Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72
Authors
Keywords
-
Journal
BRAIN
Volume 135, Issue 3, Pages 765-783
Publisher
Oxford University Press (OUP)
Online
2012-02-25
DOI
10.1093/brain/aws004
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS
- (2011) Safa Al-Sarraj et al. ACTA NEUROPATHOLOGICA
- Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72
- (2011) Melissa E. Murray et al. ACTA NEUROPATHOLOGICA
- A harmonized classification system for FTLD-TDP pathology
- (2011) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- Proposed criteria for familial amyotrophic lateral sclerosis
- (2011) Susan Byrne et al. Amyotrophic Lateral Sclerosis
- Motor Neuron dysfunction in frontotemporal dementia
- (2011) James R. Burrell et al. BRAIN
- Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
- (2011) Katya Rascovsky et al. BRAIN
- Behavioural Variant Frontotemporal Dementia—Defining Genetic and Pathological Subtypes
- (2011) Jonathan D. Rohrer JOURNAL OF MOLECULAR NEUROSCIENCE
- Antemortem differential diagnosis of dementia pathology using structural MRI: Differential-STAND
- (2011) Prashanthi Vemuri et al. NEUROIMAGE
- Classification of primary progressive aphasia and its variants
- (2011) M. L. Gorno-Tempini et al. NEUROLOGY
- Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
- (2011) Mariely DeJesus-Hernandez et al. NEURON
- A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
- (2011) Alan E. Renton et al. NEURON
- Detecting frontotemporal dysfunction in ALS: Utility of the ALS Cognitive Behavioral Screen (ALS-CBS™)
- (2010) Susan C. Woolley et al. Amyotrophic Lateral Sclerosis
- Eating and hypothalamus changes in behavioral-variant frontotemporal dementia
- (2010) Olivier Piguet et al. ANNALS OF NEUROLOGY
- Identification of 2 Loci at Chromosomes 9 and 14 in a Multiplex Family With Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis
- (2010) Ilse Gijselinck 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, 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
- Evaluation of subcortical pathology and clinical correlations in FTLD-U subtypes
- (2009) Keith A. Josephs et al. ACTA NEUROPATHOLOGICA
- A neuropsychological battery to detect specific executive and social cognitive impairments in early frontotemporal dementia
- (2009) Teresa Torralva et al. BRAIN
- Distinct anatomical subtypes of the behavioural variant of frontotemporal dementia: a cluster analysis study
- (2009) J. L. Whitwell et al. BRAIN
- Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
- (2009) I. Le Ber et al. NEUROLOGY
- Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
- (2009) C. Vance et al. SCIENCE
- Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
- (2009) T. J. Kwiatkowski et al. SCIENCE
- Pedigree with frontotemporal lobar degeneration – motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9
- (2008) Agnes A Luty et al. BMC Neurology
- TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
- (2008) Edor Kabashi et al. NATURE GENETICS
- The Mayo Clinic Study of Aging: Design and Sampling, Participation, Baseline Measures and Sample Characteristics
- (2008) Rosebud O. Roberts et al. NEUROEPIDEMIOLOGY
- TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
- (2008) J. Sreedharan et al. SCIENCE
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started