Search results for "Amy"

showing 10 items of 1486 documents

The capacity to consent to treatment in amyotrophic lateral sclerosis: a preliminary report

2020

Background: Facing the relentless worsening of their condition, ALS patients are required to make decisions on treatments and end-of-life care. A cognitive impairment showed to be a negative prognostic factor in ALS patients, perhaps affecting the ability to make informed decisions. Notwithstanding its crucial role, the capacity to consent to treatment (CCT) has never been evaluated in these patients. Objectives: To assess the CCT in an ALS cohort in comparison to a control group, and to study the effects of demographic and clinical variables on this high-level cognitive function. Methods: 102 ALS patients and 106 healthy controls (HC) were enrolled. CCT was assessed using the MacArthur Com…

medicine.medical_specialtyNeurologygenetic structuresDiseaseNeuropsychological TestsAffect (psychology)03 medical and health sciencesCognition0302 clinical medicinemedicineHumans030212 general & internal medicineAmyotrophic lateral sclerosisAmyotrophic lateral sclerosiDepression (differential diagnoses)Informed Consentbusiness.industryAmyotrophic Lateral SclerosisNeuropsychologyCognitionmedicine.diseaseeye diseases3. Good healthCognitive impairmentNeurologyCohortNeuropsychological Testsense organsNeurology (clinical)Cognition Disordersbusiness030217 neurology & neurosurgeryDecision-makingHumanClinical psychologyJournal of Neurology
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Focal elevation of liver microsomal epoxide hydrolase in early preneoplastic stages and its behaviour in the further course of hepatocarcinogenesis.

1981

Abstract Treatment of rats with N-nitrosomorpholine (NNM) for 7 weeks led to a focal increase in liver microsomal epoxide hydrolase (EH) as early as 2 weeks after withdrawal of the carcinogen. This treatment also leads to hyperplastic nodules and liver tumors, but much later. At the same early time point, ATPase activity was decreased in the same islands. Most of these areas already had increased γ-glutamyltranspeptidase activity. The increase in EH at this early time point was more distinct than the decrease in ATPase which has thus far been considered a suitable marker of the earliest stages in hepatocarcinogenesis. The focal increase in EH was also observed in all benign hepatomas, but n…

medicine.medical_specialtyNitrosaminesATPaseBiophysicsBiochemistryLiver Neoplasms ExperimentalInternal medicinemedicineAtpase activityAnimalsMolecular BiologyCarcinogenAdenosine TriphosphatasesEpoxide HydrolasesbiologyLiver NeoplasmsCell Biologygamma-GlutamyltransferaseRatsEndocrinologyLiverMicrosomal epoxide hydrolasebiology.proteinMicrosomes LiverFemaleRabbitsHyperplastic nodulesPrecancerous ConditionsBiochemical and biophysical research communications
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Macular toxoplasmosis and intravitreal clindamycin: An alternative to oral treatment

2012

medicine.medical_specialtyOral treatmentPregnancybusiness.industryMEDLINEClindamycinGeneral Medicinemedicine.diseaseToxoplasmosisPharmacotherapyInternal medicineMedicinebusinessmedicine.drugArchivos de la Sociedad Española de Oftalmología (English Edition)
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Atherosclerosis, inflammation and Chlamydia pneumoniae

2009

Coronary heart disease is the single most common cause of illness and death in the developed world. Coronary atherosclerosis is by far the most frequent cause of ischemic heart disease, and plaque disruption with superimposed thrombosis is the main cause of the acute coronary syndromes of unstable angina, myocardial infarction, and sudden death. Atherosclerosis is the result of a complex interaction between blood elements, disturbed flow, and vessel wall abnormality, involving several pathological processes: inflammation, with increased endothelial permeability, endothelial activation, and monocyte recruitment; growth, with smooth muscle cell proliferation, migration, and matrix synthesis; …

medicine.medical_specialtyPathologyATHEROSCLEROSIS INFECTIONUnstable anginabusiness.industryInflammationChlamydia Coronary atherosclerosis Coronary heart disease PhlogosisReviewmedicine.diseaseSudden deathThrombosisEndothelial activationInternal medicinemedicineCardiologyMyocardial infarctionmedicine.symptomCardiology and Cardiovascular MedicinebusinessCoronary atherosclerosisCalcification
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Inflammatory mediators as biomarkers in brain disorders.

2013

Neurodegenerative diseases such as Alzheimer, Parkinson, amyotrophic lateral sclerosis, and Huntington are incurable and debilitating conditions that result in progressive death of the neurons. The definite diagnosis of a neurodegenerative disorder is disadvantaged by the difficulty in obtaining biopsies and thereby to validate the clinical diagnosis with pathological results. Biomarkers are valuable indicators for detecting different phases of a disease such as prevention, early onset, treatment, progression, and monitoring the effect of pharmacological responses to a therapeutic intervention. Inflammation occurs in neurodegenerative diseases, and identification and validation of molecules…

medicine.medical_specialtyPathologyImmunologyPopulationInflammationDiseaseBioinformaticsInternal medicinemedicineImmunology and AllergyHumansAmyotrophic lateral sclerosiseducationPathologicalSettore MED/04 - Patologia Generaleeducation.field_of_studyInflammation biomarkersbusiness.industryNeurodegenerative Diseasesmedicine.diseaseRheumatologyinflammationmedicine.symptomAlzheimer's diseaseInflammation MediatorsbusinessBiomarkers
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Primary perireticulin amyloidosis in a 14-year-old girl.

1976

A primary perireticulin amyloidosis is reported in a 14-year-old girl, which showed the symptoms of a steroid-resistant nephrotic syndrome. The diagnosis was established by biopsies of kidney and rectum. Occurrence of amyloidosis in childhood and the clinical picture are discussed and references to clinical trials carried out are given.

medicine.medical_specialtyPathologyNephrotic SyndromeAdolescentmedia_common.quotation_subjectBiopsyRectumKidneymedicineHumansRadiology Nuclear Medicine and imagingGirlmedia_commonbusiness.industryAmyloidosisRectumGeneral MedicineAmyloidosismedicine.diseaseDermatologySteroid-resistant nephrotic syndromeClinical trialmedicine.anatomical_structurePediatrics Perinatology and Child HealthFemalebusinessNephrotic syndromeEuropean journal of pediatrics
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Asymptomatic Carotid Lesions and Aging: Role of Hypertension and Other Traditional and Emerging Risk Factors

2006

Background We evaluated the prevalence of intima-media thickening (IMT) and asymptomatic carotid plaque (ACP) in a group of subjects with or without traditional and/or emerging risk factors (RF). Methods There were 631 subjects (313 male and 318 female) aged between 19 and 97 years, asymptomatic for cerebro- and cardiovascular diseases. The following measurements were used: anamnesis, physical examination, height and sitting blood pressure. Biochemistry variables were also considered: total cholesterol, HDL-C, LDL-C, triglycerides, fibrinogen, high sensitive C-reactive protein, IgG antibodies for Helicobacter pylori (HP), cytotoxic HP, cytomegalovirus and Chlamydia pneumoniae . Finally, an …

medicine.medical_specialtyPathologyPopulationPhysical examinationCerebroFibrinogenGastroenterologyAsymptomaticInternal medicinemedicinecardiovascular diseaseseducationAnamnesiseducation.field_of_studyChlamydiamedicine.diagnostic_testbiologybusiness.industryGeneral MedicineHelicobacter pyloribiology.organism_classificationmedicine.diseasecardiovascular systemmedicine.symptombusinessmedicine.drug
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Solid organ transplantation for non-TTR hereditary amyloidosis: report from the 1st International Workshop on the Hereditary Renal Amyloidoses.

2012

Fibrinogen A α-chain (AFib) and apolipoprotein AI (AApoAI) amyloidosis due to variants in the AFib and ApoAI genes are the most common types of hereditary amyloidosis in Europe and the United States. Liver is the exclusive source of the aberrant amyloidogenic protein in AFib and responsible for supplying approximately half of the circulating variant ApoAI. Nephrotic syndrome and renal impairment due to renal amyloidosis are common disease manifestations; however, recent research provides evidence to support a more diverse and systemic disease phenotype, which in turn has implications in the management of the hereditary amyloidoses with solid organ transplantation and, in particular, liver t…

medicine.medical_specialtyPathologySystemic diseasemedicine.medical_treatmentLiver transplantationOrgan transplantationRenal amyloidosisInternal MedicineMedicineHumansbiologyApolipoprotein A-Ibusiness.industryAmyloidosisFibrinogenOrgan Transplantationmedicine.diseaseLiver TransplantationTransplantationTransthyretinTreatment OutcomeImmunologybiology.proteinbusinessNephrotic syndromeAmyloidosis FamilialAmyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
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Role of the gamma-glutamyl cycle in the regulation of amino acid translocation

1989

Amino acid translocation was studied in the mammary gland of lactating rats and in the placenta of pregnant rats. The uptake of amino acids by the mammary gland is maximal on days 10-14 of lactation and is minimal on days 19-21. However, on day 19 maximal uptake can be restored by injection of 1) small amounts of gamma-glutamyl amino acids, 2) 5-oxoproline, and 3) an inhibitor of 5-oxoprolinase. A severe decrease in uptake of amino acids at the peak of lactation is provoked by anthglutin, an inhibitor of gamma-glutamyltranspeptidase (GGT). Simultaneous injection of 5-oxoproline blocks these effects of anthglutin. In pregnant rats, inhibition (79%) of placental GGT activity by acivicin resul…

medicine.medical_specialtyPhysiologyPlacentaEndocrinology Diabetes and MetabolismMammary glandChromosomal translocationBiologychemistry.chemical_compoundFetusPregnancyPhysiology (medical)LactationInternal medicinePlacentamedicineAnimalsHomeostasisLactationAmino AcidsMaternal-Fetal Exchangechemistry.chemical_classificationAlanineUterusBiological TransportRats Inbred Strainsgamma-GlutamyltransferaseGlutathioneMetabolismRatsAmino acidGlucoseEnzymemedicine.anatomical_structureEndocrinologychemistryBiochemistryPregnancy AnimalFemaleAmerican Journal of Physiology-Endocrinology and Metabolism
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Restoration of cerebral and systemic microvascular architecture in APP/PS1 transgenic mice following treatment with Liraglutide™.

2015

OBJECTIVE: Cerebral microvascular impairments occurring in AD may reduce Aβ peptide clearance and impact upon circulatory ultrastructure and function. We hypothesized that microvascular pathologies occur in organs responsible for systemic Aβ peptide clearance in a model of AD and that Liraglutide (Victoza(®)) improves vessel architecture. METHODS: Seven-month-old APP/PS1 and age-matched wild-type mice received once-daily intraperitoneal injections of either Liraglutide or saline (n = 4 per group) for eight weeks. Casts of cerebral, splenic, hepatic, and renal microanatomy were analyzed using SEM. RESULTS: Casts from wild-type mice showed regularly spaced microvasculature with smooth lumenal…

medicine.medical_specialtyPhysiologySpleenMice TransgenicKidneyMicrocirculationAmyloid beta-Protein PrecursorMiceAlzheimer DiseaseGlucagon-Like Peptide 1Physiology (medical)Internal medicinemedicinePresenilin-1AnimalsHumansHypoglycemic AgentsMolecular BiologyKidneybusiness.industryLiraglutideMicrocirculationBrainLiraglutideGlucagon-like peptide-1Extravasationmedicine.anatomical_structureEndocrinologyCerebrovascular CirculationCirculatory systemMicrovesselsSystemic administrationCardiology and Cardiovascular MedicinebusinessSpleenmedicine.drugMicrocirculation (New York, N.Y. : 1994)
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