Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and lewy body pathology.
about
Neurodegeneration with brain iron accumulation: update on pathogenic mechanismsUpregulation of alpha-synuclein by lipopolysaccharide and interleukin-1 in human macrophagesThe miR-15/107 group of microRNA genes: evolutionary biology, cellular functions, and roles in human diseasesNeurodegeneration with brain iron accumulation: an overview.The cellular pathology of Parkinson's disease.Genetics of parkinsonism.Novel histopathologic findings in molecularly-confirmed pantothenate kinase-associated neurodegenerationFamilial Lewy body diseases.Neurodegeneration with brain iron accumulation, type 1 is characterized by alpha-, beta-, and gamma-synuclein neuropathology.Selective insolubility of alpha-synuclein in human Lewy body diseases is recapitulated in a transgenic mouse modelTau and alpha-synuclein pathology in amygdala of Parkinsonism-dementia complex patients of GuamDisrupted membrane homeostasis and accumulation of ubiquitinated proteins in a mouse model of infantile neuroaxonal dystrophy caused by PLA2G6 mutationsNovel antibodies to phosphorylated α-synuclein serine 129 and NFL serine 473 demonstrate the close molecular homology of these epitopesExtensive aggregation of α-synuclein and tau in juvenile-onset neuroaxonal dystrophy: an autopsied individual with a novel mutation in the PLA2G6 gene-splicing siteCoexistence of TDP-43 and tau pathology in neurodegeneration with brain iron accumulation type 1 (NBIA-1, formerly Hallervorden-Spatz syndrome).Neuropathology underlying clinical variability in patients with synucleinopathies.Neuroimaging features of neurodegeneration with brain iron accumulation.Syndromes of neurodegeneration with brain iron accumulation (NBIA): an update on clinical presentations, histological and genetic underpinnings, and treatment considerations.Excess iron harms the brain: the syndromes of neurodegeneration with brain iron accumulation (NBIA).The function of α-synuclein.Exploring Missense Mutations in Tyrosine Kinases Implicated with Neurodegeneration.Genetics and Pathophysiology of Neurodegeneration with Brain Iron Accumulation (NBIA).Tau and alpha-synuclein inclusions in a case of familial frontotemporal dementia and progressive aphasia.Sporadic fatal insomnia with spongiform degeneration in the thalamus and widespread PrPSc deposits in the brain.Widespread occurrence of argyrophilic glial inclusions in Parkinson's disease.Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA).Phenotypes and genotypes of patients with pantothenate kinase-associated neurodegeneration in Asian and Caucasian populations: 2 cases and literature review.
P2860
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P2860
Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and lewy body pathology.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
2000年论文
@zh
2000年论文
@zh-cn
name
Juvenile-onset generalized neu ...... llary and lewy body pathology.
@en
Juvenile-onset generalized neuroaxonal dystrophy
@nl
type
label
Juvenile-onset generalized neu ...... llary and lewy body pathology.
@en
Juvenile-onset generalized neuroaxonal dystrophy
@nl
prefLabel
Juvenile-onset generalized neu ...... llary and lewy body pathology.
@en
Juvenile-onset generalized neuroaxonal dystrophy
@nl
P2093
P356
P1476
Juvenile-onset generalized neu ...... llary and lewy body pathology.
@en
P2093
Fukushima T
Hasegawa M
Horikawa Y
Iwatsubo T
Takahashi H
Wakabayashi K
P2888
P304
P356
10.1007/S004010050049
P577
2000-03-01T00:00:00Z