Search results for "Bell"

showing 10 items of 1130 documents

CATCHING FALLING OBJECTS: THE ROLE OF THE CEREBELLUM IN PROCESSING SENSORY-MOTOR ERRORS THAT MAY INFLUENCE UPDATING OF FEEDFORWARD COMMANDS. AN fMRI …

2011

Import JabRef | WosArea Neurosciences and Neurology; International audience; The human motor system continuously adapts to changes in the environment by comparing differences between the brain's predicted outcome of a certain behavior and the observed outcome. This discrepancy signal triggers a sensory-motor error and it is assumed that the cerebellum is a key structure in updating this error and associated feedforward commands. Using fMRI, the aim of the present study was to determine the main cerebellar structures that are involved in the processing of sensory-motor errors and in updating feedforward commands when simply catching a falling ball without displacement of the hand. Subjects o…

AdultMaleCORTEXREPRESENTATIONgenetic structuresTRANSFORMATIONSMovementSpeech recognitionREACHING MOVEMENTS[ SCCO.PSYC ] Cognitive science/PsychologyImage processingSensory systemBrain mappingMECHANISMS03 medical and health sciences0302 clinical medicineCerebellumMotor systemImage Processing Computer-AssistedHumansADAPTATION030304 developmental biologyARM MOVEMENTSNeuronsBrain Mapping0303 health sciencesCommunicationbusiness.industry[SCCO.NEUR]Cognitive science/NeuroscienceGeneral NeuroscienceFeed forwardGRIPCognitionHUMAN BRAINMagnetic Resonance ImagingFunctional imagingbody regionsnervous system[SCCO.PSYC]Cognitive science/Psychology[ SCCO.NEUR ] Cognitive science/NeuroscienceBall (bearing)INTERNAL-MODELSbusinessPsychologyhuman activitiesPsychomotor Performance030217 neurology & neurosurgerypsychological phenomena and processes
researchProduct

Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.

2013

Agenesis of the corpus callosum (ACC), cerebellar hypoplasia (CBLH), and polymicrogyria (PMG) are severe congenital brain malformations with largely undiscovered causes. We conducted a large-scale chromosomal copy number variation (CNV) discovery effort in 255 ACC, 220 CBLH, and 147 PMG patients, and 2,349 controls. Compared to controls, significantly more ACC, but unexpectedly not CBLH or PMG patients, had rare genic CNVs over one megabase (p = 1.48×10−3; odds ratio [OR] = 3.19; 95% confidence interval [CI] = 1.89–5.39). Rare genic CNVs were those that impacted at least one gene in less than 1% of the combined population of patients and controls. Compared to controls, significantly more AC…

AdultMaleCancer ResearchMicrocephalycongenital hereditary and neonatal diseases and abnormalitiesAdolescentDNA Copy Number Variationslcsh:QH426-470Developmental DisabilitiesPopulationGenome-wide association studyBiologyNervous System MalformationsCorpus callosumPolymorphism Single Nucleotide03 medical and health sciences0302 clinical medicineCerebellummental disordersGeneticsPolymicrogyriamedicineHumansCopy-number variationChildAgenesis of the corpus callosumeducationMolecular BiologyGenetics (clinical)Ecology Evolution Behavior and SystematicsExome sequencing030304 developmental biologyGenetics0303 health scienceseducation.field_of_studyGenome HumanInfant NewbornInfantMiddle Agedmedicine.disease3. Good healthMalformations of Cortical Developmentlcsh:GeneticsChild PreschoolFemaleAgenesis of Corpus Callosum030217 neurology & neurosurgeryResearch ArticleGenome-Wide Association StudyPLoS Genetics
researchProduct

Structure, chromosomal localization, and brain expression of human Cx36 gene

1999

Rat connexin-36 (Cx36) is the first gap junction protein shown to be expressed predominantly in neuronal cells of the mammalian central nervous system. As a prerequisite for studies devoted to the investigation of the possible role of this connexin in human neurological diseases, we report the cloning and sequencing of the human Cx36 gene, its chromosomal localization, and its pattern of expression in the human brain analyzed by radioactive in situ hybridization. The determination of the human gene sequence revealed that the coding sequence of Cx36 is highly conserved (98% identity at the protein level with the mouse and rat Cx36 and 80% with the ortholog perch and skate Cx35), and that the…

AdultMaleCandidate geneAdolescentgenetic structuresMolecular Sequence DataIn situ hybridizationBiologyHippocampal formationPolymerase Chain ReactionConnexinsMiceCellular and Molecular NeurosciencemedicineAnimalsHumansCoding regionAmino Acid SequenceSkates FishCloning MolecularEye ProteinsPeptide Chain Initiation TranslationalGeneIn Situ Hybridization FluorescenceChromosomes Human Pair 15Genomic LibrarySequence Homology Amino Acidmedicine.diagnostic_testBrainChromosome MappingHuman brainMiddle AgedMolecular biologyIntronsRatsmedicine.anatomical_structureSpinal CordOrgan SpecificityPerchesCerebellar cortexFemalesense organsSequence AlignmentFluorescence in situ hybridizationJournal of Neuroscience Research
researchProduct

Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia

2005

Background: Mutations of oligophrenin 1, one of the first genes identified in nonspecific X-linked mental retardation (MRX), have been described in patients with moderate to severe cognitive impairment and predominant cerebellar hypoplasia, in the vermis. Objective: To further delineate the phenotypic and mutational spectrum of the syndrome, by screening oligophrenin 1 in two cohorts of male patients with mental retardation (MR) with or without known posterior fossa anomalies. Methods: Clinical examination, cognitive testing, MRI studies, and mutational analysis (denaturing gradient gel electrophoresis and direct sequencing) on blood lymphocytes were performed in 213 unrelated affected indi…

AdultMaleCerebellumAdolescentGenotypeDNA Mutational AnalysisNonsense mutationNervous System Malformationsmedicine.disease_causeCohort StudiesExonCerebellar DiseasesCerebellummedicineHumansGenetic TestingChildCerebellar hypoplasiaGeneticsMutationSplice site mutationGTPase-Activating ProteinsNuclear Proteinsmedicine.diseaseMagnetic Resonance ImagingHypoplasiaPedigreeDevelopmental disorderAlternative SplicingCytoskeletal ProteinsPhenotypemedicine.anatomical_structureFacial AsymmetryCodon NonsenseChild PreschoolMutationMental Retardation X-LinkedRNA Splice SitesNeurology (clinical)PsychologyGene DeletionNeurology
researchProduct

Cognitive and Motor Loops of the Human Cerebro-cerebellar System

2010

Abstract We applied fMRI and diffusion-weighted MRI to study the segregation of cognitive and motor functions in the human cerebro-cerebellar system. Our fMRI results show that a load increase in a nonverbal auditory working memory task is associated with enhanced brain activity in the parietal, dorsal premotor, and lateral prefrontal cortices and in lobules VII–VIII of the posterior cerebellum, whereas a sensory-motor control task activated the motor/somatosensory, medial prefrontal, and posterior cingulate cortices and lobules V/VI of the anterior cerebellum. The load-dependent activity in the crus I/II had a specific relationship with cognitive performance: This activity correlated negat…

AdultMaleCerebellumBrain activity and meditationMovementCognitive NeuroscienceStatistics as TopicSomatosensory systemFunctional Laterality050105 experimental psychologyYoung Adult03 medical and health sciencesCognition0302 clinical medicineCerebellumNeural PathwaysImage Processing Computer-AssistedReaction TimemedicineHumansta3180501 psychology and cognitive sciencesEffects of sleep deprivation on cognitive performanceta116ta515ta217Cerebral Cortexta113Brain Mappingta114Working memory05 social sciencesCognitionMagnetic Resonance ImagingOxygenDiffusion Magnetic Resonance Imagingmedicine.anatomical_structureAcoustic Stimulationnervous systemFemalePsychologyNeuroscience030217 neurology & neurosurgeryCognitive loadTractographyJournal of Cognitive Neuroscience
researchProduct

Repetitive TMS of cerebellum interferes with millisecond time processing

2007

Time processing is important in several cognitive and motor functions, but it is still unclear how the human brain perceives time intervals of different durations. Processing of time in millisecond and second intervals may depend on different neural networks and there is now considerable evidence to suggest that these intervals are possibly measured by independent brain mechanisms. Using repetitive transcranial magnetic stimulation (rTMS), we determined that the cerebellum is essential in explicit temporal processing of millisecond time intervals. In the first experiment, subjects' performance in a time reproduction task of short (400-600 ms) and long (1,600-2,400 ms) intervals, were evalua…

AdultMaleCerebellumData InterpretationTime perception; Timing; Transcranial magnetic stimulation; rTMS; Cerebellummedicine.medical_treatmentPrefrontal CortexStimulationTime perception Timing Transcranial magnetic stimulation rTMS CerebellumMagnetic Resonance Imaging; Humans; Adult; Cerebellum; Time Perception; Data Interpretation Statistical; Prefrontal Cortex; Transcranial Magnetic Stimulation; Male; Functional Laterality; FemaleFunctional LateralityNOCerebellum; rTMS; Time perception; Timing; Transcranial magnetic stimulation;CerebellumrTMSmedicineHumansTimingPrefrontal cortexMillisecondNeuroscience (all)Settore M-PSI/02 - Psicobiologia E Psicologia Fisiologicamusculoskeletal neural and ocular physiologyGeneral NeuroscienceMemoriaHuman brainTime perceptionStatisticalMagnetic Resonance ImagingTranscranial Magnetic StimulationTranscranial magnetic stimulationmedicine.anatomical_structurenervous systemData Interpretation StatisticalTime PerceptionFemaleSettore MED/26 - NeurologiaPsychologyNeuroscienceHuman
researchProduct

Hemispheric cerebellar rTMS to treat drug-resistant epilepsy: case reports.

2005

Electrical stimulation of the cerebellar cortex by implanted electrodes has been shown to ameliorate refractory epilepsy. We investigated the potential therapeutic role of high-frequency cerebellar rTMS in patients affected by refractory epilepsy due to single or multiple foci. Six patients, three with single and three with multiple epileptic foci, underwent 20 rTMS sessions. Each session was given daily, excluding weekends, and consisted of two trains of 50 stimuli (5 Hz frequency and 90% motor threshold intensity), separated by 50s interval. rTMS was delivered through a focal coil (2 cm below and lateral to the inion) bilaterally in patients with multiple foci (two trains for hemisphere: …

AdultMaleCerebellumFocus (geometry)cerebellummedicine.medical_treatmentDrug Resistancebehavioral disciplines and activitiesCentral nervous system diseaseEpilepsyCerebellar Cortexdrug-resistant epilepsymental disordersrTMSmedicineHumansEpilepsymusculoskeletal neural and ocular physiologyGeneral NeuroscienceDRECortical dysplasiamedicine.diseaseDrug Resistant EpilepsyTranscranial Magnetic StimulationTranscranial magnetic stimulationmedicine.anatomical_structurenervous systemAnesthesiaCerebellar cortexSettore MED/26 - NeurologiaFemalePsychologypsychological phenomena and processesNeuroscience letters
researchProduct

Changes in cerebellar activation pattern during two successive sequences of saccades

2002

The changes in the cerebellar activation pattern of two successive fMRI scanning runs were determined for visually guided to‐and‐fro saccades in 12 healthy volunteers familiar with the study paradigm. Group and single subject‐analyses revealed a constant activation of the paramedian cerebellar vermis (uvula, tonsils, tuber, folium/declive), which reflects constant ocular motor activity in both runs. A significant decrease in activation of the cerebellar hemispheres found in the second run is best explained by either a decrease in attention or the effects of motor optimization and learning. The significant, systematic changes of the cerebellar activation pattern in two successive runs were n…

AdultMaleCerebellumOcular motorAction PotentialsStimulationFunctional LateralityActivation patternCerebellar CortexReaction TimeSaccadesmedicineHumansRadiology Nuclear Medicine and imagingFastigial nucleusBrain MappingRadiological and Ultrasound TechnologyVisually guidedEye movementOriginal ArticlesMiddle AgedMagnetic Resonance Imagingmedicine.anatomical_structureNeurologyCerebrovascular CirculationCerebellar vermisFemaleNeurology (clinical)AnatomyPsychologyNeurosciencePhotic StimulationPsychomotor PerformanceHuman Brain Mapping
researchProduct

Alzheimer's disease: amyloid plaques in the cerebellum

1989

Two specific silver-staining methods demonstrating either extracellular amyloid and/or precursors of amyloid or intraneuronal neurofibrillary changes were used to examine cerebellar pathology in cases of presenile and senile dementia of the Alzheimer type, cases of Down's syndrome, and non-demented controls. The sensitivity of the techniques permitted visualization of large numbers of amyloid deposits in the cerebellar cortex of demented individuals. Similarly large numbers of amyloid deposits were not found in the cerebella of non-demented individuals. Neurofibrillary changes were absent. The majority of amyloid plaques occurred in the molecular layer. Quite a number of these displayed lar…

AdultMaleCerebellumPathologymedicine.medical_specialtyAdolescentAmyloidGranular layerBiologyWhite matterAlzheimer DiseaseCerebellar DiseasesCerebellummental disordersmedicineHumansSenile plaquesAgedAged 80 and overInclusion BodiesAmyloidosisAmyloidosisMiddle Agedmedicine.diseasemedicine.anatomical_structureNeurologyCerebellar cortexFemaleNeurology (clinical)Down SyndromeAlzheimer's diseaseNeuroscienceJournal of the Neurological Sciences
researchProduct

Are signs of ocular tilt reaction in patients with cerebellar lesions mediated by the dentate nucleus?

2008

A sensitive clinical sign of a vestibular tone imbalance in the roll plane is the ocular tilt reaction (OTR), a combination of skew deviation, ocular torsion and head and perceptual tilts such as tilts of the subjective visual vertical (SVV). Of these OTR components tilts of SVV are the most frequent. While these signs are regularly seen in patients with unilateral brainstem lesions, only a few case studies are available on their occurrence in patients with cerebellar lesions. Thus, the question arises whether cerebellar structures may be involved in contra- and/or ipsiversive tilts of the perceived vertical and other signs of OTR. We used lesion-mapping techniques in a total of 31 patients…

AdultMaleCerebellumPathologymedicine.medical_specialtyAdolescentFundus OculiLesionNeural PathwaysMiddle cerebellar pedunclemedicineHumansSkew deviationBiventer lobuleeducationAgedAged 80 and overVestibular systemeducation.field_of_studyChi-Square DistributionCerebral InfarctionAnatomyMiddle AgedVestibular Function TestsDentate nucleusmedicine.anatomical_structureCerebellar NucleiSpace PerceptionFemaleNeurology (clinical)Brainstemmedicine.symptomPsychologyAktuelle Neurologie
researchProduct