- Home
- Publications
- Publication Search
- Publication Details
Title
Phenotypic signatures of genetic frontotemporal dementia
Authors
Keywords
-
Journal
CURRENT OPINION IN NEUROLOGY
Volume 24, Issue 6, Pages 542-549
Publisher
Ovid Technologies (Wolters Kluwer Health)
Online
2011-10-08
DOI
10.1097/wco.0b013e32834cd442
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- 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
- A harmonized classification system for FTLD-TDP pathology
- (2011) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- Inclusion Body Myopathy With Paget Disease of Bone and Frontotemporal Dementia Linked to VCP p.Arg155Cys in a Korean Family
- (2011) Eun-Joo Kim et al. ARCHIVES OF NEUROLOGY
- Genetic and Clinical Features of Progranulin-Associated Frontotemporal Lobar Degeneration
- (2011) Alice S. Chen-Plotkin et al. ARCHIVES OF NEUROLOGY
- Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration
- (2011) J. D. Rohrer et al. BRAIN
- Familial Semantic Dementia with P301L Mutation in the Tau Gene
- (2011) Takanori Ishizuka et al. DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
- Suberoylanilide Hydroxamic Acid (Vorinostat) Up-regulates Progranulin Transcription
- (2011) Basar Cenik et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Rescue of Progranulin Deficiency Associated with Frontotemporal Lobar Degeneration by Alkalizing Reagents and Inhibition of Vacuolar ATPase
- (2011) A. Capell et al. JOURNAL OF NEUROSCIENCE
- Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson’s disease in Sardinia
- (2011) Marialuisa Quadri et al. NEUROGENETICS
- Classification of primary progressive aphasia and its variants
- (2011) M. L. Gorno-Tempini et al. NEUROLOGY
- FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration
- (2010) Hazel Urwin et al. ACTA NEUROPATHOLOGICA
- Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron disease
- (2010) Agnes A. Luty et al. ANNALS OF NEUROLOGY
- Amyotrophic Lateral Sclerosis–Frontotemporal Lobar Dementia in 3 Families With p.Ala382Thr TARDBP Mutations
- (2010) Adriano Chiò et al. ARCHIVES OF NEUROLOGY
- Alzheimer Disease–like Phenotype Associated With the c.154delA Mutation in Progranulin
- (2010) Brendan J. Kelley et al. ARCHIVES OF NEUROLOGY
- The Spectrum of Mutations in Progranulin
- (2010) Chang-En Yu et al. ARCHIVES OF NEUROLOGY
- Neurobehavioral Features in Frontotemporal Dementia With Amyotrophic Lateral Sclerosis
- (2010) Patricia Lillo et al. ARCHIVES OF NEUROLOGY
- Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p
- (2010) Justin P. Pearson et al. JOURNAL OF NEUROLOGY
- Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review
- (2010) H. Seelaar et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family
- (2010) A. L. Boxer et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- 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
- MRS in presymptomatic MAPT mutation carriers: A potential biomarker for tau-mediated pathology
- (2010) K. Kantarci et al. NEUROLOGY
- Syndromes of nonfluent primary progressive aphasia: A clinical and neurolinguistic analysis
- (2010) J. D. Rohrer et al. NEUROLOGY
- TDP-43 subtypes are associated with distinct atrophy patterns in frontotemporal dementia
- (2010) J. D. Rohrer et al. NEUROLOGY
- Does TDP-43 type confer a distinct pattern of atrophy in frontotemporal lobar degeneration?
- (2010) J. L. Whitwell et al. NEUROLOGY
- Two Australian families with inclusion-body myopathy, Paget’s disease of bone and frontotemporal dementia: Novel clinical and genetic findings
- (2010) Kishore R. Kumar et al. NEUROMUSCULAR DISORDERS
- Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
- (2010) Janel O. Johnson et al. NEURON
- Autonomic failures in Perry syndrome with DCTN1 mutation
- (2010) Sachiko Ohshima et al. PARKINSONISM & RELATED DISORDERS
- Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation
- (2010) Roberto Di Fabio et al. PARKINSONISM & RELATED DISORDERS
- In vivo detection of neuropathologic changes in presymptomatic MAPT mutation carriers: A PET and MRI study
- (2010) Michie Miyoshi et al. PARKINSONISM & RELATED DISORDERS
- Mutations in CHMP2B in Lower Motor Neuron Predominant Amyotrophic Lateral Sclerosis (ALS)
- (2010) Laura E. Cox et al. PLoS One
- TARDBP Mutations in Frontotemporal Lobar Degeneration: Frequency, Clinical Features, and Disease Course
- (2010) B. Borroni et al. REJUVENATION RESEARCH
- Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
- (2009) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- A new subtype of frontotemporal lobar degeneration with FUS pathology
- (2009) M. Neumann et al. BRAIN
- Distinct anatomical subtypes of the behavioural variant of frontotemporal dementia: a cluster analysis study
- (2009) J. L. Whitwell et al. BRAIN
- FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis
- (2009) I. P. Blair et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's disease
- (2009) Miryam Carecchio et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea
- (2009) Gabor G. Kovacs et al. MOVEMENT DISORDERS
- DCTN1 mutations in Perry syndrome
- (2009) Matthew J Farrer et al. NATURE GENETICS
- Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN
- (2009) J. L. Whitwell et al. NEUROLOGY
- Characterization of DCTN1 genetic variability in neurodegeneration
- (2009) C. Vilarino-Guell et al. NEUROLOGY
- The heritability and genetics of frontotemporal lobar degeneration
- (2009) J. D. Rohrer et al. NEUROLOGY
- Atrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutations
- (2009) J. L. Whitwell et al. NEUROLOGY
- Progranulin-associated primary progressive aphasia: A distinct phenotype?
- (2009) Jonathan D. Rohrer et al. NEUROPSYCHOLOGIA
- Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations
- (2008) Stuart M. Pickering-Brown et al. BRAIN
- Distinct genetic forms of frontotemporal dementia
- (2008) H. Seelaar et al. NEUROLOGY
- Mapping the progression of progranulin-associated frontotemporal lobar degeneration
- (2008) Jonathan D Rohrer et al. Nature clinical practice. Neurology
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExplorePublish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn More