Search results for "Pares"

showing 10 items of 163 documents

Dysynchiria is not a common feature of neuropathic pain

2006

Patients with chronic neuropathic pain (non-CRPS) and brush-evoked allodynia watched a reflected image of their corresponding but opposite skin region being brushed in a mirror. Unlike complex regional pain syndrome Type 1, this process did not evoke any sensation at the affected area ('dysynchiria'). We conclude that central nociceptive sensitisation alone is not sufficient to cause dysynchiria in neuropathic pain. The results imply a difference in cortical pain processing between complex regional pain syndrome and other chronic neuropathic pain.

MalePain Thresholdmedicine.medical_specialtyPhysical medicine and rehabilitationThreshold of painmedicineHumansParesthesiaReferred painbusiness.industrydysynchiria; CRPS; neuropathic painNociceptorsMiddle Agedmedicine.diseaseAnesthesiology and Pain MedicineComplex regional pain syndromeAllodyniaNociceptionAnesthesiaChronic DiseaseNeuropathic painOther Psychology and Cognitive SciencesNeuralgiaNociceptorNeuralgiaFemalemedicine.symptombusinessEuropean Journal of Pain
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Maternal post-natal tobacco use and current parental tobacco use is associated with higher body mass index in children and adolescents: an internatio…

2015

Background: We investigated whether maternal smoking in the first year of life or any current parental smoking is associated with childhood or adolescent body mass index (BMI). Methods: Secondary analysis of data from a multi-centre, multi-country, cross-sectional study (ISAAC Phase Three). Parents/guardians of children aged 6-7 years completed questionnaires about their children's current height and weight, whether their mother smoked in the first year of the child's life and current smoking habits of both parents. Adolescents aged 13-14 years completed questionnaires about their height, weight and current parental smoking habits. A general linear mixed model was used to determine the asso…

MaleParentsPediatricsmedicine.medical_specialtyPediatric ObesityAdolescentCross-sectional studymedicine.medical_treatmentParental smokingOverweighttabaquismeBMImedicineHumansObesityPediatrics Perinatology and Child HealthadolescentsChildtabac efectes fisiològicsBody mass indexparesbusiness.industryinfantsConfoundingSmokingOverweightmedicine.diseaseObesityClinical trialTobacco useCross-Sectional StudiesInternationalPediatrics Perinatology and Child HealthSmoking cessationObservational studyFemalemedicine.symptombusinessBody mass indexobesitatResearch ArticleDemographytrastorns de la nutrició en els infants
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Clinico-diagnostic features of neuralgic amyotrophy in childhood

2020

Neuralgic amyotrophy (NA), even known as Personage-Turner's syndrome (PTS), is a neurologic condition, affecting the lower motor neurons of brachial plexus and/or individual nerves or nerve branches, characterized by pain, muscle weakness/atrophy, and sensory symptoms. NA has an acute/subacute onset, after an infection or vaccination; it is more common in male and is rare in the pediatric population. The etiology remains uncertain, being considered heterogeneous and multifactorial. A severe acute neurologic pain around the shoulder girdle is the classic presenting symptom at onset. As the pain subsides, weakness and paresis develop. NA is usually unilateral, but sometimes, a subclinical con…

MalePediatricsmedicine.medical_specialtyWeaknessNeurologyPainNeurological examinationDermatology03 medical and health sciences0302 clinical medicineElectromyography; Neuralgic amyotrophy; Neuralgic pain; Pediatric; Personage-Turner’s syndromemedicineHumansBrachial Plexus NeuritisBrachial Plexus030212 general & internal medicineChildParesisPediatricMuscle Weaknessmedicine.diagnostic_testbusiness.industryElectromyographyPersonage-Turner’s syndromeMuscle weaknessGeneral MedicineNeuralgic amyotrophyDiagnosis of exclusionPsychiatry and Mental healthMuscular AtrophySettore MED/26 - NeurologiaNeurology (clinical)Differential diagnosismedicine.symptombusinessBrachial plexusNeuralgic pain030217 neurology & neurosurgery
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Mortality in patients with acute aortic dissection type A: analysis of pre- and intraoperative risk factors from the German Registry for Acute Aortic…

2015

Acute aortic dissection type A (AADA) is an emergency with excessive mortality if surgery is delayed. Knowledge about independent predictors of mortality on surgically treated AADA patients is scarce. Therefore, this study was conducted to identify pre- and intraoperative risk factors for death.Between July 2006 and June 2010, 2137 surgically treated patients with AADA were enrolled in a multicentre, prospective German Registry for Acute Aortic Dissection type A (GERAADA), presenting perioperative status, operative strategies, postoperative outcomes and AADA-related risk factors for death. Multiple logistic regression analysis was performed to identify the influence of different parameters …

MalePulmonary and Respiratory Medicinemedicine.medical_specialtymedicine.medical_treatmentOperative TimeMyocardial IschemiaIschemiaDisease030204 cardiovascular system & hematologyBrain Ischemia03 medical and health sciences0302 clinical medicineIschemiaRisk FactorsGermanymedicine.arteryHumansMedicineProspective StudiesRegistriesCardiopulmonary resuscitationIntraoperative ComplicationsAortic dissectionLegAortaAortic Aneurysm Thoracicbusiness.industryGeneral MedicineOdds ratioPerioperativeMiddle Agedmedicine.diseaseSurgeryAortic DissectionTreatment OutcomeHemiparesis030228 respiratory systemAcute DiseaseFemaleSurgerymedicine.symptomCardiology and Cardiovascular MedicinebusinessAortic Aneurysm AbdominalEuropean Journal of Cardio-Thoracic Surgery
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Isolated voluntary facial paresis due to pontine ischemia

1998

We describe a patient withpatientwith isolated voluntary facial paresis due to a unilateral lacunar lesion in the contralateral mediodorsal middle base of the pons. Transcranial magnetic stimulation confirmed the involvement of supranuclear corticofacial tract fibers and sparing of the corticolin-gual and corticospinal connections. This observation demonstrates that the fibers conveying voluntary orofacial activation descend mediodorsally at the level of the middle pons and that the fibers conveying emotional activation may be assumed to converge below this level.

MaleVolitionmedicine.medical_treatmentFacial ParalysisBrain IschemiaLesionMagneticsPhysical StimulationPonsmedicineHumansCranial nerve diseaseAgedParesisbusiness.industryPons VaroliiAnatomymedicine.diseaseMagnetic Resonance ImagingFacial nervePonsFacial paralysisTranscranial magnetic stimulationNeurology (clinical)medicine.symptombusinessNeurology
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Novel missense mutation in the ATP1A2 gene associated with atypical sporapedic hemiplegic migraine

2019

Hemiplegic migraine (HM) is a rare subtype of migraine with aura in which attacks include transient motor weakness or hemiparesis that can last several days. HM is linked to mutations in three different genes, CACNA1A, ATP1A2 and SCN1A, which encode for ion transporters. The clinical spectrum includes atypical symptoms such as impaired consciousness, epileptic seizures, permanent cerebellar ataxia or mental retardation. We describe a novel mutation found in the ATP1A2 gene in a patient with late-onset HM. His attacks were characterised by motor weakness associated with altered mental status, diplopia and ataxia. He also showed up MRI abnormalities and incomplete response to prophylactic the…

MaleWeaknessPediatricsmedicine.medical_specialtyAtaxiaNeurologyMigraine with AuraMutation MissenseNeuroimagingneuro geneticsDiagnosis Differential03 medical and health sciences0302 clinical medicineRare DiseaseATP1A2medicineHumansMissense mutationgenetic screening / counselling030212 general & internal medicineMigraineAgedNeurologic ExaminationGenetic counsellingCerebellar ataxiabusiness.industryHeadacheGeneral MedicineMagnetic Resonance ImagingMigraine with auraPedigreeHemiparesisNeurologySettore MED/26 - NeurologiaSodium-Potassium-Exchanging ATPasemedicine.symptombusinessheadache (including migraines)030217 neurology & neurosurgery
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The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease

2001

We identified three distinct mutations and six mutant alleles in GDAP1 in three families with axonal Charcot-Marie-Tooth (CMT) neuropathy and vocal cord paresis, which were previously linked to the CMT4A locus on chromosome 8q21.1. These results establish the molecular etiology of CMT4A (MIM 214400) and suggest that it may be associated with both axonal and demyelinating phenotypes.

Malecongenital hereditary and neonatal diseases and abnormalitiesDNA Mutational AnalysisMolecular Sequence DataMutantMutation MissenseNeural ConductionGenes RecessiveNerve Tissue ProteinsLocus (genetics)BiologyPolymerase Chain ReactionFrameshift mutationCharcot-Marie-Tooth DiseaseGeneticsHumansMissense mutationAge of OnsetAlleleChildFrameshift MutationGeneAllelesGeneticsBrainInfantExonsAnatomyPhenotypeAxonsPedigreeAmino Acid SubstitutionHaplotypesSpinal CordCodon NonsenseSpainChild PreschoolFemaleLod ScoreVocal cord paresisChromosomes Human Pair 8Demyelinating DiseasesNature Genetics
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Internuclear ophthalmoplegia of abduction: clinical and electrophysiological data on the existence of an abduction paresis of prenuclear origin.

1992

Three patients showed unilateral and five bilateral abduction paresis. Five had associated adduction nystagmus of the contralateral eye. Electrophysiological testing of masseter and blink reflexes indicated an ipsilateral rostral pontine or mesencephalic lesion, and excluded a lesion of the infranuclear portion of the abducens nerve. Abduction paresis was attributed to impaired inhibition of the tonic resting activity of the antagonistic medial rectus muscle. The prenuclear origin of the disorder is based on morphological and neurophysiological evidence of an ipsilateral inhibitory connection between the paramedian pontine reticular formation and the oculomotor nucleus running close to but …

Malegenetic structuresInternuclear ophthalmoplegiaFunctional LateralityOculomotor nucleusAbducens NerveOculomotor NervePonsmedicineHumansAbducens nerveParesisAgedOphthalmoplegiaBlinkingOculomotor nervebusiness.industryReticular FormationMedial rectus muscleAnatomyParamedian pontine reticular formationMiddle AgedMedial longitudinal fasciculusmedicine.diseasebody regionsElectrophysiologyPsychiatry and Mental healthElectrooculographymedicine.anatomical_structureSurgeryFemaleNeurology (clinical)medicine.symptombusinessResearch ArticleJournal of neurology, neurosurgery, and psychiatry
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Sudden sensorineural hearing loss associated with inner ear lesions detected by magnetic resonance imaging.

2017

Although recent advances in magnetic resonance imaging (MRI) techniques have contributed to the detection of tiny lesions in the internal auditory canal (IAC) that may be responsible for sudden sensorineural hearing loss (SSNHL), there have been relatively few studies on the clinical characteristics of intra-labyrinthine hemorrhage (ILH) and labyrinthitis versus those regarding IAC tumors. Our purpose was to investigate the frequency of those IAC lesions on MRI and their clinical characteristics. Initial MRIs of 200 patients with SSNHL (93 men, 107 women; mean age = 48.61 years, range: 18-84 years), as well as detailed clinical histories, audiological examinations, and thyroid function, lip…

Malelcsh:MedicineOtologyAudiologyDeafnessPathology and Laboratory MedicineVascular MedicineDiagnostic Radiology0302 clinical medicineVertigoMedicine and Health Sciences030223 otorhinolaryngologylcsh:ScienceHearing DisordersParesisAged 80 and overMultidisciplinarymedicine.diagnostic_testbiologyRadiology and ImagingAudiologyMiddle AgedPrognosisMagnetic Resonance ImagingInner EarVertigoFemaleRadiologymedicine.symptomThyroid functionAnatomyResearch ArticleAdultmedicine.medical_specialtyBenign paroxysmal positional vertigoAdolescentHearing lossImaging TechniquesHearing Loss SensorineuralHemorrhageResearch and Analysis Methods03 medical and health sciencesLabyrinthitisYoung AdultSigns and SymptomsDiagnostic Medicinemedicineotorhinolaryngologic diseasesHumansAgedbusiness.industrylcsh:RBiology and Life SciencesMagnetic resonance imagingbiology.organism_classificationmedicine.diseaseOtorhinolaryngologyEarsEar InnerLesionslcsh:QAudiometrybusinessHead030217 neurology & neurosurgeryPloS one
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Activity of Thigh Muscles During Static and Dynamic Stances in Stroke Patients: A Pilot Case-Control Study

2014

Impaired postural control is a key characteristic of mobility problems in stroke patients and has great impact on the incidence of falls and on the level of independence in activities of daily living. The role played by the thigh muscles in balance impairment in stroke patients has not been sufficiently investigated. This study investigated the activities of the thigh muscles in stroke patients during standing balance manipulations.Ten stroke patients and 15 healthy subjects performed 5 upright standing tasks on a force platform: normal standing with eyes open, normal standing with eyes closed, feet together, semi-tandem standing, and a dynamic measurement along a predefined route. The post…

Malemedicine.medical_specialtyActivities of daily livingPosturePilot ProjectsIsometric exercisePhysical medicine and rehabilitationHumansMedicineForce platformMuscle StrengthMuscle SkeletalPostural BalanceStrokeAgedBalance (ability)Community and Home CareElectromyographybusiness.industryRehabilitationPosturographyCase-control studyMiddle Agedmedicine.diseaseParesisStrokeThighCase-Control StudiesData Interpretation StatisticalBerg Balance ScalePhysical therapyFemaleNeurology (clinical)businessTopics in Stroke Rehabilitation
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