يعرض 1 - 5 نتائج من 5 نتيجة بحث عن '"Frontotemporal Dementia pathology"', وقت الاستعلام: 1.34s تنقيح النتائج
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    المساهمون: Netherlands Institute for Neuroscience (NIN), Clinical Genetics, Neurology, Internal Medicine, Molecular and Cellular Neurobiology, Amsterdam Neuroscience - Neurodegeneration, AIMMS, Amsterdam Neuroscience - Cellular & Molecular Mechanisms, Center for Neurogenomics and Cognitive Research

    المصدر: Acta neuropathologica communications, 10(1). BioMed Central
    Acta neuropathologica communications, 10(1):190. BioMed Central Ltd.
    Acta Neuropathologica Communications, 10:190, 1-14. BioMed Central
    Mol, M O, Miedema, S S M, Melhem, S, Li, K W, Koopmans, F, Seelaar, H, Gottmann, K, Lessmann, V, Bank, N B, Smit, A B, van Swieten, J C & van Rooij, J G J 2022, ' Proteomics of the dentate gyrus reveals semantic dementia specific molecular pathology ', Acta Neuropathologica Communications, vol. 10, 190, pp. 1-14 . https://doi.org/10.1186/s40478-022-01499-1

    وصف الملف: application/pdf

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    المساهمون: Neurology, Pathology, Amsterdam Neuroscience - Neurodegeneration, Netherlands Institute for Neuroscience (NIN)

    المصدر: Netherlands Brain Bank 2022, ' Isoform-specific patterns of tau burden and neuronal degeneration in MAPT-associated frontotemporal lobar degeneration ', Acta Neuropathologica, vol. 144, no. 6, pp. 1065-1084 . https://doi.org/10.1007/s00401-022-02487-4
    Acta Neuropathologica, 144(6), 1065-1084. Springer-Verlag
    Acta Neuropathologica, 144(6), 1065-1084. Springer Verlag
    Acta Neuropathologica, 144(6), 1065-1084. Springer Verlag GmbH

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    المساهمون: Dermaut, Bart

    المصدر: Addi. Archivo Digital para la Docencia y la Investigación
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    PLoS ONE, Vol 12, Iss 6, p e0178093 (2017)
    PLoS ONE
    PloS one, vol 12, iss 6
    Recercat. Dipósit de la Recerca de Catalunya

    مصطلحات موضوعية: Male, 0301 basic medicine, Aging, tau Proteins/genetics, Cytoplasm, Linkage disequilibrium, Mutation rate, haplotype, Heredity, Social Sciences, Neurodegenerative, Neuropsychological Tests, Alzheimer's Disease, medicine.disease_cause, Hippocampus, spectrum, Primary progressive aphasia, Frontotemporal Dementia/pathology, Progranulins, 0302 clinical medicine, Mutation Rate, Medicine and Health Sciences, 2.1 Biological and endogenous factors, Psychology, Aetiology, alzheimers-disease, Genetics, Cytoplasmic Inclusions, Multidisciplinary, TDP-43 protein, human, phenotypes, Brain, Neurodegenerative Diseases, Frontotemporal lobar degeneration, Middle Aged, Amygdala, progranulin mutation, Immunohistochemistry, DNA-Binding Proteins, Frontotemporal Dementia (FTD), Genetic Mapping, Phenotype, Neurology, frontotemporal lobar degeneration, Frontotemporal Dementia, Neurological, Intercellular Signaling Peptides and Proteins, Medicine, Female, Cellular Structures and Organelles, Anatomy, Research Article, Frontotemporal dementia, Intercellular Signaling Peptides and Proteins/genetics, Mutation/genetics, General Science & Technology, Science, MAPT protein, human, tau Proteins, Biology, 03 medical and health sciences, Rare Diseases, tau Proteins/metabolism, Clinical Research, Alzheimer Disease, Neuropsychology, Mental Health and Psychiatry, Acquired Cognitive Impairment, medicine, Humans, Dementia, Family, Demography, Haplotype, Neurosciences, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Biology and Life Sciences, Cell Biology, C9orf72 repeat expansion, medicine.disease, Brain Disorders, 030104 developmental biology, Haplotypes, variant, Spain, Mutation, GRN protein, human, Tau, 030217 neurology & neurosurgery, Neuroscience, dementia

    وصف الملف: application/pdf