Search results for "Ultra"

showing 10 items of 4451 documents

Sonoporation, a redefined ultrasound modality as therapeutic aid: a review.

2011

Traditionally a diagnostic modality, ultrasound is emerging as a promising tool for non-invasive therapy, drug delivery, and gene therapy. The ultrasound is a mechanical wave energy generated in a medium as oscillating pressure in space and time at frequencies above 20 kHz, beyond the audible range. The ultrasound exposure generates bioeffects resulting in tissue heating, shear stress, and cavitation, which have been exploited for therapeutic applications. Ultrasound cavitation, enhanced by injected micro bubbles, perturbs cell membrane structures to cause sonoporation and increases the permeability to bioactive materials. Ultrasound-mediated gene delivery has been applied to heart, blood v…

Pathologymedicine.medical_specialtyModality (human–computer interaction)business.industryGenetic enhancementUltrasoundOdontologíaGene delivery:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludDrug deliveryUNESCO::CIENCIAS MÉDICASMicrobubblesMedicinebusinessHead and neckGeneral DentistrySonoporationBiomedical engineering
researchProduct

2017

Background Catheter-based lysis with recombinant tissue plasminogen activator (rtPA) is a well-established therapy for spontaneous intracerebral hemorrhage (ICH). The effectiveness of this therapy can be increased with ultrasound, but the optimal conditions are not yet clearly established. Using a novel in vitro system of blood clots previously developed by our group, we investigated various parameters of intralesional sonothrombolysis using an endosonography catheter in combination with rtPA. Methods Standardized human blood clots were equipped with a drainage catheter and weighed before and after 4 treatments: control (drainage only), rtPA only, ultrasound only and the combination of rtPA…

Pathologymedicine.medical_specialtyMultidisciplinaryLysisbiologybusiness.industryConfocalmedicine.medical_treatmentUltrasound030204 cardiovascular system & hematologyFibrinogenmedicine.diseaseThrombosisFibrin03 medical and health sciencesCatheter0302 clinical medicineFibrinolysismedicinebiology.proteinbusiness030217 neurology & neurosurgerymedicine.drugBiomedical engineeringPLOS ONE
researchProduct

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
researchProduct

Resistance of subventricular neural stem cells to chronic hypoxemia despite structural disorganization of the germinal center and impairment of neuro…

2015

Xavier d'Anglemont de Tassigny,1,* M Salomé Sirerol-Piquer,2,3,* Ulises Gómez-Pinedo,4 Ricardo Pardal,1 Sonia Bonilla,1 Vivian Capilla-Gonzalez,2 Ivette López-López,1 Francisco Javier De la Torre-Laviana,1 José Manuel García-Verdugo,2,3 José López-Barneo1,3 1Medical Physiology and Biophysics Department, Institute of Biomedicine of Seville (IBiS), Virgen del Rocío University Hospital/CSIC/University of Seville, Seville, Spain; 2Cavanilles Institute of Biodiversity and Evolutionary Biology, University of Valencia, Valencia, Spain; 3Network Center of Biomedical Research on Neurodegenerati…

Pathologymedicine.medical_specialtyNeurogenesisSubventricular zoneBiologyHypoxia (medical)ultrastructureNeural stem cellOligodendrocyteHypoxemiachronic hypoxemiamedicine.anatomical_structurenervous systemNeuroblastImmunologymedicinesubventricular germinal nichemedicine.symptomProgenitor cellHypoxianeuronal differentiationoligodendrocyte survivalOriginal Researchneural stem cellsHypoxia
researchProduct

Granular cell ameloblastoma of jaw: report of a case with an emphasis on its characterization

2013

Ameloblastoma is a neoplasm of odontogenic epithelium, especially of enamel organ-type tissue that has not undergone differentiation to the point of hard tissue formation. It accounts for approximately 10% of all tumors originating from gnathic bones. It exhibits diverse microscopic patterns which occurs either singly or in combination with other patterns. Granular cell ameloblastoma is a rare condition, accounting for 3.5% of all ameloblastoma cases that shows marked transformation in the cytoplasm of tumor cells, which are usually stellate reticulum like cells. The transformed cells possess very coarse, granular, eosinophilic cytoplasm. The “granular change” is thought to be due to a dysf…

Pathologymedicine.medical_specialtyOral Medicine and Pathologybusiness.industryCase ReportOdontologíamedicine.disease:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludPathogenesisCytoplasmEosinophilicUNESCO::CIENCIAS MÉDICASUltrastructuremedicineNeoplasmAmeloblastomabusinessGeneral DentistryGranular Cell AmeloblastomaStellate reticulum
researchProduct

Ultrasound-based testing of tendon mechanical properties: a critical evaluation.

2015

In the past 20 years, the use of ultrasound-based methods has become a standard approach to measure tendon mechanical properties in vivo. Yet the multitude of methodological approaches adopted by various research groups probably contribute to the large variability of reported values. The technique of obtaining and relating tendon deformation to tensile force in vivo has been applied differently, depending on practical constraints or scientific points of view. Divergence can be seen in 1) methodological considerations, such as the choice of anatomical features to scan and to track, force measurements, or signal synchronization; and 2) in physiological considerations related to the viscoelas…

Pathologymedicine.medical_specialtyPhysiologybusiness.industryUltrasoundMeasure (physics)TendonBiomechanical PhenomenaTendonsmedicine.anatomical_structurePhysiology (medical)medicineHumansAponeurosisbusinessBiomedical engineeringUltrasonographyJournal of applied physiology (Bethesda, Md. : 1985)
researchProduct

Successful treatment of adult multisystemic Langerhans cell histiocytosis with psoralen-UV-A, prednisolone, mercaptopurine, and vinblastine.

2008

Background Langerhans cell histiocytosis (LCH) is a rare disease with a peak incidence in childhood. There is limited experience with treatment options for adult patients having multisystemic LCH involvement. We report successful treatment of a 70-year-old woman with adult onset of LCH and multisystem disease (diabetes insipidus centralis, bone marrow infiltration, and lung and skin involvement). Observations A 70-year-old woman with erythematous plaques and papules of the submammary and inguinal skin attended our outpatient clinic and was diagnosed as having LCH. Organ involvement was found in the infundibulum of the pituitary gland, associated with diabetes insipidus centralis, bone marro…

Pathologymedicine.medical_specialtyPrednisoloneDermatologyVinblastineUltraviolet therapyLangerhans cell histiocytosisBone MarrowMedicineOutpatient clinicHumansGlucocorticoidsLungHistiocyteAgedSkinPhotosensitizing Agentsbusiness.industryFicusinGeneral Medicinemedicine.diseaseMercaptopurineMagnetic Resonance ImagingHistiocytosisHistiocytosis Langerhans-CellTreatment OutcomePituitary GlandImmunologyDiabetes insipidusPrednisoloneDrug Therapy CombinationFemaleUltraviolet TherapybusinessTomography X-Ray Computedmedicine.drugFollow-Up StudiesArchives of dermatology
researchProduct

Comparative study of T84 and T84SF human colon carcinoma cells: in vitro and in vivo ultrastructural and functional characterization of cell culture …

2005

To better understand the relationship between tumor heterogeneity, differentiation, and metastasis, suitable experimental models permitting in vitro and in vivo studies are necessary. A new variant cell line (T84SF) exhibiting an altered phenotype was recently selected from a colon cancer cell line (T84) by repetitive plating on TNF-alpha treated human endothelial cells and subsequent selection for adherent cells. The matched pair of cell lines provides a useful system to investigate the extravasation step of the metastatic cascade. Since analysis of morphological differences can be instructive to the understanding of metastatic potential of tumor cells, we compared the ultrastructural and …

Pathologymedicine.medical_specialtyProgrammed cell deathColon carcinoma ; Tumor cells;. Ultrastructure ; Metastasis .;Apoptosis . ;Bcl-XL;Bcl-XLbcl-X ProteinColon carcinomaApoptosis. UltrastructureBiologyAdenocarcinomaMetastasis .Pathology and Forensic MedicineMetastasischemistry.chemical_compoundMicroscopy Electron TransmissionIn vivoCell Line TumorTumor cellmedicineBiomarkers TumorHumansNeoplasm MetastasisMolecular BiologyCell NucleusCytoplasmic VesiclesTyrosine phosphorylationCell BiologyGeneral Medicinemedicine.diseaseApoptosis .In vitroPhenotypechemistryPleomorphism (cytology)ApoptosisCell cultureGelatinasesColonic NeoplasmsCancer researchDisease ProgressionSignal Transduction
researchProduct

An ultrastructural study on retinal neural and pigment epithelial cells in ovine neuronal ceroid-lipofuscinosis.

1990

Ovine neuronal ceroid-lipofuscinosis represents another well studied model for human neuronal ceroid-lipofuscinosis (NCL). Accumulation of abnormal lipopigments in various retinal neurons, and loss of photoreceptors are similar to the lesions in human juvenile NCL and indicate that the sheep is a suitable model in which to study the pathogenesis of both NCL lipopigment formation and retinopathia pigmentosa. However, this latter process is not as advanced in NCL-diseased sheep as in human patients but far more obvious than in canine NCL in which retinopathy cannot be unequivocally documented. Ovine NCL shares with canine NCL peculiar lamellar inclusions in retinal pigment epithelial cells wh…

Pathologymedicine.medical_specialtySheep DiseasesBiologyRetinaLipofuscinPathogenesischemistry.chemical_compoundPigmentNeuronal Ceroid-LipofuscinosesmedicineAnimalsPhotoreceptor CellsPigment Epithelium of EyeGenetics (clinical)SheepCatabolismRetinalmedicine.diseaseCell biologyOphthalmologychemistryvisual_artPediatrics Perinatology and Child HealthUltrastructurevisual_art.visual_art_mediumNeuronal ceroid lipofuscinosissense organsRetinopathyOphthalmic paediatrics and genetics
researchProduct

AN ULTRASTRUCTURAL STUDY OF THE RETINA IN HUMAN LATE INFANTILE NEUROAXONAL DYSTROPHY

1993

A case involving a girl who died at 11 years of age and who had developed normally until the age of 18 months, at which time further psychomotor maturation stopped and then regressed, is reported. The patient appeared hypotonic and showed loss of deep tendon reflexes, as well as bulbar signs and increasing immobility. Visual impairment resulted in blindness at the age of 7 years. Her disease was diagnosed as late infantile neuroaxonal dystrophy (LINAD) after examination of sural nerve biopsy samples and after autopsy. Under electron microscopy, retinal axons were filled with tubulocisternal profiles and occasional large lamellar clefts close to or distant from synaptic complexes. These lesi…

Pathologymedicine.medical_specialtySural nerveAutopsyRetinaInfantile neuroaxonal dystrophychemistry.chemical_compoundRetinal DiseasesSural NerveHumansMedicineChildOuter nuclear layerMedulla OblongataRetinabusiness.industryMusclesRetinalHypertrophyGeneral Medicinemedicine.diseaseAxonsOphthalmologymedicine.anatomical_structurechemistryNerve DegenerationUltrastructureMedulla oblongataFemaleNervous System DiseasesbusinessRetina
researchProduct