Search results for "types"

showing 10 items of 956 documents

Integrating Telemedicine Solutions with Electronic Health Records; Evaluation of Alternatives based on the Proposed Reference Architecture for Norway…

2016

This report studies the way forward for how a telemedicine solution can be integrated for exchange of data with an existing Electronic Health Record (EHR) system. The solution used an example for this report is based on a telemedicine solution for COPD patients (Chronic Obstructive Pulmonary Disease) developed in the project “Collaborative Point-of-Care Services Agder: Follow-up of COPD patients as part of the United4Health EU Project», with financial support from the Research Council of Norway. In addition, the EHR solution from DIPS ASA is used as an example of an existing system for integration. Important parameters for choosing way forward on how to are:  urgency with regards to timeli…

OpenEHRVDP::Teknologi: 500::Medisinsk teknologi: 620FHIREHR integrationArchetypesXDSVDP::Teknologi: 500::Informasjons- og kommunikasjonsteknologi: 550TelemedicineStandardizationHL7
researchProduct

Phospho-p38 MAPK expression in COPD patients and asthmatics and in challenged bronchial epithelium

2015

<b><i>Background:</i></b> The role of mitogen-activated protein kinases (MAPK) in regulating the inflammatory response in the airways of patients with chronic obstructive pulmonary disease (COPD) and asthmatic patients is unclear. <b><i>Objectives:</i></b> To investigate the expression of activated MAPK in lungs of COPD patients and in bronchial biopsies of asthmatic patients and to study MAPK expression in bronchial epithelial cells in response to oxidative and inflammatory stimuli. <b><i>Methods:</i></b> Immunohistochemical expression of phospho (p)-p38 MAPK, p-JNK1 and p-ERK1/2 was measured in bronchial mucosa in pat…

P38 MAPKMaleMAPK/ERK pathwayAsthma phenotypeSMOKERespiratory SystemMitogen-activated protein kinases; p65; Pathology of chronic obstructive pulmonary disease; Chronic obstructive pulmonary disease phenotypes; Asthma phenotypesPathology of chronic obstructive pulmonary diseasep38 Mitogen-Activated Protein KinasesChronic obstructive pulmonary disease phenotypePulmonary Disease Chronic ObstructiveOXIDATIVE STRESSMACROPHAGESRespiratory systemMitogen-activated protein kinasesChronic obstructive pulmonary disease phenotypesMitogen-activated protein kinases; p65; pathology of chronic obstructive pulmonary disease phenotypes; asthma phenotypesCOPDp65KinaseAsthma phenotypes; Chronic obstructive pulmonary disease phenotypes; Mitogen-activated protein kinases; p65; Pathology of chronic obstructive pulmonary disease; Pulmonary and Respiratory MedicineACTIVATED PROTEIN-KINASEInterleukinMiddle AgedImmunohistochemistrypathology of chronic obstructive pulmonary disease phenotypesAsthma phenotypesFemaleLife Sciences & BiomedicinePulmonary and Respiratory Medicinep38 mitogen-activated protein kinasesBlotting WesternINHIBITIONSocio-culturaleBronchiRespiratory MucosaOBSTRUCTIVE PULMONARY-DISEASE1102 Cardiovascular Medicine And HaematologyCell LinemedicineHumansLymphocyte CountInterleukin 8AgedAsthmaScience & Technologybusiness.industryInterleukin-8Transcription Factor RelAPATHWAYSMitogen-activated protein kinasemedicine.diseaseAsthmarespiratory tract diseasesSEVERITYCase-Control StudiesCELLSImmunologybusiness
researchProduct

Paraphyly of the Blue Tit (Parus caeruleus) suggested from cytochrome b sequences

2002

The phylogenetic relationships of the Blue Tit-Azure Tit assemblage (genus Parus; Aves: Passeriformes) were studied using mitochondrial DNA sequences of 24 specimens representing seven subspecies from Eurasia and North Africa. Previous work based on comparative morphological and acoustic data suggested a division of the Blue Tit (Parus caeruleus) into two species. Our analyses clearly indicate that the Blue Tit represents a paraphyletic assemblage, including a European/Middle Asian clade that is the sister group to the Azure Tit (Parus cyanus) and a North African clade. The North African clade (teneriffae subspecies group) is a sister group to the European Blue Tit/Azure Tit clade. We sugge…

ParaphylyAsiaZoologySubspeciesBiologyDNA MitochondrialBirdsAfrica NorthernGeneticsAnimalsCladeMolecular BiologyPhylogenyEcology Evolution Behavior and SystematicsParusLikelihood FunctionsPhylogenetic treeCytochrome bEcologyGenetic VariationCytochrome b Groupbiology.organism_classificationEuropeHaplotypesSister groupMutationMolecular phylogeneticsMolecular Phylogenetics and Evolution
researchProduct

Modelling the spatial and temporal constrains of the GABAergic influence on neuronal excitability

2021

GABA (γ-amino butyric acid) is an inhibitory neurotransmitter in the adult brain that can mediate depolarizing responses during development or after neuropathological insults. Under which conditions GABAergic membrane depolarizations are sufficient to impose excitatory effects is hard to predict, as shunting inhibition and GABAergic effects on spatiotemporal filtering of excitatory inputs must be considered. To evaluate at which reversal potential a net excitatory effect was imposed by GABA (EGABAThr), we performed a detailed in-silico study using simple neuronal topologies and distinct spatiotemporal relations between GABAergic and glutamatergic inputs. These simulations revealed for GABAe…

Patch-Clamp TechniquesAction potentialPhysiologyAction PotentialsSynaptic TransmissionNervous SystemBiochemistryMiceNerve FibersAnimal CellsMedicine and Health SciencesGABAergic NeuronsBiology (General)gamma-Aminobutyric AcidNeuronsMembrane potentialEcologyChemistryPyramidal CellsDepolarizationNeurochemistryNeurotransmittersCA3 Region HippocampalElectrophysiologyReceptors GlutamateComputational Theory and MathematicsModeling and SimulationExcitatory postsynaptic potentialGABAergicAnatomyCellular TypesShunting inhibitionResearch Articlemedicine.drugQH301-705.5Models NeurologicalNeurophysiologyAMPA receptorMembrane Potentialgamma-Aminobutyric acidCellular and Molecular NeuroscienceGlutamatergicSpatio-Temporal AnalysisGeneticsmedicineAnimalsComputer SimulationReceptors AMPAReversal potentialMolecular BiologyEcology Evolution Behavior and SystematicsComputational BiologyBiology and Life SciencesNeural InhibitionDendritesCell BiologyNeuronal DendritesAxonsMice Inbred C57BLAnimals Newbornnervous systemCellular NeuroscienceSynapsesDepolarizationNeuroscienceNeurosciencePLOS Computational Biology
researchProduct

Reconstruction of Endometrium from Human Endometrial Side Population Cell Lines

2011

Endometrial regeneration is mediated, at least in part, by the existence of a specialized somatic stem cell (SSC) population recently identified by several groups using the side population (SP) technique. We previously demonstrated that endometrial SP displays genotypic, phenotypic and the functional capability to develop human endometrium after subcutaneous injection in NOD-SCID mice. We have now established seven human endometrial SP (hESP) cell lines (ICE 1-7): four from the epithelial and three from the stromal fraction, respectively. SP cell lines were generated under hypoxic conditions based on their cloning efficiency ability, cultured for 12-15 passages (20 weeks) and cryopreserved.…

PathologyAnatomy and PhysiologyCellular differentiationlcsh:MedicineVimentinCell SeparationMice SCIDEndometriumEndometriumMice0302 clinical medicineMice Inbred NODReproductive PhysiologyMolecular Cell Biologylcsh:ScienceSide-Population CellsMedicine(all)0303 health scienceseducation.field_of_study030219 obstetrics & reproductive medicineMultidisciplinaryAgricultural and Biological Sciences(all)biologyStem CellsObstetrics and GynecologyCell DifferentiationAdult Stem Cellsmedicine.anatomical_structurePhenotypeSomatic CellsMedicineFemaleCellular Types/dk/atira/pure/subjectarea/asjc/2700Receptors ProgesteroneAdult stem cellResearch Articlemedicine.medical_specialtyStromal cellPopulationCell Line/dk/atira/pure/subjectarea/asjc/130003 medical and health sciencesSide population/dk/atira/pure/subjectarea/asjc/1100medicineAnimalsHumansRegenerationeducationBiology030304 developmental biologyBiochemistry Genetics and Molecular Biology(all)lcsh:RMesenchymal stem cellEstrogen Receptor alphaReproductive SystemEpithelial CellsMesenchymal Stem CellsMolecular biologyKaryotypingbiology.proteinlcsh:QStromal CellsStem Cell LinesBiomarkersCytometry
researchProduct

Haploinsufficiency of 16.4 Mb from chromosome 22pter-q11.21 in a girl with unilateral conductive hearing loss.

2009

We present the postnatal diagnosis of a de novo der(18)t(18;22)(p11.32;q11.21)pat, resulting in an unbalanced 45,XX,der (18)t(18;22) karyotype in a girl with conductive hearing loss on the left and ptosis of the right upper eye-lid. Unilateral ptosis was also observed in the patient’s 2 years and 8 months younger sister, who grows noticeably faster and appears to be a much quicker learner. After speech therapy the patient was eventually placed in normal school. The haploinsufficient 16.4-Mb region on chromosome 22pter→q11.21 contains 10 genes as well as many predicted genes, pseudogenes, and retrotransposed sequences with unknown functions. This observation may prove useful for prenatal dia…

Pathologymedicine.medical_specialtymedia_common.quotation_subjectChromosomes Human Pair 22BiologyHearing Loss UnilateralGeneticsmedicineHumansSpeechGirlMolecular BiologyGenetics (clinical)media_commonGeneticsInfant NewbornChromosomeKaryotypemedicine.diseaseConductive hearing lossHaplotypesKaryotypingFemaleUnilateral conductive hearing lossHaploinsufficiencyChromosomes Human Pair 18Chromosome 22Cytogenetic and genome research
researchProduct

The multifaceted spectrum of liver cirrhosis in older hospitalised patients: Analysis of the REPOSI registry

2021

Abstract Background Knowledge on the main clinical and prognostic characteristics of older multimorbid subjects with liver cirrhosis (LC) admitted to acute medical wards is scarce. Objectives To estimate the prevalence of LC among older patients admitted to acute medical wards and to assess the main clinical characteristics of LC along with its association with major clinical outcomes and to explore the possibility that well-distinguished phenotypic profiles of LC have classificatory and prognostic properties. Methods A cohort of 6,193 older subjects hospitalised between 2010 and 2018 and included in the REPOSI registry was analysed. Results LC was diagnosed in 315 patients (5%). LC was ass…

Patient Discharge.RegistrieAgingmedicine.medical_specialtyCirrhosisphenotypeliver cirrhosisAftercareOlder populationNOolder people03 medical and health sciencesSocial support0302 clinical medicinePhenotypic analysisOlder patientsInternal medicinemedicineHumansRegistries030212 general & internal medicineLS4_4Hospital MortalityAgedbusiness.industryhospitalisationliver cirrhosiHazard ratioConfoundingphenotypesGeneral Medicinemedicine.diseasedisability; hospitalisation; liver cirrhosis; mortality; older people; phenotypes; Aged; Hospital Mortality; Hospitalization; Humans; Liver Cirrhosis; Registries; Aftercare; Patient DischargemortalityPatient DischargeHospitalizationdisabilityCohortdisability hospitalisation liver cirrhosis mortality older people phenotypes030211 gastroenterology & hepatologyGeriatrics and Gerontologybusinessdisability; hospitalisation; liver cirrhosis; mortality; older people; phenotypesHuman
researchProduct

Neuropsychologic phenotypes in familial hemiplegic migraine

2003

Familial hemiplegic migraine (FHM) is a rare autosomal dominant-type migraine with aura. Attacks are characterised by hemiparesis in addition to other aura and migraine symptoms. Few studies have examined the influence of FHM on cognitive functions. This study was aimed to investigate neuropsychological functions in 3 adolescent siblings suffering from FHM assessed six months after the last attack. No relevant deficits were found on a battery of multisectorial tests exploring cognitive functions. Sporadic FHM attack therefore seems not to affect cognition in these patients, at least far from the crises.

Pediatricsmedicine.medical_specialtyAurabusiness.industryOriginalNeuropsychologyCognitionGeneral MedicineNeurological disordermedicine.diseaseKey words Familial hemiplegic migraineMigraine with auraDevelopmental psychologyCognitive functionsAnesthesiology and Pain MedicineMigraineNeuropsychologiamedicineNeuropsychologic phenotypesNeurology (clinical)medicine.symptombusinessFamilial hemiplegic migraineThe Journal of Headache and Pain
researchProduct

Epidemiology of stroke and transient ischemic attacks: Current knowledge and perspectives

2015

International audience; Because of the growing size and aging of the world's population, the global burden of stroke is increasing dramatically. Current epidemiological data indicate that 16.9 million people suffer a stroke each year, which represents a global incidence of 258/100,000 year, with marked differences between high- and low-income countries, and an age-adjusted incidence 1.5 times higher in men than in women. Although primary prevention has contributed to a decrease in stroke incidence in high-income countries, the so-called 'epidemiological transition' has led to an increase in incidence in middle-to-low-income countries as well. In addition, the incidence of ischemic stroke in…

Pediatricsmedicine.medical_specialtyEpidemiologylate 20th-centuryPopulationPsychological intervention030204 cardiovascular system & hematologyGlobal Health03 medical and health sciences0302 clinical medicineetiologic subtypescaribbean population[ SDV.MHEP ] Life Sciences [q-bio]/Human health and pathologyEpidemiologymedicineGlobal healthPrevalenceHumansMortality30-day case-fatalityeducationTransient ischemic attackrisk-factorsStrokeDepression (differential diagnoses)education.field_of_studybusiness.industrycommunity strokeIncidence (epidemiology)Incidencecase-fatality ratesmedicine.disease3. Good healthStrokeEpidemiological transitionNeurologyRisk factorsIschemic Attack Transientquality-of-life1st-ever strokeNeurology (clinical)Francebusiness28-day case-fatality030217 neurology & neurosurgery[SDV.MHEP]Life Sciences [q-bio]/Human health and pathologyDemography
researchProduct

Machine learning: A modern approach to pediatric asthma

2021

Among modern methods of statistical and computational analysis, the application of machine learning (ML) to healthcare data has been gaining recognition in helping us understand the heterogeneity of asthma and predicting its progression. In pediatric research, ML approaches may provide rapid advances in uncovering asthma phenotypes with potential translational impact in clinical practice. Also, several accurate models to predict asthma and its progression have been developed using ML. Here, we provide a brief overview of ML approaches recently proposed to characterize pediatric asthma.

Phenotypemachine learningchildrenasthma children machine learning phenotypesImmunologyPediatrics Perinatology and Child Healthasthma children machine learning phenotypesphenotypesHumansImmunology and AllergyasthmaChildrespiratory tract diseases
researchProduct