The molecular basis of the frontotemporal lobar degeneration–amyotrophic lateral sclerosis spectrum
出版年份 2012 全文链接
标题
The molecular basis of the frontotemporal lobar degeneration–amyotrophic lateral sclerosis spectrum
作者
关键词
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出版物
ANNALS OF MEDICINE
Volume 44, Issue 8, Pages 817-828
出版商
Informa UK Limited
发表日期
2012-03-16
DOI
10.3109/07853890.2012.665471
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Writing Errors and Anosognosia in Amyotrophic Lateral Sclerosis with Dementia
- (2014) Hiroo Ichikawa et al. BEHAVIOURAL NEUROLOGY
- Delusion of Pregnancy in Frontotemporal Lobar Degeneration with Motor Neurone Disease (FTLD/MND)
- (2014) A. J. Larner BEHAVIOURAL NEUROLOGY
- 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
- 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
- Large Proportion of Amyotrophic Lateral Sclerosis Cases in Sardinia Due to a Single Founder Mutation of the TARDBP Gene
- (2011) Adriano Chiò ARCHIVES OF NEUROLOGY
- TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort
- (2011) Julie van der Zee et al. BRAIN
- 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
- High frequency of the TARDBP p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosis
- (2011) S Orrù et al. CLINICAL GENETICS
- Ataxin-2 repeat-length variation and neurodegeneration
- (2011) O. A. Ross et al. HUMAN MOLECULAR GENETICS
- TMEM106B a Novel Risk Factor for Frontotemporal Lobar Degeneration
- (2011) Julie van der Zee et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study
- (2011) Ilse Gijselinck et al. LANCET NEUROLOGY
- Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
- (2011) Han-Xiang Deng et al. NATURE
- VCP mutations in familial and sporadic amyotrophic lateral sclerosis
- (2011) Max Koppers et al. NEUROBIOLOGY OF AGING
- Novel p.Ile151Val mutation in VCP in a patient of African American descent with sporadic ALS
- (2011) M. DeJesus-Hernandez 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
- Expression of human FUS/TLS in yeast leads to protein aggregation and cytotoxicity, recapitulating key features of FUS proteinopathy
- (2011) Kazuo Fushimi et al. Protein & Cell
- Effect of topographical distribution of α-synuclein pathology on TDP-43 accumulation in Lewy body disease
- (2010) Osamu Yokota et al. ACTA NEUROPATHOLOGICA
- Distinct pathological subtypes of FTLD-FUS
- (2010) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- Risk genotypes at TMEM106B are associated with cognitive impairment in amyotrophic lateral sclerosis
- (2010) Ryan Vass et al. ACTA NEUROPATHOLOGICA
- FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration
- (2010) Hazel Urwin et al. ACTA NEUROPATHOLOGICA
- Enlarging clinical spectrum of FALS with TARDBP gene mutations: S393L variant in an Italian family showing phenotypic variability and relevance for genetic counselling
- (2010) Paola Origone et al. Amyotrophic Lateral Sclerosis
- How common are behavioural changes in amyotrophic lateral sclerosis?
- (2010) Patricia Lillo et al. Amyotrophic Lateral Sclerosis
- Amyotrophic Lateral Sclerosis–Frontotemporal Lobar Dementia in 3 Families With p.Ala382Thr TARDBP Mutations
- (2010) Adriano Chiò et al. ARCHIVES 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
- Novel FUS/TLS Mutations and Pathology in Familial and Sporadic Amyotrophic Lateral Sclerosis
- (2010) Christopher Hewitt et al. ARCHIVES OF NEUROLOGY
- Neurobehavioral Features in Frontotemporal Dementia With Amyotrophic Lateral Sclerosis
- (2010) Patricia Lillo et al. ARCHIVES OF NEUROLOGY
- Extensive FUS-Immunoreactive Pathology in Juvenile Amyotrophic Lateral Sclerosis with Basophilic Inclusions
- (2010) Eric J. Huang et al. BRAIN PATHOLOGY
- ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import
- (2010) Dorothee Dormann et al. EMBO JOURNAL
- Caudate atrophy on MRI is a characteristic feature of FTLD-FUS
- (2010) K. A. Josephs et al. EUROPEAN JOURNAL OF NEUROLOGY
- Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules
- (2010) Daryl A. Bosco et al. HUMAN MOLECULAR GENETICS
- TDP-43 M337V Mutation in Familial Amyotrophic Lateral Sclerosis in Japan
- (2010) Akira Tamaoka et al. INTERNAL MEDICINE
- FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion
- (2010) Naoki Suzuki et al. JOURNAL OF HUMAN GENETICS
- SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations
- (2010) S. Millecamps et al. JOURNAL OF MEDICAL GENETICS
- Writing errors as a result of frontal dysfunction in Japanese patients with amyotrophic lateral sclerosis
- (2010) Sachiko Tsuji-Akimoto et al. JOURNAL 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
- Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study
- (2010) Hannu Laaksovirta et al. LANCET NEUROLOGY
- Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study
- (2010) Aleksey Shatunov et al. LANCET NEUROLOGY
- TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia
- (2010) Ian RA Mackenzie et al. LANCET NEUROLOGY
- Fusgene mutations in familial and sporadic amyotrophic lateral sclerosis
- (2010) Rosa Rademakers et al. MUSCLE & NERVE
- Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS
- (2010) Andrew C. Elden et al. NATURE
- Mutations of optineurin in amyotrophic lateral sclerosis
- (2010) Hirofumi Maruyama et al. NATURE
- Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
- (2010) Vivianna M Van Deerlin et al. NATURE GENETICS
- Genetic contribution of FUS to frontotemporal lobar degeneration
- (2010) T. Van Langenhove et al. NEUROLOGY
- Juvenile ALS with basophilic inclusions is a FUS proteinopathy with FUS mutations
- (2010) D. Baumer et al. NEUROLOGY
- Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia
- (2010) J. Yan et al. NEUROLOGY
- TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers
- (2010) N. Finch et al. NEUROLOGY
- Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
- (2010) Janel O. Johnson et al. NEURON
- Semantic dementia with lower motor neuron disease showing FTLD-TDP type 3 pathology (sensu Mackenzie)
- (2010) Per Östberg et al. NEUROPATHOLOGY
- TDP-43 proteinopathy in familial motor neurone disease with TARDBP A315T mutation: a case report
- (2010) N. J. Cairns et al. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
- Intracellular localization and splicing regulation of FUS/TLS are variably affected by amyotrophic lateral sclerosis-linked mutations
- (2010) Yoshihiro Kino et al. NUCLEIC ACIDS RESEARCH
- 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
- Evaluation of subcortical pathology and clinical correlations in FTLD-U subtypes
- (2009) Keith A. Josephs et al. ACTA NEUROPATHOLOGICA
- FUS pathology in basophilic inclusion body disease
- (2009) David G. Munoz 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
- TARDBPmutations in motoneuron disease with frontotemporal lobar degeneration
- (2009) Lina Benajiba et al. ANNALS OF NEUROLOGY
- A new subtype of frontotemporal lobar degeneration with FUS pathology
- (2009) M. Neumann et al. BRAIN
- Absence of TARDBP Gene Mutations in an Italian Series of Patients with Frontotemporal Lobar Degeneration
- (2009) Salvatore Gallone et al. DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
- Mutation withinTARDBPleads to Frontotemporal Dementia without motor neuron disease
- (2009) B. Borroni et al. HUMAN MUTATION
- Mutations of FUS gene in sporadic amyotrophic lateral sclerosis
- (2009) L. Corrado et al. JOURNAL OF MEDICAL GENETICS
- SOD1 and cognitive dysfunction in familial amyotrophic lateral sclerosis
- (2009) P. Wicks et al. JOURNAL OF NEUROLOGY
- Amyotrophic lateral sclerosis, frontotemporal dementia and beyond: the TDP-43 diseases
- (2009) Felix Geser et al. JOURNAL OF NEUROLOGY
- Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration
- (2009) Harro Seelaar et al. JOURNAL OF 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
- TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea
- (2009) Gabor G. Kovacs et al. MOVEMENT DISORDERS
- Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
- (2009) Michael A van Es et al. NATURE GENETICS
- Genetics of motor neuron disorders: new insights into pathogenic mechanisms
- (2009) Patrick A. Dion et al. NATURE REVIEWS GENETICS
- Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
- (2009) I. Le Ber et al. NEUROLOGY
- A CASE OF ALS-FTD IN A LARGE FALS PEDIGREE WITH A K17I ANG MUTATION
- (2009) M. A. van Es et al. NEUROLOGY
- Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His
- (2009) J. van der Zee et al. NEUROLOGY
- Epidemiology of ALS in Italy: A 10-year prospective population-based study
- (2009) A. Chio et al. NEUROLOGY
- Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort
- (2009) N. Ticozzi et al. NEUROLOGY
- The heritability and genetics of frontotemporal lobar degeneration
- (2009) J. D. Rohrer et al. NEUROLOGY
- The RNA-binding protein FUS/TLS is a common aggregate-interacting protein in polyglutamine diseases
- (2009) Hiroshi Doi et al. NEUROSCIENCE RESEARCH
- 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
- TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD
- (2008) Sigrun Roeber et al. ACTA NEUROPATHOLOGICA
- Behaviour in amyotrophic lateral sclerosis
- (2008) Zoe C. Gibbons et al. Amyotrophic Lateral Sclerosis
- Aggregation of neurodegenerative disease in ALS kindreds
- (2008) Brooks A. Fallis et al. Amyotrophic Lateral Sclerosis
- TDP-43mutation in familial amyotrophic lateral sclerosis
- (2008) Akio Yokoseki et al. ANNALS OF NEUROLOGY
- VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: Review of a unique disorder
- (2008) Virginia E. Kimonis et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
- 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
- Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43-negative neuronal inclusions
- (2008) Ian R. A. Mackenzie et al. BRAIN
- New approaches to the treatment of frontotemporal lobar degeneration
- (2008) Keith A Vossel et al. CURRENT OPINION IN NEUROLOGY
- Psychotic Symptoms in Frontotemporal Dementia: Prevalence and Review
- (2008) Mario F. Mendez et al. DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
- Concomitant TAR-DNA-Binding Protein 43 Pathology Is Present in Alzheimer Disease and Corticobasal Degeneration but Not in Other Tauopathies
- (2008) Kunihiro Uryu et al. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
- TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis
- (2008) Vivianna M Van Deerlin et al. LANCET NEUROLOGY
- TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
- (2008) Edor Kabashi et al. NATURE GENETICS
- Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS
- (2008) Ilse Gijselinck et al. NEUROBIOLOGY OF AGING
- Incidence of early-onset dementias in Cambridgeshire, United Kingdom
- (2008) L. Mercy et al. NEUROLOGY
- Progranulin genetic variability contributes to amyotrophic lateral sclerosis
- (2008) K. Sleegers et al. NEUROLOGY
- Distinct genetic forms of frontotemporal dementia
- (2008) H. Seelaar et al. NEUROLOGY
- Abnormal TDP-43 immunoreactivity in AD modifies clinicopathologic and radiologic phenotype
- (2008) K. A. Josephs et al. NEUROLOGY
- TDP-43 neuropathology is similar in sporadic amyotrophic lateral sclerosis with or withoutTDP-43mutations
- (2008) NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
- TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
- (2008) J. Sreedharan et al. SCIENCE
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