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Eliana Marisa Ramos et al.
ALZHEIMERS & DEMENTIA (2020)
Age at symptom on-set and death and disease duration in genetic fronto-temporal dementia: an international retro-spective cohort study (vol 19, pg 145, 2020)
K. M. Moore et al.
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Kang Zhang et al.
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Katrina M. Moore et al.
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An update on genetic frontotemporal dementia
Caroline Greaves et al.
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Genetic and functional characters of GRN p.T487I mutation in Taiwanese patients with atypical parkinsonian disorders
Kuo-Hsuan Chang et al.
PARKINSONISM & RELATED DISORDERS (2018)
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Mario F. Mendez
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Sex differences in the prevalence of genetic mutations in FTD and ALS A meta-analysis
Ashley F. Curtis et al.
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Genetic Features of MAPT, GRN, C9orf72 and CHCHD10 Gene Mutations in Chinese Patients with Frontotemporal Dementia
Xiang-Qian Che et al.
CURRENT ALZHEIMER RESEARCH (2017)
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Zhihong Shi et al.
JOURNAL OF HUMAN GENETICS (2016)
Progranulin mutation analysis: Identification of one novel mutation in exon 12 associated with frontotemporal dementia
Peethambaran Mallika Aswathy et al.
NEUROBIOLOGY OF AGING (2016)
Analyses MAPT, GRN, and C9orf72 mutations in Chinese patients with frontotemporal dementia
Min Tang et al.
NEUROBIOLOGY OF AGING (2016)
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
Sue Richards et al.
GENETICS IN MEDICINE (2015)
Clinical and genetic analysis of MAPT, GRN, and C9orf72 genes in Korean patients with frontotemporal dementia
Eun-Joo Kim et al.
NEUROBIOLOGY OF AGING (2014)
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Paola Caroppo et al.
JAMA NEUROLOGY (2014)
Plasma progranulin levels in cortical dementia phenotypes with asymmetric perisylvian atrophy
E. Gomez-Tortosa et al.
EUROPEAN JOURNAL OF NEUROLOGY (2013)
Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS
Kotaro Ogaki et al.
PARKINSONISM & RELATED DISORDERS (2013)
Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics
Jennifer L. Whitwell et al.
BRAIN (2012)
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Anna Antonell et al.
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R. Ferrari et al.
CURRENT ALZHEIMER RESEARCH (2011)
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Harro Seelaar et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2011)
Classification of primary progressive aphasia and its variants
M. L. Gorno-Tempini et al.
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Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations
Jonathan D. Rohrer et al.
NEUROIMAGE (2010)
Asymmetric TDP-43 distribution in primary progressive aphasia with progranulin mutation
G. Gliebus et al.
NEUROLOGY (2010)
Screening for MAPT and PGRN mutations in Korean patients with PSP/CBS/FTD
Han-Joon Kim et al.
PARKINSONISM & RELATED DISORDERS (2010)
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Jonathan Beck et al.
BRAIN (2008)
Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia
Odity Mukherjee et al.
HUMAN MUTATION (2008)
Splicing in disease: disruption of the splicing code and the decoding machinery
Guey-Shin Wang et al.
NATURE REVIEWS GENETICS (2007)
Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome
Mario Masellis et al.
BRAIN (2006)
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Matt Baker et al.
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