Related references
Note: Only part of the references are listed.Are the UK genetic testing criteria for dementia too exclusive?
Annita Christodoulidou et al.
JOURNAL OF NEUROLOGY (2021)
Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p
Ging-Yuek R. Hsiung et al.
BRAIN (2012)
Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations
Julie S. Snowden et al.
BRAIN (2012)
The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions
Javier Simon-Sanchez et al.
BRAIN (2012)
Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72
Bradley F. Boeve et al.
BRAIN (2012)
Evidence for an oligogenic basis of amyotrophic lateral sclerosis
Marka van Blitterswijk et al.
HUMAN MOLECULAR GENETICS (2012)
ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutations
Adriano Chio et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2012)
Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study (vol 11, pg 232, 2012)
S. Byrne et al.
LANCET NEUROLOGY (2012)
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Elisa Majounie et al.
LANCET NEUROLOGY (2012)
Large C9orf72 repeat expansions are not a common cause of Parkinson's disease
Elisa Majounie et al.
NEUROBIOLOGY OF AGING (2012)
C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect
Antonia Ratti et al.
NEUROBIOLOGY OF AGING (2012)
Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype
Nicola J. Rutherford et al.
NEUROBIOLOGY OF AGING (2012)
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease
Serena Lattante et al.
NEUROLOGY (2012)
C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts
Carol Dobson-Stone et al.
NEUROLOGY (2012)
Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study
Susan Byrne et al.
LANCET NEUROLOGY (2012)
Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72
Melissa E. Murray et al.
ACTA NEUROPATHOLOGICA (2011)
Neuropathological background of phenotypical variability in frontotemporal dementia
Keith A. Josephs et al.
ACTA NEUROPATHOLOGICA (2011)
A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis
Amr Al-Saif et al.
ANNALS OF NEUROLOGY (2011)
Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review
Harro Seelaar et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2011)
Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
Mariely DeJesus-Hernandez et al.
NEURON (2011)
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
Alan E. Renton et al.
NEURON (2011)
Sigma Nonopioid Intracellular Receptor 1 Mutations Cause Frontotemporal Lobar Degeneration-Motor Neuron Disease
Agnes A. Luty et al.
ANNALS OF NEUROLOGY (2010)
Molecular Pathways of Frontotemporal Lobar Degeneration
Kristel Sleegers et al.
ANNUAL REVIEW OF NEUROSCIENCE, VOL 33 (2010)
Myotonic Dystrophies 1 and 2: Complex Diseases with Complex Mechanisms
Benedikt Schoser et al.
CURRENT GENOMICS (2010)
Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration
Sara Rollinson et al.
NEUROBIOLOGY OF AGING (2009)
The heritability and genetics of frontotemporal lobar degeneration
J. D. Rohrer et al.
NEUROLOGY (2009)
Pedigree with frontotemporal lobar degeneration - motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9
Agnes A. Luty et al.
BMC NEUROLOGY (2008)