Analyses MAPT, GRN, and C9orf72 mutations in Chinese patients with frontotemporal dementia
暂无分享,去创建一个
B. Tang | Xinxiang Yan | Lu Shen | Xiao-hua Gu | Bin Jiao | Jun Xu | Lin Zhou | Yafang Zhou | M. Tang | Jingya Wei | Ling Weng
[1] E. Génin,et al. A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement. , 2014, Brain : a journal of neurology.
[2] L. Schöls,et al. Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease , 2014, Neurobiology of Aging.
[3] D. Na,et al. Clinical and genetic analysis of MAPT, GRN, and C9orf72 genes in Korean patients with frontotemporal dementia , 2014, Neurobiology of Aging.
[4] K. Xia,et al. Identification of C9orf72 repeat expansions in patients with amyotrophic lateral sclerosis and frontotemporal dementia in mainland China , 2014, Neurobiology of Aging.
[5] P. S. Mathuranath,et al. Microtubule-associated protein tau genetic variations are uncommon cause of frontotemporal dementia in south India , 2014, Neurobiology of Aging.
[6] V. Meininger,et al. C9orf72 hexanucleotide repeat expansions as the causative mutation for chromosome 9p21-linked amyotrophic lateral sclerosis and frontotemporal dementia. , 2012, Archives of neurology.
[7] Janel O. Johnson,et al. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study , 2012, The Lancet Neurology.
[8] D. Galimberti,et al. Genetics of Frontotemporal Lobar Degeneration , 2012, Front. Neur..
[9] M. Nalls,et al. The chromosome 9 ALS and FTD locus is probably derived from a single founder , 2012, Neurobiology of Aging.
[10] J. Rohrer,et al. Phenotypic signatures of genetic frontotemporal dementia. , 2011, Current opinion in neurology.
[11] N. Bresolin,et al. A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia , 2011, Alzheimer's & Dementia.
[12] P. Johannsen,et al. Frontotemporal Dementia Caused by CHMP2B Mutations , 2011, Current Alzheimer research.
[13] Nick C Fox,et al. Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review , 2010, Journal of Neurology, Neurosurgery & Psychiatry.
[14] Bruce L. Miller,et al. Frontotemporal lobar degeneration , 2010, CNS drugs.
[15] K. Sleegers,et al. Genetic contribution of FUS to frontotemporal lobar degeneration , 2010, Neurology.
[16] Nick C Fox,et al. The heritability and genetics of frontotemporal lobar degeneration , 2009, Neurology.
[17] Andrew King,et al. A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series. , 2008, Brain : a journal of neurology.
[18] D. Munoz,et al. Progressive Nonfluent Aphasia Associated With a New Mutation V363I in Tau Gene , 2007, American journal of Alzheimer's disease and other dementias.
[19] M. Spillantini,et al. Hereditary Frontotemporal Dementia Caused by Tau Gene Mutations , 2007, Brain pathology.
[20] S. Melquist,et al. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 , 2006, Nature.
[21] A. Pestronk,et al. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein , 2004, Nature Genetics.
[22] R. Faber,et al. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. , 1999, Neurology.
[23] D. Geschwind,et al. Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[24] Ronald C. Petersen,et al. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 , 1998, Nature.
[25] M. Mesulam,et al. Slowly progressive aphasia without generalized dementia , 1982, Annals of neurology.
[26] N. Hattori,et al. Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS. , 2013, Parkinsonism & related disorders.