Chorea as a clinical feature of the basophilic inclusion body disease subtype of fused-in-sarcoma-associated frontotemporal lobar degeneration

Diagnosis and Treatment of Chorea Syndromes

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Distinct pathways leading to TDP-43-induced cellular dysfunctions

(2014) Makiko Yamashita et al.   HUMAN MOLECULAR GENETICS

Pathological features of FTLD-FUS in a Japanese population: Analyses of nine cases

(2013) Zen Kobayashi et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies

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Prion-like Properties of Pathological TDP-43 Aggregates from Diseased Brains

(2013) Takashi Nonaka et al.   Cell Reports

Atypical FTLD-FUS associated with ALS-TDP: A case report

(2012) Zen Kobayashi et al.   NEUROPATHOLOGY

The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene

(2011) Julie S. Snowden et al.   ACTA NEUROPATHOLOGICA

Neuropathological background of phenotypical variability in frontotemporal dementia

(2011) Keith A. Josephs et al.   ACTA NEUROPATHOLOGICA

A harmonized classification system for FTLD-TDP pathology

(2011) Ian R. A. Mackenzie et al.   ACTA NEUROPATHOLOGICA

FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations

(2011) Manuela Neumann et al.   BRAIN

Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

(2011) Katya Rascovsky et al.   BRAIN

Progressive nonfluent aphasia: A rare clinical subtype of FTLD-TDP in Japan

(2011) Naoya Aoki et al.   NEUROPATHOLOGY

Huntington's disease: a clinical review

(2011) Raymund A.C. Roos   Orphanet Journal of Rare Diseases

Distinct pathological subtypes of FTLD-FUS

(2010) Ian R. A. Mackenzie et al.   ACTA NEUROPATHOLOGICA

Very early-onset frontotemporal dementia with no family history predicts underlying fused in sarcoma pathology

(2010) Clement T. Loy et al.   BRAIN

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

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

Behavioral variant of frontotemporal dementia mimicking Huntington's disease

(2010) T. Rune Nielsen et al.   INTERNATIONAL PSYCHOGERIATRICS

Definition and classification of hyperkinetic movements in childhood

(2010) Terence D. Sanger et al.   MOVEMENT DISORDERS

The clinical approach to movement disorders

(2010) Wilson F. Abdo et al.   Nature Reviews Neurology

Spectrum of tardive syndromes: clinical recognition and management

(2010) R. Bhidayasiri et al.   POSTGRADUATE MEDICAL JOURNAL

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

(2009) Manuela Neumann et al.   ACTA NEUROPATHOLOGICA

FUS pathology in basophilic inclusion body disease

(2009) David G. Munoz et al.   ACTA NEUROPATHOLOGICA

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

(2009) Ian R. A. Mackenzie et al.   ACTA NEUROPATHOLOGICA

Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis

(2009) Michael J. Strong et al.   Amyotrophic Lateral Sclerosis

A new subtype of frontotemporal lobar degeneration with FUS pathology

(2009) M. Neumann et al.   BRAIN

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration

(2009) Harro Seelaar et al.   JOURNAL OF NEUROLOGY

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

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

Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

(2009) T. J. Kwiatkowski et al.   SCIENCE

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

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

Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

(2008) Masato Hasegawa et al.   ANNALS OF NEUROLOGY

Chorea-ballism associated with familial amyotrophic lateral sclerosis. A clinical, genetic, and neuropathological study

(2007) Josep Gamez et al.   MOVEMENT DISORDERS