Parkinsonism and Frontotemporal Dementia: The Clinical Overlap

Clinicopathological correlations in corticobasal degeneration

(2011) Suzee E. Lee et al.   ANNALS OF NEUROLOGY

An algorithm for genetic testing of frontotemporal lobar degeneration

(2011) J. S. Goldman et al.   NEUROLOGY

Neuropsychiatric symptoms of progressive supranuclear palsy in a dementia clinic

(2011) Yusuke YATABE et al.   Psychogeriatrics

Does corticobasal degeneration exist? A clinicopathological re-evaluation

(2010) H. Ling et al.   BRAIN

Caudate atrophy on MRI is a characteristic feature of FTLD-FUS

(2010) K. A. Josephs et al.   EUROPEAN JOURNAL OF NEUROLOGY

Perry syndrome due to the DCTN1 G71R mutation: A distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure

(2010) Victoria Newsway et al.   MOVEMENT DISORDERS

Novel L284R MAPT Mutation in a Family with an Autosomal Dominant Progressive Supranuclear Palsy Syndrome

(2010) Jonathan D. Rohrer et al.   Neurodegenerative Diseases

Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations

(2010) Jonathan D. Rohrer et al.   NEUROIMAGE

Does TDP-43 type confer a distinct pattern of atrophy in frontotemporal lobar degeneration?

(2010) J. L. Whitwell et al.   NEUROLOGY

Is the pathology of corticobasal syndrome predictable in life?

(2009) Bhaskara P. Shelley et al.   MOVEMENT DISORDERS

DCTN1 mutations in Perry syndrome

(2009) Matthew J Farrer et al.   NATURE GENETICS

The heritability and genetics of frontotemporal lobar degeneration

(2009) J. D. Rohrer et al.   NEUROLOGY

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

(2008) Ian R. A. Mackenzie et al.   ACTA NEUROPATHOLOGICA

Refining Frontotemporal Dementia With Parkinsonism Linked to Chromosome 17

(2008) Bradley F. Boeve et al.   ARCHIVES OF NEUROLOGY

Apraxia of speech and nonfluent aphasia: a new clinical marker for corticobasal degeneration and progressive supranuclear palsy

(2008) Keith A Josephs et al.   CURRENT OPINION IN NEUROLOGY

White Matter Tauopathy With Globular Glial Inclusions: A Distinct Sporadic Frontotemporal Lobar Degeneration

(2008) Gabor G. Kovacs et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Progranulin gene mutation with an unusual clinical and neuropathologic presentation

(2008) Christian Wider et al.   MOVEMENT DISORDERS

Novel progranulin mutation: Screening for PGRN mutations in a Portuguese series of FTD/CBS cases

(2008) Rita Joao Guerreiro et al.   MOVEMENT DISORDERS

Tau forms in CSF as a reliable biomarker for progressive supranuclear palsy

(2008) B. Borroni et al.   NEUROLOGY

Novel Mutations in TARDBP (TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis

(2008) Nicola J. Rutherford et al.   PLoS Genetics

Prominent phenotypic variability associated with mutations in Progranulin

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