Pathological and Clinical Spectrum of Progressive Supranuclear Palsy: With Special Reference to Astrocytic Tau Pathology

Cognitive–behavioural features of progressive supranuclear palsy syndrome overlap with frontotemporal dementia

(2015) Christopher Kobylecki et al.   JOURNAL OF NEUROLOGY

Astrocytic inclusions in progressive supranuclear palsy and corticobasal degeneration

(2014) Mari Yoshida   NEUROPATHOLOGY

Globular glial tauopathies (GGT): consensus recommendations

(2013) Zeshan Ahmed et al.   ACTA NEUROPATHOLOGICA

Argyrophilic Grains Are Reliable Disease-Specific Features of Corticobasal Degeneration

(2013) Shinsui Tatsumi et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Glial and Neuronal Tau Pathology in Tauopathies

(2013) Isidre Ferrer et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Characteristics of progressive supranuclear palsy presenting with corticobasal syndrome: a cortical variant

(2013) H. Ling et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Clinicopathological review of pallidonigroluysian atrophy

(2012) Janice C. Wong et al.   MOVEMENT DISORDERS

LRRK2 I2020T mutation is associated with tau pathology

(2012) Sachiko Ujiie et al.   PARKINSONISM & RELATED DISORDERS

Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS

(2012) Kotaro Ogaki et al.   PARKINSONISM & RELATED DISORDERS

Autopsy-proven progressive supranuclear palsy presenting as behavioral variant frontotemporal dementia

(2011) Anhar Hassan et al.   NEUROCASE

Atypical tauopathy in a patient with LRRK2-G2019S mutation and tremor-dominant Parkinsonism

(2011) C. Ruffmann et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entity

(2010) Yong-Juan Fu et al.   ACTA NEUROPATHOLOGICA

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

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

A Huntington's disease phenocopy characterized by pallido-nigro-luysian degeneration with brain iron accumulation and p62-positive glial inclusions

(2010) Z. Ahmed et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Screening forLRRK2R1441 mutations in a cohort of PSP patients from Germany

(2009) D. Madžar et al.   EUROPEAN JOURNAL OF NEUROLOGY

Cerebellar involvement in progressive supranuclear palsy: A clinicopathological study

(2009) Masato Kanazawa et al.   MOVEMENT DISORDERS

Mutational Analysis in Early-Onset Familial Dementia in the Japanese Population

(2008) Takeshi Ikeuchi et al.   DEMENTIA AND GERIATRIC COGNITIVE DISORDERS

Screening for the LRRK2 G2019S and codon-1441 mutations in a pathological series of parkinsonian syndromes and frontotemporal lobar degeneration

(2008) Carles Gaig et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Forme fruste or incipient form of widespread-type amyotrophic lateral sclerosis, or motor neuron disease with pallido-nigro-luysian atrophy? An autopsy case report

(2008) Tomoyo Hashimoto et al.   NEUROPATHOLOGY