Clinical features of frontotemporal dementia due to the intronic tau 10 ⁺¹⁶ mutation

“Mini-mental state”

1975 • 82,784 citations

Frontotemporal lobar degeneration

1998 • 4,937 citations

The Consortium to Establish a Registry for Alzheimer's Disease (CERAD)

1991 • 4,669 citations

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

1998 • 3,377 citations

A Modified Card Sorting Test Sensitive to Frontal Lobe Defects

1976 • 2,444 citations

Frontal-Subcortical Circuits and Human Behavior

1993 • 2,248 citations

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

1998 • 1,440 citations

Tau is a candidate gene for chromosome 17 frontotemporal dementia

1998 • 1,344 citations

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

1997 • 626 citations

Heterogeneity in dementia of the Alzheimer type: Evidence of subgroups

1985 • 507 citations

Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements

1999 • 506 citations

Frontotemporal Dementia and Corticobasal Degeneration in a Family with a P301S Mutation in Tau

1999 • 418 citations

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

1994 • 342 citations

Familial multiple system tauopathy with presenile dementia: A disease with abundant neuronal and glial tau filaments

1997 • 334 citations

Tau Pathology in Two Dutch Families with Mutations in the Microtubule-Binding Region of Tau

1998 • 281 citations

Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene

2000 • 264 citations

A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)

1999 • 214 citations

Dementia of frontal lobe type: neuropathology and immunohistochemistry.

1993 • 209 citations

TauGene Mutation G389R Causes a Tauopathy with Abundant Pick Body-like Inclusions and Axonal Deposits

1999 • 204 citations

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

1999 • 192 citations

Tau gene mutation in familial progressive subcortical gliosis

1999 • 189 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

Frequency of Tau Gene Mutations in Familial and Sporadic Cases of Non-Alzheimer Dementia

2001 • 170 citations

HETEROGENEITY IN PROGRESSIVE APHASIA DUE TO FOCAL CORTICAL ATROPHY

1990 • 152 citations

Pick's disease is associated with mutations in thetau gene

2000 • 135 citations

From genotype to phenotype: A clinical, pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation

1999 • 134 citations

Single Word Comprehension: A Concrete and Abstract Word Synonym Test

1998 • 128 citations

Familial presenile dementia with psychosis associated with cortical neurofibrillary tangles and degeneration of the amygdala

1992 • 117 citations

Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21

1997 • 92 citations

Familial progressive subcortical gliosis

1994 • 65 citations

Familial dementia with swollen achromatic neurons and corticobasal inclusion bodies: a clinical and pathological study

1996 • 58 citations

Apolipoprotein E ϵ4 Allele Has No Effect on Age at Onset or Duration of Disease in Cases of Frontotemporal Dementia with Pick- or Microvacuolar-Type Histology

2000 • 48 citations

Neuropathologic variation in frontotemporal dementia due to the intronic tau 10 ⁺¹⁶ mutation

2002 • 48 citations

Four Easy Memory Tests for Older Adults

1994 • 29 citations

A Family with Autosomal Dominant, Non-Alzheimer's Presenile Dementia

1997 • 20 citations

Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations

1999 • 20 citations