomAlzheimer's diseasePsychologyGerontologyFrontotemporal dementia
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Are postural restrictions necessary for management of posterior canal benign paroxysmal positional vertigo?

2011

Objectives: An important component of management of benign paroxysmal positional vertigo (BPPV) has been the application of postural restrictions after use of a canalith repositioning maneuver (CRM) to prevent the return of otolithic debris into the posterior semicircular canal (PSC). This study was designed to explore the effectiveness of postural restrictions in patients with BPPV caused by otolithic debris in the PSC. Methods: Seventy-four adult patients with unilateral PSC BPPV were enrolled into this study. All patients were managed with a CRM — Either the modified Epley maneuver or the Semont maneuver. The patients were divided randomly into 2 groups: Group A, with postural restrictio…

AdultMalemedicine.medical_specialtyBenign paroxysmal positional vertigoAdolescentmedicine.medical_treatmentPostureEpley maneuverlaw.inventionSemont maneuverYoung AdultPhysical medicine and rehabilitationPosterior canal vertigoRandomized controlled triallawPostural restrictionRecurrenceVertigomedicineHumansEpley maneuverBenign Paroxysmal Positional VertigoProspective StudiesProspective cohort studyAgedSemont maneuverAged 80 and overAdult patientsbiologyPosterior Semicircular Canalbusiness.industryGeneral MedicineMiddle Agedmedicine.diseasebiology.organism_classificationBPPVSurgeryTreatment OutcomeOtorhinolaryngologyVertigoFemalebusinessThe Annals of otology, rhinology, and laryngology
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Vibrational spectra and DFT calculations of PPV-oligomers

2003

The first two members of the p-phenylenevinylene- oligomer family (i. e. 1, 4-distyrylbenzene [DSB] and 4, 4'-distyrylstilbene [DSS]) were synthesized and their infrared and Raman spectra recorded and empirically assigned. Molecular geometries were optimized for the planar point group (C2h) by the density functional theory (DFT) method using the B3LYP functional and 6-31G* basis set. Calculations of vibrational spectra, including intensities, were carried out subsequently using the DFT method with the same basis set and linear scaling was applied. Calculated vibrational wavenumbers are in a fair agreement with our own experimental spectra. In order to explore changes in vibrational dynamics…

ChemistryInfraredOrganic ChemistryAnalytical chemistryPotential energyMolecular physicsHot bandAnalytical ChemistryInorganic Chemistrysymbols.namesakeMolecular geometryNormal modesymbolsDensity functional theoryPhysics::Chemical Physicsp-Phenylenevinylenes ; PPV ; Vibrational analysis ; Density functional theory ; Potential energy distributionRaman spectroscopySpectroscopyBasis setJournal of Molecular Structure
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Prediction of type 2 diabetes mellitus based on nutrition data

2021

Abstract Numerous predictive models for the risk of type 2 diabetes mellitus (T2DM) exist, but a minority of them has implemented nutrition data so far, even though the significant effect of nutrition on the pathogenesis, prevention and management of T2DM has been established. Thus, in the present study, we aimed to build a predictive model for the risk of T2DM that incorporates nutrition data and calculates its predictive performance. We analysed cross-sectional data from 1591 individuals from the population-based Cooperative Health Research in the Region of Augsburg (KORA) FF4 study (2013–14) and used a bootstrap enhanced elastic net penalised multivariate regression method in order to bu…

Elastic net regularizationFood intakeMultivariate statistics24HFL 24-h food listEndocrinology Diabetes and MetabolismPopulation030209 endocrinology & metabolismType 2 diabetesLogistic regression03 medical and health sciences0302 clinical medicinePredictive Value of TestsRisk FactorsElastic net regressionPrediction modelGermanyStatisticsmedicineHumans030212 general & internal medicineeducationNutritionMathematicseducation.field_of_studyNutrition and DieteticsReceiver operating characteristicDietary Surveys and Nutritional EpidemiologyType 2 Diabetes MellitusType 2 diabetesT2DM type 2 diabetes mellitusmedicine.diseasePPV positive predictive valueDietROC receiver operating characteristicCross-Sectional StudiesNPV negative predictive valueDiabetes Mellitus Type 2ROC CurveKORA Cooperative Health Research in the Region of Augsburg24hfl 24-h Food List ; Elastic Net Regression ; Kora Cooperative Health Research In The Region Of Augsburg ; Npv Negative Predictive Value ; Nutrition ; Ppv Positive Predictive Value ; Prediction Model ; Roc Receiver Operating Characteristic ; T2dmResearch ArticleFood ScienceJournal of Nutritional Science
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Colloidal Nanoplatelet/Conducting Polymer Hybrids: Excitonic And Material Properties

2016

WOS:000370678700053 Here we present the first account of conductive polymer/colloidal nanoplatelet hybrids. For this, we developed DEH-PPV-based polymers with two different anchor groups (sulfide and amine) acting as surfactants for CdSe nanoplatelets, which are atomically flat semiconductor nanocrystals. Hybridization of the polymers with the nanoplatelets in the solution phase was observed to cause strong photoluminescence quenching in both materials. Through steady-state photoluminescence and excitation spectrum measurements, photoluminescence quenching was shown to result from dominant exciton dissociation through charge transfer at the polymer/nanoplatelet interfaces that possess a sta…

Excitation spectrumMaterials sciencePhotoluminescenceSulfideDEH-PPV-Based PolymersSulfideExcitonCdSe NanoplateletsNanotechnology02 engineering and technologySurface active agents010402 general chemistryOptoelectronic devices01 natural sciencesDissociation (chemistry)ColloidCharge transferQuenchingHybrid optoelectronic devicesPhysical and Theoretical ChemistryPhotoluminescenceSulfur compoundsAmineSemiconductor nanocrystalsConductive polymerchemistry.chemical_classificationExcited statesBuilding blockesPolymerInterface statesEmission quenching021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPolymer/Colloidal Nanoplatelet HybridsGeneral EnergyChemical engineeringchemistryExcited stateAnchorsExcitons0210 nano-technologyDissociationConductive polymerPhotoluminescence quenchingExciton dissociation
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Observational study on risk factors determining residual dizziness after successful benign paroxysmal positional vertigo treatment: The role of subcl…

2018

Studio osservazionale sui fattori di rischio che causano residual dizziness dopo il trattamento della vertigine parossistica posizionale benigna: il ruolo della VPPB subclinica.Alcuni pazienti, dopo il trattamento della vertigine parossistica posizionale benigna concluso con successo, possono lamentare un disequilibrio residuo. La possibile spiegazione potrebbe essere: la persistenza di otoliti canalari insufficienti a provocare un nistagmo clinicamente evidente, una disfunzione utriculare, coesistenza di altri disordini del sistema vestibolare. Abbiamo condotto uno studio osservazionale prospettico caso-controllo, focalizzando l’attenzione sul ruolo di fattori di rischio che possono causar…

MalePediatricsNistagmoNystagmusResidualSettore MED/42 - Igiene Generale E ApplicataDisequilibrio residuoNystagmus0302 clinical medicineRisk FactorsMedicine030223 otorhinolaryngologyResidual dizzinessSubclinical infectionAged 80 and overHigh prevalenceDizzineMiddle AgedGeneral Energy030220 oncology & carcinogenesisCohortVPPB soggettivaFemaleBenign paroxysmal positional vertigomedicine.symptomAdultmedicine.medical_specialtyBenign paroxysmal positional vertigoAdolescentVertigine parossistica posizionale benignaResidual dizzineDizzinessNystagmuVestibologyYoung Adult03 medical and health sciencesDisequilibriootorhinolaryngologic diseasesHumansIn patientAgedbusiness.industrymedicine.diseaseLogistic ModelsOtorhinolaryngologyCase-Control StudiesObservational studysense organsbusinessSubjective BPPV
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Determining a healthy reference range and factors potentially influencing PRO-C3 – A biomarker of liver fibrosis

2021

Background & Aims Progressive fibrosis has been identified as the major predictor of mortality in patients with non-alcoholic fatty liver disease (NAFLD). Several biomarkers are currently being evaluated for their ability to substitute the liver biopsy as the reference standard. Recent clinical studies in NAFLD/NASH patients support the utility of PRO-C3, a marker of type III collagen formation, as a marker for the degree of fibrosis, disease activity, and effect of treatment. Here we establish the healthy reference range, optimal sample handling conditions for both short- and long-term serum storage, and robustness for the PRO-C3 assay. Methods PRO-C3 was measured in 269 healthy volunteers…

NASH-CRN NASH Clinical Research NetworkBiopsyDiseaseAST aspartate aminotransferaseRC799-869Ethnic groupsGastroenterologyNIMBLE Non-Invasive Biomarkers of Metabolic Liver Disease (consortium)FibrosisImmunology and AllergyBody mass indexmedicine.diagnostic_testFatty liverNAS NAFLD Activity ScoreGastroenterologyDiseases of the digestive system. GastroenterologyHospitalsNPV negative predictive valueLiver biopsyBiomarker (medicine)Research Articlemedicine.medical_specialtyNAFLD non-alcoholic fatty liver diseaseADAM A Disintegrin and MetalloproteasesNASH non-alcoholic steatohepatitisReference rangeReference valuesAUROC area under the receiver operating characteristics curveInternal medicineALT alanine aminotransferaseBiopsyInternal MedicinemedicineHumansFIB-4 fibrosis-4Healthy volunteersHepatologyALP alkaline phosphatasebusiness.industryCLSI Clinical and Laboratory Standards InstituteT2DM type 2 diabetes mellitusELF™ test Enhanced Liver Fibrosis testmedicine.diseaseLITMUS Liver Investigation: Testing Marker Utility in Steatohepatitis (consortium)Collagen type IIIFibrosisPPV positive predictive valueReference standardsbusinessBody mass indexBiomarkersNon-alcoholic fatty liver disease
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THE INTERPRETAZION OF DIAGNOSTIC TEST: A PRIMER OF ALLERGIST. PRICIPLES OF EVIDENCE BASED MEDICINE TO OBTAIN A PRECISE DIAGNOSIS

2008

Negative predictive value (NPV)Lkelihood ratio negative (LR-)SensitivitySettore MED/09 - Medicina InternaLkelihood ratio positive (LR+)SpecificityEosinophilAsthmaPositive predictive value (PPV)Rhinitis
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A multicenter observational study on the role of comorbidities in the recurrent episodes of benign paroxysmal positional vertigo

2014

Objective: Primary objective of this study was to find a statistical link between the most worldwide comorbidities affecting the elderly population (hypertension, diabetes, osteoarthrosis, osteoporosis and depression) and recurrent episodes of BPPV. Secondary objective was defining possible "groups of risk" for people suffering recurrent positional vertigo related to the presence of a well documented comorbidity. Methods: This was an observational, cross-sectional, multicenter, spontaneous, non-pharmacological study. The data of 1092 patients suffering BPPV evaluated in 11 different Departments of Otolaryngology, Otoneurology and Neurology, referring Centers for positional vertigo evaluatio…

OsteoarthrosisMalemedicine.medical_specialtyPediatricsAsiaNeurologyBenign paroxysmal positional vertigoOsteoporosisComorbidityOtolaryngologyElderlyRecurrenceRisk FactorsVertigoOsteoarthritisDiabetes Mellitusotorhinolaryngologic diseasesmedicineHumansBenign Paroxysmal Positional VertigoDepression (differential diagnoses)AgedRetrospective StudiesAged 80 and overDepressive Disorderbiologybusiness.industryDiabetesGeneral MedicineOdds ratioSouth AmericaBPPVmedicine.diseasebiology.organism_classificationComorbiditySemicircular CanalsEuropeCross-Sectional StudiesNeurologyOtorhinolaryngologyHypertensionVertigoPhysical therapyOsteoporosisFemaleSurgeryObservational studysense organsbusinessAuris Nasus Larynx
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Mosaic activating mutations in GNA11 and GNAQ are associated with phakomatosis pigmentovascularis and extensive dermal melanocytosis

2016

Common birthmarks can be an indicator of underlying genetic disease but are often overlooked. Mongolian blue spots (dermal melanocytosis) are usually localized and transient, but they can be extensive, permanent, and associated with extracutaneous abnormalities. Co-occurrence with vascular birthmarks defines a subtype of phakomatosis pigmentovascularis, a group of syndromes associated with neurovascular, ophthalmological, overgrowth, and malignant complications. Here, we discover that extensive dermal melanocytosis and phakomatosis pigmentovascularis are associated with activating mutations in GNA11 and GNAQ, genes that encode Gα subunits of heterotrimeric G proteins. The mutations were det…

WT wild typeDNA Mutational AnalysisMolecular Sequence Datapostzygotic mutationsMutation MissenseSWS Sturge-Weber syndromeDermatologycesioflammeagermlineBiochemistrySkin DiseasesAnimals Genetically Modifiedg-proteinDNA deoxyribonucleic acidMongolian Spotoculodermal melanocytosis[ SDV.MHEP ] Life Sciences [q-bio]/Human health and pathologyGeneticsAnimalsHumansddc:610Phosphorylationchoroidal melanomaMolecular BiologyAllelesZebrafishdiseaseBase SequenceNeurocutaneous Syndromessturge-weberInfantCell Biologymongolian spotPPV phakomatosis pigmentovascularisGTP-Binding Protein alpha SubunitsHEK293 CellsPhenotypeMutationGTP-Binding Protein alpha Subunits Gq-G11Original Articleuveal melanoma[SDV.MHEP]Life Sciences [q-bio]/Human health and pathologySignal Transduction
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