Frontotemporal dementia-related gene mutations in clinical dementia patients from a Chinese population

Clinical and Neuroimaging Characterization of Chinese Dementia Patients with PSEN1 and PSEN2 Mutations

(2014) Zhihong Shi et al.   DEMENTIA AND GERIATRIC COGNITIVE DISORDERS

Validation of the Chinese Version of Addenbrooke's Cognitive Examination-Revised for Screening Mild Alzheimer's Disease and Mild Cognitive Impairment

(2013) Rong Fang et al.   DEMENTIA AND GERIATRIC COGNITIVE DISORDERS

C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China

(2013) Bin Jiao et al.   Frontiers in Cellular Neuroscience

The Beijing version of the montreal cognitive assessment as a brief screening tool for mild cognitive impairment: a community-based study

(2012) Jing Yu et al.   BMC Psychiatry

A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family

(2012) Jie-Mei Gu et al.   BONE

Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia

(2012) SG Mehta et al.   CLINICAL GENETICS

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

Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS

(2011) Mariely DeJesus-Hernandez et al.   NEURON

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

(2011) Alan E. Renton et al.   NEURON

Alzheimer Disease–like Phenotype Associated With the c.154delA Mutation in Progranulin

(2010) Brendan J. Kelley et al.   ARCHIVES OF NEUROLOGY

Frontotemporal Lobar Degeneration

(2010) Gil D. Rabinovici et al.   CNS DRUGS

Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's disease

(2009) Miryam Carecchio et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Progranulin-associated primary progressive aphasia: A distinct phenotype?

(2009) Jonathan D. Rohrer et al.   NEUROPSYCHOLOGIA

Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutation

(2008) S. G. Lindquist et al.   EUROPEAN JOURNAL OF NEUROLOGY

Prominent phenotypic variability associated with mutations in Progranulin

(2007) Brendan J. Kelley et al.   NEUROBIOLOGY OF AGING