Search results for "Sensor"

showing 10 items of 4594 documents

Neuroimmunomodulatory Alterations in Non-Lesional Peritoneum Close to Peritoneal Endometriosis

2012

<b><i>Objectives:</i></b> An imbalance in the ratio of sensory to sympathetic nerve fibre (NF) density in peritoneal endometriotic lesions (pEL) has recently been demonstrated and leads to the assumption that this preponderance of the sensory pro-inflammatory milieu is a major cause of pain in endometriosis. Therefore, the density of sensory and sympathetic NFs was determined in distal unaffected peritoneum of endometriosis patients to be able to detect possible alterations in unaffected peritoneum. <b><i>Methods:</i></b> In serial pEL sections (n = 40), lesional and matching unaffected peritoneum as well as healthy peritoneum (HP) from patien…

PathologyEndometriosisSympathetic nerveSubstance PSensory nerve fibreSubstance PPeritoneal Diseaseschemistry.chemical_compoundNerve growth factorPelvic painEndocrinologyhemic and lymphatic diseasesEndometriosiintegumentary systemvirus diseasesMiddle AgedInterleukin-1βImmunohistochemistrymedicine.anatomical_structureNeurologyImmunohistochemistryFemalemedicine.symptomPeritoneal diseasesPeritoneumHumanAdultmedicine.medical_specialtyAdolescentImmunologyEndometriosisEndocrine and Autonomic SystemYoung AdultPeritoneumAdrenergic FiberInternal medicinemedicineHumansPathogenesis endometriosiEndocrine and Autonomic Systemsbusiness.industryPelvic painmedicine.diseaseNerve growth factorEndocrinologychemistrySympathetic nerve fibrePeritoneal DiseasebusinessAdrenergic Fibers
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C21orf2 is mutated in recessive early-onset retinal dystrophy with macular staphyloma and encodes a protein that localises to the photoreceptor prima…

2015

Background/aim We have noted a phenotype of early-onset retinal dystrophy with macular staphyloma but without high myopia. The aim of this study is to report the underlying genetic mutations and the subcellular localisation of the gene product in the retina. Methods Retrospective case series (2012–2015); immunohistochemical analyses of mammalian retina for in situ protein localisation. Results All three probands were first noted to have decreased vision at 3–6 years old which worsened over time. At ages 39, 37 and 12 years old, all had similar retinal findings: dystrophic changes (retinal pigment epithelium mottling, vessel narrowing), macular staphyloma (despite only mild myopia or high hy…

Pathologygenetic structuresSus scrofaPolymerase Chain ReactionPhotoreceptor cellchemistry.chemical_compoundConsanguinityMiceChildFrameshift MutationGeneticsmedicine.diagnostic_testMagnetic Resonance ImagingSensory SystemsTissue DonorsPedigreemedicine.anatomical_structureFemaleRetinal DystrophiesTomography Optical CoherenceDilatation PathologicAdultmedicine.medical_specialtyBlotting WesternMolecular Sequence DataMutation MissenseGenes RecessiveBiologyRetinaCellular and Molecular NeuroscienceRetinal DystrophiesmedicineElectroretinographyAnimalsHumansAmino Acid SequencePhotoreceptor Connecting CiliumRetrospective StudiesRetinaRetinal pigment epitheliumDystrophyProteinsRetinalmedicine.diseaseeye diseasesOphthalmologyCiliopathyCytoskeletal Proteinschemistrysense organsElectroretinographyThe British journal of ophthalmology
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Intermediate-filament expression in ocular tissue.

2002

Intermediate-filament proteins (IFPs) occur in the intracellular cytoskeleton of eukaryotic cells, and their expression in diverse tissues is related both to embryology as well as to differentiation. Although the available information concerning their functional properties in vivo is still incomplete, antibodies against individual IFPs are commonly used in immunohistochemical procedures as markers for differentiation, and these antibodies are of outstanding value in the routine histopathological evaluation of tumor specimens. This review presents a compilation of the currently available data concerning IFP expression in normal and diseased ocular tissues. Representatives of every known clas…

Pathologymedicine.medical_specialtyCell typebiologyEye DiseasesMesenchymal stem cellVimentinEyeSensory SystemsPathogenesisOphthalmologyCytokeratinmedicine.anatomical_structureIntermediate Filament ProteinsReference Valuesmedicinebiology.proteinImmunohistochemistryAnimalsHumansTissue DistributionIntermediate filamentCorneal epitheliumProgress in retinal and eye research
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3.7. Are signs of ocular tilt reaction in cerebellar lesions mediated by the dentate nucleus?

2007

Pathologymedicine.medical_specialtyDentate nucleusNeurologybusiness.industryPhysiology (medical)MedicineNeurology (clinical)Ocular tilt reactionbusinessNeuroscienceCerebellar lesionsSensory SystemsClinical Neurophysiology
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Intraepidermal formation of Merkel cells in xenografts of human fetal skin.

1990

An experimental transplantation model using human fetal skin was applied to approach the question of the embryologic origin of human Merkel cells. Palmar and plantar skin from five fetuses, between 8 and 11 weeks of estimated gestational age (EGA), was xenografted to subcutaneous beds of nude mice. After 4 or 8 weeks of growth, biopsies were taken from these xenografts and examined for the presence of Merkel cells, using immunocytochemistry with antibodies specific for simple epithelial-type cytokeratins and neuron-specific enolase (NSE) as well as using electron microscopy. Skin from the same fetuses at the time of transplantation was screened in the same way. In all fetuses, no (or very s…

Pathologymedicine.medical_specialtyImmunocytochemistryTransplantation HeterologousFluorescent Antibody TechniqueMice NudeDermatologyBiologyBiochemistryMiceDermismedicineAnimalsHumansMolecular BiologySkinFetusintegumentary systemCell BiologySkin TransplantationImmunohistochemistryNeurosecretory SystemsTransplantationMicroscopy Electronmedicine.anatomical_structureImmunohistochemistryEpidermisEpidermisMerkel cellSensory nerveThe Journal of investigative dermatology
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Isolated dysarthria due to extracerebellar lacunar stroke: a central monoparesis of the tongue

1999

OBJECTIVES—The pathophysiology of dysarthria can preferentially be studied in patients with the rare lacunar stroke syndrome of "isolated dysarthria". METHODS— A single study was carried out on seven consecutive patients with sudden onset of isolated dysarthria due to single ischaemic lesion. The localisation of the lesion was identified using MRI. The corticolingual, cortico-orofacial, and corticospinal tract functions were investigated using transcranial magnetic stimulation. Corticopontocerebellar tract function was assessed using 99mTc hexamethylpropylene amine oxime-single photon emission computerised tomography (HMPAO-SPECT) in six patients. Sensory functions were evaluated clinically…

Pathologymedicine.medical_specialtyLacunar strokeInternal capsulebusiness.industryCerebral infarctionmedicine.diseasenervous system diseasesLesionPsychiatry and Mental healthDysarthriaSomatosensory evoked potentialCorticospinal tractmedicineSurgeryNeurology (clinical)medicine.symptombusinessStrokeJournal of Neurology, Neurosurgery & Psychiatry
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Assessment of the fundamental flexural guided wave in cortical bone by an ultrasonic axial-transmission array transducer

2013

Abstract The fundamental flexural guided wave (FFGW), as modeled, for example, by the A0 Lamb mode, is a clinically useful indicator of cortical bone thickness. In the work described in this article, we tested so-called multiridge-based analysis, based on the crazy climber algorithm and short-time Fourier transform, for assessment of the FFGW component recorded by a clinical array transducer featuring a limited number of elements. Methods included numerical finite-element simulations and experiments in bone phantoms and human radius specimens ( n  = 41). The proposed approach enabled extraction of the FFGW component and determination of its group velocity. This group velocity was in good ag…

Pathologymedicine.medical_specialtyMaterials scienceLightAcoustics and UltrasonicsAcousticsTransducersBiophysicsModels BiologicalSensitivity and SpecificityHigh-Energy Shock Wavessymbols.namesakeFlexural strengthmedicineHumansScattering RadiationComputer SimulationRadiology Nuclear Medicine and imagingSensitivity (control systems)UltrasonographyGuided wave testingRadiological and Ultrasound Technologyta114Reproducibility of ResultsRadiusRadiusFourier transformmedicine.anatomical_structuresymbolsGroup velocityCortical boneUltrasonic sensorAlgorithmsUltrasound in Medicine and Biology
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2013

Neurovascular coupling (NVC) in the adult central nervous system (CNS) is a mechanism that provides regions of the brain with more oxygen and glucose upon increased levels of neural activation. Hemodynamic changes that go along with neural activation evoke a blood oxygen level-dependent (BOLD) signal in functional magnetic resonance imaging (fMRI) that can be used to study brain activity non-invasively. A correct correlation of the BOLD signal to neural activity is pivotal to understand this signal in neuronal development, health and disease. However, the function of NVC during development is largely unknown. The rodent whisker-to-barrel cortex is an experimentally well established model to…

Pathologymedicine.medical_specialtyMultidisciplinarymedicine.diagnostic_testBrain activity and meditationCentral nervous systemStimulationSensory systemBarrel cortexBiologymedicine.anatomical_structureCerebral blood flowCortex (anatomy)medicineFunctional magnetic resonance imagingNeurosciencePLOS ONE
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Neuropathologic and morphometric studies in hereditary motor and sensory neuropathy type II with neurofilament accumulation.

1986

Histological, electron microscopic and morphometric data on sural nerve, muscle, and skin biopsies of three patients affected by autosomal dominant hereditary motor and sensory neuropathy type II with neurofilament accumulation, whose neurological, cardiological and electrophysiological data have been provided in a previous paper disclosed focally enlarged myelinated axons, due to aggregation of neurofilaments in sural nerves of all 3 biopsied patients, as well as densely packed clusters of filaments in occasional non-myelinated axons without axonal enlargement, in several fibroblasts and endothelial cells in muscle and particularly in skin. This accumulation of filaments was less pronounce…

Pathologymedicine.medical_specialtyNeurofilamentNeurologyIntermediate FilamentsSural nerveDermatologyBiologylaw.invention03 medical and health sciences0302 clinical medicineSural NervelawCharcot-Marie-Tooth DiseasemedicineHumansHereditary Sensory and Autonomic NeuropathiesIntermediate filamentCytoskeletonMyelin Sheath030304 developmental biologySkinMotor Neurons0303 health sciencesGeneral NeuroscienceMusclesGeneral MedicineAnatomymedicine.diseaseAxonsPsychiatry and Mental healthElectrophysiologyMicroscopy ElectronMuscular Atrophynervous systemUltrastructureNeurology (clinical)Electron microscopeHereditary motor and sensory neuropathy030217 neurology & neurosurgeryItalian journal of neurological sciences
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S100α and S100β proteins in human cutaneous sensory corpuscles: Effects of nerve and spinal cord injury

1998

S100 protein in the vertebrate peripheral nervous system consists of homo- or heterodimers of S100α and S100β proteins, the first predominating in neurons and the second in glial cells. Recently, however, occurrence of S100β protein in neurons has been reported. The expression of S100 protein by Schwann cells, as well as their derivatives in sensory corpuscles, depends on the sensory axon (i.e., the Schwann cell–axon contact). The present study analyzed the distribution of S100α and S100β proteins in human cutaneous sensory corpuscles and the effects of peripheral or central sensory axon severance in the expression of these proteins. Simple or double immunohistochemistry was carried out usi…

Pathologymedicine.medical_specialtySensory systemBiologyConfocal scanning microscopyNerve injurymedicine.diseaseAgricultural and Biological Sciences (miscellaneous)S100 proteinmedicine.anatomical_structurePeripheral nervous systemmedicineAnatomyAxonmedicine.symptomSpinal cord injuryImmunostainingThe Anatomical Record
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