Search results for "correlation"

showing 10 items of 2282 documents

Genetic and Environmental Influences on the Relationship Between Aggression and Hyperactivity-impulsivity as Rated by Teachers and Parents

2004

This study examined genetic and environmental contributions to the covariance between aggression and hyperactivity-impulsivity as rated by twins' teachers and parents. Sex-differences in these genetic and environmental contributions and rater bias/sibling interaction effects were of interest as well. Part of an ongoing nation-wide twin-family study of behavioral development and health habits, the sample consisted of 1636 Finnish twin pairs ascertained from five consecutive and complete twin birth cohorts. Data were collected at ages 11-12, using teacher and parental rating forms of the Multidimensional Peer Nomination Inventory. Bivariate analyses were performed using structural equation mo…

MaleParents050103 clinical psychologyGenotypeTwinsChild BehaviorBivariate analysisStructural equation modelingDevelopmental psychologyCorrelationSex FactorsSurveys and QuestionnairesGenetic variationTwins DizygoticmedicineHumans0501 psychology and cognitive sciencesLongitudinal StudiesSiblingHyperactivity impulsivityFinlandGenetics (clinical)Aggression4. Education05 social sciencesGenetic VariationObstetrics and GynecologyTwins MonozygoticFacultyPhenotypeChild PreschoolPediatrics Perinatology and Child HealthFemalemedicine.symptomPsychologySocial psychologyHealth habits050104 developmental & child psychologyTwin Research
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Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9…

2012

A large hexanucleotide (GGGGCC) repeat expansion in the first intron of C9ORF72, a gene located on chromosome 9p21, has been recently reported to be responsible for 40% of familial amyotrophic lateral sclerosis cases of European ancestry. The aim of the current article was to describe the phenotype of amyotrophic lateral sclerosis cases carrying the expansion by providing a detailed clinical description of affected cases from representative multi-generational kindreds, and by analysing the age of onset, gender ratio and survival in a large cohort of patients with familial amyotrophic lateral sclerosis. We collected DNA and analysed phenotype data for 141 index Italian familial amyotrophic l…

MaleParentsPathologyphenotype-genotype correlationCohort Studies0302 clinical medicineC9orf72amyotrophic lateral sclerosigeneticsAmyotrophic lateral sclerosisAge of Onsetamyotrophic lateral sclerosis; familial als; C9Orf72; phenotype-genotype correlation0303 health sciencesSex CharacteristicsDNA Repeat ExpansionAdult Age of Onset Aged Amyotrophic Lateral Sclerosis; genetics/pathology Cohort Studies DNA Repeat Expansion DNA; genetics Female Humans Italy Male Middle Aged Mutation; genetics Parents Pedigree Phenotype Proteins; genetics Sex Characteristics Survival AnalysisMiddle Aged3. Good healthPedigreeSettore MED/26 - NEUROLOGIAPhenotypeItalyC9Orf72Settore MED/26 - NeurologiaFemaleFrontotemporal dementiaAdultmedicine.medical_specialtySOD1BiologyTARDBP03 medical and health sciencesInternal medicinemedicineHumans030304 developmental biologyAgedamyotrophic lateral sclerosis familial ALS C9ORF72 gene phenotype–genotype correlationC9orf72 ProteinAmyotrophic Lateral Sclerosisgenetics/pathologyProteinsOriginal ArticlesDNAmedicine.diseaseSurvival AnalysisC9orf72 ProteinSettore BIO/18 - Geneticaamyotrophic lateral sclerosis; familial ALS C9ORF72 gene; phenotype-genotype correlation;MutationNeurology (clinical)Age of onsetTrinucleotide repeat expansionfamilial al030217 neurology & neurosurgery
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Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease

2008

Herein we first describe a novel homozygous single nucleotide deletion in PINK1 exon 4 (889delG) which results in a loss of kinase domain on the PINK1 protein (D297fsX318). This mutation was identified in two brothers with early-onset Parkinson disease (EOPD) from a Sicilian consanguineous family. Of note, while one of the two patients developed mental deterioration and psychiatric problems, the other showed no cognitive decline. The present study supports the view that PINK1 is a pathogenic gene in some Italian families with EOPD and contributes to define the PINK1-associated phenotype. Herein we first describe a novel homozygous single nucleotide deletion in PINK1 exon 4 (889delG) which r…

MaleParkinson's diseaseGenotypeParkinson's diseaseMolecular Sequence DataPINK1DiseaseBiologyAntiparkinson AgentsLevodopaExonmedicineHumansAmino Acid SequenceAge of OnsetCognitive declineGeneAgedGeneticsGenotype–phenotype correlationPINK1Parkinson DiseaseExonsFamilial formmedicine.diseasePhenotypePedigreeSettore BIO/18 - GeneticaPhenotypeNeurologyMutationMutation (genetic algorithm)Settore MED/26 - NeurologiaNeurology (clinical)Geriatrics and GerontologyCognition DisordersProtein KinasesGene DeletionParkinsonism & Related Disorders
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A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

2012

Abstract: Background Two recent studies identified a mutation (p.Asp620Asn) in the vacuolar protein sorting 35 gene as a cause for an autosomal dominant form of Parkinson disease. Although additional missense variants were described, their pathogenic role yet remains inconclusive. Methods and results We performed the largest multi-center study to ascertain the frequency and pathogenicity of the reported vacuolar protein sorting 35 gene variants in more than 15,000 individuals worldwide. p.Asp620Asn was detected in 5 familial and 2 sporadic PD cases and not in healthy controls, p.Leu774Met in 6 cases and 1 control, p.Gly51Ser in 3 cases and 2 controls. Overall analyses did not reveal any sig…

MaleParkinson's diseasePopulationVesicular Transport ProteinsLocus (genetics)DiseaseBiologyVPS35 protein humanBioinformaticsgenetics [Vesicular Transport Proteins]genetics [Parkinson Disease]Risk Factorsmedicinemetabolism [Vesicular Transport Proteins]GeneticsMissense mutationVPS35 GeneHumansGenetic epidemiologyGenetic Predisposition to Diseaseddc:6101506Genome-wideeducationGenetics (clinical)Genetic Association StudiesGeneticsVacuolar protein sortingeducation.field_of_studyGenotype-Phenotype CorrelationsParkinson DiseaseComplex traitsmedicine.diseasePenetranceddc:MutationFemaleHuman medicineParkinson-s diseaseJournal of Medical Genetics
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Hemorragic presentation of Listeria Monocytogenes rhombencephalic abscess.

2020

Listeria monocytogenes (LM) bacterium is a cause of central nervous system (CNS) infection and the most common cause of rhombencephalitis in immunocompetent elderly. A prompt identification of this condition should be always desirable, since its clinical manifestations are often unspecific with prodromal symptoms leading to high rates of morbidity and mortality if underestimated. CNS listeriosis magnetic resonance imaging (MRI) findings are generally not specific. However, in the appropriate clinical setting, focal brainstem hyperintensity on T2-weighted pulse sequences associated with ring-enhancement pattern after i.v. contrast media injection should be suspicious of LM abscess. The diagn…

MalePathologymedicine.medical_specialtyFeverCentral nervous systemData correlationBrain AbscessHemorrhagemedicine.disease_cause030218 nuclear medicine & medical imagingDiagnosis Differential03 medical and health sciences0302 clinical medicineListeria monocytogenesMedicineHumansBrain magnetic resonance imagingListeriosisAbscessListeria monocytogeneBrain magnetic resonance imagingAgedHigh rateInfectious diseasemedicine.diagnostic_testbusiness.industryHeadacheMagnetic resonance imagingmedicine.diseaseListeria monocytogenesMagnetic Resonance ImagingHyperintensityRhombencephalonmedicine.anatomical_structurebusiness030217 neurology & neurosurgeryMRIJournal of population therapeutics and clinical pharmacology = Journal de la therapeutique des populations et de la pharmacologie clinique
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Relationship between body composition and postural control in prepubertal overweight/obese children: A cross-sectional study

2017

Abstract Background Excess body weight during childhood causes reduced motor functionality and problems in postural control, a negative influence which has been reported in the literature. Nevertheless, no information regarding the effect of body composition on the postural control of overweight and obese children is available. The objective of this study was therefore to establish these relationships. Methods A cross-sectional design was used to establish relationships between body composition and postural control variables obtained in bipedal eyes-open and eyes-closed conditions in twenty-two children. Centre of pressure signals were analysed in the temporal and frequency domains. Pearson…

MalePediatric Obesitymedicine.medical_specialtyAdolescentCorrelation coefficientCross-sectional studyPostureBiophysics030209 endocrinology & metabolismOverweightBody Mass IndexCorrelation03 medical and health sciences0302 clinical medicinePhysical medicine and rehabilitationLinear regressionmedicineHumansOrthopedics and Sports MedicineChildPostural BalancePrincipal Component Analysisbusiness.industryBody WeightRegression analysis030229 sport sciencesOverweightTrunkCross-Sectional StudiesMulticollinearityBody CompositionLinear ModelsFemalemedicine.symptombusinessClinical Biomechanics
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Validation of two portable bioelectrical impedance analyses for the assessment of body composition in school age children

2017

Background Bioelectrical impedance analysis (BIA) is a convenient and child-friendly method for longitudinal analysis of changes in body composition. However, most validation studies of BIA have been performed on adult Caucasians. The present cross-sectional study investigated the validity of two portable BIA devices, the Inbody 230 (BIA8MF) and the Tanita BC-418 (BIA8SF), in healthy Taiwanese children. Methods Children aged 7–12 years (72 boys and 78 girls) were recruited. Body composition was measured by the BIA8SF and the BIA8MF. Dual X-ray absorptiometry (DXA) was used as the reference method. Results There were strong linear correlations in body composition measurements between the BIA…

MalePediatricsResearch ValidityCross-sectional studylcsh:MedicinePediatricsDiagnostic RadiologyFamilies0302 clinical medicineMathematical and Statistical TechniquesAbsorptiometry PhotonMedicine and Health SciencesElectric ImpedanceMedicine030212 general & internal medicinelcsh:ScienceChildChildrenMusculoskeletal SystemMultidisciplinarySchool age childRadiology and ImagingLimits of agreementResearch AssessmentArmsConcordance correlation coefficientArticle-Level MetricsAdipose TissuePhysical SciencesBody CompositionRegression AnalysisFemaleAnatomyBioelectrical impedance analysisStatistics (Mathematics)Research Articlemedicine.medical_specialtyImaging Techniques030209 endocrinology & metabolismLinear Regression AnalysisResearch and Analysis MethodsFat mass03 medical and health sciencesDiagnostic MedicineLinear regressionHumansAbsorptiometryStatistical MethodsAltmetricsbusiness.industrylcsh:RLimbs (Anatomy)Biology and Life SciencesReproducibility of ResultsBiological TissueCross-Sectional StudiesAge GroupsPeople and PlacesLean body masslcsh:QPopulation GroupingsbusinessNuclear medicineMathematicsPLoS ONE
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The web-based ASSO-food frequency questionnaire for adolescents: relative and absolute reproducibility assessment

2014

Background A new food frequency questionnaire (FFQ) has been recently developed within the Italian Adolescents and Surveillance System for the Obesity prevention (ASSO) Project; it was found to be appropriate for ranking adolescents in food and nutrient levels of intake. The aim of this study was to assess the relative and absolute reproducibility of the ASSO-FFQ for 24 food groups, energy and 52 nutrients. Methods A test-retest study was performed on two ASSO-FFQs administered one month apart of each other to 185 adolescents, aged 14–17 and attending secondary schools in Palermo (Italy). Wilcoxon test assessed differences in median daily intakes between the two FFQs. Agreement was evaluate…

MalePediatricsmedicine.medical_specialtyAdolescentWilcoxon signed-rank testIntraclass correlationFood frequency questionnaireMedicine (miscellaneous)Carbonated BeveragesClinical nutritionSettore MED/42 - Igiene Generale E ApplicataDiet RecordsFood groupSurveys and QuestionnairesEnvironmental healthHumansMedicineObesityInternetReproducibilitySettore M-EDF/02 - Metodi E Didattiche Delle Attivita' SportiveNutrition and Dieteticsbusiness.industryAlcoholic BeveragesResearchdigestive oral and skin physiologyReproducibility of ResultsBreadmedicine.diseaseR1ObesityDiet RecordsReproducibilityDietItalyFood frequency questionnaire Reproducibility Adolescent Nutrient IntakeFoodIntakeFemaleEnergy IntakebusinessRAKappaNutrientNutrition Journal
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Analysis of the peri-implant microbiota in 90 dental implants and its relationship to crevicular fluid volume

2010

Objective: To evaluate the presence within the peri-implant sulcus of Tannerela forsythia (Tf), Porphyromonas gingivales (Pg), Treponema denticola (Td) and Aggregatibacter actinomycetemcomitans (Aa), and relate these bacteria to the peri-implant crevicular fluid volume (PICFV). Material and Method: A prospective and cross-sectional clinical case series study was made. For the measurement of crevicular fluid, use was made of the Periotron ® 8000 (Proflow Incorporated. New York, USA), measuring the volume in Periotron units (PU). For the detection of periodontopathogenic bacteria we used the IAI-PadoTest 4.5 (IAI Inc., IAI Institute, Zuchwil, Switzerland) - a system for the detection of Tf, P…

MalePeriDentistryPositive correlationCrevicular fluidMucositisMedicineHumansProspective StudiesGeneral DentistryAgedAged 80 and overDental ImplantsbiologyBacteriabusiness.industryAggregatibacter actinomycetemcomitansMean ageTreponema denticolaGingival Crevicular FluidMiddle Agedbiology.organism_classificationmedicine.disease:CIENCIAS MÉDICAS [UNESCO]stomatognathic diseasesCross-Sectional StudiesOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASMetagenomeSurgeryFemaleImplantbusiness
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Force-velocity profiling in athletes: Reliability and agreement across methods

2021

The aim of the study was to examine the test-retest reliability and agreement across methods for assessing individual force-velocity (FV) profiles of the lower limbs in athletes. Using a multicenter approach, 27 male athletes completed all measurements for the main analysis, with up to 82 male and female athletes on some measurements. The athletes were tested twice before and twice after a 2- to 6-month period of regular training and sport participation. The double testing sessions were separated by ~1 week. Individual FV-profiles were acquired from incremental loading protocols in squat jump (SJ), countermovement jump (CMJ) and leg press. A force plate, linear encoder and a flight time cal…

MalePhysiologyIntraclass correlationExtrapolationVelocitySocial Sciencesmedicine.disease_causeJumpingMathematical and Statistical TechniquesJumpingStatisticsMedicine and Health SciencesPsychologyRange of Motion ArticularLeg pressMathematicsMeasurementNumerical AnalysisMultidisciplinaryPhysicsStatisticsQRClassical MechanicsSoftware EngineeringVDP::Medisinske Fag: 700::Idrettsmedisinske fag: 850Sports ScienceLower ExtremityPhysical SciencessymbolsJumpLegsEngineering and TechnologyRegression AnalysisMedicineFemaleAnatomyResearch ArticleSportsAdultComputer and Information SciencesAdolescentCoefficient of variationScienceLinear Regression AnalysisResearch and Analysis MethodsComputer SoftwareMotionYoung Adultsymbols.namesakeLinear regressionmedicineHumansMuscle StrengthStatistical MethodsExerciseBehaviorBiological LocomotionBiology and Life SciencesReproducibility of ResultsPearson product-moment correlation coefficientStandard errorAthletesPhysical FitnessBody LimbsExercise TestRecreationMathematics
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