FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases

Cognitive impairment in patients with multiple system atrophy and progressive supranuclear palsy

(2010) R. G. Brown et al.   BRAIN

Sporadic corticobasal syndrome due to FTLD-TDP

(2009) Maria Carmela Tartaglia et al.   ACTA NEUROPATHOLOGICA

Evaluation of subcortical pathology and clinical correlations in FTLD-U subtypes

(2009) Keith A. Josephs et al.   ACTA NEUROPATHOLOGICA

Brain progranulin expression in GRN-associated frontotemporal lobar degeneration

(2009) Alice S. Chen-Plotkin et al.   ACTA NEUROPATHOLOGICA

TARDBP 3′-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy

(2009) Michael A. Gitcho et al.   ACTA NEUROPATHOLOGICA

TARDBPmutations in motoneuron disease with frontotemporal lobar degeneration

(2009) Lina Benajiba et al.   ANNALS OF NEUROLOGY

Amyotrophic Lateral Sclerosis–Plus Syndrome With TAR DNA-Binding Protein-43 Pathology

(2009) Leo F. McCluskey et al.   ARCHIVES OF NEUROLOGY

Clinical and Pathological Continuum of Multisystem TDP-43 Proteinopathies

(2009) Felix Geser et al.   ARCHIVES OF NEUROLOGY

Amyotrophic lateral sclerosis, frontotemporal dementia and beyond: the TDP-43 diseases

(2009) Felix Geser et al.   JOURNAL OF NEUROLOGY

Neuroanatomical substrate of visuospatial and visuoperceptual impairment in Parkinson's disease

(2009) Joana B. Pereira et al.   MOVEMENT DISORDERS

TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea

(2009) Gabor G. Kovacs et al.   MOVEMENT DISORDERS

Parietal Lobe Deficits in Frontotemporal Lobar Degeneration Caused by a Mutation in the Progranulin Gene

(2008) Jonathan D. Rohrer et al.   ARCHIVES OF NEUROLOGY

Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation

(2008) Lena Skoglund et al.   NEUROGENETICS

Prominent phenotypic variability associated with mutations in Progranulin

(2007) Brendan J. Kelley et al.   NEUROBIOLOGY OF AGING

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

(2006) Luisa Benussi et al.   NEUROBIOLOGY OF AGING