Search results for "molecular medicine"

showing 10 items of 3013 documents

Evaluation of the clonidine-suppression test in the diagnosis of pheochromocytoma

1988

In this study we examined the preoperative value of the clonidine-suppression test in 15 patients with surgically proved pheochromocytomas. The result of the clonidine-suppression test was pathological (epinephrine plus norepinephrine above 500 ng/l 3 h after clonidine) in 10 of 15 patients (66%). These patients had relatively large tumors and higher basal norepinephrine plasma levels. Out of the 5 cases without a pathological clonidine test 4 had normal basal plasma catecholamine levels with the result that the clonidine test could not be properly applied and 1 case produced a false negative result. These 5 cases generally had smaller tumors and lower plasma catecholamine levels. Two of th…

AdultMaleEpinephrineAdrenal Gland NeoplasmsPheochromocytomaClonidineNorepinephrine (medication)PheochromocytomaNorepinephrineBasal (phylogenetics)Drug DiscoverymedicineHumansPathologicalGenetics (clinical)business.industryGeneral MedicinePlasma levelsMiddle Agedmedicine.diseaseClonidineEpinephrineAnesthesiaCatecholamineMolecular MedicineFemalebusinessmedicine.drugKlinische Wochenschrift
researchProduct

Red cell enzyme polymorphisms in Bulgaria.

1972

7 human red cell enzyme polymophisms have been typed on a sample of n=138 unrelated adults from Bulgaria, which revealed the following gene frequencies: ADA1=0.8623. ADA2=0.1376; AK1=0.9637, AK2=0.0362; 6-PGDA=0.9891, 6-PGDC=0.0108; PGM11=0.8346, PGM12=0.1653; PA=0.1596, PB=0.7983, PC=0.0420. In the LDH-system one B-subunit variant was found, whilst no Peptidase A or B variant could be observed. The anthropological significance of these findings is discussed.

AdultMaleErythrocytesAcid PhosphataseElectrophoresis Starch GelBiologyGene FrequencyAminohydrolasesGeneticsHumansBulgariaGeneMolecular BiologyGenetics (clinical)GeneticsPolymorphism GeneticL-Lactate DehydrogenasePhosphogluconate DehydrogenasePhosphotransferasesBlood Protein ElectrophoresisMolecular medicineHuman geneticsAK2Red cell enzymeEnzymesGenetics PopulationPhosphoglucomutaseFemalePeptide HydrolasesHumangenetik
researchProduct

An unusual translocation associated with recurrent spontaneous abortions

1989

The authors report a case of 11;17 translocation associated with recurrent spontaneous abortions, and request contact with colleagues who have observed similar cases.

AdultMaleGeneticsAbortion HabitualChromosomes Human Pair 11Chromosomal translocationBiologyMolecular medicineTranslocation GeneticHuman geneticsPregnancyKaryotypingGeneticsHumansFemaleGenetics (clinical)Chromosomes Human Pair 17Human Genetics
researchProduct

An azoospermic male with reciprocal translocation t(1;15)(q11;p11)

1987

The authors report on a case of 1;15 translocation and request contact with any colleagues who have observed similar cases.

AdultMaleGeneticsAzoospermiaChromosomes Human Pair 15Chromosomal translocationOligospermiaBiologymedicine.diseaseMolecular medicineTranslocation GeneticHuman geneticsChromosomes Human Pair 1GeneticsmedicineHumansFemaleGenetics (clinical)Human Genetics
researchProduct

The val158met polymorphism of human catechol-O-methyltransferase (COMT) affects anterior cingulate cortex activation in response to painful laser sti…

2010

Background: Pain is a complex experience with sensory, emotional and cognitive aspects. Genetic and environmental factors contribute to pain-related phenotypes such as chronic pain states. Genetic variations in the gene coding for catechol-O-methyltransferase ( COMT) have been suggested to affect clinical and experimental pain-related phenotypes including regional μ-opioid system responses to painful stimulation as measured by ligand-PET (positron emission tomography). The functional val158met single nucleotide polymorphism has been most widely studied. However, apart from its impact on pain-induced opioid release the effect of this genetic variation on cerebral pain processing has not been…

AdultMaleGenotypePainSingle-nucleotide polymorphismStimulationCatechol O-MethyltransferaseGyrus CinguliCellular and Molecular NeuroscienceYoung Adultmedicinelcsh:PathologyHumansddc:610AlleleAnterior cingulate cortexCerebral CortexCatechol-O-methyl transferasePolymorphism Geneticmedicine.diagnostic_testResearchLasersChronic painMiddle Agedmedicine.diseaseMagnetic Resonance ImagingAnesthesiology and Pain Medicinemedicine.anatomical_structureCerebral cortexPositron-Emission TomographyMolecular MedicineFemaleFunctional magnetic resonance imagingPsychologyNeurosciencelcsh:RB1-214Molecular Pain
researchProduct

Variability in human hepatic MRP4 expression: influence of cholestasis and genotype

2007

The multidrug resistance protein 4 (MRP4) is an efflux transporter involved in the transport of endogenous substrates and xenobiotics. We measured MRP4 mRNA and protein expression in human livers and found a 38- and 45-fold variability, respectively. We sequenced 2 kb of the 5'-flanking region, all exons and intron/exon boundaries of the MRP4 gene in 95 patients and identified 74 genetic variants including 10 non-synonymous variations, seven of them being located in highly conserved regions. None of the detected polymorphisms was significantly associated with changes in the MRP4 mRNA or protein expression. Immunofluorescence microscopy indicated that none of the non-synonymous variations af…

AdultMaleGenotypeProtein ConformationBiologyPolymorphism Single NucleotideExonCholestasisTerminology as TopicGenotypeGenetic variationGeneticsmedicineHumansRNA MessengerGeneCellular localizationPharmacologyMessenger RNACholestasisPolymorphism GeneticReverse Transcriptase Polymerase Chain ReactionIntronGenetic VariationDNAmedicine.diseaseImmunohistochemistryMolecular biologyIntronsGene Expression RegulationHaplotypesLiverMicroscopy FluorescenceMolecular MedicineFemaleMultidrug Resistance-Associated ProteinsThe Pharmacogenomics Journal
researchProduct

Are medical residents a "core group" for for future improvement of influenza vaccination coverage in health-care workers? A study among medical resid…

2011

Abstract Despite international recommendations, vaccination coverage among European healthcare workers, including physicians, is widely recognized as unsatisfactory. In order to plan tailored vaccination campaigns and increase future coverage, we investigated reasons for refusing vaccination and determinants associated with influenza vaccine uptake among young health care workers. A survey was carried out during September and October 2010 on medical residents attending post-graduate Schools of the Medical Faculty at the University of Palermo (Italy). Each participant completed an anonymous web-based questionnaire including items on demographic and occupational characteristics, knowledge, at…

AdultMaleHealth Knowledge Attitudes PracticeInfluenza vaccineAttitude of Health PersonnelInfluenza vaccination acceptance healthcare workers medical residentsSettore MED/42 - Igiene Generale E ApplicataHospitals UniversityProfessional CompetenceEnvironmental healthSurveys and QuestionnairesHealth carePandemicInfluenza HumanMedical Staff HospitalMedicineHumansSicilyGeneral VeterinaryGeneral Immunology and Microbiologybusiness.industryVaccinationPublic Health Environmental and Occupational Healthvirus diseasesUniversity hospitalDrug UtilizationVaccinationInfectious DiseasesVaccination CampaignsInfluenza VaccinesVaccination coverageImmunologyHuman mortality from H5N1Molecular MedicineFemalebusiness
researchProduct

Visualizing knowledge and attitude factors related to influenza vaccination of physicians

2014

To characterize groups of primary healthcare physicians according to sociodemographic data, years of professional experience and knowledge of and attitudes to influenza, and to evaluate differences between groups with respect to influenza vaccination in the 2011-2012 season.We carried out an anonymous web survey of Spanish primary healthcare physicians in 2012. Information on vaccination, and knowledge of and attitudes to influenza was collected. Multiple correspondence analysis and cluster analysis were used to define groups of physicians.We included 835 physicians and identified three types. Type B were physicians with low professional experience of influenza. Types A and C were physician…

AdultMaleHealth Knowledge Attitudes Practicemedicine.medical_specialtyAttitude of Health PersonnelPrimary health careSevere diseaseSociodemographic dataDisease clusterMultiple correspondence analysisPhysiciansSurveys and QuestionnairesInfluenza HumanmedicineHumansGeneral VeterinaryGeneral Immunology and MicrobiologyTransmission (medicine)business.industryData CollectionVaccinationPublic Health Environmental and Occupational Healthvirus diseasesMiddle AgedVaccinationInfectious DiseasesFamily medicineMolecular MedicineFemalebusinessWeb surveyVaccine
researchProduct

Enormous hemangiosarcoma of the heart

1994

This report describes a 26-year-old patient with hemangiosarcoma of the heart and summarizes the clinicopathological features in previous reports of patients with cardiac angiosarcoma. The patient was admitted to our hospital because of a syncope and one episode of nocturnal dyspnea and hemoptysis. In his history he complained of progressive weakness and loss of weight over the past 2 months. Echocardiography and computed tomography of the chest showed inhomogeneous masses in the pericardial cavity completely surrounding the heart and involving the ascending aorta and the superior vena cava. Histological examination of the tissue obtained from the mass by fine needle technique revealed a po…

AdultMaleHemoptysismedicine.medical_specialtyLung NeoplasmsHeart diseaseRadiographyHemangiosarcomaShock CardiogenicSyncopeHeart NeoplasmsFatal OutcomeSuperior vena cavamedicine.arteryDrug DiscoveryAscending aortaHumansMedicineAngiosarcomaGenetics (clinical)business.industryVascular diseasePalliative CarePericardial cavityGeneral Medicinemedicine.diseaseSurgeryHemangiosarcomaEchocardiographyMolecular MedicineRadiologybusinessThe Clinical Investigator
researchProduct

Multislice multiecho T2* cardiac magnetic resonance for the detection of heterogeneous myocardial iron distribution in thalassaemia patients

2009

The present study investigated myocardial T2* heterogeneity in thalassaemia major (TM) patients by cardiac magnetic resonance (CMR), to determine whether is related to inhomogeneous iron overload distribution. A total of 230 TM patients consecutively referred to our laboratory were studied retrospectively. Three short-axis views (basal, medium and apical) of the left ventricle (LV) were obtained by multislice multiecho T2* CMR. T2* segmental distribution was mapped on a 16-segment LV model. The level of heterogeneity of the T2* segmental distribution, evaluated by the coefficient of variation (CoV), was compared with that of a surrogate data set, to determine whether the inhomogeneous segme…

AdultMaleIron OverloadIronCoefficient of variationMyocardial ironBasal (phylogenetics)medicineHumansDistribution (pharmacology)Radiology Nuclear Medicine and imagingMultisliceIn patientSpectroscopyChemistrybusiness.industryMyocardiumMagnetic Resonance Imagingmedicine.anatomical_structureVentricleThalassemiaMolecular MedicineFemaleCardiac magnetic resonanceNuclear medicinebusinessNMR in Biomedicine
researchProduct