Search results for "correlation"

showing 10 items of 2282 documents

Occurrence and recovery potential of rare earth elements in Finnish peat and biomass combustion fly ash

2019

Rare earth elements (REEs) are highly important in the modern society as a result of their wide use in various fields of industry. Their high supply risk and increase in demand has led to classification as critical materials, and consequently, new resources for REEs are being prospected widely. Coal fly ash has been suggested as a possible secondary resource for REEs, but very little information is available regarding REE occurrence in biomass or peat derived fly ash. In this paper, fly ash samples from commercial power plants using peat and biomass as fuel were studied for REEs. The average concentration of REEs was 530 ppm, with up to 920 ppm in one fly ash. Five out of seven fly ashes we…

PeatesiintyvyysSecondary resourcebiomassaRare earthBiomass010501 environmental sciences010502 geochemistry & geophysicsPositive correlationoccurrence01 natural sciencesturverecoveryGeochemistry and Petrologylentotuhkabiomassa (teollisuus)ta1160105 earth and related environmental sciencesbiomassharvinaiset maametallitrare earth elementfly ashBiomass combustionFly ashEnvironmental chemistrypeatEnvironmental scienceEconomic GeologyJournal of Geochemical Exploration
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Correlation between neonatal outcomes of twins depends on the outcome : Secondary analysis of twelve randomised controlled trials

2018

ObjectiveTo estimate the magnitude of the correlation between neonatal outcomes of twins and demonstrate how this information can be used in the design of randomised controlled trials (RCTs) in women with twin pregnancies.DesignSecondary analysis of data from 12 RCTs.SettingObstetric care in multiple countries, 2004-2012.Population or sample4504 twin pairs born to women who participated in RCTs to assess treatments given during pregnancy.MethodsIntraclass correlation coefficients (ICCs) were estimated using log-binomial and linear models.Main outcome measuresPerinatal death, respiratory distress syndrome, bronchopulmonary dysplasia, intraventricular haemorrhage, necrotising enterocolitis, s…

PediatricsNeonatal intensive care unitIntraclass correlationPerinatal DeathBayesian analysisintraclass correlation coefficientInfant Newborn DiseasesCorrelationpowerDOUBLE-BLIND0302 clinical medicinePregnancyMedicine030212 general & internal medicineCorrelation of DataRandomized Controlled Trials as Topiceducation.field_of_study030219 obstetrics & reproductive medicineRespiratory distressPregnancy OutcomeObstetrics and Gynecologytwinssample sizeINTRACLUSTER CORRELATIONFemaleAdultmedicine.medical_specialtyPRETERM BIRTHPopulationGestational AgeArticle03 medical and health sciencesSMALL CLUSTERSPREGNANCIESHumanseducationPregnancyModels Statisticalbusiness.industryInfant NewbornPROGESTERONEmedicine.diseasePREVENTIONmeta-analysisBronchopulmonary dysplasiaSample size determinationPregnancy TwinMULTIPLE BIRTHSbusinessCORRELATION-COEFFICIENT17-ALPHA-HYDROXYPROGESTERONE CAPROATE
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Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2

2020

Alternating Hemiplegia of Childhood (AHC) is a rare disorder characterized by frequent, transient attacks of hemiplegia involving either side of the body or both in association to several other disturbances including dystonic spells, abnormal ocular movements, autonomic manifestations, epileptic seizures and cognitive impairment. The clinical manifestations usually start before the age of 18 months. Two forms of the disorder known as AHC-1 (MIM#104290) and AHC-2 (MIM#614820) depends on mutations in ATP1A2 and ATP1A3 genes respectively, with over 75% of AHC caused by a mutation in the ATP1A3 gene. Herewith, we report serial clinical follow-up data of monozygotic (MZ) twin sisters, who presen…

Pediatricsmedicine.medical_specialtyGenotype-phenotype correlationGenotypeTwinsHemiplegiaMonozygoticEpilepsyYoung AdultSettore MED/38 - Pediatria Generale E SpecialisticaATP1A2Alternating Hemiplegia of Childhood (AHC)ATP1A3GenotypeGeneticsmedicineHumansYoung adultATPase Na+/K+ transporting subunit alpha 2 (ATP1A2)Genetics (clinical)DystoniaATPase Na+/K+ transporting subunit alpha 3 (ATP1A3)business.industryAlternating hemiplegia of childhoodp.Asn773SerGeneral MedicineTwins Monozygoticmedicine.diseasePhenotypePhenotypeMutationFemaleSodium-Potassium-Exchanging ATPasebusiness
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Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcome

2020

Abstract Introduction Autosomal recessive polycystic kidney disease (ARPKD; MIM#263200) is one of the most frequent pediatric renal cystic diseases, with an incidence of 1:20,000. It is caused by mutations of the PKHD1 gene, on chromosome 6p12. The clinical spectrum is highly variable, ranging from late-onset milder forms to severe perinatal manifestations. The management of newborns with severe pulmonary insufficiency is challenging, and causes of early death are sepsis or respiratory failure. In cases of massive renal enlargement, early bilateral nephrectomy and peritoneal dialysis may reduce infant mortality. However, there is no conclusive data on the role of surgery, and decision-makin…

Pediatricsmedicine.medical_specialtyGenotype-phenotype correlationGenotypemedicine.medical_treatmentARPKDPulmonary insufficiencyReceptors Cell SurfaceCase ReportPeritoneal dialysisSepsis03 medical and health sciencesLiver diseaseConsanguinity0302 clinical medicineFatal OutcomeNext generation sequencingmedicineHumansGenetic Predisposition to DiseaseEthicPotter sequencePolycystic Kidney Autosomal RecessiveEthicsbusiness.industrylcsh:RJ1-570Infant Newbornlcsh:Pediatricsmedicine.diseaseAutosomal Recessive Polycystic Kidney DiseaseRespiratory failure030220 oncology & carcinogenesisMutationFemalebusiness030217 neurology & neurosurgeryInfant PrematureBilateral NephrectomyPotter sequence
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2q13 microdeletion syndrome: Report on a newborn with additional features expanding the phenotype

2021

In this paper we describe an additional newborn patient with craniofacial dysmorphisms, congenital heart disease, hypotonia and a 2q13 deletion of 1.7 Mb, whose clinical and genomic findings are consistent with the diagnosis of 2q13 microdeletion syndrome.

Pediatricsmedicine.medical_specialtyMedicine (General)Heart diseaseCNVgenotype-phenotype correlationR5-920newborngenotype‐phenotype correlationsfollow-upmedicineCraniofacialGenotype-Phenotype Correlationschromosome 2newborn.GeneticsCNVsfollow‐upbusiness.industryRGeneral MedicineMicrodeletion syndromemedicine.diseasePhenotypeHypotoniaMedicinemedicine.symptombusinessClinical Case Reports
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Correlation between mutans Streptococci counts of parents and their children residing in Chandigarh, India

2013

Objectives: To determine the prevalence of Mutans Streptococci (MS) in children and to evaluate the relationship between the salivary levels of MS in children and their parents. Material and Methods: 100 children aged 3-6 years along with their parents (100 mothers and fathers each) were included in the study. The children were segregated depending upon their age and level of caries experience. The children were examined clinically on an ordinary chair in natural daylight using the Møller’s index criteria. Assays for Mutans Streptococci (MS) were done for both the children and their parents using the Dentocult SM strip mutans test. Collected data was assessed using SPSS software. Results: T…

Pediatricsmedicine.medical_specialtySalivabusiness.industryResearchOdontología:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludCommunity and Preventive DentistryCorrelationUNESCO::CIENCIAS MÉDICASmedicinebusinessCaries experienceGeneral DentistryJournal of Clinical and Experimental Dentistry
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Benefit of using an age-adjusted D-dimer cut-off

2015

Introduction: The association between a low-moderate pretest clinical probability and a negative D-dimer (DD) value is able to exclude the possibility of pulmonary embolism (PE). The value of DD seems to increase with age, reducing its specificity. Therefore, we intend to evaluate the usefulness of an age-adjusted cut-off value for age above 50 years, applying the formula suggested by Douma (age*10) set to our laboratory method (age*5) (1) . Patients and Methods: Observational, retrospective study from January to December 2011. DD test were performed to 1515 patients attended in the emergency room of our hospital according to the clinical suspicion made by the doctor who evaluated them. The…

Pediatricsmedicine.medical_specialtybusiness.industryAge adjustmentRetrospective cohort studymedicine.diseasePositive correlationPredictive valuePulmonary embolismInternal medicineD-dimermedicinePearson Correlation TestCut-offbusiness4.3 Pulmonary Circulation and Pulmonary Vascular Disease
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982 Maternal Age, History of Migration and Incidence of Infantile Hypertrophic Pyloric Stenosis in Germany in 2000-2008

2012

Background The incidence of infantile hypertrophic pyloric stenosis (IHPS) is highly variable over time and geographic regions. A decline in IHPS incidence was recently reported in Sweden, the US, Denmark, and Scotland and in Germany. Aim In further evaluation of our previous epidemiological data, we collected data on maternal age and history of migration in mothers from the regional administrations. We examined correlations between these factors and IHPS incidence. Methods Data were extracted from the public report of Health (Gesundheitsberichterstattung des Bundes) and population data from federal state governments. We collected the numbers of IHPS (International Statistical Classificatio…

Pediatricsmedicine.medical_specialtybusiness.industryIncidence (epidemiology)First birthPediatrics Perinatology and Child HealthEpidemiologyPopulation dataMedicineInternational Statistical Classification of Diseases and Related Health ProblemsNegative correlationbusinessHypertrophic Pyloric StenosisFederal stateDemographyArchives of Disease in Childhood
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Intra- and Interrater Reliability of Sagittal Spinopelvic Parameters on Full-Spine Radiographs in Adults With Symptomatic Spinal Disorders

2018

Background/Aims To evaluate the intra- and interrater reliability (I-IR) of sagittal spinopelvic parameters from digital full-spine plain radiographs with basic software tools in an unselected adult population with degenerative spinal complaints who were evaluated for surgery. Methods Forty-nine adult full-spine digital radiographs were measured twice by 3 independent observers, including an experienced spine surgeon, an experienced radiologist, and a resident orthopedic surgeon. Clinical picture archiving and communication system workstations and software tools were used and landmarks were set manually. The I-IR of the sagittal vertical axis (SVA), pelvic tilt (PT), pelvic incidence (PI), …

Pelvic tiltmedicine.medical_specialtyIntraclass correlationradiographic imagediagnostic imagingRadiographyScoliosis/diagnostic imagingskolioosiSurgical planninglcsh:RC346-42903 medical and health sciences0302 clinical medicineselkäsairaudetmedicinestandarditta315lcsh:Neurology. Diseases of the nervous systemOrthodontics030222 orthopedicsscoliosisbusiness.industrysoftwareadultröntgentutkimusta3141RepeatabilitySagittal planeobserver variationInter-rater reliabilitymedicine.anatomical_structurekuvantaminenOrthopedic surgerystandardsSoftware/standardsOriginal ArticleSurgeryNeurology (clinical)reproducibility of resultsbusinessdiagnoosi030217 neurology & neurosurgeryNeurospine
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Correlation of oscillatory behaviour in Matlab using wavelets

2014

Here we present a novel computational signal processing approach for comparing two signals of equal length and sampling rate, suitable for application across widely varying areas within the geosciences. By performing a continuous wavelet transform (CWT) followed by Spearman?s rank correlation coefficient analysis, a graphical depiction of links between periodicities present in the two signals is generated via two or three dimensional images. In comparison with alternate approaches, e.g., wavelet coherence, this technique is simpler to implement and provides far clearer visual identification of the inter-series relationships. In particular, we report on a Matlab? code which executes this tec…

PeriodicityWavelet coherenceWaveletsMachine learningcomputer.software_genreSpearman's rank correlationCorrelationWaveletDe-noisingCode (cryptography)Computers in Earth SciencesMATLABContinuous wavelet transformRank correlationMathematicscomputer.programming_languageContinuous wavelet transformSignal processingbusiness.industryContinuous wavelet transform; De-noising; Oscillation; Periodicity; Spearman's rank correlation; WaveletsOscillationArtificial intelligencebusinessAlgorithmcomputerInformation SystemsComputers and Geosciences
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