Search results for "LYN"

showing 10 items of 910 documents

Helminth parasites in faecal samples from the endangered Iberian lynx (Lynx pardinus).

2011

The Iberian lynx is the most endangered felid in the world. Enteropathogens may threaten its survival, and therefore we analysed faecal samples from 66 different individuals (37 males and 29 females), the largest population representation studied to date. The samples were obtained from November 2005 to October 2008 in the two areas where the Iberian lynx survives: Sierra Morena and Donana (Andalusia, southern Spain). A total of 56.1% samples were parasitized with at least 6 species of helminths, including two cestodes (Hymenolepis spp. and Taenia spp.) and four Nematodes (Ancylostoma spp., Toxocara spp., Toxascaris leonina, and Capillaria sp.). In this work, the presence of Hymenolepis is r…

MaleVeterinary medicineeducation.field_of_studyToxascaris leoninaGeneral VeterinarybiologyCapillariaPopulationEndangered SpeciesEndangered speciesGeneral Medicinebiology.organism_classificationFecesAncylostomaSpainLynxTaeniaHelminthsAnimalsParasitologyFemaleHelminthiasis AnimalHymenolepis (tapeworm)educationVeterinary parasitology
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Contribution of Large Genomic Rearrangements in Italian Lynch Syndrome Patients: Characterization of a Novel Alu-Mediated Deletion

2012

Lynch syndrome is associated with germ-line mutations in the DNA mismatch repair (MMR) genes, mainlyMLH1andMSH2. Most of the mutations reported in these genes to date are point mutations, small deletions, and insertions. Large genomic rearrangements in the MMR genes predisposing to Lynch syndrome also occur, but the frequency varies depending on the population studied on average from 5 to 20%. The aim of this study was to examine the contribution of large rearrangements in theMLH1andMSH2genes in a well-characterised series of 63 unrelated Southern Italian Lynch syndrome patients who were negative for pathogenic point mutations in theMLH1,MSH2, andMSH6genes. We identified a large novel delet…

Malecongenital hereditary and neonatal diseases and abnormalitiesgenomic rearragementArticle SubjectPopulationlcsh:MedicineSettore BIO/11 - Biologia MolecolareBiologyMLH1General Biochemistry Genetics and Molecular Biologynovel Alu-mediated deletionAlu ElementsmedicineHumanseducationneoplasmsAdaptor Proteins Signal TransducingSequence DeletionGene RearrangementGeneticseducation.field_of_studyGeneral Immunology and MicrobiologyPoint mutationlcsh:RNuclear ProteinsLynch syndrome; genomic rearragements; novel Alu-mediated deletionnutritional and metabolic diseasesGeneral MedicineGene rearrangementmedicine.diseaseColorectal Neoplasms Hereditary NonpolyposisMolecular biologyLynch syndromedigestive system diseasesDNA-Binding ProteinsMSH6Settore MED/18 - Chirurgia GeneraleLynch syndromeMutS Homolog 2 ProteinItalyMSH2FemaleDNA mismatch repairMutL Protein Homolog 1Research ArticleBioMed Research International
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Risk factors for depression and anxiety in painful and painless diabetic polyneuropathy: A multicentre observational cross‐sectional study

2021

BACKGROUND Despite the high prevalence of depression and anxiety in chronic pain conditions, current knowledge concerning emotional distress among painful diabetic polyneuropathy (pDSPN) and other diabetes mellitus (DM) sufferers is limited. METHODS This observational multicentre cohort study employed the Hospital Anxiety and Depression Scale, the Beck Depression Inventory II and the State-Trait Anxiety Inventory to assess symptoms of depression and anxiety in several groups with diabetes, as well as in a control group. The study cohort included 347 pDSPN patients aged 63.4 years (median), 55.9% males; 311 pain-free diabetic polyneuropathy (nDSPN) patients aged 63.7 years, 57.9% males; 50 d…

Malemedicine.medical_specialtyAnxietyHospital Anxiety and Depression ScaleCohort Studies03 medical and health sciences0302 clinical medicineDiabetic NeuropathiesRisk FactorsDiabetes mellitusInternal medicinemedicineHumans030212 general & internal medicineDepression (differential diagnoses)Depressionbusiness.industryBeck Depression InventoryChronic painMiddle Agedmedicine.disease3. Good healthCross-Sectional StudiesAnesthesiology and Pain MedicineDiabetes Mellitus Type 2NeuralgiaAnxietyFemalePain catastrophizingmedicine.symptombusinessPolyneuropathy030217 neurology & neurosurgeryEuropean Journal of Pain
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Nerve conduction velocity and circulating immunocomplexes in type 1 diabetic children.

1991

There is evidence from several laboratories of an increased prevalence of circulating immuno-complexes (CIC) in diabetic patients. It has also been suggested that CIC are pathogenetically related to chronic diabetic complications. The aim of this study was to assess peripheral nerve function in children with Type 1 diabetes and to evaluate the relationship between the neurophysiological abnormalities and the possible presence of CIC. The investigation was carried out in 25 Type 1 diabetic patients ranging in age from 7-19 years and in 20 normal controls. Neurophysiological assessment was performed to evaluate motor and sensory conduction velocity on median and tibial nerves. IgG-CIC were de…

Malemedicine.medical_specialtyDiabetic neuropathyAdolescentSensory Receptor CellsNeural ConductionSensory systemAntigen-Antibody ComplexGastroenterologyNerve conduction velocityPathogenesisDiabetic NeuropathiesInternal medicineElectroneuronographymedicineReaction TimeHumansPeripheral NervesChildMotor NeuronsType 1 diabetesbusiness.industryGeneral Medicinemedicine.diseaseEndocrinologyDiabetes Mellitus Type 1NeurologyFemaleNeurology (clinical)ComplicationbusinessPolyneuropathyActa neurologica Scandinavica
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Patient Expectations in the Treatment of Painful Diabetic Polyneuropathy: Results from a Non-Interventional Study

2014

Objective Pain control is the main objective when treating patients with painful diabetic peripheral neuropathic pain (DPNP). However, DPNP is associated with further substantial patient burden that often is not appropriately addressed. Our study identified patients' needs and asked patients what they expected from DPNP treatment. Methods Baseline data were collected in a German prospective, non-interventional study in patients with DPNP starting or switching pain medication at the discretion of the investigator. DPNP severity was evaluated using Brief Pain Inventory (BPI) and Clinician/Patient Global Impression-Severity (CGI-S/PGI-S). Primary objective of this study was to evaluate for whi…

Malemedicine.medical_specialtyDiabetic neuropathyPain medicationCohort StudiesDiabetic NeuropathiesDiabetic polyneuropathyActivities of Daily LivingHumansMedicineIn patientProspective StudiesMobility LimitationBrief Pain InventoryAgedbusiness.industryPatient PreferenceGeneral MedicineMiddle Agedmedicine.diseasehumanitiesConfidence intervalAnesthesiology and Pain MedicineMoodPatient SatisfactionNon interventionalQuality of LifePhysical therapyFemaleNeurology (clinical)businessAttitude to HealthNeeds AssessmentPain Medicine
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Restless legs syndrome in a patient with multifocal motor neuropathy

2009

Restless legs syndrome (RLS) has been frequently reported in association with peripheral neuropathy, and it is especially frequent in some forms of polyneuropathy with preferential involvement of small sensory fibers. Here, we describe a patient with multifocal motor neuropathy, who developed RLS during the course of the disease. Our findings support the notion that RLS may develop in the context of immune-mediated neuropathies and it should be specifically investigated even in those patients with preferentially or exclusive motor involvement.

Malemedicine.medical_specialtyNeurologyContext (language use)DermatologyDiseasePhysical medicine and rehabilitationRestless Legs Syndromemental disordersmedicineHumansRestless legs syndromebusiness.industryPeripheral Nervous System DiseasesRestless legs syndrome motor neuropathyGeneral MedicineMiddle Agedmedicine.diseaseSurgeryPsychiatry and Mental healthPeripheral neuropathyDisease ProgressionSettore BIO/14 - FarmacologiaNeurology (clinical)NeurosurgerybusinessPolyneuropathyMultifocal motor neuropathyNeurological Sciences
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Refsum disease. Clinical and morphological report on a case

1982

An atypical case of Refsum disease is reported together with the peripheral nerve morphological data. The body fluids must be assayed for phytanic acid whenever an atypical chronic peripheral neuropathy is observed.

Malemedicine.medical_specialtyPathologyNeurologyAdolescentPhytanic acidDermatologychemistry.chemical_compoundPeripheral nerveHumansMedicineNeuroradiologybusiness.industryGeneral NeuroscienceGeneral Medicinemedicine.diseaseChronic PolyneuropathyBody FluidsPhytanic AcidPsychiatry and Mental healthRefsum diseasePeripheral neuropathychemistryRefsum DiseaseNeurology (clinical)NeurosurgerybusinessThe Italian Journal of Neurological Sciences
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Pigment variant of neuronal ceroid-lipofuscinosis

1995

A 6-year-old girl had progressive ataxia, and visual disturbances resulting in blindness. She died in her sleep at age 22 years. She shared with her sister and paternal relatives bilateral pes cavus deformities and impaired deep-tendon reflexes which suggested Charcot-Marie-Tooth disease. Her sister, who also had both polyneuropathy and a progressive central nervous system (CNS) disease, did not have pigmentary retinopathy. At autopsy, the patient was found to have neuronal ceroid-lipofuscinosis (NCL) marked by intraneuronal accumulation of autofluorescent granular lipopigments in ballooned perikarya and conspicuous extraneuronal pigmentation of subcortical grey matter, but without axonal s…

Malemedicine.medical_specialtyPathologyPostmortem studiesNeurologyCentral nervous systemAutopsyBiologyGrey matterEpitheliumNuclear FamilyDiagnosis DifferentialCharcot-Marie-Tooth DiseaseNeuronal Ceroid-LipofuscinosesmedicineNeuropilHumansChildGenetics (clinical)Cerebral CortexNeuronsPigmentationPigments BiologicalAnatomymedicine.diseaseMicroscopy ElectronKidney Tubulesmedicine.anatomical_structureSpinal CordFemaleNeuronal ceroid lipofuscinosisPolyneuropathyAmerican Journal of Medical Genetics
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Parenteral nutrition improves nutritional status, autonomic symptoms and quality of life in transthyretin amyloid polyneuropathy

2016

Transthyretin familial amyloid polyneuropathy (TTR-FAP) is an inherited amyloidosis, leading to death in about ten years in most cases due to cardiac failure or wasting syndrome. Previous studies showed that modified body mass index was related to time before death, duration of gastrointestinal disturbances, malabsorption and functional capacity. We report two patients in whom nutritional status worsened despite diet modification, hypercaloric supplement and two relevant therapeutic approaches such as liver transplant and tafamidis meglumine, respectively. The first patient, a 52-year-old lady carrying Thr49Ala mutation, had a disease duration of twelve years and had lost weight up to 35 kg…

Malemedicine.medical_specialtyPediatricsMalabsorptionNausea030204 cardiovascular system & hematologyPediatrics03 medical and health sciences0302 clinical medicineQuality of lifeNutritional statusMedicineHumansWasting SyndromeTTR-FAPGenetics (clinical)Amyloid Neuropathies FamilialFamilial amyloid polyneuropathy; Modified body mass index (mBMI); Nutritional status; Parenteral nutrition; TTR-FAP; Neurology (clinical); Pediatrics Perinatology and Child Health; Genetics (clinical); Neurologybiologybusiness.industryAmyloidosisMiddle AgedPerinatology and Child Healthmedicine.diseaseParenteral nutritionSurgeryTransthyretinParenteral nutritionTreatment OutcomeAutonomic Nervous System DiseasesNeurologyFamilial amyloid polyneuropathyPediatrics Perinatology and Child Healthbiology.proteinQuality of LifeFemaleNeurology (clinical)medicine.symptombusinessBody mass index030217 neurology & neurosurgeryModified body mass index (mBMI)
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Differentiation between acute and chronic myocardial infarction by means of texture analysis of late gadolinium enhancement and cine cardiac magnetic…

2017

[EN] The purpose of this study was to differentiate acute from chronic myocardial infarction using machine learning techniques and texture features extracted from cardiac magnetic resonance imaging (MRI). The study group comprised 22 cases with acute myocardial infarction (AMI) and 22 cases with chronic myocardial infarction (CMI). Cine and late gadolinium enhancement (LGE) MRI were analyzed independently to differentiate AMI from CMI. A total of 279 texture features were extracted from predefined regions of interest (ROIs): the infarcted area on LGE MRI, and the entire myocardium on cine MRI. Classification performance was evaluated by a nested cross-validation approach combining a feature…

Malemedicine.medical_specialtySupport Vector MachineMyocardial InfarctionContrast MediaMagnetic Resonance Imaging CineInfarctionGadolinium030204 cardiovascular system & hematologySensitivity and Specificity030218 nuclear medicine & medical imagingDiagnosis DifferentialTECNOLOGIA ELECTRONICA03 medical and health sciences0302 clinical medicinePolynomial kernelCardiac magnetic resonance imagingmedicineHumansLate gadolinium enhancementRadiology Nuclear Medicine and imagingMyocardial infarctioncardiovascular diseasesCardiac MRIChronic myocardial infarctionReceiver operating characteristicmedicine.diagnostic_testbusiness.industryMyocardiumReproducibility of ResultsGeneral MedicineMiddle Agedmedicine.diseaseSupport vector machineClassification Myocardial infarctionROC CurveTexture analysisArea Under CurveAcute DiseaseChronic Diseasecardiovascular systemFemaleRadiologyNuclear medicinebusinessAlgorithmsMagnetic Resonance Angiography
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