Search results for "neonata"

showing 10 items of 586 documents

Audiologic profile of infants at risk: experience of a Western Sicily tertiary care centre.

2012

Objective: To identify the incidence of sensorineural hearing loss (SNHL) on infant at risk and to classify the degree and type of hearing loss describing the main causes associated in Western Sicily. To compare single TEOAE and combined TEOAE/ABR techniques studying the referral rate, the false-positive and false-negative rates through concordance test (κ coefficient), sensitivity (TPR) and specificity (TNR) for each protocol. Methods: From January 2010 to June 2011, 412 infants at risk, ranging from 4 to 20 weeks of life, transferred to Audiology Department of Palermo from the births centers of Western Sicily, underwent to audiological assessment with TEOAE, tympanometry and ABR. The foll…

MaleRiskPediatricsmedicine.medical_specialtyHearing lossHearing Loss SensorineuralAuditory neuropathySensitivity and SpecificityNeonatal screeningInfant at riskAuditory neuropathySensorineural hearing lossTertiary Care CentersNeonatal ScreeningPregnancyRisk FactorsIntensive careotorhinolaryngologic diseasesEvoked Potentials Auditory Brain StemMedicineHumansRisk factorFamily historyPregnancy Complications InfectiousSicilymedicine.diagnostic_testbusiness.industryInfant NewbornInfantGeneral MedicineAudiologymedicine.diseaseAudiometry Evoked ResponseLow birth weightOtorhinolaryngologyPediatrics Perinatology and Child HealthSensorineural hearing lossFemaleAudiometrymedicine.symptombusinessInternational journal of pediatric otorhinolaryngology
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The Role of the Unitary Prevention Delegates in the Participative Management of Occupational Risk Prevention and Its Impact on Occupational Accidents…

2020

The aim of this research was to study the impact of the unitary prevention delegates (UPDs) on the Spanish working environment. To this end, a cross-sectional study was carried out using microdata from the National Survey on Health and Safety Management in Companies (ENGE-2009) with a sample of 5147 work centres. To measure the relationship between the presence of UPD in workplaces with preventive management indicators and damage to health, individual and multiple logistic regression models were carried out, calculating the crude (cOR) and adjusted (aOR) odds ratios by sociodemographic covariates, with their corresponding 95% confidence intervals (95% CI). Ambivalent results were obtained. …

MaleSafety Managementcongenital hereditary and neonatal diseases and abnormalitiesHealth Toxicology and Mutagenesislcsh:MedicinePoison controlLogistic regressionSuicide preventionpreventive managementArticleOccupational safety and health03 medical and health sciences0302 clinical medicineEnvironmental health0502 economics and businessInjury preventionOdds RatioAccidents OccupationalHumansMedicineWorkplaceOccupational Healthcultural activationbusiness.industrylcsh:R05 social sciences050209 industrial relationsPublic Health Environmental and Occupational HealthHuman factors and ergonomicsunitary prevention delegatesOdds ratioworkers’ participation030210 environmental & occupational healthOrganizational PolicyCross-Sectional StudiesFemalebusinessRisk assessmentaccidents at workInternational Journal of Environmental Research and Public Health
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Orientation of newborn mice to lactating females: Identifying biological substrates of semiochemical interest

2013

International audience; Among mammals, odor-based communication between females and infants is decisive for neonatal survival. So far, the nature of odor substrates involved in the localization of the mother and their nipples is unknown in mice. The present study aims: (1) to evaluate the specific attractive value of lactating females to newborn mice, (2) to localize the abdominal region that is most attractive to pups, and (3) to identify odor substrates that support such attraction. Results showed that 5-6-day-old mice roam preferentially over the abdomen of lactating females than the abdomen of non-lactating females. In lactating females, pups are more attracted to abdominal areas compri…

MaleSalivamedicine.medical_specialty[ SDV.AEN ] Life Sciences [q-bio]/Food and NutritionOlfactionBiologyPheromonesMice03 medical and health sciencesBehavioral Neuroscience0302 clinical medicineDevelopmental NeurosciencenewbornOrientationInternal medicineDevelopmental and Educational PsychologymedicineAnimalsLactation0501 psychology and cognitive sciences050102 behavioral science & comparative psychologymice (Mus musculus)SemiochemicalmilksalivaBehavior AnimalNeonatal survival05 social sciencesmother-infant communicationAttractionAssociative learningSmellEndocrinologyAnimals NewbornOdorNipplesnippleChemical constituentsOdorantsFemale[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition030217 neurology & neurosurgeryolfactionDevelopmental BiologyDevelopmental Psychobiology
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Polysomnographic Findings in Fragile X Syndrome Children with EEG Abnormalities

2019

Fragile X syndrome (FXS) is a genetic syndrome with intellectual disability due to the loss of expression of the FMR1 gene located on chromosome X (Xq27.3). This mutation can suppress the fragile X mental retardation protein (FMRP) with an impact on synaptic functioning and neuronal plasticity. Among associated sign and symptoms of this genetic condition, sleep disturbances have been already described, but few polysomnographic reports in pediatric age have been reported. This multicenter case-control study is aimed at assessing the sleep macrostructure and at analyzing the presence of EEG abnormalities in a cohort of FXS children. We enrolled children with FXS and, as controls, children wit…

MaleSleep Wake Disorderscongenital hereditary and neonatal diseases and abnormalitiesPediatricsmedicine.medical_specialtyAdolescentArticle SubjectPolysomnographyNeurosciences. Biological psychiatry. NeuropsychiatryFragile X Mental Retardation Protein03 medical and health sciences0302 clinical medicinechildrenIntellectual disabilitymedicineHumansIctalCircadian rhythmChildEEG abnormalitiesPathologicalPSG030304 developmental biology0303 health sciencesNeuronal PlasticityFragile X syndrome; intellectual disability; polysomnographicbusiness.industryCase-control studyNeuropsychologyElectroencephalographyGeneral Medicinemedicine.diseasepolysomnographicFragile X syndromeNeuropsychology and Physiological PsychologyNeurologyintellectual disabilityCase-Control StudiesFragile X SyndromeCohortFemaleNeurology (clinical)FXSSleepbusiness030217 neurology & neurosurgeryRC321-571Research ArticleBehavioural Neurology
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"I Know that You Know that I Know": Neural Substrates Associated with Social Cognition Deficits in DM1 Patients.

2016

Myotonic dystrophy type-1 (DM1) is a genetic multi-systemic disorder involving several organs including the brain. Despite the heterogeneity of this condition, some patients with non-congenital DM1 can present with minimal cognitive impairment on formal testing but with severe difficulties in daily-living activities including social interactions. One explanation for this paradoxical mismatch can be found in patients' dysfunctional social cognition, which can be assessed in the framework of the Theory of Mind (ToM). We hypothesize here that specific disease driven abnormalities in DM1 brains may result in ToM impairments. We recruited 20 DM1 patients who underwent the "Reading the Mind in th…

MaleSocial CognitionMagnetic Resonance SpectroscopyTheory of MindAdult; Brain; Cognition; Female; Humans; Magnetic Resonance Spectroscopy; Male; Middle Aged; Myotonic Dystrophy; Neuropsychological Tests; Social Behavior; Theory of MindSocial Scienceslcsh:MedicineDiseaseNeuropsychological TestsDiagnostic RadiologyCognition0302 clinical medicineFunctional Magnetic Resonance ImagingTheory of mindMedicine and Health SciencesPsychologyMyotonic Dystrophylcsh:ScienceCognitive ImpairmentBrain MappingMultidisciplinarymedicine.diagnostic_testCognitive NeurologyRadiology and Imagingagricultural and biological sciences (all); biochemistry genetics and molecular biology (all); medicine (all)05 social sciencesRBrainCognitionMiddle AgedMagnetic Resonance ImagingNeurologyRC0346Genetic DiseasesPhysical SciencesFemaleSettore MED/26 - NeurologiaPsychologyResearch ArticleClinical psychologyAdultmusculoskeletal diseasesComputer and Information Sciencesmedicine.medical_specialtycongenital hereditary and neonatal diseases and abnormalitiesSocial PsychologyImaging TechniquesCognitive NeuroscienceNeuroimagingDysfunctional familyResearch and Analysis MethodsMyotonic dystrophy050105 experimental psychology03 medical and health sciencesDiagnostic MedicineSocial cognitionTheory of mind cerebral lesionGeneticsmedicineHumans0501 psychology and cognitive sciencesSocial BehaviorPsychiatryClinical GeneticsSettore M-PSI/02 - Psicobiologia E Psicologia Fisiologicalcsh:RCognitive PsychologyBiology and Life SciencesHuman Geneticsmedicine.diseaseComprehensionGraph TheoryRC0321Cognitive Sciencelcsh:QFunctional magnetic resonance imagingMathematics030217 neurology & neurosurgeryNeurosciencePLoS ONE
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A re-entry tachycardia triggered by the spontaneous interruption of an atrial tachycardia.

2015

The common atrioventricular nodal re-entry tachycardia is the most common form of paroxysmal supraventricular tachycardia. It starts frequently with a supraventricular ectopic beat that, on finding the fast pathway in refractory period, travels in the slow pathway as to appear as a prolongation of the PR interval on the ECG. In this study, we show a singular case of a common atrioventricular nodal re-entry tachycardia triggered by the spontaneous interruption of an atrial tachycardia.

MaleTachycardiacongenital hereditary and neonatal diseases and abnormalitiesmedicine.medical_specialtySettore MED/09 - Medicina InternaRefractory periodSlow pathwayEctopic beatParoxysmal supraventricular tachycardiaElectrocardiographyInternal medicineTachycardia Supraventricularmedicinere-entry tachycardia atrial tachycardiaHumansTachycardia Atrioventricular Nodal Reentrycardiovascular diseasesAtrial tachycardiaAgedFast pathwaybusiness.industryRe entryGeneral Medicinemedicine.diseasesurgical procedures operativecardiovascular systemCardiologymedicine.symptomCardiology and Cardiovascular Medicinebusiness
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Three cases of neonatal herpes simplex virus infection presenting as fulminant hepatitis

1990

We report three cases of neonatal herpes simplex virus (HSV) infection presenting as fulminant hepatitis. None of the patients had clear risk factors for HSV infection and they all died. Antiviral treatment for HSV is currently available but must be administered early in the course of the disease before irreversible liver tissue damage is present. Since the diagnosis may be difficult to establish, we wish to draw the attention of clinicians to the presentation of neonatal HSV infection and suggest that in such cases viral cultures, including culture of liver tissue, should be obtained early and antiviral treatment administered while awaiting the culture results.

MaleTime FactorsHepatitis Viral HumanvirusesAcyclovirDiseaseHSL and HSVmedicine.disease_causeDiagnosis DifferentialNeonatal herpes simplex virus infectionNecrosisLiver tissuemedicineHumansSimplexvirusFulminant hepatitisHepatitisHsv infectionbusiness.industryInfant NewbornHerpes Simplexmedicine.diseaseVirologyHerpes simplex virusAcute DiseasePediatrics Perinatology and Child HealthImmunologyFemalebusinessEuropean Journal of Pediatrics
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Using the Hemophilia Joint Health Score for assessment of children: Reliability of the Spanish version

2018

Introduction: Numerous measuring instruments for the evaluation of hemophilic arthropathy have been developed. One of the most used systems is the Hemophilia Joint Health Score (HJHS) given its sensitivity to clinical changes appearing in the joints because of recurrent hemarthrosis. Objective: Assessing the interrater reliability, using the Spanish version of the HJHS (version 2.1) in children with hemophilia. Design: Reliability study to assess the interrater reliability of the Spanish version of HJHS. Methods: A sample of 36 children aged 7–13 years diagnosed with hemophilia A or B was used. Two physiotherapists performed physical assessments with the Spanish version of the HJHS. Descrip…

Malecongenital hereditary and neonatal diseases and abnormalities030506 rehabilitationmedicine.medical_specialtyAdolescentInterobserver reliabilityHealth StatusHemophilic arthropathyPhysical Therapy Sports Therapy and RehabilitationHemophilia AHemophilia BHemofilia03 medical and health sciences0302 clinical medicinePredictive Value of Testshemic and lymphatic diseasesHemarthrosisHealth Status IndicatorsHumansMedicineHealth scoreChildJoint (geology)Reliability (statistics)Observer Variationbusiness.industryAge FactorsReproducibility of ResultsSpanish versionHemartrosisCross-Sectional StudiesSpainNiñoArtropatíasJoint damagePhysical therapyJointsLucha contra las enfermedades0305 other medical sciencebusiness030217 neurology & neurosurgeryPhysiotherapy Theory and Practice
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Psychosocial adjustment of children with spina bifida.

1998

It was the aim of the present prospective study to investigate the influence of age, sex, intellectual function, and school type as well as of hydrocephalus, the level of lesion, and of the degree of handicap on the psychosocial adjustment of children with spina bifida. Seventy-five patients with spina bifida, aged 6 to 16 years were assessed concerning their psychosocial adjustment and their intellectual function by use of standardized instruments. The findings were compared with those of nondisabled controls, matched for age and sex. Children with spina bifida showed a tendency to be at an increased risk for psychosocial maladjustment. Influencing factors were age, sex, and the degree of…

Malecongenital hereditary and neonatal diseases and abnormalitiesAdolescentAge and sexDevelopmental psychologyIntellectual function03 medical and health sciences0302 clinical medicine030225 pediatricsGermanySurveys and QuestionnairesmedicineHumansProspective StudiesProspective cohort studyChildSpinal DysraphismSchool typeSpina bifidamedicine.diseasenervous system diseasesHydrocephalusIncreased riskPediatrics Perinatology and Child HealthFemaleNeurology (clinical)Test Anxiety ScalePsychologyPsychosocialSocial Adjustment030217 neurology & neurosurgeryClinical psychologyJournal of child neurology
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Subcortical somatosensory evoked potentials after median nerve and posterior tibial nerve stimulation in high cervical cord compression of achondropl…

2008

Abstract Children with achondroplasia may have high cervical myelopathy from stenosis of the cranio-cervical junction resulting in neurological disability and an increased rate of sudden death. To detect myelopathy we recorded somatosensory evoked potentials after median nerve (MN) and posterior tibial nerve (PTN) stimulation in 77 patients with achondroplasia aged 0.3–17.8 years (mean 2.7 years). In addition to the conventional technique of recording the cortical components and the central conduction time (CCT) we employed non-cephalic and mastoid reference electrodes to record the subcortical waveforms N13b and P13 (MN-SEP) as well as P30 (PTN-SEP), respectively, which are generated near …

Malecongenital hereditary and neonatal diseases and abnormalitiesAdolescentSudden deathSensitivity and SpecificityAchondroplasiaMyelopathyDevelopmental NeuroscienceSpinal cord compressionEvoked Potentials SomatosensoryMedicineHumansTibial nerveChildbusiness.industryInfantGeneral MedicineCervical cord compressionAnatomymedicine.diseaseSpinal cordMagnetic Resonance ImagingElectric StimulationMedian Nervebody regionsmedicine.anatomical_structureSomatosensory evoked potentialChild PreschoolPediatrics Perinatology and Child HealthCervical VertebraeFemaleNeurology (clinical)Tibial NervebusinessMyelomalaciaSpinal Cord CompressionBraindevelopment
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