Refining Frontotemporal Dementia With Parkinsonism Linked to Chromosome 17

Amyloid Oligomers Exacerbate Tau Pathology in a Mouse Model of Tauopathy

2012 • 10,051 citations

Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis

2006 • 5,928 citations

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

1998 • 3,377 citations

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

2006 • 1,929 citations

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

2006 • 1,444 citations

Inhibition of glycogen synthase kinase-3 by lithium correlates with reduced tauopathy and degenerationin vivo

2005 • 673 citations

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

1997 • 626 citations

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

2006 • 544 citations

Microtubule-binding drugs offset tau sequestration by stabilizing microtubules and reversing fast axonal transport deficits in a tauopathy model

2004 • 395 citations

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene

2006 • 291 citations

Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia

2006 • 197 citations

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin‐positive, tau‐negative inclusions caused by a missense mutation in the signal peptide of progranulin

2006 • 189 citations

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome

2006 • 185 citations

Neuropathologic Features of Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions With Progranulin Gene (PGRN) Mutations

2007 • 185 citations

Prominent phenotypic variability associated with mutations in Progranulin

2007 • 173 citations

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

2001 • 170 citations

Progranulin Mutations in Primary Progressive Aphasia

2007 • 152 citations

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

1998 • 145 citations

A novel deletion in progranulin gene is associated with FTDP-17 and CBS

2006 • 126 citations

Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study

2006 • 111 citations

Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval

2002 • 107 citations

A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17

2006 • 103 citations

A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD

2006 • 91 citations

Characteristics of frontotemporal dementia patients with a Progranulin mutation

2006 • 87 citations

Clinicopathologic features of frontotemporal dementia with Progranulin sequence variation

2007 • 78 citations

Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation

2004 • 55 citations

Corticobasal Degeneration and Frontotemporal Dementia Presentations in a Kindred with Nonspecific Histopathology

2002 • 31 citations

Pick's complex and FTDP-17

2003 • 28 citations

Familial Primary Progressive Aphasia

2003 • 27 citations

Distinctive MRI findings in pallidopontonigral degeneration (PPND)

2007 • 15 citations

Progranulin Mutations in Primary Progressive Aphasia: The PPA1 and PPA3 Families

2008 • 11 citations