0000000000960090

AUTHOR

Claudia M.b. Carvalho

showing 2 related works from this author

Factorial analysis and psychometric properties of the revised Valencia scale of attitudes and beliefs towards hypnosis-client version

2007

Psychometric properties and factorial structure of the Revised Valencia Scale of Attitudes and Beliefs toward Hypnosis – Client Version using a Portuguese sample are presented. Exploratory factor analysis on a Portuguese population of undergraduate college students (N = 444) yielded 8 factors: ‘Interest/Liking’, ‘Memory/Magic’, ‘Help’, ‘Control’, ‘Cooperation’, ‘Marginal’, ‘Fear’ and ‘Automaton’. The overall 8-factor structure is similar to the one found in the therapist version of the scale, and as in the therapist version, each factor of the client version showed good internal consistency and reliability. Differences among participants that had and had not experienced hypnosis previously …

Complementary and Manual TherapyExploratory factor analysisHypnosisBeliefsContext (language use)Assessmentlanguage.human_languageExploratory factor analysisScaleClinical PsychologyAttitudesScale (social sciences)Internal consistencylanguageAssessment; Attitudes; Beliefs; Exploratory factor analysis; Hypnosis; Scale; Complementary and Manual Therapy; Clinical PsychologyPortuguese populationPortugueseFactorial analysisPsychologySocial psychologyHypnosisClinical psychologyContemporary Hypnosis
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WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome

2018

International audience; Locus heterogeneity characterizes a variety of skeletal dysplasias often due to interacting or overlapping signaling pathways. Robinow syndrome is a skeletal disorder historically refractory to molecular diagnosis, potentially stemming from substantial genetic heterogeneity. All current known pathogenic variants reside in genes within the noncanonical Wnt signaling pathway including ROR2, WNT5A, and more recently, DVL1 and DVL3. However, ∼70% of autosomal-dominant Robinow syndrome cases remain molecularly unsolved. To investigate this missing heritability, we recruited 21 families with at least one family member clinically diagnosed with Robinow or Robinow-like pheno…

Male0301 basic medicineCandidate geneFrizzledGROWTH-PLATEDEP DOMAINlnfectious Diseases and Global Health Radboud Institute for Molecular Life Sciences [Radboudumc 4]PROTEINskeletal dysplasiaCraniofacial Abnormalities0302 clinical medicineLocus heterogeneityChromosome SegregationChild[ SDV.GEN.GH ] Life Sciences [q-bio]/Genetics/Human geneticsWnt Signaling PathwayGenetics (clinical)Genes DominantGeneticsWnt signaling pathwayMiddle AgedRobinow syndromeMENDELIAN-INHERITANCEPhenotypeChild PreschoolFemaleNEURAL-TUBE DEFECTSVERTEBRATE GASTRULATIONhuman embryonic developmentRare cancers Radboud Institute for Health Sciences [Radboudumc 9]AdultAdolescentCELL POLARITYLimb Deformities CongenitalMutation MissenseDwarfismBiologyArticledual molecular diagnosisDiagnosis DifferentialGenetic Heterogeneity03 medical and health sciencesFrizzledAll institutes and research themes of the Radboud University Medical CenterSkeletal disorderGeneticsmedicineHumansGenetic Association StudiesNeurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7]Base SequenceGenetic heterogeneityMUTATIONSROR2medicine.diseaseDROSOPHILA TISSUE POLARITY030104 developmental biology[SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human geneticsUrogenital AbnormalitiesAUTOSOMAL-DOMINANT030217 neurology & neurosurgery
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