Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration.
about
Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)The genetics and neuropathology of Parkinson's diseaseInvited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimagingCreation of an open-access, mutation-defined fibroblast resource for neurological disease research.Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study.MRS in presymptomatic MAPT mutation carriers: a potential biomarker for tau-mediated pathologyHereditary frontotemporal dementia caused by Tau gene mutations.Genetics of parkinsonism.Altered functional connectivity in asymptomatic MAPT subjects: a comparison to bvFTDA network of RNA and protein interactions in Fronto Temporal Dementia.Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17Assessment of Olfactory Function in MAPT-Associated Neurodegenerative Disease Reveals Odor-Identification Irreproducibility as a Non-Disease-Specific, General Characteristic of Olfactory DysfunctionPathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRNAtrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutations.Two distinct subtypes of right temporal variant frontotemporal dementia.Anatomy of disturbed sleep in pallido-ponto-nigral degeneration.Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene.Behind the curtain of tauopathy: a show of multiple players orchestrating tau toxicity.Genetics of Frontotemporal Dementia.Interest in genetic testing in pallido-ponto-nigral degeneration (PPND): a family with frontotemporal dementia with Parkinsonism linked to chromosome 17.Compartmental analysis of dopa decarboxylation in living brain from dynamic positron emission tomograms.Novel observations with FDOPA-PET imaging after early nigrostriatal damage.Frontotemporal dementia genetics.Axonal Degeneration in Tauopathies: Disease Relevance and Underlying Mechanisms.Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease.Phenotypic variation in hereditary frontotemporal dementia with tau mutations.From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation.A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)Frontotemporal dementia and Parkinsonism linked to chromosome 17 with the N279K tau mutation.Phenotypic presentation of frontotemporal dementia with Parkinsonism-chromosome 17 type P301S in a patient of Jewish-Algerian origin.Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.On the rate of decarboxylation of dopa to dopamine in living mammalian brain.Pallidopontonigral degeneration: a deceptive familial tauopathy.In vivo 18F-AV-1451 tau-PET signal in MAPT mutation carriers varies by expected tau isoforms.
P2860
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P2860
Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Rapidly progressive autosomal ...... ido-ponto-nigral degeneration.
@en
Rapidly progressive autosomal ...... ido-ponto-nigral degeneration.
@nl
type
label
Rapidly progressive autosomal ...... ido-ponto-nigral degeneration.
@en
Rapidly progressive autosomal ...... ido-ponto-nigral degeneration.
@nl
prefLabel
Rapidly progressive autosomal ...... ido-ponto-nigral degeneration.
@en
Rapidly progressive autosomal ...... ido-ponto-nigral degeneration.
@nl
P2093
P2860
P356
P1433
P1476
Rapidly progressive autosomal ...... ido-ponto-nigral degeneration.
@en
P2093
Pfeiffer RF
Rodnitzky RL
Schelper RL
Wolters EC
P2860
P304
P356
10.1002/ANA.410320303
P577
1992-09-01T00:00:00Z