Back to search

FTDP-17: An early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation

Data up to Jan 2025

Published1999
Citations192
References25

Total Citations Per Year

Abstract

References (25)

A simple salting out procedure for extracting DNA from human nucleated cells

1988 • 20,341 citations

Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17

1998 • 3,377 citations

Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease

1989 • 2,308 citations

Tau is a candidate gene for chromosome 17 frontotemporal dementia

1998 • 1,344 citations

Clinical and neuropathological criteria for frontotemporal dementia. The Lund and Manchester Groups.

1994 • 1,291 citations

Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference

1997 • 626 citations

High Prevalence of Mutations in the Microtubule-Associated Protein Tau in a Population Study of Frontotemporal Dementia in the Netherlands

1999 • 419 citations

Genetic evidence for the involvement of τ in progressive supranuclear palsy

1997 • 387 citations

Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22.

1994 • 342 citations

Genetic dissection of Alzheimer's disease and related dementias: amyloid and its relationship to tau

1998 • 336 citations

Clinical characteristics of a family with chromosome 17‐linked disinhibition‐dementia‐ parkinsonism‐amyotrophy complex

1994 • 287 citations

Familial aggregation in frontotemporal dementia

1998 • 185 citations

Rapidly progressive autosomal dominant parkinsonism and dementia with pallido‐ponto‐nigral degeneration

1992 • 184 citations

Hereditary frontotemporal dementia is linked to chromosome 17q21—q22: A genetic and clinicopathological study of three dutch families

1997 • 175 citations

Hereditary dysphasic disinhibition dementia A frontotemporal dementia linked to 17 q21‐‐22

1998 • 145 citations

Relationship between clinical features of Parkinson's disease and presynaptic dopamine transporter binding assessed with [123I]IPT and single-photon emission tomography

1997 • 135 citations

Localization of the Gene for Rapidly Progressive Autosomal Dominant Parkinsonism and Dementia with Pallido-Ponto-Nigral Degeneration to Chromosome 17q21

1996 • 111 citations

Corticobasal degeneration: a disease with widespread appearance of abnormal tau and neurofibrillary tangles, and its relation to progressive supranuclear palsy

1994 • 108 citations

SPECT imaging of dopamine D2 receptors with 123I-IBZM

1991 • 83 citations

Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21–22

1997 • 82 citations

Familial progressive subcortical gliosis

1995 • 80 citations

Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotype.

1996 • 64 citations

Clinical Characteristics of a Chromosome 17--Linked Rapidly Progressive Familial Frontotemporal Dementia

1997 • 63 citations

Non‐Alzheimer degenerative dementias

1998 • 50 citations

Non-specific familial presenile dementia.

1968 • 22 citations

Cited By (0)

Loading...