Search results for "BN"

showing 10 items of 1136 documents

Child with repeated aspiration pneumonia and peculiar face.

1998

Pediatricsmedicine.medical_specialtyPeculiar faceHypertelorismbusiness.industryRespiratory diseaseFaciesInfantSyndromeAspiration pneumoniamedicine.diseasePneumonia AspirationSurgeryLung diseasePediatrics Perinatology and Child HealthmedicineHumansAbnormalities MultipleEsophageal Motility DisordersFemalebusinessEuropean journal of pediatrics
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Paediatric Sleep Questionnaire for Obstructive Sleep Apnoea Syndrome Screening: Is Sleep Quality Worthy of Note?

2021

Obstructive sleep apnoea syndrome (OSAS) is the most severe condition on the spectrum of sleep-related breathing disorders (SRBDs). The Paediatric Sleep Questionnaire (PSQ) is one of the most used and validated screening tools, but it lacks the comprehensive assessment of some determinants of OSAS, specifically anamnestic assessment and sleep quality. This study aims to assess the accuracy of some specific items added to the original PSQ, particularly related to the patient’s anamnestic history and to the quality of sleep, for the screening of OSAS in a paediatric population living in Sicily (Italy). Fifteen specific items, divided into “anamnestic” and “related to sleep quality” were added…

Pediatricsmedicine.medical_specialtyQuality of sleepDiseaselcsh:TechnologySettore MED/01 - Statistica Medicalcsh:Chemistry03 medical and health sciences0302 clinical medicineSettore MED/28 - Malattie OdontostomatologichePositive predicative valueMedicinescreening accuracyGeneral Materials Sciencepaediatric sleep-related breathing disorderslcsh:QH301-705.5InstrumentationObstructive sleep apnoea syndromePaediatric Sleep Questionnaire (PSQ)Fluid Flow and Transfer ProcessesSleep qualitylcsh:Tbusiness.industryProcess Chemistry and TechnologyAbnormal positionsGeneral Engineeringpaediatric obstructive sleep apnoea syndromeSleep in non-human animalslcsh:QC1-999Computer Science Applicationslcsh:Biology (General)lcsh:QD1-999030228 respiratory systemlcsh:TA1-2040sleep quality disturbancelcsh:Engineering (General). Civil engineering (General)businesspaediatric sleep-related breathing disorderlcsh:Physics030217 neurology & neurosurgeryPaediatric populationApplied Sciences
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Age- and Sex-Graded Data Evaluation of Vaccination Reactions after Initial Injection of the BNT162b2 mRNA Vaccine in a Local Vaccination Center in Ge…

2021

A high vaccination rate of older and particularly chronically ill people against coronavirus disease-2019 (COVID-19) is likely one of the most important factors in containing the pandemic. When Germany’s vaccination campaign started on December 2020, vaccination prioritization was initially carried out starting with older population groups. Side effect rates in 1065 individuals who had received the first dose of the messenger ribonucleic acid (mRNA) vaccine BNT162b2 Tozinameran from BioNTech/Pfizer three weeks earlier were examined retrospectively. An age- and gender-graded data analysis showed clear age and gender differences with regard to vaccine-related adverse effects. In 77% of all in…

Pediatricsmedicine.medical_specialtySide effectCoronavirus disease 2019 (COVID-19)COVID-19 vaccinationImmunologyage- and sex-graded data evaluationArticleHerd immunityImmunityDrug DiscoveryPandemicmedicinePharmacology (medical)Adverse effectPharmacologyvaccination strategymRNA vaccine BNT162b2business.industryRVaccinationInfectious DiseasesPopulation studyMedicinebusinessvaccination side effectsVaccines
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Early psychosis in Thauvin‐Robinet‐Faivre syndrome, a complication of the disease?

2021

Pediatricsmedicine.medical_specialtybusiness.industryEarly psychosisDiseasePhenotypePsychotic DisordersGeneticsmedicineHumansAbnormalities MultipleGenetic Predisposition to DiseaseDisease SusceptibilityAge of OnsetComplicationbusinessGenetic Association StudiesGenetics (clinical)Clinical Genetics
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Mental health perspectives of Hunter syndrome: Case reports of two biological siblings

2016

Hunter syndrome is a rare X-linked recessive disorder caused by deficiency of the lysosomal enzyme iduronate-2-sulphatase, leading to progressive accumulation of a substance called glycosaminoglycans in nearly all cell types, tissues, and organs. Hunter syndrome presents with facial dysmorphism, airway diseases, skeletal defects, cardiomyopathies, and neuropsychiatric manifestations. Mental subnormality is a cardinal feature in Hunter syndrome. This is a progressive cognitive decline that is not amenable to enzyme replacement therapy. Due to progressive cognitive decline, training the children to improve the adaptive functioning is a challenge that creates immense stress for the caregivers.…

Pediatricsmedicine.medical_specialtybusiness.industrylcsh:Reducationlcsh:MedicineHunter syndromeGeneral MedicineEnzyme replacement therapycognitive declinemedicine.diseaseMental healthProgressive cognitive declineBiological siblingsAdaptive functioningFacial dysmorphismHunter syndromeMedicineCognitive declinebusinessMental subnormalityMedical Journal of Dr. D.Y. Patil University
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Opsoclonus-myoclonus syndrome attributable to West Nile encephalitis: a case report

2014

Introduction Opsoclonus-myoclonus syndrome is a very rare neurological disorder associated with some viral infections and exceptionally with the West Nile virus. Case presentation A 57-year-old Caucasian woman presented with fever, dizziness, balance difficulties, vomiting, dancing eye, altered speech, tremor, generalized myoclonus and failure to rise or stand. Our objective is to describe a patient with West Nile infection, which was identified both in her serum and cerebrospinal fluid and was associated with encephalitis and opsoclonus-myoclonus-ataxia syndrome. Conclusions Opsoclonus-myoclonus-ataxia syndrome continued for 4 weeks after onset, when she died. There was no evidence for any…

Pediatricsmedicine.medical_specialtycongenital hereditary and neonatal diseases and abnormalitiesWest Nile virusCase ReportNeurological disordermedicine.disease_causeAntibodies ViralOpsoclonus myoclonus syndromemental disordersmedicineHumansMedicine(all)Opsoclonus-Myoclonus Syndromebusiness.industryGeneral MedicineWest Nile encephalitisMiddle Agedmedicine.diseasenervous system diseasesImmunologyVomitingEtiologyEncephalitisFemalemedicine.symptombusinessMyoclonusWest Nile virusEncephalitisWest Nile FeverJournal of Medical Case Reports
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Trends in Incidence and Survival of Myeloid Malignancies Since 1980, in the Côte D'or Department, Burgundy, France.

2009

Abstract Abstract 3122 Poster Board III-59 Objective The Registry of Haematological Malignancies (HM) has been established on January 1st, 1980 in the department of Côte d'Or (pop 500 000 inhabitants). It was the first specialized registry in haematology in the world. During the course of 25 years (1980-2004), 5026 cases of HM were recorded including 1553 Myeloid malignancies (MM) in which entities not initially considered as malignant were taken in account such as Myelodysplastic syndrome (MDS) and some Myeloproliferative neoplasms (MPN). This allow us to present trends in incidence and survival of myeloid malignancies by entities since 1980. Method MM diagnosed in the population between …

Pediatricsmedicine.medical_specialtyeducation.field_of_studyMyeloidHematologyRelative survivalbusiness.industryEssential thrombocythemiaIncidence (epidemiology)ImmunologyPopulationCell BiologyHematologymedicine.diseaseBiochemistrymedicine.anatomical_structureInternal medicinemedicineChromosome abnormalitybusinesseducationSex ratioBlood
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M. A. CORONEL RAMOS, Juan Luis Vives. El humanista y su entorno, Institució Alfons el Magnànim, Valencia, 2017. [ISBN 978-84-7822-702-0]

2019

Pedro 245 247 https://pages.uv.es/SPhV/cas/numero21.wikiUNESCO::CIENCIAS DE LAS ARTES Y LAS LETRAS1135-9560 8276 Studia philologica valentina 536436 2019 21 7225823 M. A. CORONEL RAMOS//pages.uv.es/SPhV/cas/numero21.wiki [Pedro 245 247 https]:CIENCIAS DE LAS ARTES Y LAS LETRAS [UNESCO]2017. [ISBN 978-84-7822-702-0] Fernández RequenaValenciaInstitució Alfons el MagnànimJuan Luis Vives. El humanista y su entorno
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Sylow permutable subnormal subgroups of finite groups II

2001

[EN] In this paper a local version of Agrawal's theorem about the structure of finite groups in which Sylow permutability is transitive is given. The result is used to obtain new characterisations of this class of finite groups.

Permutability conditionsTransitive relationClass (set theory)Soluble groupGeneral MathematicsSubnormal p'-perfect subgroupSylow theoremsStructure (category theory)Grups Teoria dePst_p-groupHall subgroupsCombinatoricsLocally finite groupComponent (group theory)ÀlgebraPermutable primeAlgebra over a fieldMathematicsBulletin of the Australian Mathematical Society
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The Antibody Response to the BNT162b2 mRNA COVID-19 Booster in Healthcare Workers: Association between the IgG Antibody Titers and Anthropometric and…

2022

Background: Research shows that in most people, two-dose vaccination helps to shape the humoral response to Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). Further studies are required to learn about the vaccine’s effectiveness after boosting. Methods: We conducted a prospective study among 103 healthcare workers (HCWs) from a regional multi-specialty hospital vaccinated with three doses of the BNT162b2 vaccine. We compared their immunoglobulin G (IgG) titers 14 days after the second dose with those 21 days after the booster. We also compared their anthropometric and body composition parameters with IgG concentrations at the same time points. Results: Twenty-one days aft…

PharmacologyInfectious DiseasesDrug DiscoveryImmunologyPharmacology (medical)IgG antibody; SARS-CoV-2; COVID-19; healthcare workers; humoral response; COVID-19 vaccine; BNT162b2 vaccine; immunization; body composition; boosterVaccines; Volume 10; Issue 10; Pages: 1638
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