Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles.
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Functional neuroanatomy of the noradrenergic locus coeruleus: its roles in the regulation of arousal and autonomic function part II: physiological and pharmacological manipulations and pathological alterations of locus coeruleus activity in humansFrom animal models to human disease: a genetic approach for personalized medicine in ALSDestabilizing protein polymorphisms in the genetic background direct phenotypic expression of mutant SOD1 toxicityIdentification of B6SJL mSOD1(G93A) mouse subgroups with different disease progression rates.Role of glutamate transporters in redox homeostasis of the brain.One universal common endpoint in mouse models of amyotrophic lateral sclerosis.Atypical Alzheimer's disease in an elderly United States resident with amyotrophic lateral sclerosis and pathological tau in spinal motor neurons.A cellular perspective on conformational disease: the role of genetic background and proteostasis networks.1H MRS of basal ganglia and thalamus in amyotrophic lateral sclerosisEarly onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier geneCu/Zn superoxide dismutase gene mutations in amyotrophic lateral sclerosis: correlation between genotype and clinical features.Targeting specific HATs for neurodegenerative disease treatment: translating basic biology to therapeutic possibilities.Amyotrophic lateral sclerosis-like superoxide dismutase 1 proteinopathy is associated with neuronal loss in Parkinson's disease brain.Familial amyotrophic lateral sclerosis with an I104F mutation in the SOD1 gene: Multisystem degeneration with neurofilamentous aggregates and SOD1 inclusions.An autopsy case of sporadic amyotrophic lateral sclerosis associated with the I113T SOD1 mutation.Phosphorylation of Threonine 175 Tau in the Induction of Tau Pathology in Amyotrophic Lateral Sclerosis-Frontotemporal Spectrum Disorder (ALS-FTSD). A Review.Marked intrafamilial phenotypic variation in a family with SOD1 C111Y mutationFamilial ALS with extreme phenotypic variability due to the I113T SOD1 mutation
P2860
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P2860
Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Familial amyotrophic lateral s ...... with neurofibrillary tangles.
@en
type
label
Familial amyotrophic lateral s ...... with neurofibrillary tangles.
@en
prefLabel
Familial amyotrophic lateral s ...... with neurofibrillary tangles.
@en
P2093
P2860
P356
P1476
Familial amyotrophic lateral s ...... with neurofibrillary tangles.
@en
P2093
Campbell MJ
de Belleroche JS
P2860
P304
P356
10.1136/JNNP.59.3.266
P407
P577
1995-09-01T00:00:00Z