- Home
- Publications
- Publication Search
- Publication Details
Title
Motor neuron disease-frontotemporal dementia: a clinical continuum
Authors
Keywords
-
Journal
Expert Review of Neurotherapeutics
Volume 15, Issue 5, Pages 509-522
Publisher
Informa UK Limited
Online
2015-04-11
DOI
10.1586/14737175.2015.1034108
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Multiple system atrophy is not caused by C9orf72 hexanucleotide repeat expansions
- (2015) Sonja W. Scholz et al. NEUROBIOLOGY OF AGING
- A familial ALS case carrying a novel p.G147CSOD1heterozygous missense mutation with non-executive cognitive impairment: Figure 1
- (2014) Antonio Canosa et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Safety and efficacy of ceftriaxone for amyotrophic lateral sclerosis: a multi-stage, randomised, double-blind, placebo-controlled trial
- (2014) Merit E Cudkowicz et al. LANCET NEUROLOGY
- Antisense Oligonucleotide Therapy for the Treatment of C9ORF72 ALS/FTD Diseases
- (2014) Giulietta Riboldi et al. MOLECULAR NEUROBIOLOGY
- Absence ofC9ORF72expanded or intermediate repeats in autopsy-confirmed Parkinson's disease
- (2014) Karen Nuytemans et al. MOVEMENT DISORDERS
- Prefrontal involvement related to cognitive impairment in progressive muscular atrophy
- (2014) J. Raaphorst et al. NEUROLOGY
- Discovery of a Biomarker and Lead Small Molecules to Target r(GGGGCC)-Associated Defects in c9FTD/ALS
- (2014) Zhaoming Su et al. NEURON
- Advances in treating amyotrophic lateral sclerosis: insights from pathophysiological studies
- (2014) Steve Vucic et al. TRENDS IN NEUROSCIENCES
- A novel tool to detect behavioural symptoms in ALS
- (2014) Eneida Mioshi et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Multiple System Atrophy and Amyotrophic Lateral Sclerosis in a Family With Hexanucleotide Repeat Expansions inC9orf72
- (2014) Jill S. Goldman et al. JAMA Neurology
- Frontotemporal Dementia Associated With theC9ORF72Mutation
- (2014) Emma Devenney et al. JAMA Neurology
- C9orf72 repeat expansions are a rare genetic cause of parkinsonism
- (2013) Suzanne Lesage et al. BRAIN
- Fasciculation anxiety syndrome in clinicians
- (2013) Neil G. Simon et al. JOURNAL OF NEUROLOGY
- Pathophysiological insights into ALS with C9ORF72 expansions
- (2013) K. L. Williams et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Dexpramipexole versus placebo for patients with amyotrophic lateral sclerosis (EMPOWER): a randomised, double-blind, phase 3 trial
- (2013) Merit E Cudkowicz et al. LANCET NEUROLOGY
- Memantine in patients with frontotemporal lobar degeneration: a multicentre, randomised, double-blind, placebo-controlled trial
- (2013) Adam L Boxer et al. LANCET NEUROLOGY
- Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study
- (2013) Marka van Blitterswijk et al. LANCET NEUROLOGY
- Multiparametric MRI study of ALS stratified for the C9orf72 genotype
- (2013) P. Bede et al. NEUROLOGY
- Neuropsychiatric changes precede classic motor symptoms in ALS and do not affect survival
- (2013) E. Mioshi et al. NEUROLOGY
- Cortical atrophy in ALS is critically associated with neuropsychiatric and cognitive changes
- (2013) E. Mioshi et al. NEUROLOGY
- C9ORF72 repeat expansions in cases with previously identified pathogenic mutations
- (2013) M. van Blitterswijk et al. NEUROLOGY
- A pathogenicprogranulinmutation andC9orf72repeat expansion in a family with frontotemporal dementia
- (2013) Tammaryn Lashley et al. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
- Current insights into the C9orf72 repeat expansion diseases of the FTLD/ALS spectrum
- (2013) Marc Cruts et al. TRENDS IN NEUROSCIENCES
- Frontotemporal dementia with amyotrophic lateral sclerosis: A clinical comparison of patients with and without repeat expansions inC9orf72
- (2013) Julie S. Snowden et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p
- (2012) Heather Stewart et al. ACTA NEUROPATHOLOGICA
- Amyotrophic lateral sclerosis and frontotemporal dementia: A behavioural and cognitive continuum
- (2012) Patricia Lillo et al. Amyotrophic Lateral Sclerosis
- Caregiver burden in amyotrophic lateral sclerosis is more dependent on patients’ behavioral changes than physical disability: a comparative study
- (2012) Patricia Lillo et al. BMC Neurology
- Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations
- (2012) J. S. Snowden et al. BRAIN
- Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features
- (2012) C. J. Mahoney et al. BRAIN
- Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics
- (2012) J. L. Whitwell et al. BRAIN
- The role of Nogo-A in axonal plasticity, regrowth and repair
- (2012) Vincent Pernet et al. CELL AND TISSUE RESEARCH
- Split-hand index for the diagnosis of amyotrophic lateral sclerosis
- (2012) Parvathi Menon et al. CLINICAL NEUROPHYSIOLOGY
- The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder
- (2012) Bradley N Smith et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- A Pan-European Study of theC9orf72Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
- (2012) Julie van der Zee et al. HUMAN MUTATION
- Is language impairment more common than executive dysfunction in amyotrophic lateral sclerosis?
- (2012) L. J. Taylor et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Atypical, slowly progressive behavioural variant frontotemporal dementia associated withC9ORF72hexanucleotide expansion
- (2012) Baber K Khan et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Transcranial magnetic stimulation and amyotrophic lateral sclerosis: pathophysiological insights
- (2012) Steve Vucic et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Absence of consensus in diagnostic criteria for familial neurodegenerative diseases
- (2012) Susan Byrne et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study
- (2012) Susan Byrne et al. LANCET NEUROLOGY
- Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
- (2012) Elisa Majounie et al. LANCET NEUROLOGY
- Large C9orf72 repeat expansions are not a common cause of Parkinson's disease
- (2012) Elisa Majounie et al. NEUROBIOLOGY OF AGING
- Repeat Expansion inC9ORF72in Alzheimer's Disease
- (2012) Elisa Majounie et al. NEW ENGLAND JOURNAL OF MEDICINE
- Grey and White Matter Changes across the Amyotrophic Lateral Sclerosis-Frontotemporal Dementia Continuum
- (2012) Patricia Lillo et al. PLoS One
- Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72
- (2011) Melissa E. Murray 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
- The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study
- (2011) Julie Phukan et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Amyotrophic lateral sclerosis
- (2011) Matthew C Kiernan et al. LANCET
- Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
- (2011) Han-Xiang Deng et al. NATURE
- Clinical genetics of amyotrophic lateral sclerosis: what do we really know?
- (2011) Peter M. Andersen et al. Nature Reviews Neurology
- Executive dysfunction is a negative prognostic indicator in patients with ALS without dementia
- (2011) M. Elamin et al. NEUROLOGY
- 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
- Evidence of Social Understanding Impairment in Patients with Amyotrophic Lateral Sclerosis
- (2011) Marco Cavallo et al. PLoS One
- Detecting frontotemporal dysfunction in ALS: Utility of the ALS Cognitive Behavioral Screen (ALS-CBS™)
- (2010) Susan C. Woolley et al. Amyotrophic Lateral Sclerosis
- Neurobehavioral Features in Frontotemporal Dementia With Amyotrophic Lateral Sclerosis
- (2010) Patricia Lillo et al. ARCHIVES OF NEUROLOGY
- Amyotrophic lateral sclerosis patients show executive impairments on standard neuropsychological measures and an ecologically valid motor-free test of executive functions
- (2010) Vita Štukovnik et al. JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY
- Phenomenology and anatomy of abnormal behaviours in primary progressive aphasia
- (2010) Jonathan D. Rohrer et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Behavioural-variant frontotemporal dementia: diagnosis, clinical staging, and management
- (2010) Olivier Piguet et al. LANCET NEUROLOGY
- Mutations of optineurin in amyotrophic lateral sclerosis
- (2010) Hirofumi Maruyama et al. NATURE
- Genetic contribution of FUS to frontotemporal lobar degeneration
- (2010) T. Van Langenhove et al. NEUROLOGY
- How preserved is episodic memory in behavioral variant frontotemporal dementia?
- (2010) M. Hornberger et al. NEUROLOGY
- Deficits in emotional and social cognition in amyotrophic lateral sclerosis.
- (2010) Alessandra Girardi et al. NEUROPSYCHOLOGY
- The multiple roles of TDP-43 in pre-mRNA processing and gene expression regulation
- (2010) Emanuele Buratti et al. RNA Biology
- Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis
- (2009) Michael J. Strong et al. Amyotrophic Lateral Sclerosis
- Mesenchymal stem cell transplantation in amyotrophic lateral sclerosis: A Phase I clinical trial
- (2009) L. Mazzini et al. EXPERIMENTAL NEUROLOGY
- FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis
- (2009) I. P. Blair et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Incidence of amyotrophic lateral sclerosis in Europe
- (2009) G. Logroscino et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Alzheimer and frontotemporal pathology in subsets of primary progressive aphasia
- (2008) Marsel Mesulam et al. ANNALS OF NEUROLOGY
- Refining Frontotemporal Dementia With Parkinsonism Linked to Chromosome 17
- (2008) Bradley F. Boeve et al. ARCHIVES OF NEUROLOGY
- Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis
- (2008) Steve Vucic et al. BRAIN
- Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia
- (2008) John C van Swieten et al. LANCET NEUROLOGY
- TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
- (2008) Edor Kabashi et al. NATURE GENETICS
- Incidence of early-onset dementias in Cambridgeshire, United Kingdom
- (2008) L. Mercy et al. NEUROLOGY
- TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
- (2008) J. Sreedharan et al. SCIENCE
- Stem cell treatment in Amyotrophic Lateral Sclerosis
- (2007) Letizia Mazzini et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now