Search results for "Urologia"

showing 10 items of 1005 documents

Wuhan, the second MPAU meeting: our society is progressing

2010

Urology society ChinaSettore MED/24 - Urologia
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Recurrence and progression according to stage at re-TUR in t1g3 bladder cancer patients treated with BCG: Not as bad as previously thought

2017

Introduction & Objectives The goals of transurethral resection of a bladder tumour (TUR) are to completely resect the lesions and to make a correct diagnosis in order to adequately stage the patient. Persistent disease after TUR is not uncommon and is the reason why re-TUR is recommended in T1G3 patients. When there is T1 tumour in the re-TUR specimen, very high risks of progression (82%) have been reported1 and therefore cystectomy is considered to be mandatory. We analyse the tumour stage at re-TUR and the risk of recurrence, progression to muscle invasive disease and cancer specific mortality (CSM) in T1G3 patients treated with BCG. Material & Methods In our retrospective cohort …

Urologybladder camcer BCGSettore MED/24 - Urologia
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LA VARICOCELECTOMIA SUBINGUINALE SECONDO MARMAR: IMMAGINI INEDITE

2006

VARICOCELECTOMIASettore MED/24 - Urologia
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LA CISTECTOMIA “PROSTATE E SEMINAL SPARING” Pro: (Trieste) Contro: V. Serretta (Palermo)

2013

Il tumore della vescica rimane una delle neoplasie più frequenti nell’ambito dell’oncologia urologica. Le strategie diagnostiche si stanno sempre più evolvendo e ci permettono di caratterizzare sempre meglio la neoplasia. Durante il corso verranno illustrate alcune nuovissime tecniche diagnostiche apparse recentemente. Dal punto di vista terapeutico l’intervento chirurgico demolitivo, la cistectomia, è sicuramente l’approccio di scelta per i tumori non muscolo invasivi ad alto ed altissimo rischio e per i tumori infiltranti. Tuttavia le tecniche si sono evolute come pure la preparazione del paziente. Durante il corso verranno discusse e dibattute due delle più interessanti e recenti tecnich…

Vescica cistectomiaSettore MED/24 - Urologia
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Use of virtual reality to explore the decision making in obsessive–compulsive disorder and Parkinson’s disease

2013

Virtual reality Obsessive compulsive disorder Parkinson desease decision makingSettore M-PSI/08 - Psicologia ClinicaSettore MED/48 -Scienze Infermierist. e Tecn. Neuro-Psichiatriche e Riabilitat.Settore MED/26 - NeurologiaSettore MED/25 - Psichiatria
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Suppression of extinction with TMS in humans: from healthy controls to patients.

2006

We review a series of studies exemplifying some applications of single-pulse and paired-transcranial magnetic stimulation (TMS) in the study of spatial attention and of its deficits. We will focus primarily on sensory extinction, the failure to consciously perceive a contralesional sensory stimulus only during bilateral stimulation of homologous surfaces. TMS studies in healthy controls show that it is possible either to interfere or modulate the excitability of the parietal cortex during sensory (i.e. tactile and visual) attentional tasks, thus reproducing a condition of virtual extinction. TMS studies in patients with unilateral (mainly right) brain damage show that the modulation of the …

Visual perceptionmedicine.medical_treatmentINHIBITIONPosterior parietal cortexNeurosciences. Biological psychiatry. NeuropsychiatrySensory systemStimulationTACTILE SPACEBrain damageFunctional LateralityExtinction PsychologicalPARIETAL CORTEXParietal LobemedicineHumansCUTANEOUS STIMULIMOTOR CORTEXTRANSCRANIAL MAGNETIC STIMULATION; CUTANEOUS STIMULI; PULSE STIMULATION; PARIETAL CORTEX; TACTILE SPACE; MOTOR CORTEX; HUMAN BRAIN; NEGLECT; INHIBITION; PERCEPTIONPERCEPTIONSettore M-PSI/02 - Psicobiologia E Psicologia FisiologicaParietal lobeExtinctionGeneral Medicinemedicine.diseaseHUMAN BRAINTranscranial Magnetic StimulationSensation Disorders; Extinction Psychological; Humans; Space Perception; Transcranial Magnetic Stimulation; Parietal Lobe; Visual Perception; Touch; Functional LateralityTranscranial magnetic stimulationNeuropsychology and Physiological PsychologyNeurologyNEGLECTTouchExtinction (neurology)Space PerceptionPULSE STIMULATIONSensation DisordersVisual PerceptionPsychologicalSettore MED/26 - NeurologiaNeurology (clinical)medicine.symptomPsychologyNeuroscienceRC321-571Research ArticleBehavioural neurology
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Unusual Presentation of Bilateral Carotid Artery Dissection: The Importance of Reasoning Outside the Box

2021

A bilateral internal carotid artery dissection presenting with atypical symptoms of cerebral hypoperfusion has been rarely reported, especially in the absence of obvious precipitating factors. A middle-aged woman presented to the emergency department with a 2-day-history of progressive left arm numbness and weakness, confusion, disorientation and clumsiness worsened by upright position. A cerebral hypoperfusion condition was hypothesized and confirmed by a CT angiography, which showed bilateral internal carotid dissection with uncertain etiology. Screening for predisposing conditions to spontaneous carotid arteries dissection was basically negative. Regarding potential precipitating factors…

Weaknessmedicine.medical_specialtyCerebrovascular disordersUnusual PresentationNeuroimagingDissection (medical)030204 cardiovascular system & hematology030218 nuclear medicine & medical imaging03 medical and health sciences0302 clinical medicinemedicineBilateral carotid artery dissectionInternal carotid artery dissectionmedicine.diagnostic_testbusiness.industryGeneral MedicineEmergency departmentmedicine.diseaseBilateral Carotid Artery DissectionAngiographyEtiologySettore MED/26 - NeurologiaSurgeryRadiologyPresentation (obstetrics)medicine.symptomCardiology and Cardiovascular MedicinebusinessAnnals of Vascular Surgery
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Diagnostic and therapeutic aspects of hemiplegic migraine

2020

Hemiplegic migraine (HM) is a clinically and genetically heterogeneous condition with attacks of headache and motor weakness which may be associated with impaired consciousness, cerebellar ataxia and intellectual disability. Motor symptoms usually last <72 hours and are associated with visual or sensory manifestations, speech impairment or brainstem aura. HM can occur as a sporadic HM or familiar HM with an autosomal dominant mode of inheritance. Mutations in CACNA1A, ATP1A2 and SCN1A encoding proteins involved in ion transport are implicated. The pathophysiology of HM is close to the process of typical migraine with aura, but appearing with a lower threshold and more severity. We review…

Weaknessmedicine.medical_specialtyMigraine with AuraElectroencephalographyMotor symptomsDiagnosis Differentialclinical neurology; EEG; headache; ion transportion transport03 medical and health sciences0302 clinical medicinePhysical medicine and rehabilitationIntellectual disabilitymedicineHumansclinical neurology1506EEGMigraine030304 developmental biology0303 health sciencesCerebellar ataxiamedicine.diagnostic_testbusiness.industryDisease ManagementEEG; clinical neurology; headache; ion transportmedicine.diseasePedigreeClinical neurologyImpaired consciousnessPsychiatry and Mental healthMutationHemiplegic migraineSettore MED/26 - NeurologiaSurgeryCalcium ChannelsNeurology (clinical)medicine.symptombusinessheadache030217 neurology & neurosurgeryJournal of Neurology, Neurosurgery & Psychiatry
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Editorial: The Incredible Challenge of Digitizing the Human Brain

2022

The world we live in is drastically different from previous decades in terms of digitalization expansion. Logically, one might expect that these changes modify the way we behave, our habits, the way we do tasks, communicate and access information (Moret-Tatay et al., 2018; Wang et al., 2021). And, therefore, the functioning of the brain and even its anatomy. If so, it seems imperative to examine how it affects our cognition. Furthermore, based on the assumption that the brain is plastic and adaptable, some alterations and changes are expected to optimize resources or even compensations by improving other skills (Oliveira et al., 2018; Bubbico et al., 2020; Della Gatta et al., 2021).

Xarxes socialsNeurologiaPsicologia de la cognicióNeuropsicologiaEducacióGeneral PsychologyFrontiers in Psychology
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Age-dependent epileptic encephalopathy associated with an unusual co-occurrence of ZEB2 and SCN1A variants.

2020

Mowat-Wilson syndrome is a genetic disorder associated with a variable phenotype including peculiar facial features associated with intellectual disability, epilepsy, language impairment, and multiple congenital anomalies caused by heterozygous mutation of the ZEB2 gene. The ZEB2 protein is a complex transcription factor that encompasses multiple functional domains that interact with the regulatory regions of target genes including those involved in brain development. Recently, it has been documented that ZEB2 regulates the differentiation of interneuron progenitors migrating from the medial ganglionic eminence to cortical layers by repression of the Nkx2-1 homeobox transcription factor. It…

ZEB2genotype-phenotype correlationSettore MED/38 - Pediatria Generale E SpecialisticaSettore M-PSI/08 - Psicologia ClinicaIntellectual DisabilityHumansMowat-Wilson syndromeEEGgenotype-phenotype correlationSCN1AHirschsprung DiseaseEEGChildGenetic Association StudiesZEB2Zinc Finger E-box Binding Homeobox 2EpilepsyEEG; epilepsy; GABAergic interneurons; genotype-phenotype correlation; Mowat-Wilson syndrome; SCN1A; ZEB2FaciesElectroencephalographySettore MED/39 - Neuropsichiatria InfantileGABAergic interneuronsMowat-Wilson syndromeepilepsyNAV1.1 Voltage-Gated Sodium ChannelGABAergic interneuronsMicrocephalySettore MED/26 - NeurologiaFemaleEpileptic disorders : international epilepsy journal with videotape
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