Search results for "BERT"

showing 10 items of 1789 documents

Design and Implementation of a Data Acquisition System for R Peak Detection in Electrocardiograms

2018

This paper presents a data acquisition system for the R peak detection in electrocardiograms. R wave is one of the most important sections of the QRS complex, which has an essential role in diagnosis of heart rhythm irregularities. This paper employs Hilbert transform and adaptive threshold technique for the detection of R-peak. The performance of the system was tested using standard ECG waveform records from the MIT-BIH arrhythmia database. In addition, tests were carried out using the sensors Single Lead Heart Rate Monitor for real-time data processing Design and Implementation of a Data Acquisition System for R Peak Detection in Electrocardiograms | Request PDF. Available from: https://w…

Adaptive ThresholdHilbert TransformElectrocardiogram
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Predicting the Short-Term Exchange Rate Between United State Dollar and Czech Koruna Using Hilbert-Huang Transform and Fuzzy Logic

2017

In this paper, the combination of the Hilbert-Huang Transform, fuzzy logic and an embedding theorem is described to predict the short-term exchange rate from United States dollar to Czech Koruna. By Using the Hilbert-Huang Transform as an adaptive filter, the proposed method decreases the embedding dimension space from five (original samples) to four (de-noising samples). This dimension space provides the number of inputs to the fuzzy rule base system, which causes the number of rules, the time for training and the inference process to decrease. Experimental results indicated that this method achieves higher accuracy prediction than the direct use of original data.

Adaptive filterExchange rateFuzzy ruleDimension (vector space)Financial economicsEconomicsInferenceEmbeddingAlgorithmFuzzy logicHilbert–Huang transform
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Una ciencia admirable: filosofía y admiración en Descartes

2021

RESUMEN Aunque Descartes pretende hablar de cuestiones morales en general, y de las pasiones en particular, como si nadie hubiera escrito antes sobre ellas, lo cierto es que, en el caso de la admiración, es clara su referencia al mundo antiguo. En concreto, en este caso el pensador francés se sitúa críticamente en contra de la postura aristotélica, que entiende la admiración como el inicio de la filosofía. Frente a la propuesta clásica, que convierte dicha emoción en el motor permanente de la investigación de las primeras causas, para Descartes la curiosidad excesiva y el estupor del asombro son rechazables. No obstante, algunos han señalado el carácter ambivalente de las declaraciones cart…

Admiracióncuriositylibre albedríoEmocionspasiónLlibertatVida intel·lectualFilosofiaPhilosophypassionWondercuriosidadamazementfree willasombro
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TCTN3 Mutations Cause Mohr-Majewski Syndrome

2012

Orofaciodigital syndromes (OFDSs) consist of a group of heterogeneous disorders characterized by abnormalities in the oral cavity, face, and digits and associated phenotypic abnormalities that lead to the delineation of 13 OFDS subtypes. Here, by a combined approach of homozygozity mapping and exome ciliary sequencing, we identified truncating TCTN3 mutations as the cause of an extreme form of OFD associated with bone dysplasia, tibial defect, cystic kidneys, and brain anomalies (OFD IV, Mohr-Majewski syndrome). Analysis of 184 individuals with various ciliopathies (OFD, Meckel, Joubert, and short rib polydactyly syndromes) led us to identify four additional truncating TCTN3 mutations in un…

AdolescentFoot Deformities CongenitalMolecular Sequence DataCiliopathiesJoubert syndromeYoung AdultFetusReportCerebellumGLI3medicineGeneticsHumansExomeHedgehog ProteinsGenetics(clinical)Sonic hedgehogChildExomeGenetics (clinical)Adaptor Proteins Signal TransducingCystic kidneyGeneticsBase SequencebiologyHomozygoteIntracellular Signaling Peptides and ProteinsMembrane ProteinsCiliary transition zoneSequence Analysis DNAOrofaciodigital Syndromesmedicine.diseaseCleft PalateCiliopathyPhenotypeMutationbiology.proteinApoptosis Regulatory ProteinsHand Deformities CongenitalSignal TransductionThe American Journal of Human Genetics
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Physical activity and aerobic fitness in relation to local and interhemispheric functional connectivity in adolescents' brains

2021

Abstract Introduction Adolescents have experienced decreased aerobic fitness levels and insufficient physical activity levels over the past decades. While both physical activity and aerobic fitness are related to physical and mental health, little is known concerning how they manifest in the brain during this stage of development, characterized by significant physical and psychosocial changes. The aim of the study is to examine the associations between both physical activity and aerobic fitness with brains’ functional connectivity. Methods Here, we examined how physical activity and aerobic fitness are associated with local and interhemispheric functional connectivity of the adolescent brai…

AdolescentbrainROBUSTphysical activityEXERCISElcsh:RC321-571toiminnallinen magneettikuvausnuoretHumansExerciselcsh:Neurosciences. Biological psychiatry. NeuropsychiatryOriginal Researchaerobic fitnessRESTING-STATE NETWORKSfMRIfunctional connectivityMOTION CORRECTIONNeurosciencesPUBERTAL CHANGESMagnetic Resonance Imagingfyysinen kuntoMental HealthRIGHT SUPRAMARGINAL GYRUSREGISTRATIONREGIONAL HOMOGENEITYadolescenceaivotCARDIORESPIRATORY FITNESSfyysinen aktiivisuusNeurovetenskaper
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Abnormal pentagastrin response in a patient with pseudohypoparathyroidism

2002

The case of a 25 year old female patient with pseudohypoparathyroidism type I (PHP) and hypercalcitoninaemia is reported. She was referred to our clinic because of recurrent hypocalcaemia associated with paraesthesias and muscle cramps. She had no signs of Albright hereditary osteodystrophy (AHO), a normal mental status and no family history of hypocalcaemia or any other endocrine disease. Considering the laboratory results with hypocalcaemia, hyperphosphataemia, normal vitamin D and normal creatinine with an extraordinary elevated PTH we diagnosed pseudohypoparathyroidism type I. She had delayed pubertal development with menarche in the age of 20 and hypothyroidism with an atrophic thyroid…

AdultCalcitoninmusculoskeletal diseasesmedicine.medical_specialtyendocrine system diseasesEndocrinology Diabetes and MetabolismGastroenterologyPhosphatesEndocrinologyHypothyroidismInternal medicineInternal MedicinemedicineHumansHypocalcaemiaFamily historyPseudohypoparathyroidismPuberty DelayedEndocrine diseaseHypocalcemiabusiness.industryThyroidGeneral MedicineAlkaline Phosphatasemedicine.diseasePentagastrinmedicine.anatomical_structureEndocrinologyCalcitoninPseudohypoparathyroidismCalciumFemalePentagastrinmedicine.symptombusinessMuscle crampmedicine.drugExperimental and Clinical Endocrinology & Diabetes
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Bone and body segment lengthening and widening: a 7-year follow-up study in pubertal girls.

2010

Abstract During growth bone increases in length and width as does the body size. The aim of this paper was to examine the growth pattern of body height and weight, and the width and length of various body segments, and to establish the timing of peak growth velocity (PV) in relation to time of menarche in a cohort of Finnish girls followed from age 10 until 18. The study was a 7-year longitudinal cohort study. Widths and lengths of body segments and bones were measured from DXA scan images using bone landmarks in 396 girls aged 10 to 13 years at baseline, and in 255 mothers and 159 grandmothers. The girls' growth velocities (rate of change with time) peaked at 13.5 months prior to menarche …

AdultHistologyAdolescentPhysiologyEndocrinology Diabetes and MetabolismBody Mass IndexMedicineHumansFemurHumerusTibiaLongitudinal StudiesChildDual-energy X-ray absorptiometryPelvisFinlandAgedAged 80 and overMenarcheBone Developmentmedicine.diagnostic_testbusiness.industryBody WeightPubertyAnatomyMiddle AgedTrunkBody Heightmedicine.anatomical_structureMenarcheFemalebusinessBody mass indexFollow-Up StudiesBone
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Declining Sexual Activity and Desire in Men—Findings From Representative German Surveys, 2005 and 2016

2017

Abstract Background Surveys have indicated an increase of sexual activity in aging men; recently, however, a decrease of sexual activity has been reported in young men. Aim To assess (i) sexual activity and desire and their determinants across the age range in a population-based male sample and (ii) their changes over 11 years. Methods A representative survey of men (N = 1,095) 18 to 93 years old from 2016 was compared with a survey from 2005 (N = 1,106 men) with the same age range. Samples were drawn from the German population at random using standardized sampling procedures. Questions were filled out by participants in the presence of a trained interviewer. Sexual activity was compared us…

AdultMaleAdolescentLongitudinal dataLibidoSexual BehaviorUrologyEndocrinology Diabetes and MetabolismPopulation030232 urology & nephrologyPuberty PrecociousLogistic regressionGermanYoung Adult03 medical and health sciencesSexually active0302 clinical medicineEndocrinologyGerman populationGermanySurveys and QuestionnairesHumans030212 general & internal medicineeducationAgedAged 80 and overeducation.field_of_studyMiddle Agedlanguage.human_languagePsychiatry and Mental healthSexual desireLogistic ModelsSocioeconomic FactorsReproductive MedicinelanguagePsychologyDemographyThe Journal of Sexual Medicine
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Femininity and Fertility in Sisters with Twin Brothers: Prenatal Androgenization? Cross-Sex Socialization?

2002

Are sisters of twin brothers behaviorally or physiologically masculinized? Prenatal exposure to their brothers' androgens and postnatal socialization experiences unique to girls growing up with twin brothers might influence their attitudes, pubertal development, and reproductive histories. To investigate, we studied age- and cohort-matched samples of Finnish sisters from same-sex and opposite-sex twin pairs. Using data from two ongoing longitudinal studies of consecutive birth cohorts of Finnish twins, we assessed pubertal development at ages 11 and 14 and endorsement of attitudes associated with femininity at age 16. We also studied fertility in Finnish women from same- and opposite-sex t…

AdultMaleAdolescentmedia_common.quotation_subjectFertility050105 experimental psychologyDevelopmental psychologyCohort Studies5. Gender equalityPregnancyTwins DizygoticHumans0501 psychology and cognitive sciencesLongitudinal StudiesChildGonadal Steroid HormonesPrenatal exposureFinlandGeneral Psychologymedia_commonPubertySocialization05 social sciencesSocializationGender IdentityTwins MonozygoticFemininityFertilityPrenatal Exposure Delayed EffectsFemaleReproductive HistoriesBirth cohortPsychology050104 developmental & child psychologyPsychological Science
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Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.

2007

Peters, T.A./0000-0001-8443-5500; van Beersum, Sylvia E.C./0000-0002-4552-2908; Cremers, Frans/0000-0002-4954-5592; Roepman, Ronald/0000-0002-5178-8163 WOS: 000247619800019 PubMed: 17558407 Protein- protein interaction analyses have uncovered a ciliary and basal body protein network that, when disrupted, can result in nephronophthisis ( NPHP), Leber congenital amaurosis, Senior- Loken syndrome ( SLSN) or Joubert syndrome ( JBTS)(1-6). However, details of the molecular mechanisms underlying these disorders remain poorly understood. RPGRIP1- like protein ( RPGRIP1L) is a homolog of RPGRIP1 ( RPGR-interacting protein 1), a ciliary protein defective in Leber congenital amaurosis(7,8). We show t…

AdultMaleHealth aging / healthy living [IGMD 5]Eye DiseasesGenetics and epigenetic pathways of disease [NCMLS 6]TMEM67Molecular Sequence DataMembrane transport and intracellular motility [NCMLS 5]Biologymedicine.disease_causeJoubert syndromeCell LineGenomic disorders and inherited multi-system disorders [IGMD 3]NephronophthisisCerebellar DiseasesGeneticsmedicinePerception and Action [DCN 1]Basal bodyAnimalsHumansNeurosensory disorders [UMCN 3.3]CiliaAdaptor Proteins Signal TransducingRenal disorder [IGMD 9]GeneticsMutationCiliumCiliary transition zoneProteinsSyndromemedicine.diseasePedigreeRatsCytoskeletal ProteinsGenetic defects of metabolism [UMCN 5.1]RPGRIP1LFemaleKidney DiseasesFunctional Neurogenomics [DCN 2]Ciliary Motility Disorders
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