Search results for "psichiatria"

showing 10 items of 426 documents

Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination

2019

See Karakaya and Wirth (doi:10.1093/brain/awz273) for a scientific commentary on this article. Neurofascin (NFASC) isoforms are immunoglobulin cell adhesion molecules involved in node of Ranvier assembly. Efthymiou et al. identify biallelic NFASC variants in ten unrelated patients with a neurodevelopmental disorder characterized by variable degrees of central and peripheral involvement. Abnormal expression of Nfasc155 is accompanied by severe loss of myelinated fibres.

Male[SDV]Life Sciences [q-bio][SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/NeurobiologyNerve Fibers MyelinatedGene FrequencyNeurodevelopmental Disorder[SDV.BC.IC]Life Sciences [q-bio]/Cellular Biology/Cell Behavior [q-bio.CB]Nerve Growth FactorProtein IsoformsChildComputingMilieux_MISCELLANEOUSMyelin Sheathneurofascin; neurodevelopment; peripheral demyelinationAlleleneurodevelopmentDemyelinating DiseaseGenomicsneurodevelopment neurofascin peripheral demyelinationSettore MED/39 - Neuropsichiatria InfantilePedigree[SDV.IMM.IA]Life Sciences [q-bio]/Immunology/Adaptive immunologyChild PreschoolPeripheral Nerve[SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]Femaleneurodevelopment; neurofascin; peripheral demyelinationNeurogliaHumanAdultAdolescentNervous System MalformationsGuillain-Barre SyndromeAxonNervous System MalformationneurofascinRanvier's NodesHumansNerve Growth FactorsPeripheral NervesAllelesAutoantibodiesperipheral demyelinationInfantProtein IsoformOriginal ArticlesAxonsnervous systemNeurodevelopmental DisordersCell Adhesion MoleculeMutationCell Adhesion MoleculesDemyelinating Diseases
researchProduct

Premorbid Adjustment and IQ in Patients With First-Episode Psychosis: A Multisite Case-Control Study of Their Relationship With Cannabis Use

2020

Abstract Psychotic patients with a lifetime history of cannabis use generally show better cognitive functioning than other psychotic patients. Some authors suggest that cannabis-using patients may have been less cognitively impaired and less socially withdrawn in their premorbid life. Using a dataset comprising 948 patients with first-episode psychosis (FEP) and 1313 population controls across 6 countries, we examined the extent to which IQ and both early academic (Academic Factor [AF]) and social adjustment (Social Factor [SF]) are related to the lifetime frequency of cannabis use in both patients and controls. We expected a higher IQ and a better premorbid social adjustment in psychotic p…

MalecognitionIntelligenceComorbiditySUBSTANCE USE DISORDERS0302 clinical medicineSettore MED/48 -Scienze Infermierist. e Tecn. Neuro-Psichiatriche e Riabilitat.MedicinePREDICTORSRISKeducationeducation.field_of_studybiologyCognitionMiddle AgedPsychosocial FunctioningsociabilityPsychiatry and Mental healthSchizophreniaFemaleMarijuana UseSocial AdjustmentMENTAL-HEALTHAdultmedicine.medical_specialtyPsychosisAdolescentPopulation1ST EPISODEDRUG-USEpreillnessSettore MED/01 - Statistica MedicaYoung Adult03 medical and health sciencesAGESettore M-PSI/08 - Psicologia ClinicaHumansCognitive skilleducationPsychiatrySettore MED/25 - Psichiatriabusiness.industryCase-control studypreillnebiology.organism_classificationmedicine.diseaseEDUCAÇÃO030227 psychiatryschizophreniaPsychotic DisordersCase-Control StudiesONSETCannabisNEUROCOGNITIONbusinessmarijuanaNeurocognitive030217 neurology & neurosurgeryRegular ArticlesSchizophrenia Bulletin
researchProduct

Xq27 FRAXA Locus is a Strong Candidate for Dyslexia: Evidence from a Genome-Wide Scan in French Families

2012

Dyslexia is a frequent neurodevelopmental learning disorder. To date, nine susceptibility loci have been identified, one of them being DYX9, located in Xq27. We performed the first French SNP linkage study followed by candidate gene investigation in dyslexia by studying 12 multiplex families (58 subjects) with at least two children affected, according to categorical restrictive criteria for phenotype definition. Significant results emerged on Xq27.3 within DYX9. The maximum multipoint LOD score reached 3,884 between rs12558359 and rs454992. Within this region, seven candidate genes were investigated for mutations in exonic sequences (CXORF1, CXORF51, SLITRK2, FMR1, FMR2, ASFMR1, FMR1NB), al…

Malecongenital hereditary and neonatal diseases and abnormalitiesCandidate geneGenotypeGenome-wide association studyLocus (genetics)BiologyPolymorphism Single NucleotideGenomeDyslexiaFragile X Mental Retardation ProteinGenes X-LinkedGenotypeGeneticsmedicineHumansSNPGenetic Predisposition to DiseaseChildGenetics (clinical)Ecology Evolution Behavior and SystematicsGeneticsChromosomes Human XDyslexiamedicine.diseaseFMR1Settore MED/39 - Neuropsichiatria InfantilePedigreeGenetic LociFemaleFranceDyslexia Linkage study Multiplex families Fmr1 Dyx 9 loci InLod ScoreGenome-Wide Association StudyBehavior Genetics
researchProduct

Sleep in children with autistic spectrum disorder: a questionnaire and polysomnographic study.

2007

Abstract Objective To evaluate sleep in children with autistic spectrum disorder (ASD) by means of sleep questionnaires and polysomnography; moreover, to analyze their cyclic alternating pattern (CAP). Methods Thirty-one patients with ASD (28 males, 3 females, aged 3.7–19 years) and age-matched normal controls were included. ASD children were evaluated by a standard sleep questionnaire that consisted of 45 items in a Likert-type scale covering several areas of sleep disorders and by overnight polysomnography in the sleep laboratory after one adaptation night. Results The questionnaire results showed that parents of ASD children reported a high prevalence of disorders of initiating and maint…

Malemedicine.medical_specialtyAdolescentcyclic alternating patternPolysomnographySleep REMPolysomnographyComorbidityAudiologyNon-rapid eye movement sleepactigraphy polysomnographyEnuresisSleep Disorders Circadian RhythmSurveys and Questionnairesmental disordersActivities of Daily LivingmedicineHumansAutistic DisorderParent-Child RelationsChildSleep disorderSleep StagesSleep stagemedicine.diagnostic_testautistic spectrum disorderActigraphyGeneral Medicinemedicine.diseaseComorbiditySleep in non-human animalsSettore MED/39 - Neuropsichiatria Infantilesleep questionnaireactigraphy; actigraphy polysomnography; autistic spectrum disorder; cyclic alternating pattern; polysomnography; sleep questionnaire; sleep stagesLogistic ModelsChild PreschoolPhysical therapyFemaleSleep Stagesmedicine.symptomPsychologyactigraphySleep medicine
researchProduct

Minor physical anomalies in children with autism spectrum disorder.

2007

Abstract Aim To investigate the rate and topological profile of minor physical anomalies (MPAs) (prenatal errors of morphogenesis) in a group of children with Autism Spectrum Disorder (ASD), in order to better set a temporal framing of embryological factors involved in the neurodevelopmental etiology. Method A new modified Waldrop scale and a mixed approach of computerized photogrammetry and classic anthroposcopy was used to detect the presence or absence of 41 MPAs in 24 children (mean age: 7 years; sex ratio: 22M:2F) with ASD and 24 healthy comparison subjects (mean age: 7 years; sex ratio: 19M:5F) selected with DSM IV and CARS. Results We found that children with ASD presenting MPAs (n =…

Malemedicine.medical_specialtyAudiologyCongenital AbnormalitiesPregnancymental disordersmedicineHumansMinor physical anomaliesAutistic DisorderPsychiatryChildPregnancyAutism spectrum disorder Minor physical anomalies NeurodevelopmentCephalic indexfungiObstetrics and Gynecologymedicine.diseaseSettore MED/39 - Neuropsichiatria InfantileDevelopmental disorderEl NiñoAutism spectrum disorderPediatrics Perinatology and Child HealthEtiologyAutismFemalePsychology
researchProduct

Electroencephalographic Abnormalities in Autism Spectrum Disorder: Characteristics and Therapeutic Implications.

2020

A large body of literature reports the higher prevalence of epilepsy in subjects with Autism Spectrum Disorder (ASD) compared to the general population. Similarly, several studies report an increased rate of Subclinical Electroencephalographic Abnormalities (SEAs) in seizure-free patients with ASD rather than healthy controls, although with varying percentages. SEAs include both several epileptiform discharges and different non-epileptiform electroencephalographic abnormalities. They are more frequently associated with lower intellectual functioning, more serious dysfunctional behaviors, and they are often sign of severer forms of autism. However, SEAs clinical implications remain controver…

Malemedicine.medical_specialtyMedicine (General)Autism Spectrum Disorderautism spectrum disordersPopulationEpiphenomenonDysfunctional familyChild Behavior DisordersReviewAudiologybehavioral disciplines and activities03 medical and health sciencesEpilepsy0302 clinical medicineBorderline intellectual functioningR5-920mental disordersmedicineHumansCognitive DysfunctioneducationChildSubclinical infectioneducation.field_of_studyEpilepsyEvidence-Based MedicineEpileptogenic abnormalitiebusiness.industryepileptogenic abnormalitiesElectroencephalographyGeneral Medicineelectroencephalogrammedicine.diseaseSettore MED/39 - Neuropsichiatria Infantile030227 psychiatryAutism spectrum disorderAutismAnticonvulsantsFemaleAutism spectrum disorders Electroencephalogram Epilepsy Epileptogenic abnormalities Non-epileptiform abnormalitiesbusinessnon-epileptiform abnormalities030217 neurology & neurosurgeryMedicina (Kaunas, Lithuania)
researchProduct

Ischemic hypoxic encephalopathy: The role of MRI of neonatal injury and medico-legal implication

2021

Hypoxic ischemic encephalopathy is one of the major causes of neonatal death and neurological disability in the child, and represents the most common birth injury claim. Intrapartum asphyxia often leads to several long-term sequalae, such as cerebral palsy and/or developmental delay, epilepsy. Through the neuroimaging it's possible to identify and define the different lesioned pictures and provide useful elements to establish the moment in which the damage occurred; indeed, timing of injury is a key element in the legal arena. Magnetic resonance imaging (MRI) is emerging as one of the most important tools in identifying the etiologic of neonatal encephalopathy as well as in predicting long-…

Malemedicine.medical_specialtyNeuroimagingHypoxic Ischemic EncephalopathyPathology and Forensic MedicineCerebral palsyMedico-legalEpilepsySettore MED/38 - Pediatria Generale E SpecialisticaNeuroimagingSettore MED/43 - Medicina LegaleMalpractice litigationMalpracticemedicineHumansIschemic Hypoxic encephalopathyIntensive care medicineAsphyxia Neonatorummedicine.diagnostic_testNeonatal encephalopathybusiness.industryInfant NewbornInfantMagnetic resonance imagingForensic Medicinemedicine.diseaseMagnetic Resonance ImagingBirth injurySettore MED/39 - Neuropsichiatria InfantileItalyMRI brainHypoxia-Ischemia BrainCerebral palsyFemalebusinessSettore MED/36 - Diagnostica Per Immagini E RadioterapiaLawHuman
researchProduct

West syndrome followed by juvenile myoclonic epilepsy: a coincidental occurrence?

2013

Background: West syndrome is an age-dependent epilepsy with onset peak in the first year of life whose aetiology may be symptomatic or cryptogenic. Long-term cognitive and neurological prognosis is usually poor and seizure outcome is also variable. Over the past two decades a few patients with favourable cognitive outcome and with total recovery from seizures were identified among the cryptogenic group suggesting an idiopathic aetiology. Recent research has described two children with idiopathic WS who later developed a childhood absence epilepsy. Case presentation: We reviewed the medical records of patients with West syndrome admitted to the our Child Neuropsychiatry Unit in the last 15 y…

Malemedicine.medical_specialtyPediatricsNeurologyLevetiracetamAdolescentHairy elbows syndromeMyoclonic JerkClinical NeurologyCase ReportEpilepsyChildhood absence epilepsyJuvenile myoclonic epilepsySettore M-PSI/08 - Psicologia ClinicamedicineHumansEpilepsy evolutionPsychiatrySettore M-PSI/02 - Psicobiologia E Psicologia Fisiologicabusiness.industryGenetic predispositionMyoclonic Epilepsy JuvenileBrainInfantWest SyndromeGeneral MedicineWest syndromemedicine.diseaseMagnetic Resonance ImagingPiracetamSettore MED/39 - Neuropsichiatria InfantileWest syndrome Juvenile myoclonic epilepsy Epilepsy evolution Genetic predisposition Hairy elbows syndromeDisease ProgressionMyoclonic epilepsyNeurology (clinical)LevetiracetamJuvenile myoclonic epilepsybusinessSpasms Infantilemedicine.drugBMC neurology
researchProduct

Rates and correlates of suicidal ideation among stroke survivors: a meta-Analysis

2017

BACKGROUND: A better understanding of the epidemiological impact of suicidal ideation after stroke is required to identify subjects needing personalised interventions. OBJECTIVE: The aim of this meta-analysis was to estimate rates and correlates of suicidal ideation among stroke survivors. METHODS: We searched via Ovid, Medline, Embase and PsycInfo from database inception until August 2016. Predefined outcomes were (1) rates of suicidal ideation based on random-effects pooled proportion and (2) relevant sociodemographic and clinical correlates, using random-effects odds ratio (OR) or standardised mean difference (SMD) for categorical and continuous variables, respectively. RESULTS: Fifteen …

Malemedicine.medical_specialtyStatistics as TopicMEDLINEPsychological interventionPsycINFOmeta-analysisurgery03 medical and health sciences0302 clinical medicineRecurrenceEpidemiologyOdds RatiomedicineHumansSurvivors030212 general & internal medicinePsychiatryStrokeSuicidal ideationSettore MED/25 - PsichiatriaAgedarts and humanitiesDepressive DisorderneurologyOdds ratioMiddle Agedmedicine.diseasestrokedepression; epidemiology; meta-analysis; stroke; suicidal ideation; surgery; arts and humanities ; neurology; psychiatry and mental healthmeta-analysissuicidal ideationpsychiatry and mental healthObservational Studies as TopicCross-Sectional StudiesMeta-analysisdepressionFemaleSettore MED/26 - NeurologiaepidemiologyNeurology (clinical)medicine.symptomPsychology030217 neurology & neurosurgeryClinical psychology
researchProduct

Reading–writing disorder in children with idiopathic epilepsy

2020

Abstract Several studies have documented learning disabilities (LDs) in subjects with epilepsy, who have been shown to be at greater risk of mild neuropsychological damage, with the consequent risk of academic failure. This retrospective study aimed to investigate the peculiarities of reading and writing disorders in subjects with idiopathic epilepsy. The reading and writing performance of 35 children affected by reading and writing disorders and idiopathic epilepsy (R/WD + E group) has been compared with the performance of 37 children with only reading and writing disorders (R/WD group). A comparison group of 22 typical developing healthy children (TDC group) was also included in the study…

Malemedicine.medical_specialtymedia_common.quotation_subjectWritingeducationShort-term memoryAudiologyNeuropsychological TestsWriting disorderDyslexiaEpilepsy Reading Short-term memory Writing disorder03 medical and health sciencesBehavioral NeuroscienceEpilepsy0302 clinical medicineReading (process)Memory spanmedicineHumansShort-term memory030212 general & internal medicineChildmedia_commonRetrospective StudiesEpilepsyDictationLearning DisabilitiesDyslexiaNeuropsychologymedicine.diseaseSettore MED/39 - Neuropsichiatria InfantileMemory Short-TermNeurologyLearning disabilityFemaleNeurology (clinical)medicine.symptomReading disorderPsychologyReading disorder Writing disorder Epilepsy Short-term memory030217 neurology & neurosurgery
researchProduct