The Right Temporal Variant of Frontotemporal Dementia is Not Genetically Sporadic: A Case Series
Published 2021 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
The Right Temporal Variant of Frontotemporal Dementia is Not Genetically Sporadic: A Case Series
Authors
Keywords
-
Journal
JOURNAL OF ALZHEIMERS DISEASE
Volume -, Issue -, Pages 1-7
Publisher
IOS Press
Online
2021-01-09
DOI
10.3233/jad-201191
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- A clinical-radiological framework of the right temporal variant of frontotemporal dementia
- (2020) Hulya Ulugut Erkoyun et al. BRAIN
- TARDBP mutation associated with semantic variant primary progressive aphasia, case report and review of the literature
- (2019) M. González-Sánchez et al. NEUROCASE
- An update on genetic frontotemporal dementia
- (2019) Caroline V. Greaves et al. JOURNAL OF NEUROLOGY
- Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia
- (2019) Luke W. Bonham et al. Scientific Reports
- Amsterdam Dementia Cohort: Performing Research to Optimize Care
- (2018) Wiesje M. van der Flier et al. JOURNAL OF ALZHEIMERS DISEASE
- Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review
- (2018) Emil Ygland et al. Alzheimers Research & Therapy
- Phenotypic Heterogeneity of the GRN Asp22fs Mutation in a Large Italian Kindred
- (2018) Anna M. Pietroboni et al. JOURNAL OF ALZHEIMERS DISEASE
- Frontotemporal dementia-related gene mutations in clinical dementia patients from a Chinese population
- (2016) Zhihong Shi et al. JOURNAL OF HUMAN GENETICS
- An update on semantic dementia: genetics, imaging, and pathology
- (2016) Ramon Landin-Romero et al. Alzheimers Research & Therapy
- Neurofilament light chain: a biomarker for genetic frontotemporal dementia
- (2016) Lieke H. Meeter et al. Annals of Clinical and Translational Neurology
- Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients
- (2016) Gamze Guven et al. PLoS One
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- Using visual rating to diagnose dementia: a critical evaluation of MRI atrophy scales
- (2015) Lorna Harper et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Invited review: Neuropathology of tauopathies: principles and practice
- (2015) G. G. Kovacs NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
- A single nucleotide TDP-43 mutation within a Taiwanese family: A multifaceted demon
- (2015) Yu-Wen Cheng et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- A novel mutation P112H in the TARDBP gene associated with frontotemporal lobar degeneration without motor neuron disease and abundant neuritic amyloid plaques
- (2015) Fermin Moreno et al. Acta Neuropathologica Communications
- The genetics of primary progressive aphasia
- (2014) Jonathan D. Rohrer APHASIOLOGY
- Clinical phenotypes and radiological findings in frontotemporal dementia related to TARDBP mutations
- (2014) Gianluca Floris et al. JOURNAL OF NEUROLOGY
- Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis
- (2013) A. Cannon et al. NEUROLOGY
- TARDBPmutation p.Ile383Val associated with semantic dementia and complex proteinopathy
- (2013) E. Gelpi et al. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
- Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics
- (2012) J. L. Whitwell et al. BRAIN
- Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
- (2011) Katya Rascovsky et al. BRAIN
- Classification of primary progressive aphasia and its variants
- (2011) M. L. Gorno-Tempini et al. NEUROLOGY
- Progressive supranuclear palsy syndrome presenting as progressive nonfluent aphasia: A neuropsychological and neuroimaging analysis
- (2010) Jonathan D. Rohrer et al. MOVEMENT DISORDERS
- The clinical profile of right temporal lobe atrophy
- (2009) D. Chan et al. BRAIN
- Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN
- (2009) J. L. Whitwell et al. NEUROLOGY
- The heritability and genetics of frontotemporal lobar degeneration
- (2009) J. D. Rohrer et al. NEUROLOGY
- Two distinct subtypes of right temporal variant frontotemporal dementia
- (2009) K. A. Josephs et al. NEUROLOGY
- TDP-43mutation in familial amyotrophic lateral sclerosis
- (2008) Akio Yokoseki et al. ANNALS OF NEUROLOGY
- TDP-43A315T mutation in familial motor neuron disease
- (2008) Michael A. Gitcho et al. ANNALS OF NEUROLOGY
- A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series
- (2008) J. Beck et al. BRAIN
- Atrophy progression in semantic dementia with asymmetric temporal involvement: A tensor-based morphometry study
- (2007) S.M. Brambati et al. NEUROBIOLOGY OF AGING
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now