Search results for "BELLA"

showing 10 items of 388 documents

Anatomical Correlate of Impaired Covert Visual Attentional Processes in Patients with Cerebellar Lesions

2010

In the past years, claims of cognitive and attentional function of the cerebellum have first been raised but were later refuted. One reason for this controversy might be that attentional deficits only occur when specific cerebellar structures are affected. To further elucidate this matter and to determine which cerebellar regions might be involved in deficits of covert visual attention, we used new brain imaging tools of lesion mapping that allow a direct comparison with control patients. A total of 26 patients with unilateral right-sided cerebellar infarcts were tested on a covert visual attention task. Eight (31%) patients showed markedly slowed responses, especially in trials in which an…

AdultMaleCerebellumgenetic structuresCerebellar lesionsNeuroimagingCerebellumReaction TimemedicineHumansVisual attentionAttentionIn patientAgedAged 80 and overGeneral NeuroscienceCognitionArticlesMiddle Agedmedicine.anatomical_structureOculomotor controlCovertVisual PerceptionFemalePsychologyNeurosciencePhotic StimulationPsychomotor PerformanceCognitive psychologyThe Journal of Neuroscience
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Role of the cerebellum in time perception: A TMS study in normal subjects

2007

The aim of this study was to investigate the role of the cerebellum in a temporal-discrimination task without movement production in healthy subjects. Ten healthy subjects underwent a time-perception task with somatosensory stimuli. Two pairs of electrical stimuli: the first considered the reference pair (rp) with a standard interval of 400 ms and the second, the test pair (tp), with variable intervals ranging from 300 to 500 ms, were applied by surface electrodes on the right forearm. Subjects were instructed to compare time intervals of rp and tp and to estimate whether the tp interval was shorter than, equal to, or longer than that of rp. The task was performed in baseline and after 1 Hz…

AdultMaleCerebellummedicine.medical_specialtyTime FactorsAdolescentmedicine.medical_treatmentTime perceptionNeuropsychological TestsAudiologySomatosensory stimuliSomatosensory systembehavioral disciplines and activitiesFunctional LateralityDiscrimination PsychologicalCognitionCerebellumCerebellar hemispheremedicineHumansAnalysis of VarianceCognitionTime perceptionTranscranial Magnetic StimulationElectric StimulationTime intervalTranscranial magnetic stimulationInterval (music)medicine.anatomical_structurenervous systemNeurologyTMSFemaleSettore MED/26 - NeurologiaNeurology (clinical)Analysis of variancePsychologyNeurosciencepsychological phenomena and processesJournal of the Neurological Sciences
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Surgical Treatment in Symptomatic Chiari Malformation Type I: A Series of 25 Adult Patients Treated with Cerebellar Tonsil Shrinkage

2019

Background: The variety of symptoms and radiological findings in patients with Chiari malformation type I makes both the indication for surgery and the technical modality controversial. We report our 5-year experience, describing our technique and critically evaluating the clinical results. Methods: Between 2012 and 2016, 25 patients (15 female and 10 male; mean age 39.2 years) underwent posterior fossa decompression for Chiari malformation type I. Their clinical complaints included headache, nuchalgia, upper limb weakness or numbness, instability, dizziness and diplopia. Syringomyelia was present in 12 patients (48%). Suboccipital craniectomy was completed in all cases with C1 laminectomy …

AdultMaleDecompressive Craniectomymedicine.medical_specialtyCerebellar Vermi030218 nuclear medicine & medical imaging03 medical and health sciencesChiari malformation type I0302 clinical medicineCHIARI MALFORMATION TYPE IElectrocoagulationmedicineDuraplastyIn patientSurgical treatmentCerebellar tonsil shrinkageAdult patientsSettore MED/27 - Neurochirurgiabusiness.industryLaminectomyDecompression Surgicalmedicine.diseaseMagnetic Resonance ImagingSyringomyeliaArnold-Chiari MalformationSurgeryPosterior fossa decompressionTreatment Outcomemedicine.anatomical_structureRadiological weaponCerebellar tonsilFemalebusiness030217 neurology & neurosurgerySyringomyeliaHuman
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Cognitive and social cognitive functioning in spinocerebellar ataxia : a preliminary characterization

2006

INTRODUCTION : The spinocerebellar ataxias (SCAs), are rare neurodegenerative disorders caused by distinct genetic mutations. Clinically, the SCAs are characterised by progressive ataxia and a variety of other features, including cognitive dysfunction. The latter is consistent with a growing body of evidence supporting a cognitive as well as motor role for the cerebellum. Recent suggestions of cerebellar involvement in social cognition have not been extensively explored in these conditions. The availability of definitive molecular diagnosis allows genetically defined subgroups of SCA patients, with distinct patterns of cerebellar and extracerebellar involvement, to be tested comparatively u…

AdultMaleEmotionsNeuropsychological TestsSocial Environmentcognitive functioningDisability EvaluationCognitionSocial cognitionCerebellumTheory of mindmedicineHumansSpinocerebellar AtaxiasCognitive skillSocial BehaviorAgedIntelligence TestsVerbal BehaviorCognitive disorderNeuropsychologyRecognition PsychologyCognitionMachado-Joseph DiseaseMiddle Agedmedicine.diseaseNeurologyMental RecallSpinocerebellar ataxiaAutismFemaleAtaxiaNeurology (clinical)PsychologyNeurosciencePsychomotor Performance
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A preliminary characterisation of cognition and social cognition in spinocerebellar ataxia types 2, 1, and 7.

2010

Over the last decade, studies have implicated the cerebellum not only in motor functioning, but also in cognition and social cognition. Although some aspects of cognition have been explored in the five most common forms of Spinocerebellar Ataxia (SCA), social cognition in these patients has rarely been examined. The present study provides a preliminary characterisation of the severity of cognitive and social cognitive impairments in patients with SCA2, SCA1 and SCA7 using an identical battery to the one previously used in SCA3 and SCA6 patients for comparison. The cognitive profiles of SCA1 and SCA7 patients were comparable to that of SCA6 patients; SCA1 patients had relatively intact profi…

AdultMaleEmotionsTheory of MindemotionNeurosciences. Biological psychiatry. NeuropsychiatryGeneral MedicineMiddle AgedNeuropsychological TestsNeuropsychology and Physiological PsychologyCognitionNeurologySocial PerceptionHumansSpinocerebellar AtaxiasSpinocerebellar ataxia (SCA)FemaleOtherNeurology (clinical)EmpathyErratumSocial BehaviorPsychomotor PerformanceRC321-571Behavioural neurology
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Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.

2007

Peters, T.A./0000-0001-8443-5500; van Beersum, Sylvia E.C./0000-0002-4552-2908; Cremers, Frans/0000-0002-4954-5592; Roepman, Ronald/0000-0002-5178-8163 WOS: 000247619800019 PubMed: 17558407 Protein- protein interaction analyses have uncovered a ciliary and basal body protein network that, when disrupted, can result in nephronophthisis ( NPHP), Leber congenital amaurosis, Senior- Loken syndrome ( SLSN) or Joubert syndrome ( JBTS)(1-6). However, details of the molecular mechanisms underlying these disorders remain poorly understood. RPGRIP1- like protein ( RPGRIP1L) is a homolog of RPGRIP1 ( RPGR-interacting protein 1), a ciliary protein defective in Leber congenital amaurosis(7,8). We show t…

AdultMaleHealth aging / healthy living [IGMD 5]Eye DiseasesGenetics and epigenetic pathways of disease [NCMLS 6]TMEM67Molecular Sequence DataMembrane transport and intracellular motility [NCMLS 5]Biologymedicine.disease_causeJoubert syndromeCell LineGenomic disorders and inherited multi-system disorders [IGMD 3]NephronophthisisCerebellar DiseasesGeneticsmedicinePerception and Action [DCN 1]Basal bodyAnimalsHumansNeurosensory disorders [UMCN 3.3]CiliaAdaptor Proteins Signal TransducingRenal disorder [IGMD 9]GeneticsMutationCiliumCiliary transition zoneProteinsSyndromemedicine.diseasePedigreeRatsCytoskeletal ProteinsGenetic defects of metabolism [UMCN 5.1]RPGRIP1LFemaleKidney DiseasesFunctional Neurogenomics [DCN 2]Ciliary Motility Disorders
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Evidence of Wallerian degeneration in normal appearing white matter in the early stages of relapsing-remitting multiple sclerosis

2003

Objective: Wallerian degeneration in normal appearing white matter in early relapsing-remitting multiple sclerosis (RRMS), and its correlation with the number of relapses and disease duration. Background Recent pathological studies have demonstrated Wallerian degeneration in normal appearing white matter (NAWM) in multiple sclerosis (MS), in established RRMS, and in chronic MS. However, the presence of Wallerian degeneration early in the disease and its correlation with relapse and with disease duration has not been studied. Methods: We performed proton magnetic resonance spectroscopic imaging in 21 MS patients, and 4 healthy controls, age and gender matched, aged under 45 years, with a max…

AdultMaleIn vivo magnetic resonance spectroscopyWallerian degenerationPathologymedicine.medical_specialtyMagnetic Resonance SpectroscopyTime FactorsNeurologyAdolescentWhite matterCentral nervous system diseaseMultiple Sclerosis Relapsing-RemittingmedicineHumansAspartic AcidMultiple sclerosisBrainmedicine.diseaseMagnetic Resonance ImagingPonsRadiographymedicine.anatomical_structurenervous systemNeurologyCerebellar peduncleCreatinineFemaleNeurology (clinical)Wallerian DegenerationPsychologyJournal of Neurology
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A longitudinal investigation into cognition and disease progression in spinocerebellar ataxia types 1, 2, 3, 6, and 7

2016

Background The natural history of clinical symptoms in the spinocerebellar ataxias (SCA)s has been well characterised. However there is little longitudinal data comparing cognitive changes in the most common SCA subtypes over time. The present study provides a preliminary longitudinal characterisation of the clinical and cognitive profiles in patients with SCA1, SCA2, SCA3, SCA6 and SCA7, with the aim of elucidating the role of the cerebellum in cognition. Methods 13 patients with different SCAs all caused by CAG repeat expansion (SCA1, n = 2; SCA2, n = 2; SCA3, n = 2; SCA6, n = 4; and SCA7, n = 3) completed a comprehensive battery of cognitive and mood assessments at two time points, a mea…

AdultMaleMedicine(all)Settore M-PSI/02 - Psicobiologia E Psicologia FisiologicaResearchNeuroimagingMiddle AgedCognitionNeuropsychologyDisease ProgressionHumansSpinocerebellar AtaxiasFemaleAtaxiaGenetics(clinical)Pharmacology (medical)Longitudinal StudiesSpinocerebellar ataxiaAgedAtaxia; Cognition; Spinocerebellar ataxiaOrphanet Journal of Rare Diseases
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Factors associated with poor adherence to MMR vaccination in parents who follow vaccination schedule.

2014

Due to median vaccination coverage far from elimination level, Italy is still an European country with high number of measles cases per million of people. In this study we explored potential socioeconomic, medical and demographic factors which could influence the propensity of family members for measles vaccination schedule. A cross-sectional study was performed through a questionnaire administered to the parents of children who received the first dose of MMR vaccine in two different vaccination centers in the Palermo area from November 2012 to May 2013. Overall, the role played by internet (OR 19.8 P = 0.001) and the large number of children in a family (OR 7.3 P ≤ 0.001) were the factors …

AdultMaleParentsPediatricsmedicine.medical_specialtyMeasles-Mumps-Rubella VaccineVaccination scheduleCross-sectional studyImmunologyMMR vaccineSettore MED/42 - Igiene Generale E ApplicataMeaslesMedication AdherencechildrenSurveys and QuestionnairesmedicineImmunology and AllergyHumansmeaslebirth orderSocioeconomic statusPharmacologypersonal decisionbusiness.industryVaccinationInfant NewbornInfantmedicine.diseaseVaccinationBirth orderCross-Sectional Studiesvaccination refuseSocioeconomic FactorsItalyfamily memberChild PreschoolFemaleinternetbusinessMeasles-Mumps-Rubella VaccineDemographyResearch PaperMeasles
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Differentiation in medulloblastomas: correlation between the immunocytochemical demonstration of photoreceptor markers (S-antigen, rod-opsin) and the…

1989

Biopsy specimens of 66 medulloblastomas were investigated by means of S-antigen and rod-opsin immunocytochemistry. The patients were operated between 1969 and 1988 and the medical records were retrospectively evaluated to correlate the immunocytochemical features of the tumors to the course of the disease. S-antigen- and rod-opsin-immunoreactive tumor cells were found in 19 out of 66 cases. Since in the normal non-neoplastic state immunoreactive S-antigen and rod-opsin are restricted to retinal photoreceptors and a class of pinealocytes derived from photoreceptor cells, the occurrence of these proteins in certain tumor cells of medulloblastomas suggests a differentiation of these cells alon…

AdultMalePathologymedicine.medical_specialtyAdolescentgenetic structuresCellular differentiationImmunocytochemistryBiologyPhotoreceptor cellPathology and Forensic MedicinePinealocyteCellular and Molecular NeuroscienceAntigenBiopsymedicineHumansPhotoreceptor CellsAntigensCerebellar NeoplasmsChildEye ProteinsSurvival rateRetrospective StudiesMedulloblastomaArrestinmedicine.diagnostic_testInfantMiddle AgedPrognosismedicine.diseaseeye diseasesmedicine.anatomical_structureChild PreschoolFemalesense organsNeurology (clinical)Retinal PigmentsMedulloblastomaActa Neuropathologica
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