Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis
Published 2016 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis
Authors
Keywords
Movement disorders, Clinical genetics, Human genetics, Genetics of disease, Meta-analysis, Levodopa, Parkinson disease, Gene mapping
Journal
PLoS One
Volume 11, Issue 4, Pages e0153852
Publisher
Public Library of Science (PLoS)
Online
2016-04-22
DOI
10.1371/journal.pone.0153852
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Treatment of Frontotemporal Dementia
- (2014) Richard M. Tsai et al. Current Treatment Options in Neurology
- Absence ofC9ORF72expanded or intermediate repeats in autopsy-confirmed Parkinson's disease
- (2014) Karen Nuytemans et al. MOVEMENT DISORDERS
- Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease
- (2014) J. Theuns et al. NEUROLOGY
- Parkinsonian syndrome in familial frontotemporal dementia
- (2014) Joanna Siuda et al. PARKINSONISM & RELATED DISORDERS
- Neurodegenerative Disease Phenotypes in Carriers of MAPT p.A152T, A Risk Factor for Frontotemporal Dementia Spectrum Disorders and Alzheimer Disease
- (2013) Suzee E. Lee et al. ALZHEIMER DISEASE & ASSOCIATED DISORDERS
- Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation
- (2013) Regina M. Carney et al. Alzheimers & Dementia
- Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation
- (2013) Daniela Galimberti et al. BIOLOGICAL PSYCHIATRY
- C9orf72 repeat expansions are a rare genetic cause of parkinsonism
- (2013) Suzanne Lesage et al. BRAIN
- Motor neuron disease and frontotemporal dementia: sometimes related, sometimes not
- (2013) John Hardy et al. EXPERIMENTAL NEUROLOGY
- Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia
- (2013) O. Dols-Icardo et al. HUMAN MOLECULAR GENETICS
- Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis
- (2013) A. Cannon et al. NEUROLOGY
- Screening for progranulin mutations by serum protein dosage in common neurodegenerative disorders
- (2013) Eloy Rodríguez-Rodríguez et al. PARKINSONISM & RELATED DISORDERS
- A Re-Analysis of the Cochrane Library Data: The Dangers of Unobserved Heterogeneity in Meta-Analyses
- (2013) Evangelos Kontopantelis et al. PLoS One
- Frontotemporal dementia
- (2013) J. D. Warren et al. BMJ-British Medical Journal
- Enlarging the clinical spectrum associated with C9orf 72 repeat expansions: Findings in an Italian cohort of patients with Parkinsonian syndromes and relevance for genetic counselling
- (2013) Paola Origone et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review
- (2013) Xiao-dong Pan et al. Translational Neurodegeneration
- The genetics and neuropathology of frontotemporal lobar degeneration
- (2012) Anne Sieben et al. ACTA NEUROPATHOLOGICA
- Characterization of a Family With c9FTD/ALS Associated With the GGGGCC Repeat Expansion in C9ORF72
- (2012) Rodolfo Savica et al. ARCHIVES OF NEUROLOGY
- Frontotemporal Dementia in a Brazilian Kindred With the C9orf72 Mutation
- (2012) Leonel T. Takada ARCHIVES OF NEUROLOGY
- 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 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
- Psychosis,C9ORF72and dementia with Lewy bodies: Table 1
- (2012) Julie S Snowden et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- The frontotemporal dementias in a tertiary referral center: Classification and demographic characteristics in a series of 232 cases
- (2012) Panagiotis Ioannidis et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- 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
- Pallidopontonigral degeneration: A deceptive familial tauopathy
- (2012) Seán O'Dowd et al. MOVEMENT 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
- Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion
- (2012) Marco Luigetti et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Sporadic Corticobasal Syndrome With Progranulin Mutation Presenting as Progressive Apraxic Agraphia
- (2011) Victoria Passov et al. ARCHIVES OF NEUROLOGY
- Genetic and Clinical Features of Progranulin-Associated Frontotemporal Lobar Degeneration
- (2011) Alice S. Chen-Plotkin et al. ARCHIVES OF NEUROLOGY
- 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
- Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration
- (2011) J. D. Rohrer et al. BRAIN
- Symmetrical Corticobasal Syndrome Caused by a Novel c.314dup Progranulin Mutation
- (2011) Elise G. P. Dopper et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- Clinical Aspects of Familial Forms of Frontotemporal Dementia Associated with Parkinsonism
- (2011) Shinsuke Fujioka et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- Parkinsonism and Frontotemporal Dementia: The Clinical Overlap
- (2011) Alberto J. Espay et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- Extrapyramidal Syndromes in Frontotemporal Degeneration
- (2011) Andrew Kertesz et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- Progressive supranuclear palsy-like phenotype caused by progranulin p.Thr272fs mutation
- (2011) Lucio Tremolizzo et al. MOVEMENT DISORDERS
- G303V tau mutation presenting with progressive supranuclear palsy-like features
- (2011) Ariane Choumert et al. MOVEMENT DISORDERS
- Frontotemporal dementia with parkinsonism presenting as posterior cortical atrophy
- (2011) Francesca Spagnolo et al. MOVEMENT DISORDERS
- A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration
- (2011) Cinzia Coppola et al. NEUROLOGICAL SCIENCES
- Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
- (2011) Mariely DeJesus-Hernandez et al. NEURON
- Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entity
- (2010) Yong-Juan Fu et al. ACTA NEUROPATHOLOGICA
- Anatomy of disturbed sleep in pallido-ponto-nigral degeneration
- (2010) Andrew R. Spector et al. ANNALS OF NEUROLOGY
- Familial early onset frontotemporal dementia caused by a novel S356T MAPT mutation, initially diagnosed as schizophrenia
- (2010) Parastoo Momeni et al. CLINICAL NEUROLOGY AND NEUROSURGERY
- Frontotemporal dementia and parkinsonism linked to chromosome 17 - the first Polish family
- (2010) E. Narożańska et al. EUROPEAN 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
- Progressive supranuclear palsy syndrome presenting as progressive nonfluent aphasia: A neuropsychological and neuroimaging analysis
- (2010) Jonathan D. Rohrer et al. MOVEMENT DISORDERS
- Novel L284R MAPT Mutation in a Family with an Autosomal Dominant Progressive Supranuclear Palsy Syndrome
- (2010) Jonathan D. Rohrer et al. Neurodegenerative Diseases
- TDP-43 subtypes are associated with distinct atrophy patterns in frontotemporal dementia
- (2010) J. D. Rohrer et al. NEUROLOGY
- Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation
- (2010) Roberto Di Fabio et al. PARKINSONISM & RELATED DISORDERS
- Unilateral neglect in a patient diagnosed with frontotemporal dementia and parkinsonism linked to chromosome 17
- (2009) Emilia J. Sitek et al. ACTA NEUROPSYCHIATRICA
- The heritability and genetics of frontotemporal lobar degeneration
- (2009) J. D. Rohrer et al. NEUROLOGY
- Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study
- (2008) Isabelle Le Ber et al. BRAIN
- 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
- In vivo and Postmortem Clinicoanatomical Correlations in Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17
- (2008) Bernardino Ghetti et al. Neurodegenerative Diseases
- 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
- Prominent phenotypic variability associated with mutations in Progranulin
- (2007) Brendan J. Kelley et al. NEUROBIOLOGY OF AGING
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExplorePublish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn More