Search results for "adolescent"

showing 10 items of 6718 documents

Sexting in adolescence: what are the reasons? An empirical study

2022

Objectives: This study aims to provide an in-depth analysis on the phenomenon of sexting through the investigation of the motivations that lead adolescents to such practice. We took account of gender differences and the more used varieties of sexting behaviors. Recent studies have pointed out that sexual purposes, instrumental motivations and body image reinforcement, as well as the pressure exerted by partners and friends, seem to be the reasons that push teenager to resort to sexting. The aim of our research is to evaluate which of these motivations are mainly associated to sexting behaviors. Method: Our sample involved 157 teenagers aged from 13 and 20 years (M=17,39), among which 110 we…

motivationssextinggenderinstrumental/aggravatedAdolescents
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Dampness and student-reported social climate: two multilevel mediation models.

2021

Background Little previous research has analysed the relationship between schools' indoor air problems and schools' social climate. In this study, we analysed a) whether observed mould and dampness in a school building relates to students' perceptions of school climate (i.e. teacher-student relationships and class spirit) and b) whether reported subjective indoor air quality (IAQ) at the school level mediates this relationship. Methods The data analysed was created by merging two nationwide data sets: survey data from students, including information on subjective IAQ (N = 25,101 students), and data from schools, including information on mould and dampness in school buildings (N = 222). The …

mouldMaledampnessAdolescenteducationkosteusvauriotIndoor environmental problemsteacher-student relationshipsMultilevel analysislcsh:RC963-969HumansIndoor air qualityStudentsopettaja-oppilassuhdeMouldrakennuksetSchoolskoulutNegotiatingsisäilmalcsh:Public aspects of medicineResearchFungiClass spiritlcsh:RA1-1270Humidityhomeilmapiiri3142 Public health care science environmental and occupational healthTeacher-student relationshipsSocial ConditionskoulurakennuksetAir Pollution Indoor5141 Sociologyindoor environmental problemslcsh:Industrial medicine. Industrial hygieneclass spiritmultilevel analysisFemaleDampnessindoor air qualityEnvironmental health : a global access science source
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The assessment of skeletal status in young patients with Turner syndrome by 2 densitometric techniques: Phalangeal quantitative ultrasound and dual e…

2018

Background. Studies using dual energy X-ray absorptiometry (DXA) demonstrate a reduction in bone mineral density (BMD) in children and adolescents with Turner syndrome (TS). However, these studies do not take into account changes in bone size, which influence BMD in the case of short-statured patients. Phalangeal quantitative ultrasound (phQUS) measurements have shown an ability to reveal changes due to skeletal growth, aging, and bone and mineral disorders. There is limited data on bone mineral status in girls with TS assessed by 2 different techniques, i.e., DXA and phQUS. Objectives. The aim of this study was to investigate the potential negative impact of TS on bone status and to assess…

musculoskeletal diseases0301 basic medicineAdolescentmedicine.medical_treatmentMedicine (miscellaneous)Turner Syndromedual energy X-ray absorptiometry030209 endocrinology & metabolismGeneral Biochemistry Genetics and Molecular BiologyBone and Bones03 medical and health sciencesFinger PhalangesFractures Bonequantitative ultrasound0302 clinical medicineAbsorptiometry PhotonBone DensityTurner syndromeInternal MedicinemedicinePrevalenceHumansPharmacology (medical)Reference populationChildGenetics (clinical)Dual-energy X-ray absorptiometryReduction (orthopedic surgery)UltrasonographyBone mineralmedicine.diagnostic_testbusiness.industryfracturesmedicine.diseaseQuantitative ultrasound030104 developmental biologyNormal boneChild PreschoolReviews and References (medical)Lumbar spineFemalebusinessNuclear medicineAdvances in clinical and experimental medicine : official organ Wroclaw Medical University
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Assessment of the tibia using ultrasonic guided waves in pubertal girls

2002

The purpose of this study was to compare low frequency ultrasonic guided wave measurements with established ultrasound and bone density measurements in terms of their ability to characterize the tibia in pubertal girls. Subjects were 12-14-year-old girls ( n=106) who were participating in a calcium and vitamin D intervention study. A prototype low frequency pulse transmission device consisting of a uniaxial scanning mechanism and low frequency transducers orientated perpendicularly to the limb was used to measure two ultrasound velocities in the tibia. The first velocity, V1, was that of the first arriving signal, similar to that measured by existing commercial tibial ultrasound devices. Th…

musculoskeletal diseasesAdolescentBone densityEndocrinology Diabetes and MetabolismOsteoporosisBone DensitymedicineHumansUltrasonicsTibiaChildGuided wave testingTibiabusiness.industryBody WeightPubertyUltrasoundAnatomymusculoskeletal systemmedicine.diseaseBody HeightCalcaneusRadiusmedicine.anatomical_structureRegression AnalysisFemaleCortical boneUltrasonic sensorCalcaneusTomography X-Ray ComputedbusinessBiomedical engineeringOsteoporosis International
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Does δ-sarcoglycan-associated autosomal-dominant cardiomyopathy exist?

2009

In this study we clinically and genetically characterize a consanguineous family with a homozygous novel missense mutation in the delta-sarcoglycan gene and a second delta-sarcoglycan mutation that has previously been reported to cause severe autosomal-dominant dilated cardiomyopathy. We identified a novel missense mutation in exon 6 (p.A131P) of the delta-sarcoglycan gene, which in a homozygous state leads to the clinical picture of a limb girdle muscular dystrophy. In four heterozygous carriers for the mutation, aged 3-64 years, a second sequence variant in exon 6 (p.S151A) of the delta-sarcoglycan gene was detected on the other allele. This second missense change had previously been repo…

musculoskeletal diseasesAdultCardiomyopathy DilatedMalemedicine.medical_specialtyAdolescentBiopsyDNA Mutational AnalysisCardiomyopathyMutation MissenseCompound heterozygosityArticleExonConsanguinityElectrocardiographyYoung AdultInternal medicineSarcoglycansGeneticsMedicineMissense mutationHumansMuscular dystrophyChildGenetics (clinical)Genes DominantGeneticsFamily Healthbusiness.industryMusclesMyocardiumDilated cardiomyopathyMiddle Agedmedicine.diseasePedigreeEndocrinologyEchocardiographyChild PreschoolMutation (genetic algorithm)FemalebusinessLimb-girdle muscular dystrophy
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Pfeiffer syndrome: clinical and genetic findings in five Brazilian families

2014

Pfeiffer syndrome (PS) is mainly characterized by craniosysnostosis, midface hypoplasia, great toes with partial syndactyly of the digits and broad and medially deviated thumbs. It is caused by allelic mutations in the fibroblast growth factor receptor 1 and 2 (FGFR1 and 2) genes. This study describes the clinical and genetic features of five Brazilian families affected by PS. All patients exhibited the classical phenotypes related to PS. The genetic analysis was able to detect the mutations Cys278Phe, Cys342Arg, and Val359Leu in three of these families. Two mutations were de novo, with one familial. We identified pathogenic mutations in four PS cases in five Brazilian families by PCR seque…

musculoskeletal diseasesAdultMaleAdolescentAcrocephalosyndactyliaOdontologíaBiologymedicine.disease_causeGenetic analysisExonmedicineHumansAlleleChildGeneral DentistryGeneticsMutationOral Medicine and PathologyResearchFibroblast growth factor receptor 1Crouzon syndromeAcrocephalosyndactyliaMiddle Agedmedicine.disease:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludPedigreePhenotypeOtorhinolaryngologyChild PreschoolMutationUNESCO::CIENCIAS MÉDICASPfeiffer syndromeFemaleSurgeryBrazil
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Transcriptional profiles from patients with dystrophinopathies and limb girdle muscular dystrophies as determined by qRT-PCR.

2003

Mutations in genes coding for the dystrophin-glycoprotein complex (DGC) cause inherited muscular dystrophies (MD), including Morbus Duchenne (DMD) and M. Becker (BMB) as well as limb-girdle muscular dystrophies (LGMD). New insights into the pathophysiology of the dystrophic muscle, the identification of compensatory mechanisms and additional proteins interacting with dystrophin are essential for developing new treatments. In order to define molecular mechanisms induced by lack of dystrophin and the subsequent counter-regulatory transcriptional response of degenerating muscle fibres, we have investigated the mRNA expression of 19 functionally linked genes in biopsies of patients with MD by m…

musculoskeletal diseasesAdultMaleAdolescentTranscription GeneticGene Expressionmedicine.disease_causeMuscular DystrophiesStatistics NonparametricDystrophinGenetic linkageGene expressionmedicineHumansRNA MessengerMuscular dystrophyChildGeneGlycoproteinsMutationbiologyReverse Transcriptase Polymerase Chain ReactionGene Expression ProfilingMusclesMiddle Agedmedicine.diseaseCell biologyGene expression profilingMuscular Dystrophy DuchenneNeurologyChild PreschoolMutationbiology.proteinFemaleNeurology (clinical)DystrophinNeuroscienceLimb-girdle muscular dystrophyJournal of neurology
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An Optoelectronic System for Measuring the Range of Motion in Healthy Volunteers: A Cross-Sectional Study.

2019

Background and Objectives: Within the clinical evaluation of multiple pathologies of the lower limb, the measurement of range of motion (ROM) of its joints is fundamental. To this end, there are various tools, from the goniometer as a reference to more recent devices such as inclinometry-based applications, photo capture applications, or motion capture systems. This study aimed to assess the validity, intra-rater, and inter-rater reliability of the VeloFlex system (VS), which is a new camera-based tool designed for tracking joint trajectories and measuring joint ROM. Materials and Methods: Thirty-five healthy volunteers (16 females

musculoskeletal diseasesAdultMaleMedicine (General)AdolescentCross-sectional studyConcurrent validityeducationMesurament -- InstrumentsArticlerange of motionsymbols.namesakeYoung AdultR5-920articular goniometryHealthy volunteersMedicineHumanslower extremity; range of motion; reproducibility of results; articular goniometryRange of Motion ArticularReliability (statistics)Leg -- DiseasesOrthodonticsObserver VariationArthrometry Articularbusiness.industryOrthopedic EquipmentReproducibility of ResultsGeneral MedicineMiddle AgedPearson product-moment correlation coefficientHealthy VolunteersStandard errorCross-Sectional StudiesLower ExtremityCames -- MalaltiesGoniometersymbolsMeasuring instrumentsFemaleRange of motionbusinessMedicina (Kaunas, Lithuania)
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Detection of bifid mandibular condyle using computed tomography

2011

Objective: To determine the frequency and characteristics of bifid mandibular condyle (BMC) using computed tomography (CT) evaluation. Study Design: A retrospective study was carried out using the CT records of 550 patients referred to the Medical School of Erciyes University (Kayseri, Turkey) between 2007 and 2010. T-tests were used to compare frequency of BMC between the left and right sides and between female and male patients. Statistical analysis was performed using SPSS software and a chi-squared test. Results: Of the 550 Patients, 10 patients (1.82%) were found to have BMCs. Five patients were female (50%) and five were male (50%). Of these 10 patients, 7 (70%) had unilateral and 3 (…

musculoskeletal diseasesAdultMaleTurkish populationAdolescentDentistryComputed tomographyOdontologíaCondyleYoung Adultstomatognathic systemmedicineHumansStatistical analysisChildGeneral DentistryAgedRetrospective StudiesAged 80 and overOral Medicine and Pathologymedicine.diagnostic_testbusiness.industryMedical schoolMandibular CondyleRetrospective cohort studyMiddle Agedmusculoskeletal system:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludhumanitiesstomatognathic diseasesOtorhinolaryngologyMale patientUNESCO::CIENCIAS MÉDICASSurgeryFemaleResearch-ArticleNuclear medicinebusinessTomography X-Ray ComputedBifid mandibular condyle
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Effectiveness of adalimumab for ulcerative colitis: A multicentre, retrospective study of clinical practice in Italy.

2022

Abstract Background Adalimumab is used to treat ulcerative colitis, but additional effectiveness and safety data are needed. Patients and methods This retrospective study considered adults with ulcerative colitis treated with adalimumab at 19 hospitals. Clinical data were collected from the start of treatment, after 2, 6 and 12 months, and at the last visit. Outcome measures of effectiveness were treatment duration, reasons for discontinuation and colectomy. Results We studied 381 patients treated with adalimumab for a median of 12.1 months. Disease activity at the start of treatment was moderate to severe in 262 cases (68.8%) and endoscopic activity was moderate to severe in 339 cases (89.…

musculoskeletal diseasesAdultMalemedicine.medical_specialtyAdolescentmedicine.medical_treatmentEffectivenessYoung AdultInternal medicineAdalimumabMedicineHumansAdverse effectskin and connective tissue diseasesColectomyColectomyAgedRetrospective StudiesReal-world evidenceHepatologybusiness.industryGastroenterologyEffectiveneAdalimumabRetrospective cohort studyInduction ChemotherapyMiddle Agedmedicine.diseaseUlcerative colitisDiscontinuationClinical PracticeTreatment OutcomeUlcerative colitisItalyAdalimumab; Effectiveness; Real-world evidence; Safety; Ulcerative colitisConcomitantColitis UlcerativeFemaleTumor Necrosis Factor InhibitorsSafetybusinessmedicine.drugDigestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver
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