Abnormal Paraplegin Expression in Swollen Neurites, τ- and α-Synuclein Pathology in a Case of Hereditary Spastic Paraplegia SPG7 with an Ala510Val Mutation.
第一作者:
Dietmar R,Thal
第一单位:
Laboratory of Neuropathology-Institute of Pathology, Center of Clinical Research, University of Ulm, Helmholtzstraße 8/1, D-89081 Ulm, Germany. Dietmar.Thal@kuleuven.be.;Department of Neuroscience, Katholieke Universiteit Leuven, B-3000 Leuven, Belgium. Dietmar.Thal@kuleuven.be.
作者:
医学主题词
老年人(Aged);迈内特基底核(Basal Nucleus of Meynert);小脑核(Cerebellar Nuclei);基因频率(Gene Frequency);神经胶质增生(Gliosis);人类(Humans);Lewy体(Lewy Bodies);男(雄)性(Male);金属内肽酶类(Metalloendopeptidases);肌痉挛状态(Muscle Spasticity);神经突(Neurites);神经原纤维缠结(Neurofibrillary Tangles);神经元(Neurons);橄榄核(Olivary Nucleus);视神经萎缩(Optic Atrophy);痉挛性截瘫, 遗传性(Spastic Paraplegia, Hereditary);脊髓小脑共济失调(Spinocerebellar Ataxias);黑质(Substantia Nigra);α突触核蛋白(alpha-Synuclein);tau蛋白质类(tau Proteins)
DOI
10.3390/ijms161025050
PMID
26506339
发布时间
2022-03-30
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