Search results for "Norm"

showing 10 items of 4018 documents

Assessing Planning Ability Across the Adult Life Span in a Large Population-Representative Sample: Reliability Estimates and Normative Data for the T…

2019

AbstractObjectives:The Tower of London (TOL) test has probably become the most often used task to assess planning ability in clinical and experimental settings. Since its implementation, efforts were made to provide a task version with adequate psychometric properties, but extensive normative data are not publicly available until now. The computerized TOL-Freiburg Version (TOL-F) was developed based on theory-grounded task analyses, and its psychometric adequacy has been repeatedly demonstrated in several studies but often with small and selective samples.Method:In the present study, we now report reliability estimates and normative data for the TOL-F stratified for age, sex, and education …

AdultMale050103 clinical psychologyHuman DevelopmentApplied psychologyNormative dataLarge populationTower of LondonSample (statistics)Neuropsychological TestsGutenberg Health Study (GHS)Task (project management)Cohort StudiesExecutive Function03 medical and health sciences0302 clinical medicineReference ValuesGermanyHumans0501 psychology and cognitive sciencesReliability (statistics)AgedAged 80 and overRegular Researchorganic chemicalsGeneral Neuroscience05 social sciencesReproducibility of ResultsMiddle AgedReliabilityTest (assessment)PlanningPsychiatry and Mental healthClinical PsychologyAdult lifeTOL-FbacteriaNormativeFemaleNeurology (clinical)PsychologyTower030217 neurology & neurosurgeryJournal of the International Neuropsychological Society
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Incompleteness and not just right experiences in the explanation of Obsessive-Compulsive Disorder.

2015

In the past decade, not just right experiences (NJRE) and incompleteness (INC) have attracted renewed interest as putative motivators of symptoms in obsessive-compulsive disorder (OCD), beyond harm avoidance (HA). This study examines, in 267 non-clinical undergraduates and 47 OCD patients, the differential contributions of HA, INC, and NJRE to the different OCD symptom dimensions and the propensity to have the disorder. The results indicate that although both the NJRE and INC range from normality to OCD, their number and intensity significantly increase as the obsessional tendencies increase, which suggests that they are vulnerability markers for OCD. Although they cannot be considered full…

AdultMale050103 clinical psychologyObsessive-Compulsive DisorderPsychotherapistmedia_common.quotation_subjectbehavioral disciplines and activities03 medical and health sciencesYoung Adult0302 clinical medicineObsessive compulsiveSurveys and Questionnairesmental disordersmedicineHumans0501 psychology and cognitive sciencesBiological PsychiatryNormalitymedia_commonMotivationOperationalization05 social sciencesMiddle Agedmedicine.diseasehumanities030227 psychiatryPsychiatry and Mental healthGeneral distressCompulsive behaviorTraitCompulsive BehaviorHarm avoidanceFemalemedicine.symptomObsessive BehaviorConstruct (philosophy)PsychologyPsychiatry research
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Interpersonal Self-Efficacy, Goals, and Problems of Persistently Depressed Outpatients: Prototypical Circumplex Profiles and Distinctive Subgroups.

2016

Severely and persistently depressed outpatients ( n = 138) completed interpersonal circumplex measures of self-efficacy, problems, and values/goals. Compared with normative samples, patients showed deficits in agency: They reported less self-efficacy, especially for being assertive, tough, and influential; stronger goals, especially to avoid conflict or humiliation; and more problems, especially with being too timid, inhibited, and accommodating. Circular and structural summary indices suggested greater variability among patients in goal profiles than in efficacy or problem profiles; nonetheless, latent profile analyses identified coherent subgroups of patients with distinct patterns of ef…

AdultMale050103 clinical psychologyPsychometricsmedia_common.quotation_subjectPsychological intervention050109 social psychologyInterpersonal communicationInterpersonal circumplexModels PsychologicalDevelopmental psychologySurveys and QuestionnairesAgency (sociology)Humans0501 psychology and cognitive sciencesAssertivenessInterpersonal RelationsApplied Psychologymedia_commonSelf-efficacyDepression05 social sciencesHumiliationMiddle AgedSelf EfficacyClinical PsychologyCase-Control StudiesNormativeFemalePsychologyGoalsClinical psychologyPersonalityAssessment
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Phenotypical features of two patients diagnosed with PHARC syndrome and carriers of a new homozygous mutation in the ABHD12 gene.

2018

Abstract PHARC (Polyneuropathy, Hearing loss, Ataxia, Retinitis pigmentosa and Cataracts) (MIM# 612674 ) is an autosomal recessive neurodegenerative disease caused by mutations in the ABHD12 gene. We evaluated two Spanish siblings affected with pes cavus, sensorimotor neuropathy, hearing loss, retinitis pigmentosa and juvenile cataracts in whom the genetic test of ABHD12 revealed a novel homozygous frameshift mutation, c.211_223del (p.Arg71Tyrfs*26). The earliest clinical manifestation in these patients was a demyelinating neuropathy manifested with a Charcot-Marie-Tooth phenotype over three decades. Progressive hearing loss, cataracts and retinitis pigmentosa appeared after the age of 30. …

AdultMaleARLID12 genecongenital hereditary and neonatal diseases and abnormalitiesmedicine.medical_specialtyAtaxiagenetic structuresHearing lossUsher syndromeCharcot-Marie-Tooth diseaseCataractFrameshift mutation03 medical and health sciencesPolyneuropathies0302 clinical medicineCataractsRetinitis pigmentosaotorhinolaryngologic diseasesmedicineHumansMuscle SkeletalDeaf-blindnessbusiness.industryPHARCBrainmedicine.diseaseDermatologyMagnetic Resonance Imagingeye diseasesMonoacylglycerol LipasesPedigreePhenotypeNeurologySpainMutation030221 ophthalmology & optometryAtaxiasense organsNeurology (clinical)medicine.symptombusinessUsher syndromePolyneuropathy030217 neurology & neurosurgeryRetinitis PigmentosaRetinopathyJournal of the neurological sciences
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A new set of 299 pictures for psycholinguistic studies : French norms for name agreement, image agreement, conceptual familiarity, visual complexity,…

2003

Pictures are often used as stimuli in studies of perception, language, and memory. Since performances on different sets of pictures are generally contrasted, stimulus selection requires the use of standardized material to match pictures across different variables. Unfortunately, the number of standardized pictures available for empirical research is rather limited. The aim of the present study is to provide French normative data for a new set of 299 black-and-white drawings. Alario and Ferrand (1999) were closely followed in that the pictures were standardized on six variables: name agreement, image agreement, conceptual familiarity, visual complexity, image variability, and age of acquisit…

AdultMaleAdolescentComputer sciencemedia_common.quotation_subjectExperimental and Cognitive Psychologycomputer.software_genreLanguage Development050105 experimental psychologyVisual complexity03 medical and health sciences0302 clinical medicineEmpirical researchPerceptionHumans0501 psychology and cognitive sciencesGeneral PsychologyLanguagemedia_commonName agreementPsycholinguisticsPsychology Experimentalbusiness.industry05 social sciencesAge of AcquisitionPictorial stimuli[SCCO.PSYC]Cognitive science/Psychology[SCCO.PSYC] Cognitive science/PsychologyVisual PerceptionNormativeFemalePsychology (miscellaneous)Artificial intelligenceFactor Analysis Statisticalbusinesscomputer030217 neurology & neurosurgeryNatural language processing
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Dental anomalies inside the cleft region in individuals with nonsyndromic cleft lip with or without cleft palate

2015

Background Individuals with non syndromic cleft lip with or without cleft palate (NSCL±P) present high frequency of dental anomalies, which may represent complicating factors for dental treatment. The aim of this study was to investigate the prevalence of dental anomalies inside cleft area in a group of Brazilians with NSCL±P. Material and Methods Retrospective analysis of 178 panoramic radiographs of patients aged from 12 to 45 years old and without history of tooth extraction or orthodontic treatment was performed. Association between cleft type and the prevalence of dental anomalies was assessed by chi-square test with a significance level set at p≤ 0.05. Results Dental anomalies were fo…

AdultMaleAdolescentCross-sectional studyCleft LipDentistryOdontologíaYoung Adult03 medical and health sciences0302 clinical medicinestomatognathic systemStatistical significancePrevalenceMicrodontiamedicineRetrospective analysisHumansChild030223 otorhinolaryngologyGeneral DentistryRetrospective StudiesOrthodonticsDental anomaliesOral Medicine and PathologyTooth Abnormalitiesbusiness.industryResearchRetrospective cohort study030206 dentistryMiddle Aged:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseCiencias de la saludUnilateral complete cleft lipstomatognathic diseasesCross-Sectional StudiesOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASFemaleSurgeryTooth agenesisbusiness
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Fever of Unclear Origin and Cytopenia Because of Acute Splenic Sequestration in a Young Immunocompetent Carrier of Beta-Globin Mutation for Hb Vallet…

2008

Fever of unclear origin is a clinical challenge in medical practice. Infectious diseases, neoplasms, and collagen vascular illnesses are its main causes in adults and children. Acute splenic sequestration crises, a known potentially fatal complication of sickle cell disease and sickle beta-thalassemia, are uncommon in beta-heterozygosis. We describe a case of prolonged recurrent episodes of fever with spontaneous resolution, commencing at age 10 in a 15-year-old boy with a history of hypochromic microcytic anemia attributed to a thalassemic trait. He was admitted twice to our university hospital for continuous-remittent fever with a pruritic, macular evanescent Still's skin rash, severe spl…

AdultMaleAdolescentFeverAnemiaHemoglobins AbnormalThalassemiaHepatosplenomegalybeta-Globinshemic and lymphatic diseasesmedicineHumansChildCytopeniabusiness.industryBeta thalassemiaAnemiaGeneral Medicinemedicine.diseaseHematologic DiseasesHypochromic microcytic anemiaHemoglobinopathyMutationImmunologymedicine.symptomSplenic diseasebusinessImmunocompetenceSpleenThe American Journal of the Medical Sciences
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Translocations Disrupting PHF21A in the Potocki-Shaffer-Syndrome Region Are Associated with Intellectual Disability and Craniofacial Anomalies

2012

Contains fulltext : 110038.pdf (Publisher’s version ) (Closed access) Potocki-Shaffer syndrome (PSS) is a contiguous gene disorder due to the interstitial deletion of band p11.2 of chromosome 11 and is characterized by multiple exostoses, parietal foramina, intellectual disability (ID), and craniofacial anomalies (CFAs). Despite the identification of individual genes responsible for multiple exostoses and parietal foramina in PSS, the identity of the gene(s) associated with the ID and CFA phenotypes has remained elusive. Through characterization of independent subjects with balanced translocations and supportive comparative deletion mapping of PSS subjects, we have uncovered evidence that t…

AdultMaleAdolescentGenotypePotocki–Shaffer syndromeChromosome DisordersHaploinsufficiencyBiologyHistone DeacetylasesSodium ChannelsTranslocation GeneticArticleChromatin remodelingCraniofacial Abnormalities03 medical and health sciencesSCN3A0302 clinical medicineIntellectual DisabilityNAV1.3 Voltage-Gated Sodium ChannelmedicineTranscriptional regulationGeneticsAnimalsHumansDeletion mappingGenetics(clinical)CraniofacialZebrafishGenetics (clinical)030304 developmental biologyGenetics0303 health sciencesChromosomes Human Pair 11Infant Newbornmedicine.diseaseGenetics and epigenetic pathways of disease DCN MP - Plasticity and memory [NCMLS 6]Child PreschoolHomeoboxFemaleChromosome DeletionHaploinsufficiencyExostoses Multiple Hereditary030217 neurology & neurosurgeryThe American Journal of Human Genetics
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Psycholinguistic norms for 320 fixed expressions (idioms and proverbs) in French

2018

International audience; We provide psycholinguistic norms for a new set of 160 French idiomatic expressions and 160 proverbs: knowledge, predictability, literality, compositionality, subjective and objective frequency, familiarity, age of acquisition (AoA), and length. Different analyses (reliability, descriptive statistics, correlations) performed on the norms are reported and discussed. The norms can be downloaded as supplemental material.

AdultMaleAdolescentPhysiologyPrinciple of compositionalityStatistics as TopicExperimental and Cognitive Psychology[ SCCO.PSYC ] Cognitive science/PsychologyIdiomsVocabulary050105 experimental psychologyYoung Adult03 medical and health sciences0302 clinical medicineIdiomatic expressionsReference ValuesPhysiology (medical)Humans0501 psychology and cognitive sciencesPredictability[SHS.LANGUE]Humanities and Social Sciences/LinguisticsSet (psychology)General PsychologyMathematicsPrincipal Component AnalysisLanguage TestsPsycholinguistics4. Education05 social sciences[ SCCO.LING ] Cognitive science/LinguisticsGeneral Medicine[SCCO.LING]Cognitive science/LinguisticsLinguisticsSemanticsKnowledgeNeuropsychology and Physiological PsychologyPsycholinguistic norms[SCCO.PSYC]Cognitive science/Psychology[ SHS.LANGUE ] Humanities and Social Sciences/LinguisticsFemaleFranceProverbs030217 neurology & neurosurgery
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Single-Nucleotide Polymorphism Array-Based Characterization of Ring Chromosome 18

2012

Objective To study genotype–phenotype correlation of ring chromosome 18 [r(18)] in 9 patients with 46,XN karyotype. Study design In 9 patients with a de novo 46,XN,r(18) karyotype (7 females, 2 males), we performed high-resolution single-nucleotide polymorphism array analysis (Illumina Human Omni1-QuadV1 array in 6 patients, Affymetrix 6.0 array in 3 patients), investigation of parental origin, and genotype–phenotype correlation. Results No breakpoint was recurrent. Single metaphases with loss of the ring, double rings, or secondarily rearranged rings were found in some cases, but true mosaicism was present in none of these cases. In 3 patients, additional duplications in 18p (of 1.4 Mb, 2 …

AdultMaleAdolescentRing chromosomeSingle-nucleotide polymorphismBiologyPolymorphism Single NucleotideCROMOSSOMOS HUMANOS (ANORMALIDADES;COMPLICAÇÕES)Young AdultMeiosisPolymorphism (computer science)SNPBody SizeHumansRing ChromosomesChildGenetic Association StudiesOligonucleotide Array Sequence AnalysisGeneticsBreakpointInfant NewbornInfantKaryotypeMiddle AgedPhenotypeChild PreschoolKaryotypingPediatrics Perinatology and Child HealthFemaleChromosome DeletionChromosomes Human Pair 18HeadMaternal AgeMicrosatellite Repeats
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