Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review. - Wikidata - awgldk - TriplyDB

Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review.

Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review.

http://www.wikidata.org/entity/Q36803576

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The Use of Stem Cells to Model Amyotrophic Lateral Sclerosis and Frontotemporal Dementia: From Basic Research to Regenerative Medicine Parkinsonian syndrome in familial frontotemporal dementia Genetic markers in biological fluids for aging-related major neurocognitive disorder Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis.ALS-FTD complex disorder due to C9ORF72 gene mutation: description of first Polish family.An Assessment of Possible Neuropathology and Clinical Relationships in 46 Sporadic Amyotrophic Lateral Sclerosis Patient Autopsies The neuropathology and cerebrovascular mechanisms of dementia An advanced white matter tract analysis in frontotemporal dementia and early-onset Alzheimer's disease.Altered sleep and EEG power in the P301S Tau transgenic mouse model.Opening up the DNA methylome of dementia Sensitivity of the Wechsler Abbreviated Scale of Intelligence-Second Edition (WASI-II) to the neurocognitive deficits associated with the semantic dementia variant of frontotemporal lobar degeneration: A case study.The role of CHMP2BIntron5 in autophagy and frontotemporal dementia.Updated meta-analysis of the role of APOE ε2/ε3/ε4 alleles in frontotemporal lobar degeneration.Prognosis of Patients with Behavioral Variant Frontotemporal Dementia Who have Focal Versus Diffuse Frontal Atrophy.Disulfide cross-linked multimers of TDP-43 and spinal motoneuron loss in a TDP-43A315T ALS/FTD mouse model.Clinical Spectrum of Amyotrophic Lateral Sclerosis (ALS).Sleep in Alzheimer's Disease - Beyond Amyloid.Are Major Dementias Triggered by Poor Blood Flow to the Brain? Theoretical Considerations.FOXP2 Expression in Frontotemporal Lobar Degeneration-Tau.Unclassified cases of behavioral variant of major frontotemporal neurocognitive disorder in the Diagnostic and Statistical Manual of Mental Disorders, 5th edition.Pathomechanisms of TDP-43 in neurodegeneration.Gray matter changes in asymptomatic C9orf72 and GRN mutation carriers.Molecular Genetics of Frontotemporal Dementia Elucidated by Drosophila Models-Defects in Endosomal⁻Lysosomal Pathway.

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Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review.

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name

Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review.

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Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review.

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Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review.

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Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review.

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Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review.

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Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review.

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Translational Neurodegeneration

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Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review.

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Xiao-Dong Pan

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P2860

Valosin-containing protein is a multi-ubiquitin chain-targeting factor required in ubiquitin-proteasome degradation

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

Classification of primary progressive aphasia and its variants

Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease

Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

The genetics and neuropathology of frontotemporal lobar degeneration

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

A harmonized classification system for FTLD-TDP pathology

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

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