Search results for "IGM"

showing 10 items of 1928 documents

Determinants of mental health stigma among pharmacy students in Australia, Belgium, Estonia, Finland, India and Latvia.

2009

Background: Healthcare professionals commonly exhibit negative attitudes toward people with mental disorders. Few international studies have sought to investigate the determinants of stigma. Objective: To conduct an international comparison of pharmacy students’ stigma towards people with schizophrenia, and to determine whether stigma is consistently associated with stereotypical attributes of people with schizophrenia. Method: Students (n = 649) at eight universities in Australia, Belgium, India, Finland, Estonia and Latvia completed a seven-item Social Distance Scale (SDS) and six items related to stereotypical attributes of people with schizophrenia. Method: Students (n = 649) at eight u…

AdultCross-Cultural ComparisonMalemedicine.medical_specialtyInternational studiesAttitude of Health PersonnelStigma (botany)Indiasocial distancePharmacy03 medical and health sciencesYoung Adultpharmaceutical services0302 clinical medicineSurveys and QuestionnairesDangerous BehaviormedicineHumans030212 general & internal medicinePsychiatryStereotypingbusiness.industry4. EducationPublic healthSocial distanceAustraliaSocial environmentMental healthCross-cultural studies030227 psychiatry3. Good healthschizophreniaEuropePsychiatry and Mental healthPsychological DistanceStudents PharmacyFamily medicineSchizophreniaFemaleSchizophrenic PsychologybusinessPrejudiceThe International journal of social psychiatry
researchProduct

Cruoricaptor ignavus gen. nov., sp. nov., a novel bacterium of the family Flavobacteriaceae isolated from blood culture of a man with bacteraemia.

2012

Abstract A Gram-reaction-negative bacterium, strain IMMIB L-12475 T , was isolated from blood cultures of a human with septicaemia. The yellowish orange pigmented strain contained flexirubin pigment. Phylogenetic analysis based on 16S rRNA gene sequence revealed that strain IMMIB L-12475 T belonged to the family Flavobacteriaceae , forming a distinct phyletic line that is distantly related (79.1–89.4% sequence similarity) to described genera of this family. Membership to the family was confirmed by a fatty acid profile consisting of branched-chain and 3-hydroxy fatty acids with major amounts of iso-C 17:0 3-OH and iso-C 15:0 , by the presence of menaquinone MK-6 as the only respiratory quin…

AdultDNA BacterialMaleMolecular Sequence DataBacteremiaApplied Microbiology and BiotechnologyMicrobiologyDNA RibosomalMicrobiologyGenusFlavobacteriaceae InfectionsRNA Ribosomal 16SPolyaminesCluster AnalysisHumansEcology Evolution Behavior and SystematicsPhospholipidsPhylogenychemistry.chemical_classificationBase CompositionbiologyPhylogenetic treeFatty AcidsQuinonesFatty acidPigments BiologicalSequence Analysis DNAbiology.organism_classification16S ribosomal RNAFlavobacteriaceaeBacterial Typing Techniquesgenomic DNABloodchemistryChemotaxonomyFlavobacteriaceaeBacteriaSystematic and applied microbiology
researchProduct

How the Context Matters. Literal and Figurative Meaning in the Embodied Language Paradigm

2014

The involvement of the sensorimotor system in language understanding has been widely demonstrated. However, the role of context in these studies has only recently started to be addressed. Though words are bearers of a semantic potential, meaning is the product of a pragmatic process. It needs to be situated in a context to be disambiguated. The aim of this study was to test the hypothesis that embodied simulation occurring during linguistic processing is contextually modulated to the extent that the same sentence, depending on the context of utterance, leads to the activation of different effector-specific brain motor areas. In order to test this hypothesis, we asked subjects to give a moto…

AdultDeep linguistic processinglcsh:MedicineSocial SciencesContext (language use)Literal and figurative languageEmbodied Language ParadigmSentence processingYoung AdultNeurolinguisticsPsychologyHumanslcsh:Scienceidioms.Settore M-FIL/05 - Filosofia E Teoria Dei LinguaggiLanguageMultidisciplinarymotor simjulationFootlcsh:RContextCognitive PsychologyBiology and Life SciencesHandPhilosophyMetaphorCognitive Sciencelcsh:QPsychologyPsychomotor PerformanceUtteranceSentenceResearch ArticleNeuroscienceMeaning (linguistics)Cognitive psychologyPLoS ONE
researchProduct

Homozygous variants in the gene SCAPER cause syndromic intellectual disability

2019

The S-Phase Cyclin A Associated Protein In The ER (SCAPER) gene is a ubiquitously expressed gene with unknown function in the brain. Recently, biallelic SCAPER variants were described in four patients from three families with retinitis pigmentosa (RP) and intellectual disability (ID). Here, we expand the spectrum of pathogenic variants in SCAPER and report on 10 further patients from four families with ID, RP, and additional dysmorphic features carrying homozygous variants in SCAPER. The variants found comprise frameshift, nonsense, and missense variants as well as an intragenic homozygous deletion, which spans SCAPER exons 15 and 16 and introduces a frameshift and a premature stop codon. A…

AdultMale0301 basic medicineAdolescentmedia_common.quotation_subjectCyclin ANonsenseGene Expression030105 genetics & heredityFrameshift mutationConsanguinityMice03 medical and health sciencesExonNeural Stem CellsIntellectual DisabilityRetinitis pigmentosaGene expressionGeneticsmedicineAnimalsHumansMissense mutationFamilyChildGeneGenetics (clinical)media_commonCerebral CortexNeuronsGeneticsbiologyHomozygoteSyndromemedicine.diseasePedigree030104 developmental biologyMutationbiology.proteinFemaleCarrier ProteinsRetinitis PigmentosaAmerican Journal of Medical Genetics Part A
researchProduct

Dermatitis due to Mesostigmatic mites (Dermanyssus gallinae, Ornithonyssus [O.] bacoti, O. bursa, O. sylviarum ) in residential settings

2018

No abstract available (letter to the Editor)

AdultMale0301 basic medicineMite InfestationsVeterinary medicineDermanyssus gallinae040301 veterinary sciencesDermatitisDermatologyBiologymedicine.disease_causeDermatiti0403 veterinary scienceResidential settings.03 medical and health sciencesInfestationSettore MED/35 - Malattie Cutanee E VenereemedicineAnimalsHumansOrnithonyssusRetrospective StudiesMite InfestationsOutbreak04 agricultural and veterinary sciencesMiddle Agedbiology.organism_classification030104 developmental biologyMesostigmatic miteFemaleJDDG: Journal der Deutschen Dermatologischen Gesellschaft
researchProduct

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
researchProduct

PORCN mutations in focal dermal hypoplasia: coping with lethality.

2009

Contains fulltext : 81709.pdf (Publisher’s version ) (Closed access) The X-linked dominant trait focal dermal hypoplasia (FDH, Goltz syndrome) is a developmental defect with focal distribution of affected tissues due to a block of Wnt signal transmission from cells carrying a detrimental PORCN mutation on an active X-chromosome. Molecular characterization of 24 unrelated patients from different ethnic backgrounds revealed 23 different mutations of the PORCN gene in Xp11.23. Three were microdeletions eliminating PORCN and encompassing neighboring genes such as EBP, the gene associated with Conradi-Hunermann-Happle syndrome (CDPX2). 12/24 patients carried nonsense mutations resulting in loss …

AdultMaleAdolescentBase SequenceDNA Mutational AnalysisMolecular Sequence DataInfant NewbornInfantMembrane ProteinsGenomic disorders and inherited multi-system disorders [IGMD 3]Focal Dermal HypoplasiaSettore MED/38 - Pediatria Generale E SpecialisticaSettore MED/03 - Genetica MedicaChild PreschoolMutationGoltz syndrome FDH PORCN WNT skewed X-inactivation postzygotic mosaicHumansProtein IsoformsFemaleAmino Acid SequenceChildAcyltransferasesHuman Mutation
researchProduct

Resources to cope with stigma related to HIV status, gender identity, and sexual orientation in gay men and transgender women

2017

The stigma related to HIV status, gender identity, and sexual orientation has negative implications for the quality of life of individuals. A qualitative study was conducted to explore the resources that these stigmatized groups recognize as tools to cope with stigma and maintain their psychological well-being. Four focus groups were conducted with gay men and transgender women divided by HIV status. A thematic analysis revealed that individual, interpersonal, and institutional resources are commonly recognized as coping resources. This article discusses the importance of enhancing self-acceptance, social support, and a legal framework that legitimizes these groups as right holders.

AdultMaleAdolescentHuman RightsSexual BehaviorSocial StigmaHIV InfectionsInterpersonal communicationTransgender PersonsYoung Adult03 medical and health sciencesSocial support0302 clinical medicineAdaptation PsychologicalHumans030212 general & internal medicineHomosexuality MaleQualitative ResearchApplied Psychology030505 public healthGender IdentitySocial SupportFocus GroupsMiddle AgedFocus groupPsychological well-beingQuality of LifeSexual orientationHealth ResourcesFemaleThematic analysisLesbian0305 other medical sciencePsychologySocial psychologyClinical psychologyQualitative researchJournal of Health Psychology
researchProduct

Corneal and Refractive Astigmatism in Adults: A Power Vectors Analysis

2009

Purpose. In this article, we examine the relationship between corneal and refractive astigmatism (including with the rule, against-the-rule, and oblique astigmatism) in an adult population using power vectors. Methods. Refractive and keratometric measures of astigmatism were conducted on right eyes of 105 white subjects aged 18 to 59 years. We performed a linear regression of refractive astigmatic error on corneal astigmatism, using the J0 and J45 components of the astigmatism. Results. We obtained a statistically significant regression relationship between the corneal (C) and refractive (R) astigmatism for both J0 and J45 components, namely, RJ0 = 1.07 × CJ0 − 0.28; and RJ45 = 1.46 × CJ45 …

AdultMaleAdolescentbusiness.industryAdult populationAstigmatismReproducibility of ResultsDiagnostic Techniques OphthalmologicalMiddle AgedRefraction OcularRefractionOblique astigmatismCorneaYoung AdultOphthalmologyAberrations of the eyeOpticsLinear regressionLinear ModelsHumansFemalebusinessCorneal astigmatismOptometryMathematicsOptometry and Vision Science
researchProduct

Contrast sensitivity and glare disability by halogen light after monofocal and multifocal lens implantation

2000

BACKGROUND—Standard examination of contrast sensitivity under conditions of glare disability is performed with incandescent light. A new halogen glare test that simulates glare as seen with oncoming vehicle headlights was used to measure glare disability in patients implanted with multifocal and monofocal intraocular lenses (IOLs). METHODS—28 patients with an average age of 69 years (SD 12 years) were implanted with a monofocal IOL (SI-40NB, Allergan) and 28 patients with an average of 66 years (12 years) were implanted with a refractive multifocal IOL (Array-SA-40N, Allergan). All patients were followed for 5 months postoperatively. Contrast sensitivity at four spatial frequencies (3, 6, 1…

AdultMaleAgingAutomobile Drivingmedicine.medical_specialtygenetic structuresEye diseasemedicine.medical_treatmentmedia_common.quotation_subjecteducationPoison controlIntraocular lensAstigmatismGlareContrast SensitivityVision disorderCellular and Molecular NeuroscienceHalogensOphthalmologymedicineHumansContrast (vision)Postoperative PeriodDioptreAgedmedia_commonAged 80 and overLenses Intraocularbusiness.industryGlare (vision)Middle AgedOriginal articles - Clinical sciencemedicine.diseaseeye diseasesSensory SystemsSurgeryOphthalmologyFemalesense organsmedicine.symptombusinessFollow-Up StudiesBritish Journal of Ophthalmology
researchProduct