Search results for "brain stem"

showing 10 items of 86 documents

Somatosensory evoked potentials in Arnold-Chiari malformation.

2002

Abstract Nearly all patients with repaired myelomeningoceles have an Arnold–Chiari (AC) malformation and about 20% of these patients develop clinical signs of brainstem dysfunction. The management of symptomatic AC malformation is still controversial and techniques are needed to provide an objective assessment of brainstem function. We recorded somatosensory evoked potentials (SEPs) in 52 patients aged between 8 months and 20 years (median 7.3 years) with AC malformation, to determine whether the SEPs discriminate patients with symptomatic AC malformation from those without symptoms. The subcortical far-field components P13, P14 and N18, which are generated within the brainstem, were record…

AdultYounger ageMeningomyeloceleAdolescentNeural ConductionSigns and symptomsLate onsetSomatosensory systemSensitivity and SpecificityDevelopmental NeurosciencePredictive Value of TestsEvoked Potentials SomatosensoryMedicineHumansIn patientChildbusiness.industryInfantReproducibility of ResultsGeneral MedicineArnold-Chiari MalformationSpinal CordSomatosensory evoked potentialAnesthesiaChild PreschoolPediatrics Perinatology and Child HealthNeurology (clinical)BrainstemArnold chiaribusinessBrain StemBraindevelopment
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Early auditory evoked potentials: developmental aspects and validity in neuropaediatric and audiologic disorders.

1984

Auditory evoked potentials and in this context especially five waves in the first 10 ms (early auditory evoked potentials = EAEP) are a diagnostic aid in topodiagnosis of posterior fossa diseases. This is due to waves I to V which arise along the acoustic nerve and in brain stem structures such as medulla, pons and mid-brain. Besides an indication about the site of a lesion in the posterior fossa, wave V allows an objective threshold determination. The present results were gained in normal children aged 1-3 years and in children with neuropaediatric and audiologic disorders.

Adultmedicine.medical_specialtyAgingAdolescentPosterior fossaNeural ConductionContext (language use)AudiologyDiagnostic aidLesionChild DevelopmentMedicineHumansChildHearing DisordersMedullaNeural Conductionbusiness.industryBrain NeoplasmsInfant NewbornInfantDiffuse Cerebral Sclerosis of SchilderLeukodystrophy MetachromaticPonsChild PreschoolPediatrics Perinatology and Child HealthNormal childrenEvoked Potentials Auditorymedicine.symptomNervous System DiseasesbusinessBrain StemEuropean journal of pediatrics
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Bickerstaff brainstem encephalitis. A case report

1992

A 33-year-old woman three weeks after a febrile illness presented with a syndrome of ophthalmoplegia, ataxia and areflexia (SOAA) that characterizes clinically both Bickerstaff and Miller Fisher syndromes. The normality of the electrophysiological tests performed, the CSF findings and the magnetic resonance images proved that the syndrome stemmed from brainstem pathology.

Adultmedicine.medical_specialtyPathologyAtaxiaNeurologyBickerstaff brainstem encephalitisDermatologyotorhinolaryngologic diseasesmedicineHumansNeuroradiologyOphthalmoplegiaReflex Abnormalmedicine.diagnostic_testbusiness.industryGeneral NeuroscienceFebrile illnessMagnetic resonance imagingSyndromeGeneral Medicinemedicine.diseaseMagnetic Resonance ImagingPsychiatry and Mental healthEncephalitisAtaxiaFemaleNeurology (clinical)NeurosurgeryBrainstemmedicine.symptombusinessBrain StemThe Italian Journal of Neurological Sciences
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Brainstem reflex circuits revisited

2004

Our current understanding of brainstem reflex physiology comes chiefly from the classic anatomical-functional correlation studies that traced the central circuits underlying brainstem reflexes and establishing reflex abnormalities as markers for specific areas of lesion. These studies nevertheless had the disadvantage of deriving from post-mortem findings in only a few patients. We developed a voxel-based model of the human brainstem designed to import and normalize MRIs, select groups of patients with or without a given dysfunction, compare their MRIs statistically, and construct three-plane maps showing the statistical probability of lesion. Using this method, we studied 180 patients with…

Adult; Aged; 80 and over; Blinking; Brain Stem Infarctions; diagnosis/physiopathology; Brain Stem; physiopathology; Electromyography; Female; Humans; Jaw; Magnetic Resonance Imaging; Male; Masseter Muscle; Middle Aged; Reflex; AbnormalAdultMalemedicine.medical_specialtyBrain Stem InfarctionsClinical neurophysiologyReflex80 and overmedicineHumansCorneal reflexAgedAged 80 and overBlinkingReflex AbnormalElectromyographyMasseter MuscleDental occlusionAnatomyMiddle AgedMagnetic Resonance Imagingdiagnosis/physiopathologyPonsJawCiliospinal reflexAbnormalReflexFemaleNeurology (clinical)BrainstemphysiopathologyPsychologyJaw jerk reflexBrain StemBrain
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The brainstem efferent acoustic chiasm in pigmented and albino rats

2015

Abstract The present study examined whether structural peculiarities in the brain-efferent pathway to the organ of Corti may underlie functional differences in hearing between pigmented and albino individuals of the same mammalian species. Pigmented Brown-Norway rats and albino Wistar rats received unilateral injections of an aqueous solution of the retrograde neuronal tracer Fluorogold (FG) into the scala tympani of the cochlea to identify olivocochlear neurons (OCN) in the brainstem superior olivary complex. After five days, brains were perfusion-fixed and brainstem sections were cut and analyzed with respect to retrogradely labeled neurons. Intrinsic neurons of the lateral system were lo…

Auditory PathwaysStilbamidinesAlbinismEfferentOlivary NucleusBiologyInjections03 medical and health sciences0302 clinical medicineRats Inbred BNotorhinolaryngologic diseasesmedicineAnimalsTrapezoid bodyRats Wistar030223 otorhinolaryngologyCochlear NerveOrgan of CortiNeuronal Tract-TracersCochleaAnatomySensory SystemsCochleaNeuroanatomical Tract-Tracing TechniquesNeuronal tracingDisease Models Animalmedicine.anatomical_structureOrgan of CortiSuperior olivary complexsense organsBrainstemNucleus030217 neurology & neurosurgeryBrain StemHearing Research
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The Oculo-auricular Phenomenon in Brain-Stem Disease

1993

The oculo-auricular phenomenon (OAP), as described by Wilson in 1908 [26], consists of bilateral coactivation of external ear muscles during lateral gaze. Two ear muscles are innervated by motoneurons of the medial part of the facial nucleus [9, 25]: the transverse auricular muscle (TAM) (Fig. 1), which adducts and curls the helix of the auricle, and the posterior auricular muscle (Fig. 2), which moves the whole auricle backwards [3, 16, 22].

AuricleFacial NucleusFacial motor nucleusbusiness.industryAnatomyMedial longitudinal fasciculusCoactivationstomatognathic diseasesEar musclemedicine.anatomical_structurePosterior auricular muscleotorhinolaryngologic diseasesmedicinesense organsbusinessBrain stem disease
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A low repeat length in oligodendrocyte chromatin

1985

Abstract: The behavior of oligodendrocyte chromatin after micrococcal nuclease digestion of nuclei was assayed in brains of rats of four different ages. During oligodendrocyte differentiation, a decreasing sensitivity of the chromatin to enzymatic attack was observed. On the other hand, the nucleosomal repeat length showed a slight tendency to increase during development. It is worth noting that even the highest values reported here for “oligodendrocyte’ chromatin repeat lengths are significantly lower than 200 base pairs, the value previously reported by others for “non‐astrocytic glia.” Copyright © 1985, Wiley Blackwell. All rights reserved

Base pairCellular differentiationFluorescent Antibody TechniqueOligodendrocyte differentiationBiochemistryCellular and Molecular NeuroscienceSettore BIO/10 - BiochimicamedicineAnimalsMicrococcal NucleaseNucleosomeRepetitive Sequences Nucleic AcidElectrophoresis Agar GelGeneticsNucleosomal Repeat LengthbiologyAge FactorsOligodendrocyte differentiationDNAMolecular biologyChromatinOligodendrocyteNucleosomesRatsChromatinOligodendrogliamedicine.anatomical_structureLiverbiology.proteinSettore MED/26 - NeurologiaNucleosomal repeat lengthNeurogliaBrain StemMicrococcal nuclease
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Determination of Brain Death/Death by Neurologic Criteria

2020

Importance: There are inconsistencies in concept, criteria, practice, and documentation of brain death/death by neurologic criteria (BD/DNC) both internationally and within countries. Objective: To formulate a consensus statement of recommendations on determination of BD/DNC based on review of the literature and expert opinion of a large multidisciplinary, international panel. Process: Relevant international professional societies were recruited to develop recommendations regarding determination of BD/DNC. Literature searches of the Cochrane, Embase, and MEDLINE databases included January 1, 1992, through April 2020 identified pertinent articles for review. Because of the lack of high-quali…

Brain Deathmedicine.medical_specialtyBiomedical ResearchNeurologyBrain Death Death by Neurologic CriteriaApneaPhysical examination01 natural scienceslaw.inventionDiagnosis Differential03 medical and health sciences0302 clinical medicinePharyngeal reflexRandomized controlled triallawmedicineHumansNervous System Physiological Phenomena030212 general & internal medicineComa0101 mathematicsIntensive care medicineComamedicine.diagnostic_testbusiness.industry010102 general mathematicsApneaGeneral MedicineObservational studyNeurosurgerymedicine.symptombusinessBrain StemJAMA
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Natural Course, Clinical Profile, and Treatment Strategies for Cerebral Cavernous Malformations

2022

A large body of evidence has suggested that the natural biology for symptomatic cerebral cavernous malformations (CCMs) is dynamic. These lesions exhibit a temporal clustering epiphenomenon and usually manifest with multispectral clinical patterns, the most relevant being hemorrhagic and seizurogenic events. Most patients with cerebral cavernous malformations are asymptomatic, and the lesions are detected as incidentalomas. However, association with the CCM3 gene, Zabramski type I and II lesions, and brainstem location have the propensity to increase the bleeding events. The rebleeding risk is 20%/year per lesion, which supports the need for surgical strategies for brainstem cavernous malfo…

CavernomaHemangioma Cavernous Central Nervous SystemSeizuresHumansAnticonvulsantsSurgeryNeurology (clinical)PresentationCourseRadiosurgeryBrain StemManagementWorld Neurosurgery
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A critical role for the cholesterol-associated proteolipids PLP and M6B in myelination of the central nervous system.

2012

The formation of central nervous system myelin by oligodendrocytes requires sterol synthesis and is associated with a significant enrichment of cholesterol in the myelin membrane. However, it is unknown how oligodendrocytes concentrate cholesterol above the level found in nonmyelin membranes. Here, we demonstrate a critical role for proteolipids in cholesterol accumulation. Mice lacking the most abundant myelin protein, proteolipid protein (PLP), are fully myelinated, but PLP-deficient myelin exhibits a reduced cholesterol content. We therefore hypothesized that "high cholesterol" is not essential in the myelin sheath itself but is required for an earlier step of myelin biogenesis that is f…

Central Nervous SystemProteolipid protein 1Nerve Tissue ProteinsBiologyCell Line03 medical and health sciencesCellular and Molecular Neurosciencechemistry.chemical_compoundMyelinMice0302 clinical medicineimmune system diseasesmedicineEvoked Potentials Auditory Brain StemAnimalsMyelin Proteolipid ProteinMyelin Sheath030304 developmental biology0303 health sciencesMembrane GlycoproteinsCholesterolProteolipidsLeukodystrophyPelizaeus–Merzbacher diseasemedicine.diseaseOligodendrocytenervous system diseasesMyelin proteolipid proteinmedicine.anatomical_structureCholesterolnervous systemNeurologychemistryBiochemistryEvoked Potentials Visuallipids (amino acids peptides and proteins)Vomeronasal Organ030217 neurology & neurosurgeryGlia
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