نتائج البحث - "ETIOLOGY of diseases"

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المؤلفون: Birgit Ertl-Wagner, Franziska Dorn, Steffen Tiedt, Martin Dichgans, Marco Duering, Christian Barro, Benno Gesierich, Felix J. Bode, Asli Gizem Kaya, Gabor C. Petzold, Jens Kuhle, Lars Kellert, Matthias Klein, Julia Boeck, Frank A. Wollenweber, Nils Peters, Michael W. Goertler

المصدر: Neurology 91(14), e1338-e1347 (2018). doi:10.1212/WNL.0000000000006282

مصطلحات موضوعية: Male, 0301 basic medicine, diagnostic imaging [Neurodegenerative Diseases], blood [Neurofilament Proteins], Gastroenterology, Brain Ischemia, etiology [Neurodegenerative Diseases], 0302 clinical medicine, Neurofilament Proteins, Modified Rankin Scale, Neural Pathways, diagnostic imaging [Stroke], complications [Stroke], blood [Brain Ischemia], blood [Biomarkers], medicine.diagnostic_test, Brain, Neurodegenerative Diseases, complications [Brain Ischemia], Prognosis, Magnetic Resonance Imaging, diagnostic imaging [Neural Pathways], Stroke, Biomarker (medicine), Female, medicine.medical_specialty, Neurofilament light, 03 medical and health sciences, Internal medicine, medicine, Humans, ddc:610, neurofilament protein L, diagnostic imaging [Brain], Aged, business.industry, Magnetic resonance imaging, Odds ratio, Axons, Confidence interval, blood [Stroke], 030104 developmental biology, diagnostic imaging [Brain Ischemia], blood [Neurodegenerative Diseases], Ischemic stroke, Neurology (clinical), business, Biomarkers, 030217 neurology & neurosurgery, Follow-Up Studies, Diffusion MRI

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9fbe5138aef4bd3216fe3eaf39e712c
https://doi.org/10.1212/wnl.0000000000006282

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Potential human transmission of amyloid β pathology: surveillance and risks

المصدر: Lauwers, E, Lalli, G, Brandner, S, Collinge, J, Compernolle, V, Duyckaerts, C, Edgren, G, Haïk, S, Hardy, J, Helmy, A, Ivinson, A J, Jaunmuktane, Z, Jucker, M, Knight, R, Lemmens, R, Lin, I, Love, S, Mead, S, Perry, V H, Pickett, J, Poppy, G, Radford, S E, Rousseau, F, Routledge, C, Schiavo, G, Schymkowitz, J, Selkoe, D J, Smith, C, Thal, D R, Theys, T, Tiberghien, P, Van Den Burg, P, Vandekerckhove, P, Walton, C, Zaaijer, H L, Zetterberg, H & De Strooper, B 2020, ' Potential human transmission of amyloid β pathology: surveillance and risks ', Lancet Neurology, vol. 19, no. 10, pp. 872-878 . https://doi.org/10.1016/S1474-4422(20)30238-6
The lancet / Neurology 19(10), 872-878 (2020). doi:10.1016/S1474-4422(20)30238-6
Lauwers, E, Lalli, G, Brandner, S, Collinge, J, Compernolle, V, Duyckaerts, C, Edgren, G, Haik, S, Hardy, J, Helmy, A, Ivinson, A, Jaunmuktane, Z, Jucker, M, Knight, R, Lemmens, R, Love, S, Mead, S & de Strooper, B 2020, ' Potential human transmission of amyloid beta pathology : surveillance and risks ', Lancet Neurology, vol. 19, no. 10, pp. 872-878 . https://doi.org/10.1016/S1474-4422(20)30238-6

مصطلحات موضوعية: 0301 basic medicine, Pathology, Amyloid β, etiology [Alzheimer Disease], Disease, metabolism [Neurodegenerative Diseases], Creutzfeldt-Jakob Syndrome, etiology [Neurodegenerative Diseases], pathology [Alzheimer Disease], 0302 clinical medicine, Risk Factors, metabolism [Creutzfeldt-Jakob Syndrome], neurosurgery, Iatrogenic transmission, biology, Transmission (medicine), pathology [Neurodegenerative Diseases], Neurodegenerative Diseases, Parkinson Disease, Population Surveillance, transmission [Creutzfeldt-Jakob Syndrome], etiology [Parkinson Disease], Cerebral amyloid angiopathy, Amyloid-beta, metabolism [Alzheimer Disease], medicine.medical_specialty, Amyloid, Amyloid beta, metabolism [Parkinson Disease], metabolism [Amyloid beta-Peptides], blood transfusion, prion, 03 medical and health sciences, Alzheimer Disease, mental disorders, medicine, Dementia, Animals, Humans, ddc:610, proteopathic seed, pathology [Creutzfeldt-Jakob Syndrome], Amyloid beta-Peptides, iatrogenic transmission, business.industry, medicine.disease, toxicity [Amyloid beta-Peptides], pathology [Parkinson Disease], 030104 developmental biology, biology.protein, Neurology (clinical), business, 030217 neurology & neurosurgery

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https://eprints.whiterose.ac.uk/161306/1/THELANCETNEUROLOGY-D-20-00204R3_Main_text_CLEAN.pdf

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Distribution of microRNA profiles in pre-clinical and clinical forms of murine and human prion disease

المؤلفون: Mitch Shambrook, Laura J Ellett, Xia Li, Saima Zafar, Lesley Cheng, Andrew F. Hill, Inga Zerr, Shayne A. Bellingham, Camelia Quek, Victoria A. Lawson

المصدر: Communications Biology
Communications Biology, Vol 4, Iss 1, Pp 1-12 (2021)
Communications biology 4(1), 411 (2021). doi:10.1038/s42003-021-01868-x

مصطلحات موضوعية: 0301 basic medicine, Male, animal diseases, Medicine (miscellaneous), blood [Creutzfeldt-Jakob Syndrome], Disease, analysis [MicroRNAs], Creutzfeldt-Jakob Syndrome, Prion Diseases, Mice, 0302 clinical medicine, pathology [Brain], etiology [Creutzfeldt-Jakob Syndrome], etiology [Prion Diseases], Biology (General), Aged, 80 and over, Mice, Inbred BALB C, blood [Biomarkers], Neurodegeneration, Brain, Middle Aged, Alzheimer's disease, Mechanisms of disease, Female, General Agricultural and Biological Sciences, QH301-705.5, Thalamus, Biology, General Biochemistry, Genetics and Molecular Biology, Article, 03 medical and health sciences, ddc:570, mental disorders, microRNA, medicine, Distribution (pharmacology), Dementia, Animals, Humans, Aged, blood [MicroRNAs], medicine.disease, Serum samples, nervous system diseases, MicroRNAs, 030104 developmental biology, blood [Prion Diseases], Immunology, Gene expression, 030217 neurology & neurosurgery, Biomarkers

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::965ec9c52039203d11f1dcba9bcf08a5
https://pubmed.ncbi.nlm.nih.gov/33767334

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4

Microglia Biology: One Century of Evolving Concepts

المؤلفون: Josef Priller, Steffen Jung, Marco Prinz

المصدر: Cell 179(2), 292-311 (2019). doi:10.1016/j.cell.2019.08.053

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56cd80219e17839add40396b0f519a8f
https://pubmed.ncbi.nlm.nih.gov/31585077

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miRNAs Identify Shared Pathways in Alzheimer's and Parkinson's Diseases

المؤلفون: Robert Perneczky, Panagiotis Alexopoulos, Inga Prokopenko, Petros Takousis, Evangelos Evangelou, Angélique Sadlon

المصدر: Trends in molecular medicine 25(8), 662-672 (2019). doi:10.1016/j.molmed.2019.05.006

مصطلحات موضوعية: 0301 basic medicine, ALPHA-SYNUCLEIN, L1, diagnosis, etiology [Alzheimer Disease], Disease, metabolism [Neurodegenerative Diseases], Research & Experimental Medicine, WIDE IDENTIFICATION, etiology [Neurodegenerative Diseases], pathology [Alzheimer Disease], chemistry.chemical_compound, 0302 clinical medicine, Gene Regulatory Networks, genetics [MicroRNAs], ADHESION MOLECULE, pathophysiology, 11 Medical and Health Sciences, Caspase, biology, DEMENTIA, Neurodegeneration, pathology [Neurodegenerative Diseases], neurodegeneration, Neurodegenerative Diseases, Parkinson Disease, LEWY BODIES, Medicine, Research & Experimental, MESSENGER-RNA TRANSLATION, Caspases, etiology [Parkinson Disease], biomarker, Molecular Medicine, Disease Susceptibility, Life Sciences & Biomedicine, metabolism [Alzheimer Disease], Signal Transduction, EXPRESSION, Biochemistry & Molecular Biology, Immunology, Neuronal Outgrowth, metabolism [Parkinson Disease], 03 medical and health sciences, Alzheimer Disease, microRNA, medicine, metabolism [Caspases], Dementia, Animals, Humans, ddc:610, Molecular Biology, CHRONIC BRAIN HYPOPERFUSION, Alpha-synuclein, therapy, Science & Technology, Cell Biology, 06 Biological Sciences, DOPAMINERGIC-NEURONS, medicine.disease, pathology [Parkinson Disease], Biomarker (cell), MicroRNAs, 030104 developmental biology, chemistry, Gene Expression Regulation, biology.protein, MICRORNA DYSREGULATION, Neuroscience, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee9b15a4507d7d2098d402345e53488b
https://pubmed.ncbi.nlm.nih.gov/31221572

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Biallelic variants in the transcription factor PAX7 are a new genetic cause of myopathy

المساهمون: Universidade do Minho

المصدر: Genetics in medicine 21(11), 2521-2531 (2019). doi:10.1038/s41436-019-0532-z
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP

مصطلحات موضوعية: 0301 basic medicine, Male, Pathology, metabolism [Muscle, Skeletal], Myopathy, Medicina Básica [Ciências Médicas], 030105 genetics & heredity, Muscle Development, Whole Exome Sequencing, Myoblasts, Myocyte, Child, Genetics (clinical), Exome sequencing, education.field_of_study, metabolism [Satellite Cells, Skeletal Muscle], PAX7 Transcription Factor, metabolism [PAX7 Transcription Factor], genetics [Transcription Factors], musculoskeletal system, Hypotonia, 3. Good health, Pedigree, medicine.anatomical_structure, Child, Preschool, Ciências Médicas::Medicina Básica, Female, Stem cell, medicine.symptom, tissues, medicine.medical_specialty, Adolescent, Satellite Cells, Skeletal Muscle, Population, Biology, etiology [Muscular Diseases], 03 medical and health sciences, Atrophy, Muscular Diseases, Exome Sequencing, medicine, genetics [Muscular Diseases], genetics [PAX7 Transcription Factor], Humans, Regeneration, ddc:610, skeletal muscle, education, Muscle, Skeletal, Alleles, Muscle stem cell, Science & Technology, Skeletal muscle, medicine.disease, PAX7, 030104 developmental biology, methods [Exome Sequencing], Transcription Factors

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::974e0cb8d7282fa5111b507fc8c8fa45
https://hdl.handle.net/1822/67260

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Transcutaneous vagal nerve stimulation improves gastroenteric complaints in Parkinson's disease patients

المؤلفون: Ullrich Wüllner, Laura Janocha, Oliver Kaut, Tobias J. Weismüller

المصدر: Neurorehabilitation 45(4), 449-451 (2019). doi:10.3233/NRE-192909

مصطلحات موضوعية: Male, 030506 rehabilitation, therapy [Parkinson Disease], Parkinson's disease, Vagus Nerve Stimulation, Gastrointestinal Diseases, Vagal nerve, adverse effects [Vagus Nerve Stimulation], Physical Therapy, Sports Therapy and Rehabilitation, Stimulation, adverse effects [Transcutaneous Electric Nerve Stimulation], Disease, Sham group, methods [Vagus Nerve Stimulation], 03 medical and health sciences, 0302 clinical medicine, Double-Blind Method, Rating scale, Medicine, Humans, In patient, ddc:610, Aged, Breath test, medicine.diagnostic_test, business.industry, therapy [Gastrointestinal Diseases], Rehabilitation, Parkinson Disease, Middle Aged, medicine.disease, etiology [Gastrointestinal Diseases], Anesthesia, Transcutaneous Electric Nerve Stimulation, methods [Transcutaneous Electric Nerve Stimulation], Female, Neurology (clinical), complications [Parkinson Disease], 0305 other medical science, business, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35efffa90528140bd3dd8d6b1c99abf0

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Gut Microbiota-Dependent Trimethylamine N-Oxide Predicts Risk of Cardiovascular Events in Patients With Stroke and Is Related to Proinflammatory Monocytes

المصدر: Arteriosclerosis, thrombosis, and vascular biology 38(9), 2225-2235 (2018). doi:10.1161/ATVBAHA.118.311023

مصطلحات موضوعية: 0301 basic medicine, Antigens, Differentiation, T-Lymphocyte, Male, metabolism [Stroke], Trimethylamine N-oxide, etiology [Cardiovascular Diseases], Monocytes, Brain Ischemia, chemistry.chemical_compound, Recurrence, Risk Factors, physiology [Gastrointestinal Microbiome], Choline, complications [Stroke], Prospective Studies, Stroke, Hazard ratio, complications [Brain Ischemia], etiology [Death, Sudden, Cardiac], Cardiovascular Diseases, CD4 Antigens, CD6 antigen, Female, Cardiology and Cardiovascular Medicine, medicine.medical_specialty, metabolism [Brain Ischemia], CD14, trimethyloxamine, blood [Methylamines], Article, Proinflammatory cytokine, immunology [Monocytes], 03 medical and health sciences, Methylamines, Antigens, CD, Diabetes mellitus, Internal medicine, medicine, Animals, Humans, ddc:610, Inflammation, Cholesterol, business.industry, medicine.disease, Gastrointestinal Microbiome, Mice, Inbred C57BL, 030104 developmental biology, Endocrinology, Death, Sudden, Cardiac, chemistry, business, metabolism [Monocytes]

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdd3ed9add4b75e23c236b434248e17b
https://pubmed.ncbi.nlm.nih.gov/29976769

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Friedreich and dominant ataxias: quantitative differences in cerebellar dysfunction measurements

المساهمون: Tezenas du Montcel, Sophie, CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Fondazione IRCCS Istituto Neurologico 'Carlo Besta', Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), University College of London [London] (UCL), Leopold Franzens Universität Innsbruck - University of Innsbruck, Munich Cluster for systems neurology [Munich] (SyNergy), Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM)-Ludwig-Maximilians-Universität München (LMU), University of Tübingen, German Research Center for Neurodegenerative Diseases - Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Philipps Universität Marburg = Philipps University of Marburg, Universitätsklinikum RWTH Aachen - University Hospital Aachen [Aachen, Germany] (UKA), Rheinisch-Westfälische Technische Hochschule Aachen University (RWTH), Jülich Aachen Research Alliance (JARA), Hôpital Erasme [Bruxelles], Institut du Cerveau = Paris Brain Institute (ICM), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Sorbonne Université (SU), Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP), Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)

المصدر: Journal of neurology, neurosurgery, and psychiatry 89(6), 559-565 (2018). doi:10.1136/jnnp-2017-316964
Journal of neurology, neurosurgery, and psychiatry 89(6), 559-565 (2017). doi:10.1136/jnnp-2017-316964
Journal of Neurology, Neurosurgery and Psychiatry
Journal of Neurology, Neurosurgery and Psychiatry, 2018, 89 (6), pp.559-565. ⟨10.1136/jnnp-2017-316964⟩

مصطلحات موضوعية: 0301 basic medicine, Male, Time Factors, physiopathology [Spinocerebellar Ataxias], Severity of Illness Index, 0302 clinical medicine, Medicine, Age of Onset, Child, etiology [Cerebellar Diseases], Aged, 80 and over, Outcome measures, Middle Aged, Psychiatry and Mental health, Spinocerebellar ataxia, Cardiology, Female, medicine.symptom, Adult, medicine.medical_specialty, Ataxia, Adolescent, Disease duration, physiopathology [Friedreich Ataxia], Context (language use), 03 medical and health sciences, Young Adult, Cerebellar Diseases, Internal medicine, Humans, Spinocerebellar Ataxias, In patient, ddc:610, Trial registration, Aged, complications [Spinocerebellar Ataxias], diagnosis [Cerebellar Diseases], business.industry, Cerebellar dysfunction, medicine.disease, complications [Friedreich Ataxia], 030104 developmental biology, [SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologie, Friedreich Ataxia, Case-Control Studies, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, Surgery, Neurology (clinical), business, 030217 neurology & neurosurgery

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f83aa958b0096bec2cc5837bc0b48bb1
https://pubmed.ncbi.nlm.nih.gov/29279305

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10

First symptom and initial diagnosis in sporadic CJD patients in Germany

المؤلفون: Inga Zerr, Anna Krasnianski, Hans A. Kretzschmar, Judith Kaune, Klaus Jung

المصدر: Journal of neurology 261(9), 1811-1817 (2014). doi:10.1007/s00415-014-7410-z

مصطلحات موضوعية: Male, Pediatrics, Pathology, Neurology, Photophobia, Disease, Creutzfeldt-Jakob Syndrome, Polymorphism (computer science), Germany, Genotype, Medicine, Young adult, Child, etiology [Cerebellar Diseases], epidemiology [Vision Disorders], Diagnostic Techniques and Procedures, Neuroradiology, physiopathology [Creutzfeldt-Jakob Syndrome], Aged, 80 and over, Mental Disorders, genetics [Creutzfeldt-Jakob Syndrome], Middle Aged, Female, medicine.symptom, etiology [Mental Disorders], Adult, medicine.medical_specialty, Adolescent, psychology [Dementia], Prions, Vision Disorders, diagnosis [Creutzfeldt-Jakob Syndrome], psychology [Creutzfeldt-Jakob Syndrome], statistics & numerical data [Diagnostic Errors], diagnosis [Mental Disorders], epidemiology [Dementia], Polymorphism, Single Nucleotide, Diagnosis, Differential, Young Adult, complications [Creutzfeldt-Jakob Syndrome], Cerebellar Diseases, mental disorders, Humans, Dementia, ddc:610, Diagnostic Errors, Aged, diagnosis [Cerebellar Diseases], genetics [Prions], business.industry, medicine.disease, epidemiology [Mental Disorders], diagnosis [Dementia], etiology [Vision Disorders], nervous system diseases, epidemiology [Cerebellar Diseases], Neurology (clinical), etiology [Dementia], diagnosis [Vision Disorders], business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d851b6af55d7e10036e4c96120e1abf7
https://doi.org/10.1007/s00415-014-7410-z

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