标题
Parkinsonism, movement disorders and genetics in frontotemporal dementia
作者
关键词
-
出版物
Nature Reviews Neurology
Volume 12, Issue 3, Pages 175-185
出版商
Springer Nature
发表日期
2016-02-19
DOI
10.1038/nrneurol.2016.14
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Imaging biomarkers in tauopathies
- (2016) Melanie Dani et al. PARKINSONISM & RELATED DISORDERS
- The Spectrum of Recurrent Thoughts and Behaviors in Frontotemporal Dementia
- (2016) Mario F. Mendez et al. CNS SPECTRUMS
- A novel tau mutation, p.K317N, causes globular glial tauopathy
- (2015) Pawel Tacik et al. ACTA NEUROPATHOLOGICA
- Cerebrospinal Fluid Biomarkers in Familial Forms of Alzheimer's Disease and Frontotemporal Dementia
- (2015) Nina Rostgaard et al. DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
- Mapping neuroinflammation in frontotemporal dementia with molecular PET imaging
- (2015) Jing Zhang Journal of Neuroinflammation
- A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease
- (2015) Pawel Tacik et al. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
- Frontotemporal dementia
- (2015) Jee Bang et al. LANCET
- The impact of rare variants inFUSin essential tremor
- (2015) Franziska Hopfner et al. MOVEMENT DISORDERS
- The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype
- (2014) Johnathan Cooper-Knock et al. ACTA NEUROPATHOLOGICA
- PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology
- (2014) Tsz Hang Wong et al. BRAIN
- Imaging Frontotemporal Lobar Degeneration
- (2014) Janine Diehl-Schmid et al. Current Neurology and Neuroscience Reports
- C9ORF72in Dementia with Lewy bodies
- (2014) Andrew Robinson et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- The phenotypic spectrum of progressive supranuclear palsy: A retrospective multicenter study of 100 definite cases
- (2014) Gesine Respondek et al. MOVEMENT DISORDERS
- The role of FUS gene variants in neurodegenerative diseases
- (2014) Hao Deng et al. Nature Reviews Neurology
- Homozygous TREM2 mutation in a family with atypical frontotemporal dementia
- (2014) Isabelle Le Ber et al. NEUROBIOLOGY OF AGING
- Parkinsonian syndrome in familial frontotemporal dementia
- (2014) Joanna Siuda et al. PARKINSONISM & RELATED DISORDERS
- Multiple System Atrophy and Amyotrophic Lateral Sclerosis in a Family With Hexanucleotide Repeat Expansions inC9orf72
- (2014) Jill S. Goldman et al. JAMA Neurology
- Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration
- (2013) Naomi Kouri et al. ACTA NEUROPATHOLOGICA
- C9ORF72Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease
- (2013) Karen Nuytemans et al. ANNALS OF HUMAN GENETICS
- C9orf72 repeat expansions are a rare genetic cause of parkinsonism
- (2013) Suzanne Lesage et al. BRAIN
- Deciphering logopenic primary progressive aphasia: a clinical, imaging and biomarker investigation
- (2013) M. Teichmann et al. BRAIN
- Plasma progranulin levels in cortical dementia phenotypes with asymmetric perisylvian atrophy
- (2013) E. Gómez-Tortosa et al. EUROPEAN JOURNAL OF NEUROLOGY
- Generalized myoclonus as a prominent symptom in a patient with FTLD-TDP
- (2013) Martin Pail et al. JOURNAL OF NEUROLOGY
- Tetrabenazine Treatment for Stereotypies and Tics Associated With Dementia
- (2013) William G. Ondo JOURNAL OF NEUROPSYCHIATRY AND CLINICAL NEUROSCIENCES
- TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson’s disease
- (2013) Sruti Rayaprolu et al. Molecular Neurodegeneration
- “Atypical” atypical parkinsonism: New genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-A diagnostic guide
- (2013) Maria Stamelou et al. MOVEMENT DISORDERS
- Sortilin receptor 1 predicts longitudinal cognitive change
- (2013) Chandra A. Reynolds et al. NEUROBIOLOGY OF AGING
- Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease
- (2013) Margarita Giraldo et al. NEUROBIOLOGY OF AGING
- C9ORF72 expansions, parkinsonism, and Parkinson disease: A clinicopathologic study
- (2013) J. Cooper-Knock et al. NEUROLOGY
- C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies
- (2013) D. J. Hensman Moss et al. NEUROLOGY
- Criteria for the diagnosis of corticobasal degeneration
- (2013) M. J. Armstrong et al. NEUROLOGY
- Exome sequencing in familial corticobasal degeneration
- (2013) Robert Fekete et al. PARKINSONISM & RELATED DISORDERS
- Genetics of frontotemporal lobar degeneration: An up-date and diagnosis algorithm
- (2013) I. Le Ber REVUE NEUROLOGIQUE
- Frontotemporal Dementia
- (2013) Bruce Miller et al. SEMINARS IN NEUROLOGY
- Distinct Clinical Characteristics of C9orf72 Expansion Carriers Compared With GRN, MAPT, and Nonmutation Carriers in a Flanders-Belgian FTLD Cohort
- (2013) Tim Van Langenhove et al. JAMA Neurology
- Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement
- (2013) Rita João Guerreiro et al. JAMA Neurology
- C9orf72 Hexanucleotide Repeat Expansion and Guam Amyotrophic Lateral Sclerosis–Parkinsonism-Dementia Complex
- (2013) Beth A. Dombroski et al. JAMA Neurology
- F-Box Only Protein 7 Gene in Parkinsonian-Pyramidal Disease
- (2013) Hao Deng et al. JAMA Neurology
- Patterns of Striatal Degeneration in Frontotemporal Dementia
- (2012) Cathra Halabi et al. ALZHEIMER DISEASE & ASSOCIATED DISORDERS
- Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor
- (2012) Nancy D. Merner et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Investigation of C9orf72 in 4 Neurodegenerative Disorders
- (2012) Zhengrui Xi et al. ARCHIVES OF NEUROLOGY
- Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations
- (2012) J. S. Snowden et al. BRAIN
- Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72
- (2012) Bradley F. Boeve et al. BRAIN
- Corticobasal and ataxia syndromes widen the spectrum ofC9ORF72hexanucleotide expansion disease
- (2012) SG Lindquist et al. CLINICAL GENETICS
- Frontotemporal Lobar Degeneration
- (2012) Rachel E. Seltman et al. CNS DRUGS
- Phenotypic variability in three families withvalosin-containing proteinmutation
- (2012) S. Spina et al. EUROPEAN JOURNAL OF NEUROLOGY
- Frontotemporal dementia with psychosis, parkinsonism, visuo-spatial dysfunction, upper motor neuron involvement associated to expansion of C9ORF72: a peculiar phenotype?
- (2012) Gianluca Floris et al. JOURNAL OF NEUROLOGY
- Stereotypic behaviors in degenerative dementias
- (2012) S. Prioni et al. JOURNAL OF NEUROLOGY
- Psychosis,C9ORF72and dementia with Lewy bodies: Table 1
- (2012) Julie S Snowden 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
- Differentiation of frontotemporal dementia from dementia with Lewy bodies using FP-CIT SPECT
- (2012) Shirlony Morgan et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- 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
- C9ORF72 expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism
- (2012) Seán O'Dowd et al. MOVEMENT DISORDERS
- Dystonia in corticobasal degeneration: A review of the literature on 404 pathologically proven cases
- (2012) Maria Stamelou et al. MOVEMENT DISORDERS
- Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject
- (2012) Lorena Mosca et al. NEUROBIOLOGY OF AGING
- Repeat expansions in the C9ORF72 gene contribute to Alzheimer's disease in Caucasians
- (2012) Martin A. Kohli et al. NEUROBIOLOGY OF AGING
- TREM2 Variants in Alzheimer's Disease
- (2012) Rita Guerreiro et al. NEW ENGLAND JOURNAL OF MEDICINE
- Analysis of the C9orf72 repeat in Parkinson's disease, essential tremor and restless legs syndrome
- (2012) Mariely DeJesus-Hernandez et al. PARKINSONISM & RELATED DISORDERS
- TARDBP mutations in Parkinson's disease
- (2012) Sruti Rayaprolu et al. PARKINSONISM & RELATED DISORDERS
- Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS
- (2012) Kotaro Ogaki et al. PARKINSONISM & RELATED DISORDERS
- No GGGGCC-hexanucleotide repeat expansion inC9ORF72in parkinsonism patients in Sweden
- (2012) Chizuru Akimoto et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases
- (2011) Robert Rusina et al. BMC Neurology
- Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
- (2011) Katya Rascovsky et al. BRAIN
- Frontotemporal Dementia Caused by CHMP2B Mutations
- (2011) A. M. Isaacs et al. Current Alzheimer Research
- Tetrabenazine for the treatment of chorea and other hyperkinetic movement disorders
- (2011) Joseph Jankovic et al. Expert Review of Neurotherapeutics
- Clinical Aspects of Familial Forms of Frontotemporal Dementia Associated with Parkinsonism
- (2011) Shinsuke Fujioka et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- Diagnostic criteria for corticobasal syndrome: a comparative study
- (2011) Robert Mathew et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Stereotypies: A critical appraisal and suggestion of a clinically useful definition
- (2011) Mark J. Edwards et al. MOVEMENT DISORDERS
- The Met-allele of the BDNF Val66Met polymorphism enhances task switching in elderly
- (2011) Patrick D. Gajewski et al. NEUROBIOLOGY OF AGING
- The chromosome 9 ALS and FTD locus is probably derived from a single founder
- (2011) Kin Mok et al. NEUROBIOLOGY OF AGING
- Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson’s disease in Sardinia
- (2011) Marialuisa Quadri et al. NEUROGENETICS
- Different clinical and neuropathologic phenotypes of familial ALS with A315E TARDBP mutation
- (2011) Y. Fujita et al. NEUROLOGY
- A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
- (2011) Alan E. Renton et al. NEURON
- Does corticobasal degeneration exist? A clinicopathological re-evaluation
- (2010) H. Ling et al. BRAIN
- Neuropathology of variants of progressive supranuclear palsy
- (2010) Dennis W Dickson et al. CURRENT OPINION IN NEUROLOGY
- Caudate atrophy on MRI is a characteristic feature of FTLD-FUS
- (2010) K. A. Josephs et al. EUROPEAN JOURNAL OF NEUROLOGY
- Behavioral variant of frontotemporal dementia mimicking Huntington's disease
- (2010) T. Rune Nielsen et al. INTERNATIONAL PSYCHOGERIATRICS
- Rapidly progressive atypical parkinsonism associated with frontotemporal lobar degeneration and motor neuron disease
- (2010) A. J. Espay et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Novel L284R MAPT Mutation in a Family with an Autosomal Dominant Progressive Supranuclear Palsy Syndrome
- (2010) Jonathan D. Rohrer et al. Neurodegenerative Diseases
- Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia
- (2010) J. Yan et al. NEUROLOGY
- Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
- (2010) Janel O. Johnson et al. NEURON
- Putaminal Volume in Frontotemporal Lobar Degeneration and Alzheimer Disease: Differential Volumes in Dementia Subtypes and Controls
- (2009) J.C.L. Looi et al. AMERICAN JOURNAL OF NEURORADIOLOGY
- No TARDBP Mutations in a French Canadian Population of Patients With Parkinson Disease
- (2009) Edor Kabashi et al. ARCHIVES OF NEUROLOGY
- Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members
- (2009) N. Finch et al. BRAIN
- Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options
- (2009) A. C. Ludolph et al. EUROPEAN JOURNAL OF NEUROLOGY
- Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration
- (2009) Harro Seelaar et al. JOURNAL OF NEUROLOGY
- The clinical spectrum of stereotypies in frontotemporal lobar degeneration
- (2009) Farrah J. Mateen et al. MOVEMENT DISORDERS
- TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea
- (2009) Gabor G. Kovacs et al. MOVEMENT DISORDERS
- Mutational analysis of TARDBP in neurodegenerative diseases
- (2009) Nicola Ticozzi et al. NEUROBIOLOGY OF AGING
- Subcortical and deep cortical atrophy in Frontotemporal Lobar Degeneration
- (2009) Valentina Garibotto et al. NEUROBIOLOGY OF AGING
- The heritability and genetics of frontotemporal lobar degeneration
- (2009) J. D. Rohrer et al. NEUROLOGY
- Caudate Nucleus Volumes in Frontotemporal Lobar Degeneration: Differential Atrophy in Subtypes
- (2008) J.C.L. Looi et al. AMERICAN JOURNAL OF NEURORADIOLOGY
- Refining Frontotemporal Dementia With Parkinsonism Linked to Chromosome 17
- (2008) Bradley F. Boeve et al. ARCHIVES OF NEUROLOGY
- Clinical and Pathological Heterogeneity of Neuronal Intermediate Filament Inclusion Disease
- (2008) Laura Molina-Porcel et al. ARCHIVES OF NEUROLOGY
- Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study
- (2008) Isabelle Le Ber 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
- Progranulin gene mutation with an unusual clinical and neuropathologic presentation
- (2008) Christian Wider et al. MOVEMENT DISORDERS
- The G389R mutation in theMAPTgene presenting as sporadic corticobasal syndrome
- (2008) Giacomina Rossi et al. MOVEMENT DISORDERS
- Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide
- (2008) Luisa Benussi et al. NEUROBIOLOGY OF DISEASE
- Incidence of early-onset dementias in Cambridgeshire, United Kingdom
- (2008) L. Mercy et al. NEUROLOGY
- Frontotemporal dementia and Parkinsonism linked to chromosome 17 in a young Australian patient with the G389R Tau mutation
- (2008) N. Bermingham et al. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
- Parkinsonism and impaired axonal transport in a mouse model of frontotemporal dementia
- (2008) L. M. Ittner et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Anatomic correlates of stereotypies in frontotemporal lobar degeneration
- (2007) Keith A. Josephs et al. NEUROBIOLOGY OF AGING
- Prominent phenotypic variability associated with mutations in Progranulin
- (2007) Brendan J. Kelley et al. NEUROBIOLOGY OF AGING
- A novel deletion in progranulin gene is associated with FTDP-17 and CBS
- (2006) Luisa Benussi et al. NEUROBIOLOGY OF AGING
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