Keywords: سندرم کورتیکوباسال; Corticobasal syndrome; Dopaminergic degeneration; Cerebrovascular disease; Carotid endarterectomy; Atypical parkinsonism;
مقالات ISI سندرم کورتیکوباسال (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: سندرم کورتیکوباسال; Alzheimer's disease; Dementia with lewy bodies; Progressive supranuclear palsy; Corticobasal syndrome; Transcranial magnetic stimulation; Intracortical connectivity; Short interval intracortical inhibition; Intracortical facilitation; Short latency affere
Keywords: سندرم کورتیکوباسال; Non-amnestic Alzheimer's disease; Alzheimer's disease; Atrophy; Magnetic resonance imaging; Braak staging; tau; Disease progression; Logopenic-variant primary progressive aphasia; Posterior cortical atrophy; Corticobasal syndrome; Frontalvariant Alzheimer
Keywords: سندرم کورتیکوباسال; Parkinson's Disease; Corticobasal Syndrome; Progressive Supranuclear Palsy; Noun; Verb;
Keywords: سندرم کورتیکوباسال; Corticobasal syndrome; Hashimoto encephalopathy; cortical ribboning;
Keywords: سندرم کورتیکوباسال; Parkinsonian disorders; Parkinson's disease; Progressive supranuclear palsy; Multiple system atrophy; Corticobasal syndrome; Biomarker; Proteomics; Cerebrospinal fluid; Isobaric labelling;
Keywords: سندرم کورتیکوباسال; Aβ; β-amyloid; AD; Alzheimer's disease; APD; atipical parkinsonian diseases; α-syn; α-synuclein; CBS; corticobasal syndrome; DLB; dementia with lewy bodies; DLN; dorsolateral tegmental nucleus; MCI; mild cognitive impairment; HD; Huntington's dise
Keywords: سندرم کورتیکوباسال; Progressive supranuclear palsy; Corticobasal syndrome; Functional connectivity; Thalamus; Dentate nucleus;
Keywords: سندرم کورتیکوباسال; Corticobasal syndrome; Dystonia; Basal ganglia;
Keywords: سندرم کورتیکوباسال; Corticobasal syndrome; Cortical thickness; Diffusion tensor imaging; Tractography;
Keywords: سندرم کورتیکوباسال; Corticobasal syndrome; Alzheimer's disease; Neuroimaging; CSF biomarkers; Aphasia;
Keywords: سندرم کورتیکوباسال; Alzheimer's disease; Semantic dementia; Corticobasal degeneration; Mechanical problem-solving; Apraxia; AD; Alzheimer's disease (as a group); BEC; “Batterie d'Evaluation Cognitive” (a French neuropsychological battery); CBS; Corticobasal syndrome; F
Keywords: سندرم کورتیکوباسال; Corticobasal syndrome; Swallowing; Dysphagia; Atypical parkinsonism
Keywords: سندرم کورتیکوباسال; Number knowledge; Corticobasal syndrome; Posterior cortical atrophy; Chunking; Parietal; Prefrontal;
Keywords: سندرم کورتیکوباسال; Posterior cortical atrophy; Corticobasal syndrome; Alzheimer's disease; Phenotype; Asymmetric atrophy;
Keywords: سندرم کورتیکوباسال; Corticobasal syndrome; Corticobasal degeneration; Multiple system atrophy; Parkinsonism; Atypical parkinsonism; Asymmetry;
Keywords: سندرم کورتیکوباسال; Corticobasal syndrome; Progressive supranuclear palsy; Primary progressive aphasia-nonfluent variant; Activities of daily living; Functional disability; Apraxia; Memory; Cognitive deficits; Behavioural changes;
CSF biomarkers β-amyloid, tau proteins and a-synuclein in the differential diagnosis of Parkinson-plus syndromes
Keywords: سندرم کورتیکوباسال; Aβ42; beta-amyloid; AD; Alzheimer's disease; ANCOVA; analysis of covariance; ANOVA; analysis of variance; a-syn; a-synuclein; CBD; Corticobasal degeneration; CBS; corticobasal syndrome; CBS-AD; corticobasal syndrome with underlying AD pathology; CBS-non-
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations
Keywords: سندرم کورتیکوباسال; Frontotemporal lobar degeneration; Corticobasal syndrome; GRN; Progranulin protein; Mutation; Founder effect;
IgLON5 autoimmunity tested negative in patients with progressive supranuclear palsy and corticobasal syndrome
Keywords: سندرم کورتیکوباسال; Progressive supranuclear palsy; Corticobasal syndrome; Autoimmune diseases; Sleep disorders; IgLON5;
Mutation analysis of C9orf72 in patients with corticobasal syndrome
Keywords: سندرم کورتیکوباسال; C9orf72; Corticobasal syndrome; oral stereotypies;
C9orf72 repeat expansions are restricted to the ALS-FTD spectrum
Keywords: سندرم کورتیکوباسال; Amyotrophic lateral sclerosis; Frontotemporal lobar degeneration; C9orf72; Progressive supranuclear palsy; Corticobasal syndrome; Neurogenetics;
Exome sequencing in familial corticobasal degeneration
Keywords: سندرم کورتیکوباسال; Corticobasal degeneration; Corticobasal syndrome; Apraxia; Genetics; Progressive supranuclear palsy;
Dopamine D2 receptor SPECT in corticobasal syndrome and autopsy-confirmed corticobasal degeneration
Keywords: سندرم کورتیکوباسال; Atypical parkinsonism; Corticobasal syndrome; Corticobasal degeneration; Dopamine D2 receptors; Single photon emission computerized tomography;
FUS and TDP43 genetic variability in FTD and CBS
Keywords: سندرم کورتیکوباسال; Frontotemporal dementia; Corticobasal syndrome; Genetics; FUS; TDP-43;
Limb apraxia in corticobasal syndrome
Keywords: سندرم کورتیکوباسال; Limb apraxia; Corticobasal degeneration; Corticobasal syndrome; Pantomime; Imitation; Transitive gestures; Intransitive gestures; Non-representational gestures; Skilled movement; Action; Motor control; Objects; Naming; Gesture identification
Diffusion tensor imaging of the corpus callosum differentiates corticobasal syndrome from Parkinson’s disease
Keywords: سندرم کورتیکوباسال; Corticobasal syndrome; Parkinson’s disease; Corpus callosum; Diffusion tensor imaging
Symmetric corticobasal degeneration (S-CBD)
Keywords: سندرم کورتیکوباسال; Corticobasal degeneration; Corticobasal syndrome; Symmetric CBD; Atlas based parcellation; Pathology
Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide
Keywords: سندرم کورتیکوباسال; Frontotemporal dementia; Corticobasal syndrome; Progressive supranuclear palsy; Motorneuron disease; PGRN; MAPT haplotype; Deletion; Mutation prevalence; Mutation penetrance
A novel deletion in progranulin gene is associated with FTDP-17 and CBS
Keywords: سندرم کورتیکوباسال; Frontotemporal dementia; Corticobasal syndrome; Linkage analysis; PGRN; Mutation; Genotype–phenotype correlation