Search results for "newborn"

showing 10 items of 1435 documents

The Relationship between Fatigue in Mothers and the Age of Their Less-Than-24-Month-Old Newborns

2021

The birth of a child marks the beginning of a new developmental period for the parents. These changes have positive but also negative aspects, such as the increase in fatigue experienced by mothers during this period of time, which can be very limiting and lead them to postpone other life or work goals. However, despite the widespread nature of this problem, there is a lack of information about the duration of this fatigue, with estimates ranging from three months to six years

030504 nursingbusiness.industryHealth Toxicology and MutagenesismotherhoodRPublic Health Environmental and Occupational HealthInfant NewbornInfantMothersLimitingArticle03 medical and health sciences0302 clinical medicineChild PreschoolMedicineMedicineHumansfatigueFemale030212 general & internal medicine0305 other medical sciencebusinessChildDemographyInternational Journal of Environmental Research and Public Health
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Effects of maternal singing during kangaroo care on maternal anxiety, wellbeing, and mother-infant relationship after preterm birth: a mixed methods …

2020

Introduction: Preterm birth may disturb the typical development of the mother– infant relationship, when physical separation and emotional distress in the neonatal intensive care unit may increase maternal anxiety and create challenges for early interaction. This cluster-randomized controlled trial examined the effects of maternal singing during kangaroo care on mothers’ anxiety, wellbeing, and the early mother– infant relationship after preterm birth. Method: In the singing intervention group, a certified music therapist guided the mothers (n = 24) to sing or hum during daily kangaroo care during 33–40 gestational weeks (GW). In the control group, the mothers (n = 12) conducted daily kanga…

030506 rehabilitationNeonatal intensive care unitMother infantmusiikkiterapiaMUSIC-THERAPYvanhempi-lapsisuhdePARENTSEmotional distressMedicineEarly interactionWEIGHT INFANTSPREMATURE-INFANTSmaternal singingearly interactionKangaroo careNEWBORNS05 social sciencesEXPERIENCEShumanities3. Good healthemotional connectionkeskosetennenaikainen synnytysPshychiatric Mental HealthMaternal anxietySinging0305 other medical scienceClinical psychologyNICUMusic therapy515 Psychology050105 experimental psychologypreterm infant03 medical and health sciencesArts and Humanities (miscellaneous)tunteetahdistus0501 psychology and cognitive sciencesEXPOSUREvarhainen vuorovaikutusmaternal anxietybusiness.industryVOICEpreterm birthlaulaminenComplementary and alternative medicineAnthropologyPhysical separationäitiysFATHERSbusinessNordic Journal of Music Therapy
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Paternal uniparental disomy chromosome 14-like syndrome due a maternal de novo 160 kb deletion at the 14q32.2 region not encompassing the IG- and the…

2015

The human chromosome 14q32 carries a cluster of imprinted genes which include the paternally expressed genes (PEGs) DLK1 and RTL1, as well as the maternally expressed genes (MEGs) MEG3, RTL1as, and MEG8. PEGs and MEGs expression at the 14q32.2-imprinted region are regulated by two differentially methylated regions (DMRs): the IG-DMR and the MEG3-DMR, which are respectively methylated on the paternal and unmethylated on the maternal chromosome 14 in most cells. Genetic and epigenetic abnormalities affecting these imprinted gene clusters result in two different phenotypes currently known as maternal upd(14) syndrome and paternal upd(14) syndrome. However, only few patients carrying a maternal…

14q32.2 imprinted regionGenotypeBiologyPregnancy ProteinsMEG3-DMRGenomic ImprintingPaternal uniparental disomy chromosome 14 [upd(14)pat]GeneticsmedicineHumans14q32.2 maternal deletionEpigenetics"coat-hanger" rib signGeneGenetics (clinical)Sequence DeletionGeneticsMEG3Chromosomes Human Pair 14Comparative Genomic HybridizationIG-DMRMEG3 geneCalcium-Binding ProteinsInfant NewbornChromosomeMembrane ProteinsSyndromeDNA MethylationUniparental Disomymedicine.diseasePrognosisPhenotypeMolecular biologyUniparental disomyDifferentially methylated regionsPhenotypeSkeletal dysplasiaIntercellular Signaling Peptides and ProteinsFemaleRNA Long NoncodingRTL1as geneGenomic imprintingAmerican journal of medical genetics. Part A
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Layer-Specific Refinement of Sensory Coding in Developing Mouse Barrel Cortex

2017

Rodent rhythmic whisking behavior matures during a critical period around 2 weeks after birth. The functional adaptations of neocortical circuitry during this developmental period remain poorly understood. Here, we characterized stimulus-evoked neuronal activity across all layers of mouse barrel cortex before, during, and after the onset of whisking behavior. Employing multi-electrode recordings and 2-photon calcium imaging in anesthetized mice, we tested responses to rostro-caudal whisker deflections, axial "tapping" stimuli, and their combination from postnatal day 10 (P10) to P28. Within this period, whisker-evoked activity of neurons displayed a general decrease in layer 2/3 (L2/3) and …

2805 Cognitive NeuroscienceMale0301 basic medicineNeurogenesisCognitive NeurosciencePeriod (gene)2804 Cellular and Molecular Neuroscience610 Medicine & healthSensory systemStimulationBiologySomatosensory system03 medical and health sciencesCellular and Molecular Neuroscience0302 clinical medicineCalcium imagingPhysical StimulationAnimalsPremovement neuronal activityNeuronsAfferent PathwaysNeuronal Plasticity10242 Brain Research InstituteWhisking in animalsSomatosensory CortexBarrel cortexMice Inbred C57BL030104 developmental biologyAnimals NewbornVibrissae570 Life sciences; biologyFemaleSensory DeprivationNeuroscience030217 neurology & neurosurgery
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Nanodesign of new self-assembling core-shell gellan-transfersomes loading baicalin and in vivo evaluation of repair response in skin

2017

Gellan nanohydrogel and phospholipid vesicles were combined to incorporate baicalin in new self-assembling core-shell gellan-transfersomes obtained by an easy, scalable method. The vesicles were small in size (~107 nm) and monodispersed (P.I. ≤ 0.24), forming a viscous system (~24 mPa/s) as compared to transfersomes (~1.6 mPa/s), as confirmed by rheological studies. Gellan was anchored to the bilayer domains through cholesterol, and the polymer chains were distributed onto the outer surface of the bilayer, thus forming a core-shell structure, as suggested by SAXS analyses. The optimal carrier ability of core-shell gellan-transfersomes was established by the high deposition of baicalin in th…

3003SwinePharmaceutical ScienceMedicine (miscellaneous)02 engineering and technology01 natural sciencesMicechemistry.chemical_compoundDrug Delivery Systemsmaterials science (all)skin deliveryGeneral Materials ScienceSkinchemistry.chemical_classificationSkin repairSmall-angle X-ray scatteringBilayerVesicleAnti-Inflammatory Agents Non-SteroidalPolysaccharides BacterialPolymer021001 nanoscience & nanotechnologymedicine.anatomical_structureMolecular MedicineFemale0210 nano-technologytransfersomesSkin AbsorptionBiomedical EngineeringgellanBioengineeringAdministration Cutaneous010402 general chemistryIn vivo studiesDermisIn vivoSAXS analysismedicineAnimalsgellan; In vivo studies; rheological studies; SAXS analysis; skin delivery; transfersomes; bioengineering; medicine (miscellaneous); molecular medicine; biomedical engineering; materials science (all); 3003rheological studiesFlavonoidsInflammationWound Healing0104 chemical sciencesAnimals NewbornchemistryLiposomesBiophysicsNanoparticlesBaicalin
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A 3D‑scaffold of PLLA induces the morphological differentiation and migration of primary astrocytes and promotes the production of extracellular vesi…

2019

The present study analyzed the ability of primary rat astrocytes to colonize a porous scaffold, mimicking the reticular structure of the brain parenchyma extracellular matrix, as well as their ability to grow, survive and differentiate on the scaffold. Scaffolds were prepared using poly-L-lactic acid (PLLA) via thermally-induced phase separation. Firstly, the present study studied the effects of scaffold morphology on the growth of astrocytes, evaluating their capability to colonize. Specifically, two different morphologies were tested, which were obtained by changing the polymer concentration in the starting solution. The structures were characterized by scanning electron microscopy, and a…

3D culture0301 basic medicineCancer ResearchScaffoldCell SurvivalPolyestersneural tissue engineeringBiochemistryNeural tissue engineeringExtracellular matrixExtracellular Vesicles03 medical and health sciences0302 clinical medicineSettore BIO/13 - Biologia ApplicataCell MovementSettore BIO/10 - BiochimicaGeneticsExtracellularAnimalsSettore BIO/06 - Anatomia Comparata E CitologiaRats WistarCell ShapeMolecular BiologyCells CulturedNeural tissue engineering astrocytes 3D cultures poly‑L‑ lactic acid scaffold extracellular vesicles.Cell ProliferationSettore ING-IND/24 - Principi Di Ingegneria Chimica3D culturesTissue ScaffoldsbiologyChemistryastrocytesCell DifferentiationArticlesMicrovesiclesFibronectin030104 developmental biologyAnimals NewbornOncology030220 oncology & carcinogenesisReticular connective tissuepoly-L-lactic acid scaffoldbiology.proteinBiophysicsMolecular MedicineExtracellular vesicleAstrocyteIntracellularMolecular Medicine Reports
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Two-dimensional and three-dimensional sonography of conjoined twins.

2002

Purpose The aim of this study was to evaluate and compare the diagnostic capabilities of 2-dimensional (2D) and 3-dimensional (3D) sonography for the study of conjoined twins. Methods Four pregnant women with an initial 2D sonographic diagnosis of conjoined twins were examined with color Doppler sonography, 3D multiplanar sonography, and orthogonal plane imaging and 3D surface rendering. Results All 4 cases of conjoined twins were initially diagnosed with either transvaginal or transabdominal 2D sonography. 3D sonography afforded more realistic views and demonstrated more clearly the linking areas and surface anomalies, but 2D and color Doppler sonography provided more definitive and specif…

3d sonographyAdultMalemedicine.medical_specialty3 dimensional ultrasonographybusiness.industryOrthogonal planeUltrasoundInfant NewbornColor dopplermedicine.diseaseSurgeryPregnancyConjoined twinsmedicineHumansRadiology Nuclear Medicine and imagingSurface renderingFemaleRadiologyUltrasonographyUltrasonography Doppler ColorbusinessTwins ConjoinedUltrasonographyJournal of clinical ultrasound : JCU
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An extensive pattern of atypical neural speech-sound discrimination in newborns at risk of dyslexia.

2019

Objective: Identifying early signs of developmental dyslexia, associated with deficient speech-sound processing, is paramount to establish early interventions. We aimed to find early speech-sound processing deficiencies in dyslexia, expecting diminished and atypically lateralized event-related potentials (ERP) and mismatch responses (MMR) in newborns at dyslexia risk. Methods: ERPs were recorded to a pseudoword and its variants (vowel-duration, vowel-identity, and syllable-frequency changes) from 88 newborns at high or no familial risk. The response significance was tested, and group, laterality, and frontality effects were assessed with repeated-measures ANOVA. Results: An early positive a…

6162 Cognitive scienceMaleSpeech soundAudiologyEvent-related potential (ERP)Dyslexia0302 clinical medicineEARLY LANGUAGE-ACQUISITIONnewbornMedicineFAMILIAL RISKAuditoryBRAIN RESPONSES05 social sciencesevent-related potential (ERP)ElectroencephalographySensory SystemsLanguage developmentNeurologyLateralityEvoked Potentials AuditorySpeech PerceptionFemaleAnalysis of variancespeech soundpsychological phenomena and processesmedicine.medical_specialty515 PsychologyMISMATCH NEGATIVITY MMNCORTICAL RESPONSESEVENT-RELATED POTENTIALSGENETIC RISKbehavioral disciplines and activities050105 experimental psychology03 medical and health sciencesSpeech discriminationEvent-related potentialPhoneticsPhysiology (medical)Vowelotorhinolaryngologic diseasesdysleksiaHumansSpeech0501 psychology and cognitive sciencesauditoryAUDITORY-DISCRIMINATIONMismatch response (MMR)vastasyntyneetAuditory Cortexbusiness.industrypuheääni3112 NeurosciencesDyslexiaInfant NewbornNewbornmismatch response (MMR)medicine.diseaseta3124PseudowordPHONEME MISMATCHAcoustic StimulationDEVELOPMENTAL DYSLEXIANeurology (clinical)business030217 neurology & neurosurgeryClinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
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Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study.

2015

INTRODUCTION: Published prevalence rates of congenital diaphragmatic hernia (CDH) vary. This study aims to describe the epidemiology of CDH using data from high-quality, population-based registers belonging to the European Surveillance of Congenital Anomalies (EUROCAT).METHODS: Cases of CDH delivered between 1980 and 2009 notified to 31 EUROCAT registers formed the population-based case series. Prevalence over time was estimated using multilevel Poisson regression, and heterogeneity between registers was evaluated from the random component of the intercept.RESULTS: There were 3373 CDH cases reported among 12 155 491 registered births. Of 3131 singleton cases, 353 (10.4%) were associated wit…

ANOMALIESAdultMalePediatricsmedicine.medical_specialtyAUSTRALIAAdolescentPopulationPrevalencePrenatal diagnosisGestational AgeEurope/epidemiologysymbols.namesakeYoung AdultEpidemiologyPrevalenceMedicineBirth WeightHumansMALFORMATIONSAbnormalities MultiplePoisson regressionRegistriesPRENATAL-DIAGNOSISeducationeducation.field_of_studybusiness.industryMORTALITYInfant NewbornObstetrics and GynecologyCongenital diaphragmatic herniaGestational ageGeneral MedicineDEFECTSmedicine.diseaseSurvival AnalysisCongenital anomalies ; Diaphragmal hernia ; Epidemiology ; EuropeEuropeHernias Diaphragmatic Congenital/epidemiologyRelative riskPopulation SurveillancePediatrics Perinatology and Child HealthsymbolsAbnormalities Multiple/epidemiologyFemalebusinessHernias Diaphragmatic CongenitalMaternal AgeArchives of disease in childhood. Fetal and neonatal edition
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Anorectal malformations and pregnancy-related disorders: a registry-based case-control study in 17 European regions

2013

Objective To identify pregnancy-related risk factors for different manifestations of congenital anorectal malformations (ARMs).Design A population-based case-control study.Setting Seventeen EUROCAT (European Surveillance of Congenital Anomalies) registries, 1980-2008.Population The study population consisted of 1417 cases with ARM, including 648 cases of isolated ARM, 601 cases of ARM with additional congenital anomalies, and 168 cases of ARM-VACTERL (vertebral, anal, cardiac, tracheo-esophageal, renal, and limb defects), along with 13371 controls with recognised syndromes or chromosomal abnormalities.Methods Multiple logistic regression analyses were used to calculate adjusted odds ratios …

ANOMALIESaetiologyMaternalLogistic regressionAnus ImperforateEpilepsyPre-EclampsiaMEDICATION USEPregnancyRisk FactorsOdds RatioAetiologymedia_commoneducation.field_of_studyObstetricsMATERNAL EXPOSUREObstetrics and GynecologyAnal atresiaCONGENITAL-MALFORMATIONSAnorectal MalformationsEuropeParityHuman Reproduction Renal disorder [NCEBP 12]Population studyFemaleAnal Atresiamedicine.medical_specialtyFeverReproductive Techniques Assistedmedia_common.quotation_subjectPopulationFertilityGenomic disorders and inherited multi-system disorders [IGMD 3]VACTERLmedicineanorectal malformations; anal atresia; birth defects; aetiology; maternal; pregnancy; VACTERLHumansAbnormalities MultipleBirth DefectseducationPregnancyEpilepsybusiness.industryRENACCase-control studyInfant NewbornAbortion InducedOdds ratioBIRTH-DEFECTS PREVENTIONBECKWITH-WIEDEMANN-SYNDROMEHuman Reproducion Genomic disorders and inherited multi-system disorders [NCEBP 12]Estados de Saúde e de Doençamedicine.diseasePregnancy Complicationsmaternalbirth defectsEvaluation of complex medical interventions [NCEBP 2]Case-Control StudiesRISK-FACTORSPregnancy TwinMULTIPLE BIRTHSbusinessIN-VITRO FERTILIZATION
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