The multiple phenotypes of corticobasal syndrome and corticobasal degeneration: implications for further study.
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Neuronal network disintegration: common pathways linking neurodegenerative diseasesCortical Activation During Levitation and Tentacular Movements of Corticobasal Syndrome.Validation of the new consensus criteria for the diagnosis of corticobasal degenerationDisentangling the neural correlates of corticobasal syndrome and corticobasal degeneration with systematic and quantitative ALE meta-analysesThe progression of posterior cortical atrophy to corticobasal syndrome: lumping or splitting neurodegenerative diseases?A disease-specific metabolic brain network associated with corticobasal degeneration.FUS and TDP43 genetic variability in FTD and CBSTranscranial Magnetic Stimulation (TMS) as a Tool for Early Diagnosis and Prognostication in Cortico-Basal Ganglia Degeneration (CBD) Syndromes: Review of Literature and Case ReportClinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review.Dystonia in corticobasal degeneration: a review of the literature on 404 pathologically proven cases.Frontotemporal lobar degeneration: epidemiology, pathology, diagnosis and management.Cognitive dysfunction in corticobasal degeneration.Car drivers with dementia: Different complications due to different etiologies?Atypical association of semantic dementia, corticobasal syndrome, and 4R tauopathy.Cerebral Glucose Metabolism and Dopaminergic Function in Patients with Corticobasal Syndrome.Brain Perfusion in Corticobasal Syndrome with Progressive Aphasia.An autopsied case of corticobasal degeneration showing severe cerebral atrophy over a protracted disease course of 16 years.Posterior cortical atrophy as a primary clinical phenotype of corticobasal syndrome with a progranulin gene rs5848 TT genotype.Emerging Diagnostic and Therapeutic Strategies for Tauopathies.Corticobasal degeneration: clinical characteristics and multidisciplinary therapeutic approach in 26 patients.Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies.Neocortical origin and progression of gray matter atrophy in nonamnestic Alzheimer's disease.Neurodegenerative disease: can synucleinopathy and tauopathy be identified during life?The association of aphasia and right-sided motor impairment in corticobasal syndrome.An autopsied case of corticobasal degeneration presenting with frontotemporal dementia followed by myoclonus.Diffuse lewy body disease presenting as corticobasal syndrome and progressive supranuclear palsy syndrome.Cortical limb myoclonus in pathologically proven progressive supranuclear palsy.Neurophysiology and neurochemistry of corticobasal syndrome.Progressive Dopamine Transporter Binding Loss in Autopsy-Confirmed Corticobasal Degeneration.
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The multiple phenotypes of corticobasal syndrome and corticobasal degeneration: implications for further study.
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article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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The multiple phenotypes of cor ...... mplications for further study.
@en
The multiple phenotypes of cor ...... mplications for further study.
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type
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The multiple phenotypes of cor ...... mplications for further study.
@en
The multiple phenotypes of cor ...... mplications for further study.
@nl
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The multiple phenotypes of cor ...... mplications for further study.
@en
The multiple phenotypes of cor ...... mplications for further study.
@nl
P2860
P1476
The multiple phenotypes of cor ...... mplications for further study.
@en
P2093
Bradley F Boeve
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P2888
P304
P356
10.1007/S12031-011-9624-1
P577
2011-08-19T00:00:00Z