Frontotemporal dementia and parkinsonism associated with the IVSI+IG→A mutation in progranulin : a clinicopathologic study
- Author
- GOEDERT, Michel1 ; GRAZIA SPILLANTINI, Maria2 ; RADEMAKERS, Rosa5 ; TANG-WAI, David8 ; JACK, Clifford R4 9 ; KANTARCI, Kejal9 ; SHIUNG, Maria M9 ; GOLDE, Todd4 5 ; SMITH, Glenn E10 4 ; GEDA, Yonas E10 4 ; KNOPMAN, David S3 4 ; PETERSEN, Ronald C3 4 ; BOEVE, Bradley F3 4 ; BAKER, Matt5 ; DICKSON, Dennis W4 6 ; PARISI, Joseph E3 4 7 ; GIANNINI, Caterina7 ; JOSEPHS, Keith A3 4 ; HUTTON, Michael4 5 ; PICKERING-BROWN, Stuart M5
[1] MRC Laboratory of Molecular Biology, University of Cambridge, Cambridge, United Kingdom
[2] Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom
[3] Department of Neurology, Mayo Clinic, Rochester, MN, United States
[4] Robert H. and Clarice Smith and Abigail Van Buren Alzheimer's Disease Research Program of the Mayo Foundation, United States
[5] Neurogenetics Laboratory, Mayo Clinic, Jacksonville, FL, United States
[6] Neuropathology Laboratory, Mayo Clinic, Jacksonville, FL, United States
[7] Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, United States
[8] Department of Medicine, University of Toronto, Toronto, Ontario, Canada
[9] Department of Diagnostic Radiology-Neuroradiology, Mayo Clinic, Rochester, MN, United States
[10] Department of Psychiatry and Psychology, Mayo Clinic, Rochester, MN, United States - Source
Brain. 2006, Vol 129 ; 2808-2810,3103-3114 [15 p.] ; 11 ; ref : dissem
- Publisher
- Oxford University Press, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Author keyword
- frontotemporal dementia neurodegenerative disease neurogenetics presenilin progranulin
- Keyword (fr)
- Démence frontotemporale Mutation Parkinsonisme Préséniline Système nerveux pathologie
- Keyword (en)
- Frontotemporal dementia Mutation Parkinsonism Presenilin Nervous system diseases
- Keyword (es)
- Demencia frontotemporal Mutación Parkinson síndrome Presenilina Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17H Diseases of striated muscles. Neuromuscular diseases
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18281563
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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