Search results for "newborn."

showing 10 items of 1433 documents

Age-related changes in the expression of CD95 (APO1/FAS) on blood lymphocytes☆

1999

Abstract Aging is associated with alterations of the immune system, thought to be related to an increased susceptibility to infectious diseases, and possibly to cancer and autoimmunity in the elderly. In the present paper we report data obtained on freshly collected blood from 148 healthy subjects of different ages (from cord blood to 102 years old). The subjects were divided into seven age classes (cord blood, 3–11 years, 15–39 years, 41–60 years, 61–74 years, 75–84 years, 85–102 years) and their lymphocyte subsets and the expression of the apoptosis-related molecule CD95 were evaluated. In respect of lymphocyte subsets, the major differences were found in the cord-blood samples compared w…

AdultMaleAgingAdolescentT-LymphocytesPopulationchemical and pharmacologic phenomenaBiologymedicine.disease_causeBiochemistryCD19AutoimmunityLeukocyte CountEndocrinologyImmune systemAntigens CDGeneticsmedicineHumansLymphocyte CountLymphocytesfas ReceptorChildeducationMolecular BiologyAgedAged 80 and overeducation.field_of_studyAge FactorsInfant NewbornGene Expression Regulation Developmentalhemic and immune systemsCell BiologyImmunosenescenceMiddle AgedFetal BloodFas receptorLymphocyte SubsetsChild PreschoolCord bloodImmunologybiology.proteinFemaleCD8Experimental Gerontology
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Maturation of near-field and far-field somatosensory evoked potentials after median nerve stimulation in children under 4 years of age

2000

Abstract Objectives : The maturation of subcortical SEPs in young children. Methods : Median nerve SEPs were recorded during sleep in 42 subjects aged 0–48 months. Active electrodes were at the ipsilateral Erb's point, the lower and upper dorsal neck, and the frontal and contralateral centroparietal scalp; reference electrodes were at the contralateral Erb's point, the ipsilateral earlobe and the frontal scalp; bandpass was 10–3000 Hz. The peaks were labelled by their latencies in adults. Results : The peak latencies of N9 (brachial plexus potential) decreased exponentially with age during the first year, but increased with height thereafter. The interpeak latencies (IPLs) N9–N11, which mea…

AdultMaleAgingCentral nervous systemSomatosensory systemFunctional LateralityEvoked Potentials SomatosensoryPhysiology (medical)Reaction TimemedicineHumansBrachial PlexusEarlobeScalpbusiness.industryInfant NewbornInfantAnatomyElectric StimulationSensory SystemsMedian nerveMedian Nervebody regionsElectrophysiologymedicine.anatomical_structureNeurologySomatosensory evoked potentialChild PreschoolScalpFemaleNeurology (clinical)businessBrachial plexusNeckClinical Neurophysiology
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Diet supplementation during early lactation with non-alcoholic beer increases the antioxidant properties of breastmilk and decreases the oxidative da…

2013

After delivery and birth, mothers and neonates are exposed to oxidative stress. We tested whether supplementing the diet of breastfeeding mothers with non-alcoholic beer, a product rich in antioxidants, could improve their oxidative status and the antioxidant content of their milk. A prospective trial begun on Day 2 postpartum was conducted in mother-infant dyads.Sixty breastfeeding mothers and their infants were allocated to either a control group (n=30) on a free diet or a study group (n=30) on a free diet supplemented with 660 mL of non-alcoholic beer/day. The oxidative status of the mothers' breastmilk, plasma, and urine and the infant's urine was analyzed on Days 2 and 30 postpartum. T…

AdultMaleAntioxidantUbiquinonemedicine.medical_treatmentBreastfeedingPhysiologyMothersCarbonated BeveragesUrinemedicine.disease_causePediatricsAntioxidantschemistry.chemical_compoundLactationMaternity and MidwiferyMedicineHumansLactationProspective StudiesProspective cohort studyCoenzyme Q10Milk Humanbusiness.industryHealth PolicyInfant NewbornObstetrics and GynecologyBeerInfantPolyphenolsNon alcoholicOxidative Stressmedicine.anatomical_structureBreast FeedingchemistryDietary SupplementsFemalebusinessOxidative stressFollow-Up StudiesBreastfeeding medicine : the official journal of the Academy of Breastfeeding Medicine
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Learning-induced neural plasticity of speech processing before birth

2013

Learning, the foundation of adaptive and intelligent behavior, is based on plastic changes in neural assemblies, reflected by the modulation of electric brain responses. In infancy, auditory learning implicates the formation and strengthening of neural long-term memory traces, improving discrimination skills, in particular those forming the prerequisites for speech perception and understanding. Although previous behavioral observations show that newborns react differentially to unfamiliar sounds vs. familiar sound material that they were exposed to as fetuses, the neural basis of fetal learning has not thus far been investigated. Here we demonstrate direct neural correlates of human fetal l…

AdultMaleAuditory perceptionmedicine.medical_specialtySpeech perceptionMULTIFEATURE MMN PARADIGMBrain activity and meditation515 PsychologyAuditory learningeducationMismatch negativityLANGUAGEEVENT-RELATED POTENTIALSAudiologyPRINCIPAL-COMPONENTS-ANALYSISYoung Adult03 medical and health sciencesFetus0302 clinical medicineNeural ensembleMemoryPhoneticsPregnancyotorhinolaryngologic diseasesmedicineHumansLearning030304 developmental biology0303 health sciencesNeural correlates of consciousnessPERCEPTIONNeuronal PlasticityMultidisciplinaryBRAIN RESPONSESInfant NewbornElectroencephalographyBiological SciencesSpeech processingHUMAN-FETUSAcoustic StimulationDISCRIMINATIONSpeech Perceptionmismatch negativityFemalePHONEME REPRESENTATIONSPsychology030217 neurology & neurosurgeryCognitive psychology
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Association of Low Birth Weight With Altered Corneal Geometry and Axial Length in Adulthood in the German Gutenberg Health Study

2019

IMPORTANCE: Low birth weight is associated with altered ocular organ development in childhood, including the morphology of the eye. However, no population-based data exist about this association in adulthood. OBJECTIVE: To evaluate whether low birth weight has a long-term association with anterior segment anatomy and axial length in adulthood. DESIGN, SETTING, AND PARTICIPANTS: The Gutenberg Health Study is a population-based, observational cohort study in Germany. All participants underwent ocular biometry. Among the participants with follow-up and self-reported birth weight available, associations were assessed between low birth weight and anterior segment anatomy and axial length using m…

AdultMaleBirth weightPopulationGeometry01 natural sciencesCohort StudiesCornea03 medical and health sciences0302 clinical medicineCorneaGermanymedicineHumansIn patient0101 mathematicseducationOriginal InvestigationAgedAged 80 and overeducation.field_of_studybusiness.industry010102 general mathematicsInfant NewbornRetinopathy of prematurityAxial lengthInfant Low Birth WeightMiddle Agedmedicine.diseaseOphthalmologyLow birth weightAxial Length Eyemedicine.anatomical_structure030221 ophthalmology & optometryFemalemedicine.symptombusinessCohort study
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Burden of disease assessment with summary measures of population health for the Region of Valencia, Spain: a population-based study

2011

Abstract Background and objective An important input to decision-making and health planning is a consistent and comparative description of the population health status. The purpose of this study was to describe the burden of disease in the Region of Valencia (Spain). Material and methods Disability-adjusted life years (DALYs) were calculated and divided into years of life lost (YLLs) and years lived with disability (YLDs). Using death registry data and Valencian population estimates in 2008, we calculated the number of deaths and YLLs. YLDs were based on age- and sex-specific data for countries of the EURO-A subregional level (which includes the Region of Valencia) from the Global Burden of…

AdultMaleBurden of diseaseAdolescentSense organHealth StatusPopulationPopulation healthValencianYoung AdultAge DistributionLife ExpectancyCost of IllnessCause of DeathHumansMedicineDisabled PersonsSex DistributionChildeducationDiagnosis-Related GroupsDisease burdenDepression (differential diagnoses)AgedAged 80 and overeducation.field_of_studybusiness.industryInfant NewbornInfantGeneral MedicineMiddle Agedlanguage.human_languageYears of potential life lostSpainChild PreschoolChronic DiseaselanguageFemalebusinessDemographyMedicina Clínica
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New data from the Italian National Register of Congenital Coagulopathies, 2016 Annual Survey

2018

BACKGROUND: In Italy, the National Register of Congenital Coagulopathies (NRCC) collects epidemiological and therapeutic data from patients affected by haemophilia A (HA), haemophilia B (HB), von Willebrand’s disease (vWD) and other rare coagulation disorders. Here we present data from the 2016 annual survey. MATERIALS AND METHODS: Data are provided by the Italian Haemophilia Centres, on a voluntary basis. Information flows from every Centre to a web-based platform of the Italian Association of Haemophilia Centres, shared with the Italian National Institute of Health, in accordance with current privacy laws. Patients are classified by diagnosis, disease severity, age, gender and treatment-r…

AdultMaleCanadaAdolescentAdolescent Adult Aged Blood Coagulation Factors Canada Child Coagulation Protein Disorders Factor IX Factor VIII Female France HIV Infections Hemophilia A Hemophilia B Hepatitis CHumans Infant Infant Newborn Italy Male Middle Aged Prevalence Registries Surveys and Questionnaires United Kingdom von Willebrand DiseasesHIV InfectionsCoagulation Protein DisordersHemophilia AHemophilia BFactor IXhemic and lymphatic diseasesSurveys and QuestionnairesPrevalenceHumansRegistriesChildAgedFactor VIIIInfant NewbornInfantMiddle AgedHepatitis CBlood Coagulation FactorsUnited Kingdomvon Willebrand DiseasesItalyChild PreschoolFemaleOriginal ArticleFrance
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Is the risk of childhood leukaemia associated with socioeconomic measures in Denmark? A nationwide register‐based case‐control study

2021

The aetiology of childhood leukaemia is poorly understood. Knowledge about differences in risk by socioeconomic status (SES) may enhance etiologic insights. We conducted a nationwide register-based case-control study to evaluate socioeconomic differences in the risk of childhood leukaemia in Denmark and to access whether associations varied by different measures of SES, time point of assessment, leukaemia type and age at diagnosis. We identified all cases of leukaemia in children aged 0 to 19 years, born and diagnosed between 1980 and 2013 from the Danish Cancer Registry (N = 1336) and sampled four individually matched controls per case (N = 5330). We used conditional logistic regression mo…

AdultMaleCancer ResearchAdolescentOffspringDenmark610 Medizinsocioeconomic factorsDiseasesocioeconomic statusDanishYoung Adult03 medical and health sciencesmyeloid leukaemia0302 clinical medicinechildhood leukaemiaRisk Factors610 Medical scienceschildhood cancerHumansMedicineRegistriesChildSocioeconomic statusbusiness.industryInfant NewbornCase-control studyInfantOdds ratiolymphoid leukaemiaConfidence intervallanguage.human_languageregister-based studyCancer registryLeukemia Myeloid AcuteSocial ClassOncologyCase-Control StudiesChild Preschool030220 oncology & carcinogenesislanguageFemalebusinessDemographyInternational Journal of Cancer
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Antibodies against lytic and latent Kaposi's sarcoma-associated herpes virus antigens and lymphoma in the European EpiLymph case-control study.

2011

Background: Kaposi's sarcoma-associated herpes virus is associated with primary effusion lymphoma and multicentric Castleman's disease. Methods: Seropositivity to lytic and latent Kaposi's sarcoma herpes virus (KSHV) antigens were examined in 2083 lymphomas and 2013 controls from six European countries. Results: Antibodies against KSHV latent and lytic antigens were detectable in 4.5% and 3.4% of controls, respectively, and 3.6% of cases (P>0.05). The KSHV seropositivity was associated with splenic marginal zone lymphoma (SMZL) (odds ratio (OR)=4.11, 95% confidence interval (CI)=1.57–10.83) and multiple myeloma (OR=0.31, 95% CI=0.11–0.85). Conclusion: The KSHV is unlikely to contribute impo…

AdultMaleCancer ResearchAdolescentvirusesShort CommunicationserologylymphomaAntibodiesSerologyhuman herpes virus 8Young AdultHerpes virusAntigenhemic and lymphatic diseasesLymphoma Primary EffusionmedicineHumansChildKaposi's sarcomaAntigens ViralSarcoma KaposiAgedAged 80 and overbiologybusiness.industryCastleman DiseaseLymphoma Non-HodgkinCase-control studyInfant Newbornvirus diseasesInfantMiddle Agedmedicine.diseaseVirologyLymphomaEuropeOncologyLytic cycleKaposi's sarcoma-associated herpes virusCase-Control StudiesChild PreschoolImmunologyHerpesvirus 8 Humanbiology.proteinFemaleepidemiologyAntibodybusinessBritish journal of cancer
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Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.

2013

Agenesis of the corpus callosum (ACC), cerebellar hypoplasia (CBLH), and polymicrogyria (PMG) are severe congenital brain malformations with largely undiscovered causes. We conducted a large-scale chromosomal copy number variation (CNV) discovery effort in 255 ACC, 220 CBLH, and 147 PMG patients, and 2,349 controls. Compared to controls, significantly more ACC, but unexpectedly not CBLH or PMG patients, had rare genic CNVs over one megabase (p = 1.48×10−3; odds ratio [OR] = 3.19; 95% confidence interval [CI] = 1.89–5.39). Rare genic CNVs were those that impacted at least one gene in less than 1% of the combined population of patients and controls. Compared to controls, significantly more AC…

AdultMaleCancer ResearchMicrocephalycongenital hereditary and neonatal diseases and abnormalitiesAdolescentDNA Copy Number Variationslcsh:QH426-470Developmental DisabilitiesPopulationGenome-wide association studyBiologyNervous System MalformationsCorpus callosumPolymorphism Single Nucleotide03 medical and health sciences0302 clinical medicineCerebellummental disordersGeneticsPolymicrogyriamedicineHumansCopy-number variationChildAgenesis of the corpus callosumeducationMolecular BiologyGenetics (clinical)Ecology Evolution Behavior and SystematicsExome sequencing030304 developmental biologyGenetics0303 health scienceseducation.field_of_studyGenome HumanInfant NewbornInfantMiddle Agedmedicine.disease3. Good healthMalformations of Cortical Developmentlcsh:GeneticsChild PreschoolFemaleAgenesis of Corpus Callosum030217 neurology & neurosurgeryResearch ArticleGenome-Wide Association StudyPLoS Genetics
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