Symmetrical corticobasal syndrome caused by a novel c.314dup progranulin mutation

Journal of Molecular Neuroscience

Volumn 45, Issue 3, 2011, Pages 354-358

  Dopper, Elise G P ^a   Seelaar, Harro ^a   Chiu, Wang Zheng ^a   De Koning, Inge ^a   Van Minkelen, Rick ^a   Baker, Matthew C ^b   Rozemuller, Annemieke J M ^c   Rademakers, Rosa ^b   Van Swieten, John C ^a,c  

^a ERASMUS MEDICAL CENTER   (Netherlands)

^b MAYO CLINIC   (United States)

^c VU UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Corticobasal syndrome (CBS); Frontotemporal lobar degeneration (FTLD); Progranulin (GRN); TDP 43

Indexed keywords

HEXAMETHYLPROPYLENE AMINE OXIME TECHNETIUM TC 99M; MESSENGER RNA; PROGRANULIN;

ADULT; AMNESIA; APHASIA; APRAXIA; AUTOPSY; BEHAVIOR CHANGE; BRAIN RADIOGRAPHY; CASE REPORT; CONFERENCE PAPER; CORTICOBASAL DEGENERATION; CORTICOBASAL SYNDROME; DEGENERATIVE DISEASE; DYSPHAGIA; DYSTONIA; FRONTOTEMPORAL DEMENTIA; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; HUMAN; HUMAN TISSUE; LANGUAGE DISABILITY; MALE; NEUROIMAGING; NEUROLOGIC EXAMINATION; NEUROPSYCHOLOGICAL TEST; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOLOGICAL CRYING; SINGLE PHOTON EMISSION COMPUTER TOMOGRAPHY; WALKING DIFFICULTY;

AUTOPSY; BASAL GANGLIA DISEASES; CEREBRAL CORTEX; FATAL OUTCOME; HUMANS; INTERCELLULAR SIGNALING PEPTIDES AND PROTEINS; MALE; MIDDLE AGED; MUTATION; NEURODEGENERATIVE DISEASES; SYNDROME;

EID: 84860390154     PISSN: 08958696     EISSN: 15591166     Source Type: Journal    
DOI: 10.1007/s12031-011-9626-z     Document Type: Conference Paper

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