Search results for "rema"

showing 10 items of 911 documents

The effect of radiofrequency catheter ablation of frequent premature ventricular complexes and arrhythmia burden on left ventricular function

2016

Background: Frequent premature ventricular complexes (PVC) are related to reversible tachycardia-induced cardiomyopathy. However, the role of arrhythmia burden on the outcome of the catheter ablation has not been fully recognised. Aim: The aim of this study was to assess the effect of catheter ablation and PVC burden in patients with and without structural heart disease (SHD) on left ventricular ejection fraction (LVEF). Methods: Transthoracic echocardiography was done before and six months after radiofrequency catheter ablation in 109 consecutive patients (61 men, age 55 ± 17 years) with frequent PVCs. Sixty-five (59.6%) patients had underlying SHD. Results: The catheter ablation procedure…

AdultMalemedicine.medical_specialtyHeart diseasemedicine.medical_treatmentCardiomyopathyCatheter ablation030204 cardiovascular system & hematologyVentricular Dysfunction Left03 medical and health sciencesQRS complex0302 clinical medicineInternal medicinemedicineHumanscardiovascular diseases030212 general & internal medicineventricular arrhythmiaAgedEjection fractionbusiness.industryleft ventricular ejection fractionStroke VolumeStroke volumeMiddle Agedmedicine.diseaseAblationstructural heart diseaseVentricular Premature ComplexesTreatment OutcomeEchocardiographyConcomitantMultivariate AnalysisCatheter Ablationcardiovascular systemCardiologyFemalepremature ventricular complexCardiology and Cardiovascular MedicinebusinessKardiologia Polska
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Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders

2004

Mutations in ABCA1 have been shown to be the cause of Tangier disease (TD) and some forms of familial hypoalphalipoproteinemia (HA), two genetic disorders characterized by low plasma HDL levels. Here we report six subjects with low HDL, carrying seven ABCA1 mutations, six of which are previously unreported. Two mutations (R557X and H160FsX173) were predicted to generate short truncated proteins; two mutations (E284K and Y482C) were located in the first extracellular loop and two (R1901S and Q2196H) in the C-terminal cytoplasmic domain of ABCA1. Two subjects found to be compound heterozygotes for ABCA1 mutations did not have overt clinical manifestations of TD. Three subjects, all with prema…

AdultMalemedicine.medical_specialtyHeterozygoteSettore MED/09 - Medicina InternaApolipoprotein BAdolescentPremature coronary artery diseaseTangier diseaseCoronary DiseaseBiologyGene mutationmedicine.disease_causeCompound heterozygosityTangier diseaseInternal medicineGenotypeABCA1 genemedicineHumansChildHypoalphalipoproteinemiaSelection BiasAgedApolipoproteins BGeneticsMutationFamilial defective Apo B (FDB)Apolipoprotein A-ICholesterol HDLnutritional and metabolic diseasesMiddle Agedmedicine.diseaseLipoprotein lipaseTangier disease; Familial HDL deficiency; ABCA1 gene; Familial defective Apo B (FDB); Lipoprotein lipase; Premature coronary artery diseaseEndocrinologyChild PreschoolMutationbiology.proteinlipids (amino acids peptides and proteins)Allelic heterogeneityATP-Binding Cassette TransportersFemaleCardiology and Cardiovascular MedicineFamilial HDL deficiencyATP Binding Cassette Transporter 1
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Perinatal cerebral insults alter auditory event-related potentials.

2011

Background: Auditory event-related potentials (AERPs) can be used as indices of neural information processing. Altered AERPs have been reported in children and young adults with frontal lobe infarction. Aim: To test the hypothesis that perinatal brain injury affects cortical auditory processing. Methods: We assessed AERPs at term. 6 and 12 months of age in preterm infants [n = 9. median gestational age (GA) 27.9, range 23.9-30.0 wk], term infants with perinatal intracerebral hemorrhage (ICH) [n = 5, GA 40.3, range 37.4-42.3 wk], and term infants with perinatal asphyxia In [n = 4. GA 39.4. range 37.9-40.3 wk]. Healthy preterm (n = 16) and term infants (n = 22) served as controls. A harmonic …

AdultMalemedicine.medical_specialtyMismatch negativityInfant Newborn DiseasesCentral nervous system disease03 medical and health sciencesYoung Adult0302 clinical medicinePregnancy030225 pediatricsInternal medicinemedicineHumansYoung adultCerebral HemorrhageIntracerebral hemorrhageAsphyxiaAuditory CortexInfant NewbornObstetrics and GynecologyGestational agemedicine.diseasePrognosisSurgeryPerinatal asphyxiaFrontal lobeAcoustic StimulationBrain InjuriesPediatrics Perinatology and Child HealthCardiologyEvoked Potentials AuditoryFemalemedicine.symptomPsychology030217 neurology & neurosurgeryInfant PrematureFollow-Up StudiesEarly human development
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Pre-Prosthetic surgical alterations in maxillectomy to enhance the prosthetic prognoses as part of rehabilitation of oral cancer patient

2011

Objectives: After maxillectomy, prosthetic restoration of the resulting defect is an essential step because it signals the beginning of patient’s rehabilitation. The obturator used to restore the defect should be comfortable, restore adequate speech, deglutition, mastication, and be cosmetically acceptable, success will depend on the size and location of the defect and the quantity and integrity of the remaining structures, in addition to pre-prosthetic surgical preparation of defect site. Preoperative cooperation between the oncologist surgeon and the maxillofacial surgeon may allow obturation of a resultant defect by preservation of the premaxilla or the tuberosity on the defect side and …

AdultMalemedicine.medical_specialtyPremaxillamedicine.medical_treatmentDentistryProsthodontistSwallowingmedicineMaxillaHumansGeneral DentistryDental alveolusAgedMaxillary NeoplasmsRehabilitationbusiness.industryMaxillary NeoplasmsCancerProstheses and ImplantsMiddle AgedPlastic Surgery Proceduresmedicine.diseasePrognosis:CIENCIAS MÉDICAS [UNESCO]Surgerymedicine.anatomical_structureOtorhinolaryngologyMaxillaUNESCO::CIENCIAS MÉDICASSurgeryResearch-ArticleFemaleOral Surgerybusiness
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Inter-hemispheric remapping between arm proprioception and vision of the hand is disrupted by single pulse TMS on the left parietal cortex.

2013

International audience; Parietal cortical areas are involved in sensori-motor transformations for their respective contralateral hemifield/body. When arms of the subjects are crossed while their gaze is fixed straight ahead, vision of the hand is processed by the hemisphere ipsilateral to the arm position and proprioception of the arm by the contralateral hemisphere. It induces interhemispheric transfer and remapping. Our objective was to investigate whether a single pulse TMS applied to the left parietal cortical area would disturb interhemispheric remapping in a similar case, and would increase a simple reaction time (RT) with respect to a control single pulse TMS applied to the frontal c…

AdultMalemedicine.medical_specialtygenetic structuresCognitive NeurosciencePosterior parietal cortexExperimental and Cognitive PsychologyAudiology050105 experimental psychologyFunctional Laterality[SPI.AUTO]Engineering Sciences [physics]/Automatic03 medical and health sciencesInterhemispheric transfer0302 clinical medicineArts and Humanities (miscellaneous)Transcranial magnetic stimulation (TMS)Remapping[ SPI.AUTO ] Engineering Sciences [physics]/AutomaticParietal LobeMoro reflexDevelopmental and Educational PsychologymedicineLeft parietal areaReaction TimeVisual attentionHumans0501 psychology and cognitive sciencesAttentionSimple reaction time (RT)Brain MappingProprioception[SCCO.NEUR]Cognitive science/Neuroscience05 social sciencesContralateral hemisphereSingle pulseHandProprioceptionGazeTranscranial Magnetic StimulationNeuropsychology and Physiological PsychologyStartle reflex[ SCCO.NEUR ] Cognitive science/NeuroscienceArmVisual PerceptionPsychologyNeuroscience030217 neurology & neurosurgeryArm positionPsychomotor PerformanceBrain and cognition
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The temperament of preterm infant in preschool age

2010

Abstract Background The study deals with the characteristics of temperament of preterm infants during their preschool age in order to not only investigate likely "difficult or problematic profiles", guided by impairments driven by their preterm birth, but also to provide guidelines for the activation of interventions of prevention, functional to improve the quality of preterm infant's life. Methods The study involved a group of 105 children where 50 preterm children at the average age of 5 years and 2 months, enrolled in preschools of Palermo. The research planned the child reference teachers to be administered a specific questionnaire, the QUIT, made up of 60 items investigating six specif…

AdultMalemedicine.medical_specialtymedia_common.quotation_subjectPsychological interventionMotor ActivityStimulus (physiology)Developmental psychologyYoung AdultChild DevelopmentSurveys and Questionnairestemperament preterm preschool agemedicineHumansAttentionNeonatologyTemperamentPsychiatrymedia_commonbusiness.industryResearchInfant Newbornlcsh:RJ1-570NoveltyInfantMotor controllcsh:PediatricsCognitionFeelingChild PreschoolFemaleTemperamentbusinessInfant PrematureFollow-Up StudiesItalian Journal of Pediatrics
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Perinatal and newborn care in a two years retrospective study in a first level peripheral hospital in Sicily (Italy)

2019

Abstract Background Two hundred seventy-five thousand maternal deaths, 2.7 million neonatal deaths, and 2.6 million stillbirths have been estimated in 2015 worldwide, almost all in low-income countries (LICs). Moreover, more than 20 million severe disabilities result from the complications of pregnancy, childbirth or its management each year. A significant decrease of mortality/morbidity rates could be achieved by providing effective perinatal and newborn care also in high-income countries (HICs), especially in peripheral hospitals and/or rural areas, where the number of childbirths per year is often under the minimal threshold recognized by the reference legislation. We report on a 2 years…

AdultPatient Transfermedicine.medical_specialtyComplications of pregnancyAdolescentTerm BirthCohort StudiesYoung Adult03 medical and health sciences0302 clinical medicinePregnancyHealth caremedicineHumansChildbirth030212 general & internal medicineRetrospective StudiesPerinatal mortalityPregnancy030219 obstetrics & reproductive medicinebusiness.industryObstetricsResearchPublic healthInfant NewbornQuality of carelcsh:RJ1-570Gestational agelcsh:PediatricsRetrospective cohort studyMiddle AgedStillbirthDelivery ObstetricNewbornmedicine.diseaseInfant FormulaObstetric Labor ComplicationsPerinatal CareBreast FeedingItalyPremature BirthFemaleMaternal deathbusinessItalian Journal of Pediatrics
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Variations in breastfeeding rates for very preterm infants between regions and neonatal units in Europe: results from the MOSAIC cohort

2010

Abstract: Objectives To compare breastfeeding rates at discharge for very preterm infants between European regions and neonatal units, and to identify characteristics associated with breast feeding using multilevel models. Methods Population-based cohort of 3006 very preterm births (2231 weeks of gestation) discharged home from neonatal units in eight European regions in 2003. Results Breastfeeding rates varied from 19% in Burgundy to 70% in Lazio, and were correlated with national rates in the entire newborn population. Women were more likely to breast feed if they were older, primiparous and European; more premature, smaller and multiple babies or those with bronchopulmonary dysplasia wer…

AdultPediatricsmedicine.medical_specialtyBreastfeedingGestational AgeCohort StudiesYoung AdultIntensive careHumansMedicineBronchopulmonary DysplasiaPregnancybusiness.industryObstetricsAge FactorsInfant NewbornObstetrics and GynecologyGestational ageGeneral Medicinemedicine.diseaseEuropeParityBreast FeedingBronchopulmonary dysplasiaPediatrics Perinatology and Child HealthCohortIntensive Care NeonatalFemaleHuman medicinebusinessBreast feedingInfant PrematureCohort studyArchives of Disease in Childhood - Fetal and Neonatal Edition
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Interferon-beta exposure during first trimester is safe in women with multiple sclerosis-A prospective cohort study from the German Multiple Sclerosi…

2015

Background: Available data suggest that pregnancy exposure to interferon-beta might result in lower mean birth weight and preterm birth. Objective: To determine the effect of interferon-beta exposure during pregnancy on pregnancy outcomes in multiple sclerosis patients. Methods: We compared the pregnancy outcomes of women exposed to interferon-beta with pregnancies unexposed to disease-modifying therapies. Women were enrolled into the German Multiple Sclerosis and Pregnancy Registry. A standardized questionnaire was administered during pregnancy and postpartum. Detailed information on course of multiple sclerosis and pregnancy, concomitant medications, delivery, and outcome of pregnancy was…

AdultPediatricsmedicine.medical_specialtyMultiple SclerosisBirth weightGerman03 medical and health sciences0302 clinical medicinePregnancyGermanymedicineBirth WeightHumansImmunologic Factors030212 general & internal medicineProspective StudiesRegistriesProspective cohort studyPregnancy registryPregnancyInterferon betabusiness.industryMultiple sclerosisInfant NewbornAbnormalities Drug-InducedInterferon-betamedicine.diseaselanguage.human_languageBody HeightAbortion SpontaneousPregnancy ComplicationsFirst trimesterPregnancy Trimester FirstNeurologylanguagePremature BirthFemaleNeurology (clinical)business030217 neurology & neurosurgeryMultiple sclerosis (Houndmills, Basingstoke, England)
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[Fetal pseudohypoaldosteronism: rare cause of hydramnios].

2005

PHA is a rare cause of hydramnios, characterized by increased amniotic fluid levels of aldosterone and sodium. Two distinct genetic entities (PHA type I and PHA type II) are included. Both are stemmed by a target organ defect with diminished renal tubular responsiveness to aldosterone. The AA present a case in which pregnancy resulted in a preterm infant with severe hydramnios, metabolic acidosis, hyponatriemia, hyperkaliemia. Salt and fluid replacement significantly improved clinical and metabolic condition. However a growth deficiency (-2 SDS) persists at follow-up.

AdultPolyhydramniosFetal DiseasesPolyhydramnioCesarean SectionPregnancyPseudohypoaldosteronismInfant NewbornHumansFemalePrognosisGrowth DisordersInfant PrematureLa Pediatria medica e chirurgica : Medical and surgical pediatrics
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