Search results for "Edema"

showing 10 items of 625 documents

Skeletal muscle oedema and muscle fibre necrosis during septic shock. Observations with a porcine septic shock model

1994

In domestic pigs, intermitted application of Escherichia coli-endotoxin was used to create an animal model for a prolonged hypo- and hyperdynamic septic shock-like state and to investigate mechanisms of multiple organ failure. Here, we describe the changes in skeletal muscle after 18 h (2 animals) and 48 h (6 animals) of septic shock. Two pigs for each observation period that received physiologic saline solutions instead of endotoxin served as controls. The earliest lesions were endothelial cell damage with endomysial oedema and swelling of mitochondria in muscle fibres. With increasing degree of endothelial cell damage, pericytes showed degenerative changes with cytoplasmic fragmentation a…

KaryolysisPathologymedicine.medical_specialtyTime FactorsNecrosisSwineBiologyPathology and Forensic MedicineNecrosisHypoproteinemiaMuscular DiseasesmedicineAnimalsEdemaMolecular BiologyTumor Necrosis Factor-alphaSeptic shockSkeletal muscleCell BiologyGeneral MedicineAnatomymedicine.diseaseShock SepticEndothelial stem cellDisease Models AnimalMicroscopy Electronmedicine.anatomical_structureShock (circulatory)Tumor necrosis factor alphamedicine.symptomVirchows Archiv
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New acetophenone glucosides isolated from extracts of Helichrysum italicum with antiinflammatory activity.

2001

Three new acetophenone glucosides (4-6), three known aglycons (1-3), and a benzo-gamma-pyrone glucoside (7) were isolated from the CH(2)Cl(2), EtOAc, and BuOH extracts from the aerial parts of Helichrysum italicum. All the compounds tested showed antiinflammatory activity in a 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced mouse ear edema test, and the ID(50) value of compound 2, the most active compound, was determined.

KetoneMagnetic Resonance SpectroscopySpectrophotometry InfraredStereochemistryIndomethacinPharmaceutical SciencePharmacognosyAsteraceaeHelichrysum italicumAnalytical Chemistrychemistry.chemical_compoundMiceGlucosideGlucosidesPhenolsDrug DiscoverySpectroscopy Fourier Transform InfraredAnimalsEdemaBenzopyransPharmacologychemistry.chemical_classificationPlants MedicinalbiologyDose-Response Relationship DrugPlant Extractsbeta-GlucosidaseOrganic ChemistryAnti-Inflammatory Agents Non-SteroidalGlycosideAcetophenonesbiology.organism_classificationComplementary and alternative medicinechemistryAldoseActive compoundSpainMolecular MedicineTetradecanoylphorbol AcetateSpectrophotometry UltravioletChromatography Thin LayerAcetophenoneJournal of natural products
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Comparison of the efficacy of low doses of methylprednisolone, acetaminophen, and dexketoprofen trometamol on the swelling developed after the remova…

2015

WOS: 000365269900016

KetoprofenMolarmedicine.medical_specialtyAnalgesicAnti-Inflammatory AgentsOdontologíaMethylprednisoloneswellingEdemamedicinedexketoprofen trometamolEdemaHumansTromethamineGeneral DentistryAcetaminophenbusiness.industryResearchdigestive oral and skin physiologyTooth ImpactedAnalgesics Non-Narcotic:CIENCIAS MÉDICAS [UNESCO]DexketoprofenCiencias de la saludSurgeryAcetaminophenthird molar extractionOtorhinolaryngologyMethylprednisoloneKetoprofenAnesthesiaUNESCO::CIENCIAS MÉDICASTooth ExtractionMolar ThirdSurgeryOral Surgerymedicine.symptomSwellingMouth Diseasesbusinessmedicine.drugMedicina Oral Patología Oral y Cirugia Bucal
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Hereditary angioedema cosegregating with a novel kininogen 1 gene mutation changing the N‐terminal cleavage site of bradykinin

2019

Kininogen 1 Genechemistry.chemical_compoundchemistrybusiness.industryImmunologyHereditary angioedemamedicineImmunology and AllergyBradykininmedicine.diseasebusinessCleavage (embryo)Molecular biologyAllergy
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The Expanding Spectrum of Mutations in Hereditary Angioedema.

2021

The evolution in the knowledge of rare genetic diseases such as hereditary angioedema (HAE) has increased at a parallel pace with the development of new molecular tools. The deficiency of C1 inhibitor (C1-INH) has been recognized as the main cause of HAE (HAE-C1-INH) since the 1960s, but the discovery of the wide spectrum of mutations affecting the C1-INH gene (SERPING1) was possible only from the late 1980s, when Sanger sequencing became available and more accessible worldwide. Nevertheless, the involvement of other genes in HAE was discovered only in 2006 with the description of mutations in the F12 gene in patients with HAE and normal C1-INH. In the last 3 years, advanced next-generation…

Kininogen 1Muscle ProteinsGenomicsSeverity of Illness IndexDNA sequencingC1-inhibitorPathogenesis03 medical and health sciencessymbols.namesake0302 clinical medicineImmunology and AllergyMedicineHumans030212 general & internal medicineGeneSanger sequencingGeneticsbiologybusiness.industryCalcium-Binding ProteinsAngioedemas HereditaryMembrane Proteinsmedicine.disease030228 respiratory systemHereditary angioedemaMutationbiology.proteinsymbolsbusinessComplement C1 Inhibitor ProteinThe journal of allergy and clinical immunology. In practice
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In ricordo di Klaus Tiedemann

2019

Brief biography of Klaus Tiedeman, German professor of criminal law, with an international scientific relevance. His studies in the fields of economic criminal law, European criminal law, criminology and comparative criminal law have represented decisive contributions to the development of the related sectors.

Klaus Tiedemann - BiographySettore IUS/17 - Diritto Penale
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Clinical studies of sudden upper airway obstruction in patients with hereditary angioedema due to C1 esterase inhibitor deficiency.

2003

Background Hereditary angioedema due to C1 esterase inhibitor deficiency is clinically characterized by recurrent and self-limiting skin, intestinal, and laryngeal edema. Asphyxiation by laryngeal edema is the main cause of death among patients who die of hereditary angioedema. This study describes the age at which laryngeal edema first occurs, the time between onset and full development, and the effectiveness of therapy and prophylaxis. Methods Information on 123 patients with hereditary angioedema was obtained from medical histories and reports by the general practitioners, emergency physicians, and hospitals involved. Results Sixty-one patients (49.6%) experienced a total of 596 laryngea…

LarynxAdultAbdominal painAdolescentComplement C1 Inactivator ProteinsLaryngeal EdemaEcallantideRisk FactorsEdemaInternal MedicinemedicineHumansAge of OnsetAngioedemaChildAgedbusiness.industryAirway obstructionLaryngeal EdemaMiddle Agedmedicine.diseasemedicine.anatomical_structureAnesthesiaChild PreschoolHereditary angioedemaAge of onsetmedicine.symptombusinessmedicine.drugArchives of internal medicine
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Risk of laryngeal edema and facial swellings after tooth extraction in patients with hereditary angioedema with and without prophylaxis with C1 inhib…

2010

Objective Tooth extractions may trigger clinical symptoms of hereditary angioedema due to C1 inhibitor deficiency (HAE-C1-INH). The aim of this study was to determine how many tooth extractions were followed by symptoms of HAE-C1-INH in patients with and without preoperative short-term prophylaxis with C1 inhibitor concentrate. Study design Tooth extractions and clinical symptoms of HAE-C1-INH were determined from clinical record files of 171 patients with HAE-C1-INH. Results Facial swelling or potentially life-threatening laryngeal edema, or both, occurred in 124/577 tooth extractions (21.5%) without prophylaxis. Similar symptoms occurred in a fewer proportion of patients undergoing extrac…

LarynxAdultMalemedicine.medical_specialtyTime FactorsPremedicationComplement C1 Inactivator ProteinsLaryngeal EdemaChemopreventionC1-inhibitorRisk FactorsEdemamedicineEdemaHumansRisk factorGeneral DentistryRetrospective StudiesbiologyDose-Response Relationship Drugbusiness.industryAngioedemas HereditaryRetrospective cohort studyLaryngeal Edemamedicine.diseaseSurgerymedicine.anatomical_structureTreatment OutcomeOtorhinolaryngologyFaceHereditary angioedemaInjections IntravenousTooth Extractionbiology.proteinSurgeryPremedicationFemaleOral Surgerymedicine.symptombusinessComplement C1 Inhibitor ProteinFollow-Up StudiesOral surgery, oral medicine, oral pathology, oral radiology, and endodontics
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Recurrent angioedema and the threat of asphyxiation.

2009

Angioedema (also known as Quincke disease) is the name given to edema lasting 1–7 days that recurs at irregular intervals. Target organs are the skin, tongue, glottis and larynx, gastrointestinal tract, and sometimes other soft organs. The clinical symptom referred to as angioedema forms part of a variety of disease entities (Box 1, Figure 1). In Germany, according to the present author’s estimate, several thousand patients suffer from one of the forms of recurrent angioedema. Cases of sudden asphyxiation are rare, but do occur every now and again (1). This review aims to draw attention to the various clinical features of recurrent angioedema and the practical steps for dealing with it, and…

Larynxmedicine.medical_specialtyDNA Mutational AnalysisReview ArticleC1-inhibitorAsphyxiaimmune system diseasesRecurrenceRisk FactorsEdemamedicineAmbulatory CareHumanscardiovascular diseasesAngioedemaskin and connective tissue diseasesPseudoallergic reactionChronic urticariabiologyAngioedemabusiness.industryfood and beveragesGeneral MedicineAirway obstructionmedicine.diseaseDermatologyAirway Obstructionmedicine.anatomical_structureImmunologyHereditary angioedemaFactor XIIbiology.proteinmedicine.symptombusinessComplement C1 Inhibitor ProteinDeutsches Arzteblatt international
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EDEMA EMORRAGICO ACUTO DEL LATTANTE: DESCRIZIONE DI UN CASO

2009

Lattante edema emorragicoSettore MED/38 - Pediatria Generale E Specialistica
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