Search results for "abnormal"

showing 10 items of 761 documents

Relationship Between Glucocerebrosidase Activity and Clinical Response to Enzyme Replacement Therapy in Patients With Gaucher Disease Type I

2019

The quantification of enzyme activity in the patient treated with enzyme replacement therapy (ERT) has been suggested as a tool for dosage individualization, so we conducted a study to evaluate the relationship between glucocerebrosidase activity and clinical response in patients with Gaucher disease type I (GD1) to ERT. The study included patients diagnosed with GD1, who were being treated with ERT, and healthy individuals. Markers based on glucocerebrosidase activity measurement in patients' leucocytes were studied: enzyme activity at 15 min. post-infusion (Act(75)) reflects the amount of enzyme that is distributed in the body post-ERT infusion, and accumulated glucocerebrosidase activity…

congenital hereditary and neonatal diseases and abnormalitiesnutritional and metabolic diseases
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Corporate entrepreneurship and governance: Mergers and acquisitions in Europe

2022

Mergers and acquisitions (M&A) are a form of corporate entrepreneurship involving strategic decisions that require discussion and approval by the board of directors of the acquiring firm. We focus on board attributes to analyze the entrepreneurial function of the board of directors and its involvement in corporate entrepreneurship. Building on different theories (agency theory, resource dependence theory, stewardship theory, and stakeholder theory), we examine whether board composition affects the number of acquisitions, the risk involved in bids, and the creation of value for the acquirer's shareholders. For a sample of European firms over the period 2002 to 2020, we find that board size a…

corporate boardabnormal returnManagement of Technology and InnovationM&A performanceUNESCO::CIENCIAS ECONÓMICASBusiness and International Managementboard of directorsApplied Psychologymergers and acquisitions
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Evaluation of menstrual irregularities after COVID-19 vaccination: Results of the MECOVAC survey

2022

Abstract We investigated menstrual irregularities after the first and second doses of the COVID-19 vaccine. Women answered a customised online questionnaire (ClinicalTrial.gov ID: NCT05083065) aimed to assess the vaccine type, the phase of the menstrual cycle during which the vaccine was administered, the occurrence of menstrual irregularities after the first and second doses, and how long this effect lasted. We excluded women with gynaecological and non-gynaecological diseases, undergoing hormonal and non-hormonal treatments, in perimenopause or menopause, as well as those who had irregular menstrual cycles in the last 12 months before vaccine administration. According to our data analysis…

covid19mestrual irregularitymenstrual irregularitiesadverse effectvaccineabnormal uterine bleedingCOVID-19General MedicineMenstrual irregularitieabnormal uterine bleeding; adverse effect; COVID-19; menstrual irregularities; vaccine
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Juridiskā zinātne, Nr. 12

2019

The publishing of Journal “Law” of the University of Latvia is financed by the Faculty of Law of the University of Latvia. The publishing of issue No. 11 is supported by “Eversheds Sutherland Bitāns” Law Office.

eIDAS Regulationlegal education - University of Latviapublic assets - Latvia:LAW/JURISPRUDENCE [Research Subject Categories]principle of duty of care - Latviaseparated ownershipaccessorinesStaatsfreiheit der Parteien - Deutschlandabnormally dangerous activitiesgender equality - Latviacriminal procedure - directives of the European Parliament and of the Council procedural guaranteestax law - Latviaconstitutional changes - Polandpolitical party funding - Germanylaw making - Estonia
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De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome

2014

Activating mutations in genes encoding phosphatidylinositol 3-kinase (PI3K)-AKT pathway components cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome (MPPH, OMIM 603387)(1-3). Here we report that individuals with MPPH lacking upstream PI3K-AKT pathway mutations carry de novo mutations in CCND2 (encoding cyclin D2) that are clustered around a residue that can be phosphorylated by glycogen synthase kinase 313 (GSK-3 beta)(4). Mutant CCND2 was resistant to proteasomal degradation in vitro compared to wild-type CCND2. The PI3K-AKT pathway modulates GSK-3 beta activity(4), and cells from individuals with PIK3CA, PIK3R2 or AKT3 mutations showed similar CCND2 accumulation. CCND…

endocrine systemBlotting WesternMolecular Sequence DataMutantMedizinBiologymedicine.disease_causeArticleAKT3Mice03 medical and health sciences0302 clinical medicineCyclin D2GSK-3GeneticsmedicineAnimalsCyclin D2HumansAbnormalities MultipleExomeMegalencephalyPI3K/AKT/mTOR pathway030304 developmental biology0303 health sciencesMutationBase SequenceSequence Analysis DNASyndromeCell cyclemedicine.diseaseImmunohistochemistryMolecular biologyMegalencephalyMalformations of Cortical DevelopmentPolydactylyElectroporationHEK293 CellsBromodeoxyuridineMicroscopy FluorescenceMutagenesis Site-DirectedFemale030217 neurology & neurosurgeryHydrocephalusNature Genetics
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Epileptiform activity in the acute phase of stroke predicts the outcomes in patients without seizures

2023

Background and purposeThe abnormalities in EEG of stroke-patients increase the risk of epilepsy but their significancy for poststroke outcome is unclear. This presented study was aimed at determining the prevalence and nature of changes in EEG recordings from the stroke hemisphere and from the contralateral hemisphere. Another objective was to determine the significance of abnormalities in EEG in the first days of stroke for the post-stroke functional status on the acute and chronic phase of disease.MethodsIn all qualified stroke-patients, EEG was performed during the first 3 days of hospitalization and at discharge. The correlation between EEG abnormalities both in the stroke hemisphere an…

epileptiform abnormalitiesNeurologybrain activityRankinEEGNeurology (clinical)strokeFrontiers in Neurology
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New Frontiers in Cancer Imaging and Therapy Based on Radiolabeled Fibroblast Activation Protein Inhibitors: A Rational Review and Current Progress.

2021

Over the past decade, the tumor microenvironment (TME) has become a new paradigm of cancer diagnosis and therapy due to its unique biological features, mainly the interconnection between cancer and stromal cells. Within the TME, cancer-associated fibroblasts (CAFs) demonstrate as one of the most critical stromal cells that regulate tumor cell growth, progression, immunosuppression, and metastasis. CAFs are identified by various biomarkers that are expressed on their surfaces, such as fibroblast activation protein (FAP), which could be utilized as a useful target for diagnostic imaging and treatment. One of the advantages of targeting FAP-expressing CAFs is the absence of FAP expression in q…

fibroblast activation proteincongenital hereditary and neonatal diseases and abnormalitiesStromal cellmedicine.medical_treatmentcancer-associated fibroblastPharmaceutical Science610 Medicine & healthCancer imagingReviewfibroblast activation protein inhibitorMetastasisPharmacy and materia medicaFibroblast activation protein alphaDrug Discoverymedicinetumor microenvironment610 Medicine & healthneoplasmsradiotherapynuclear imagingTumor microenvironmentbusiness.industryRCancerImmunosuppressionmedicine.diseasedigestive system diseasesRadiation therapyRS1-441Cancer researchMolecular MedicineMedicinebusiness
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Psychological factors and defective colour vision

1995

In this study, involving students between 14 and 16 years old, the psychological dimensions of cognition and personality affected by red-green colour vision deficiencies were investigated. From the results of a factorial analysis it appears that the influence of colour vision abnormality on the psychological factors that we tested is always minor. Colour vision defect is correlated with such cognitive variables as spatial aptitude and visual difference perception, and with such personality variables as praxemia and submission. The weighting of the cognition and personality factors linked to colour vision abnormality, however, varies considerably and does not in any case contribute more than…

genetic structuresColor visionmedia_common.quotation_subjectColour VisionCognitioneye diseasesDevelopmental psychologyPersonality factorsPerceptionPersonalityAptitudeAbnormalityPsychologymedia_common
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Electrofunctional features of the tilted disc syndrome.

1986

The ERG, EOG and VEPs of 15 patients with tilted disc syndrome were studied. The ERG showed abnormal amplitudes in about 1/4 of the eyes and the EOG values were pathological in 3 patients. It is probable that the abnormality of the inferior-nasal portion of the retina and retinal pigment epithelium seen in the tilted disc syndrome causes the changes in the ERG and EOG. Pattern VEPs latency was delayed in most patients. This finding is probably due to the poor focusing of the light in the retina.

genetic structuresEye DiseasesEye diseaseOptic DiskVisual evoked potentialsPhysiology (medical)medicineElectroretinographyHumansRetinaRetinal pigment epitheliummedicine.diagnostic_testbusiness.industryAnatomyElectrooculographySyndromemedicine.diseaseeye diseasesSensory SystemsOphthalmologyElectrooculographymedicine.anatomical_structureEvoked Potentials Visualsense organsAbnormalitybusinessErgElectroretinographyDocumenta ophthalmologica. Advances in ophthalmology
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Unmixing methods in novel applications of spectral imaging

2014

hyperspectral imagingrikospaikkaimaging spectrometryspektrografilaskennallinen vaativuusympäristön tilaanalysmetoderihosyöpäskin abnormalitiesesitutkintaspectral unmixinghudcancerbrottsplatsenvironmental monitoringspektrografiamiljöövervakningspektral avbildningtarget detectionmiljöns tillståndspektrikuvausanalyysimenetelmätförundersökningforensicskuvantaminenympäristövalvontahyperspektrikuvaus
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