Corticobasal syndrome associated with the A9D Progranulin mutation

Journal of Neuropathology and Experimental Neurology

Volumn 66, Issue 10, 2007, Pages 892-900

  Spina, Salvatore ^a,b   Murrell, Jill R ^a   Huey, Edward D ^c   Wassermann, Eric M ^c   Pietrini, Pietro ^d   Grafman, Jordan ^c   Ghetti, Bernardino ^a  

^a INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF SIENA   (Italy)

^c NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

^d UNIVERSITY OF PISA   (Italy)

Author keywords

Alien limb; Apraxia; Frontotemporal lobar degeneration; Hemineglect; Parietal lobe; Progranulin; TDP 43

Indexed keywords

FLUORODEOXYGLUCOSE F 18; PROGRANULIN;

ADULT; AMNESIA; APRAXIA; ARTICLE; BRAIN ATROPHY; CASE REPORT; CORTICOBASAL DEGENERATION; DEMENTIA; DYSTONIA; GENE MUTATION; GENETIC ANALYSIS; HUMAN; MALE; MOTOR DYSFUNCTION; NERVE DEGENERATION; NEUROPATHOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; PARKINSONISM; POSITRON EMISSION TOMOGRAPHY; PRIORITY JOURNAL;

ALLELES; APRAXIAS; BRAIN; COGNITION DISORDERS; DEMENTIA; DNA; DNA-BINDING PROTEINS; FLUORODEOXYGLUCOSE F18; HUMANS; INTERCELLULAR SIGNALING PEPTIDES AND PROTEINS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; NEUROPSYCHOLOGICAL TESTS; POSITRON-EMISSION TOMOGRAPHY; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SYNDROME;

EID: 34948898536     PISSN: 00223069     EISSN: None     Source Type: Journal    
DOI: 10.1097/nen.0b013e3181567873     Document Type: Article

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