Search results for "normal"

showing 10 items of 2571 documents

Severe beak deformity in Melopsittacus undulatus caused by Knemidocoptes pilae

2014

An outbreak of knemidocoptic mange caused by Knemidocoptes pilae is described in caged Australian budgerigars (Melopsittacus undulatus) in a public park in L´Eliana (Valencia, Spain). Five individuals (5 out of 70) displayed severe malformation of the beak, with the rhamphotheca, rhinotheca, and gnathotheca affected and a slight lateral deviation of the jawbone, which did not, however, impede feeding or grooming.

Public parkGeneral VeterinaryKey words: Knemidocoptes pilaemangeMelopsittacus undulatusabnormal beak growthSpainLateral deviationMangeOutbreakAnatomyBiologyMelopsittacusmedicine.diseaseBeakDeformitymedicinemedicine.symptomKnemidocoptes pilae
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FVIII production by human lung microvascular endothelial cells

2006

While extrahepatic factor VIII (FVIII) synthesis suffices for hemostasis, the extrahepatic production sites are not well defined. We therefore investigated the ability of the human lungs to produce FVIII. Lungs from heart-beating donors who were declined for transplantation were perfused and ventilated in an isolated reperfusion model for 2 hours. A progressive accumulation of FVIII and von Willebrand factor (VWF) was recorded in the perfusion medium in 3 of 4 experiments. By contrast, factor V, fibrinogen, and immunoglobulin G (IgG) levels remained constant during the perfusion period, indicating that the accumulation of FVIII and VWF was not due to diffusion from the intercellular medium …

Pulmonary Circulationcongenital hereditary and neonatal diseases and abnormalitiesmedicine.medical_specialtyEndotheliumanimal diseasesImmunologyIn Vitro TechniquesFibrinogenBiochemistryImmunoglobulin GMicrocirculationVon Willebrand factorhemic and lymphatic diseasesInternal medicinevon Willebrand FactormedicineHumansLungFactor VIIILungbiologybusiness.industryMicrocirculationEndothelial CellsCell BiologyHematologyTransplantationKineticsEndocrinologymedicine.anatomical_structureHemostasisReperfusionImmunologybiology.proteinEndothelium Vascularbusinessmedicine.drugBlood
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The disease-specific clinical trial network for primary ciliary dyskinesia: PCD-CTN

2022

Primary ciliary dyskinesia; Rare genetic disorder; Lung diseases Discinesia ciliar primaria; Trastorno genético raro; Enfermedades pulmonares Discinesia ciliar primària; Trastorn genètic rar; Malalties pulmonars Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by impaired mucociliary clearance leading to irreversible lung damage. In contrast to other rare lung diseases like cystic fibrosis (CF), there are only few clinical trials and limited evidence-based treatments. Management is mainly based on expert opinions and treatment is challenging due to a wide range of clinical manifestations and disease severity. To improve clinical and translational research and facili…

Pulmonary and Respiratory Medicine:enfermedades respiratorias::trastornos de la motilidad ciliar [ENFERMEDADES]:Health Occupations::Medicine::Pediatrics [DISCIPLINES AND OCCUPATIONS]Respiratory SystemSağlık BilimleriClinical Medicine (MED)SOLUNUM SİSTEMİRespiratory CareHealth SciencesMANAGEMENTKlinik Tıp (MED)Chest Diseases and Allergy:profesiones sanitarias::medicina::pediatría [DISCIPLINAS Y OCUPACIONES]:Otros calificadores::/terapia [Otros calificadores]:Respiratory Tract Diseases::Ciliary Motility Disorders [DISEASES]Internal Medicine SciencesScience & TechnologyKlinik TıpMUTATIONSRESPIRATORY SYSTEM:Other subheadings::/therapy [Other subheadings]Dahili Tıp BilimleriGöğüs Hastalıkları ve AllerjiCLINICAL MEDICINECèl·lules - Motilitat:Congenital Hereditary and Neonatal Diseases and Abnormalities::Genetic Diseases Inborn [DISEASES]TıpPulmons - Malalties - TractamentAkciğer ve Solunum TıbbıMedicineMalalties congènites:enfermedades y anomalías neonatales congénitas y hereditarias::enfermedades genéticas congénitas [ENFERMEDADES]Solunum BakımıLife Sciences & BiomedicinePulmons Malalties
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Childhood intermittent and persistent rhinitis prevalence and climate and vegetation: a global ecologic analysis

2014

Abstract Background The effect of climate change and its effects on vegetation growth, and consequently on rhinitis, are uncertain. Objective To examine between- and within-country associations of climate measures and the normalized difference vegetation index with intermittent and persistent rhinitis symptoms in a global context. Methods Questionnaire data from 6- to 7-year-olds and 13- to 14-year-olds were collected in phase 3 of the International Study of Asthma and Allergies in Childhood. Associations of intermittent (>1 symptom report but not for 2 consecutive months) and persistent (symptoms for ≥2 consecutive months) rhinitis symptom prevalences with temperature, precipitation, vapor…

Pulmonary and Respiratory MedicineAllergyRhinitis Allergic PerennialAdolescentClimate ChangeImmunologyEczemaClimate changeContext (language use)Normalized Difference Vegetation IndexAdolescent; Asthma; Child; Eczema; Humans; Plants; Questionnaires; Rhinitis Allergic Perennial; Rhinitis Allergic Seasonal; Climate Change; Immunology and Allergy; Pulmonary and Respiratory Medicine; Medicine (all)Interquartile rangeSurveys and QuestionnairesmedicineHumansImmunology and AllergyChildAsthmaQuestionnairebusiness.industryMedicine (all)Rhinitis Allergic SeasonalRegression analysisPlantPlantsmedicine.diseaseAsthmaConfidence intervalbusinessHumanDemographyAnnals of Allergy, Asthma & Immunology
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Design and Simulation of Measurement-Based Correlation Models for Shadow Fading

2011

This paper deals with the design of measurement-based correlation models for shadow fading. Based on the correlation model, we design a simulation model using the sum-of-sinusoids (SOS) method to enable the simulation of spatial lognormal processes characterizing real-world shadow fading scenarios. The model parameters of the simulation model are computed by applying the Lp-norm method (LPNM). This method facilitates an excellent fitting of the simulation model’s autocorrelation function (ACF) to that of measured channels. Our study includes an evaluation of all important statistical quantities of the proposed measurement-based simulation model, such as the probability density function (PDF…

Pulmonary and Respiratory MedicineEngineeringbusiness.industryAutocorrelationProbability density functionCorrelationGoodness of fitPediatrics Perinatology and Child HealthLog-normal distributionCoherence (signal processing)FadingbusinessDecorrelationAlgorithmSimulationComputer Science::Information TheoryREV Journal on Electronics and Communications
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Spanish multicentre study on morbidity and pathogenicity of tracheal bronchus in children.

2019

Tracheal bronchus (TRB) has been generally considered an anatomical variant of the tracheobronchial tree without a precise pathological effect. Its prevalence is estimated to be between 0.2% to 3% of all children undergoing bronchoscopy and scientific information has been limited to case reports or small case series. Our working hypothesis was that TRB could trigger by itself recurrent or persistent respiratory symptoms. The objective of this retrospective and multicentre study of children with a diagnosis of TRB, coming from the main paediatric pulmonology units of Spain, was to determine the anatomical and clinical characteristics, including comorbidities, of TRB in childhood and their im…

Pulmonary and Respiratory MedicineMaleDown syndromePediatricsmedicine.medical_specialtyAdolescentCardiovascular AbnormalitiesBronchi03 medical and health sciences0302 clinical medicineBronchoscopy030225 pediatricsBronchoscopymedicinePrevalenceHumansRespiratory systemBronchitisChildPathologicalTracheal Diseasesmedicine.diagnostic_testbusiness.industryRefluxInfantPneumoniamedicine.diseasePathogenicityTrachea030228 respiratory systemTracheomalaciaSpainTracheal bronchusChild PreschoolPediatrics Perinatology and Child HealthGastroesophageal RefluxFemaleDown SyndromebusinessPediatric pulmonology
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Pulmonary microvascular architecture in hereditary haemorrhagic telangiectasia

2017

A 24-year-old Caucasian man was admitted with a known hereditary haemorrhagic telangiectasia (HHT) and heterozygous mutation of factor V Leiden following episodes of cerebral infarctions in occipital lobes, cerebellum and brainstem. In his case history, the patient underwent several interventional embolisation of arteriovenous (AV) malformations in the middle and lower lobes (figure 1). However, those were not completely successful as the malformations were diffuse. We performed video-assisted thoracoscopic surgery with a resection of the middle lobe and a wedge resection of segment 10. Figure 1 CT scans depict the pulmonary arteriovenous malformations after re-embolisation in the middle lo…

Pulmonary and Respiratory MedicineMalecongenital hereditary and neonatal diseases and abnormalitiesmedicine.medical_specialtyMucocutaneous zoneMedizinArticleResection03 medical and health sciencesYoung Adult0302 clinical medicineMicroscopy Electron Transmissionhemic and lymphatic diseasesotorhinolaryngologic diseasesmedicineFactor V LeidenHumans030223 otorhinolaryngologyLungHeterozygous mutationHereditary haemorrhagic telangiectasiabusiness.industryMiddle LobeMicrovascular architecturemedicine.diseaseSurgery030228 respiratory systemMicrovesselsTelangiectasia Hereditary HemorrhagicRadiologybusinessTomography X-Ray ComputedWedge resection (lung)
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Shedding some light on tricuspid intervention

2021

Background More than 1.6 million Americans have at least moderate to severe valvular tricuspid regurgitation, yet fewer than 8000 tricuspid valve operations are performed annually in the USA. The undertreatment for isolated tricuspid regurgitation might be related to the fact that in the past years no clear guidelines on 'how' and 'when' to treat tricuspid regurgitation were issued. Aims Sarris-Michopoulos and colleagues carried out a meta-analysis with the aim to investigate the role of tricuspid valve repair versus tricuspid valve replacement in patients with isolated tricuspid valve regurgitation. Material and methods Outcomes of patients with first-time surgery for isolated tricuspid va…

Pulmonary and Respiratory MedicineModerate to severecongenital hereditary and neonatal diseases and abnormalitiesmedicine.medical_specialtyPercutaneousContext (language use)Regurgitation (circulation)Intervention (counseling)Internal medicineHumansMedicinecardiovascular diseasesRetrospective StudiesHeart Valve Prosthesis ImplantationTricuspid valvebusiness.industryTricuspid Valve InsufficiencySurgeryTreatment Outcomemedicine.anatomical_structureVentricleCohortcardiovascular systemCardiologySurgeryTricuspid ValveTricuspid Valve RegurgitationCardiology and Cardiovascular Medicinebusiness
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The Contribution of Small-Airway Abnormalities in Chronic Obstructive Pulmonary Disease Clinical Manifestations: More than a Functional Issue.

2016

Pulmonary and Respiratory Medicinemedicine.medical_specialtybusiness.industryMEDLINESocio-culturalePulmonary diseaseSettore MED/10 - Malattie Dell'Apparato Respiratorio03 medical and health sciencesPulmonary Disease Chronic Obstructive0302 clinical medicineText mining030228 respiratory systemAirway abnormalitiesmedicineHumans030212 general & internal medicineIntensive care medicinebusinessHumanRespiration; international review of thoracic diseases
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Generically split projective homogeneous varieties. II

2012

AbstractThis article gives a complete classification of generically split projective homogeneous varieties. This project was begun in our previous article [PS10], but here we remove all restrictions on the characteristic of the base field, give a new uniform proof that works in all cases and in particular includes the case PGO2n+ which was missing in [PS10].

Pure mathematicsAlgebra and Number TheoryCollineationComplex projective spaceProjective lineProjective spaceGeometry and TopologyRational normal curveQuaternionic projective spaceProjective varietyMathematicsTwisted cubicJournal of K-Theory
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