Search results for "Neurologi"

showing 10 items of 1189 documents

The pterygoid reflex in man and its clinical application

1992

A technique for eliciting and recording the stretch reflex (R) of the medial pterygoid muscle (Pter) is described. The latency was 6.9 ± 0.43 ms in 23 healthy volunteers (mean age 23.7 years) showing a side-to-side difference of 0.29 ± 0.21 ms. The PterR latencies were little shorter and side-to-side difference little greater than of the masseter reflex. Observations in 5 selected patients with small brainstem lesions suggest that the neurons of the PterR afferents form a cluster within the caudal portion of the trigeminal mesencephalic nucleus. Testing the masseter and pterygoid reflexes provides a more precise localization of small ponto-mesencephalic lesions. © 1992 John Wiley & Sons, In…

AdultMaleReflex StretchPhysiologyElectromyographyNeurological disorderCellular and Molecular NeuroscienceTrigeminal Caudal NucleusMesencephalonReference ValuesPonsPhysiology (medical)medicineHumansStretch reflexSmall brainstemAgedBrain DiseasesBlinkingmedicine.diagnostic_testMasseter Musclebusiness.industryElectrodiagnosisPterygoid MusclesMean ageAnatomyMiddle Agedmedicine.diseaseMagnetic Resonance Imagingmedicine.anatomical_structureReflexMedial pterygoid muscleFemaleNeurology (clinical)Tomography X-Ray ComputedbusinessJaw jerk reflexBrain StemMuscle & Nerve
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Migraine and Sport in a Physically Active Population of Students: Results of a Cross‐Sectional Study

2020

Abstract Objective: In this study, we explored the relationship between migraine and sport in a physically active population of students, analyzing the risk of migraine among sporty students. Background: The relationship between sport and migraine is controversial; moreover, several studies report on sport as a migraine trigger, but there is evidence that physical activity could have a relevant role in migraine prevention. Methods: A cross-sectional survey was conducted using the validated ID-migraine questionnaire including specific demo-anthropometric (gender, age, weight, height) and sports variables on a potentially active student population of the University of Palermo. Evaluation in p…

AdultMaleRiskUniversitiesCross-sectional studyMigraine DisordersPopulationPhysical activityphysical activityPhysical exerciseLogistic regressionDisability assessmentYoung Adult03 medical and health sciencesSex Factors0302 clinical medicineID-migrainephysical exercisePrevalenceHumansMedicineDisabled Personsmigraine030212 general & internal medicineStudentseducationExerciseeducation.field_of_studybusiness.industrygender medicineProtective Factorsmedicine.diseasesport.Cross-Sectional StudiesIncreased riskItalyNeurologyMigraineFemaleSettore MED/26 - NeurologiaNeurology (clinical)business030217 neurology & neurosurgerySportsClinical psychologyHeadache: The Journal of Head and Face Pain
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Migraine mediates the influence of C677T MTHFR genotypes on ischemic stroke risk with a stroke-subtype effect.

2007

Background and Purpose— The objective was to investigate the role of C677T MTHFR polymorphism in migraine pathogenesis and in the migraine–ischemic stroke pathway. Methods— A first genotype–migraine association study was conducted on 100 patients with migraine with aura (MA), 106 with migraine without aura (MO), and 105 subjects without migraine, which provided evidence in favor of association of the TT677 MTHFR genotype with increased risk of MA compared with both control subjects (OR, 2.48; 95% CI, 1.11 to 5.58) and patients with MO (OR, 2.21; 95% CI, 1.01 to 4.82). Based on these findings, mediational models of the genotype–migraine–stroke pathway were fitted on a group of 106 patients …

AdultMaleRiskmedicine.medical_specialtyGenotypeAuraMigraine DisordersCADASILGastroenterologyRisk FactorsInternal medicineOdds RatiomedicineHumansmigraineRisk factorStrokeMethylenetetrahydrofolate Reductase (NADPH2)Advanced and Specialized NursingPolymorphism Geneticbiologybusiness.industryCerebral infarctionOdds ratioMiddle Agedmedicine.diseaseMigraine with auraStrokePhenotyperisk factorMigraineAnesthesiaMethylenetetrahydrofolate reductaseMutationbiology.proteinBlood VesselsSettore MED/26 - NeurologiaFemalestroke in young adultsNeurology (clinical)geneticmedicine.symptomCardiology and Cardiovascular Medicinebusiness
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The HLA locus and multiple sclerosis in Sicily

2005

The authors report the analysis of HLA-class II allelic heterogeneity in a well characterized multiple sclerosis (MS) Sicilian dataset. Family-based association analysis revealed evidence for excess transmission to affected individuals for alleles HLA-DRB1*1501, DRB1*04, and DQB1*0302. When analyzed as haplotypes, the authors observed excess transmission for the DRB1*0400-DQB1*0302 haplotype. Sicilian patients share the HLA-DRB1*1501 susceptibility allele with affecteds living in continental Italy, but also display the allelic heterogeneity that characterizes Mediterranean populations.

AdultMaleRiskmusculoskeletal diseasesMultiple SclerosisAdolescentGenes MHC Class IILocus (genetics)Human leukocyte antigenBiologySeverity of Illness IndexLinkage DisequilibriumCohort StudiesDisability EvaluationGene Frequencyimmune system diseasesMultiple Sclerosis/epidemiologyPrevalencemedicineHumansGenetic Predisposition to DiseaseAge of OnsetAlleleskin and connective tissue diseasesSicilyAllelesGenetic associationGeneticsHLA-D AntigensIncidenceMultiple sclerosisHaplotypeGene Poolmedicine.diseaselanguage.human_languageSettore BIO/18 - GeneticaHaplotypeslanguageFemaleAllelic heterogeneitySettore MED/26 - NeurologiaNeurology (clinical)Sicilian
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Chronic sacral neuromodulation for treatment of neurogenic bladder dysfunction: long-term results with unilateral implants

2001

Abstract Objectives. To investigate the therapeutic value of sacral neuromodulation in patients with neurogenic disorders in whom conservative treatment options were unsuccessful. Neurogenic disorders may result in various forms of lower urinary tract dysfunction. Methods. Twenty-seven patients (19 women, 8 men) aged 18 to 63 years (mean 44.9 years) were subjected to percutaneous test stimulation of the sacral spinal nerves. Their urologic symptoms consisted of bladder storage failure (n = 15) due to detrusor hyperreflexia and/or bladder hypersensitivity, failure to empty due to detrusor areflexia (n = 11), and combined bladder hypersensitivity and detrusor areflexia (n = 1). Twelve patient…

AdultMaleSacrummedicine.medical_specialtyPercutaneousAdolescentUrologyUrinary systemElectric Stimulation TherapyStimulationNeurological disordermedicineHumansUrinary Bladder NeurogenicNeurogenic bladder dysfunctionbusiness.industryLong term resultsMiddle AgedUrination Disordersmusculoskeletal systemmedicine.diseaseElectrodes ImplantedSurgerySacral nerve stimulationAnesthesiaFemaleImplantbusinessUrology
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Prevalence of headache in patients with Behçet's disease without overt neurological involvement

2003

The aims of the present study were to evaluate the prevalence of headache and the frequency of different headache syndromes in patients with Behçet's Disease (BD) without neurological involvement and to investigate the relationship with other clinical, and behavioural variables. Twenty-seven BD patients and 27 control subjects underwent a validated semistructured questionnaire based on the International Headache Society criteria. Levels of anxiety and depression, disease activity, and current medication were collected. Headache occurred in 88.9% of BD patients. There was no difference in the prevalence of the different headache syndromes between BD patients and controls. Only migraine witho…

AdultMaleSelf-AssessmentBehçet's diseaseBehcet SyndromeHeadacheGeneral MedicineHealth SurveysTension-type headacheItalyPrevalenceHumansFemaleSettore MED/26 - NeurologiaNeurology (clinical)Nervous System DiseasesMigraine
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Excitability and susceptibility of the brain's electrical activity during sleep: an analysis of late components of AEPs and VEPs.

1991

We investigated ten healthy male subjects and measured late components of AEPs and VEPs during sleep. According to Rechtschaffen and Kales (1968) we performed an off-line scoring procedure of sleep-EEG and averaged the AEPs and VEPs of five different periods, corresponding to sleep stages I, II, III, IV and REM. From the averaged evoked potentials we computed the amplitude-frequency-characteristic (AFC) of the brain (Basar, 1980) during different sleep stages. These AFCs characterize transfer properties of an oscillating system. A comparison of different AFCs has shown that the excitability of the brain depicts a clear alpha resonance during stage I, a pronounced delta resonance during stag…

AdultMaleSleep Stagesmedicine.diagnostic_testGeneral Neurosciencemedia_common.quotation_subjectModels NeurologicalBrainGeneral MedicineElectroencephalographyElectrophysiologyCorrelation analysismedicineEvoked Potentials AuditoryEvoked Potentials VisualHumansSpectral analysisSleep StagesPsychologySleepNeuroscienceSleep eegVigilance (psychology)media_commonThe International journal of neuroscience
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Fatigue in multiple sclerosis is closely related to sleep disorders: a polysomnographic cross-sectional study.

2011

Background: Sleep disorders can cause tiredness. The relationship between sleep disorders and fatigue in patients with multiple sclerosis (MS) has not yet been investigated systematically. Objective: To investigate the relationship between fatigue and sleep disorders in patients with MS. Methods: Some 66 MS patients 20 to 66 years old were studied by overnight polysomnography. Using a cut-off point of 45 in the Modified Fatigue Impact Scale (MFIS), the entire cohort was stratified into a fatigued MS subgroup ( n = 26) and a non-fatigued MS subgroup ( n = 40). Results: Of the fatigued MS patients, 96% ( n = 25) were suffering from a relevant sleep disorder, along with 60% of the non-fatigue…

AdultMaleSleep Wake Disordersmedicine.medical_specialtyPeriodic limb movement disorderMultiple SclerosisPolysomnographyNeurological disorderPolysomnographyRisk AssessmentCentral nervous system diseaseYoung AdultRisk FactorsInternal medicineGermanySurveys and QuestionnairesmedicineInsomniaOdds RatioHumansRestless legs syndromeFatigueAgedSleep disordermedicine.diagnostic_testbusiness.industryMiddle Agedmedicine.diseaseCross-Sectional StudiesLogistic ModelsNeurologyCohortPhysical therapyFemaleNeurology (clinical)medicine.symptombusinessSleepMultiple sclerosis (Houndmills, Basingstoke, England)
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Increased frequency of migraine in narcoleptic patients

1999

We explored the relationship between narcolepsy and different types of headaches. We interviewed 68 patients with idiopathic narcolepsy for the presence of headache symptoms based on the criteria of the International Headache Society (IHS). Eighty-one percent of the patients reported headaches that warranted an IHS headache diagnosis. Fifty-four percent of the patients (64% women, 35% men) had migraine with all IHS criteria fulfilled.

AdultMaleSleep disorderPediatricsmedicine.medical_specialtybusiness.industryVascular diseaseMigraine DisordersMEDLINENeurological disorderMiddle Agedmedicine.diseaseCentral nervous system diseaseMigraineAnesthesiamedicineHumansFemaleNeurology (clinical)Sex DistributionHeadachesmedicine.symptombusinessNarcolepsyNarcolepsyNeurology
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Autosomal dominant hereditary spastic paraplegia: report of a large italian family with R581X spastin mutation

2007

We describe a large kindred with a typical pure form of autosomal dominant hereditary spastic paraplegia (ADHSP). On the basis of maximum LOD score of 1.94 at theta (max)=0 with marker D2S367, we obtained suggestive evidence for linkage of ADHSP to SPG4 locus. Denaturing high-performance liquid chromatography (DHPLC) and direct sequence analysis allowed us to identify a nonsense mutation (1741* C > T) in exon 17 of the Spastin gene. This transition, carried by all the affected family members and two apparently healthy individuals, lead to truncation of the last 36 amino acids in the C-terminus of the protein. These results confirm the existence of mutation in the SPG4 gene with a reduced pe…

AdultMaleSpastinGenotypeSequence analysisHereditary spastic paraplegiaDNA Mutational AnalysisNonsense mutationLocus (genetics)DermatologyBiologyArginineSpastinExonHereditary spastic paraplegia Spastin Neurological diseasemedicineHumansGeneAgedAdenosine TriphosphatasesFamily HealthGeneticsSpastic Paraplegia HereditaryGeneral MedicineMiddle Agedmedicine.diseaseMolecular biologyPenetrancePsychiatry and Mental healthItalyMutationFemaleNeurology (clinical)Lod ScoreNeurological Sciences
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