Search

Author/Creator Parisi, J. E.

1. Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP‐17) due to microtubule‐associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathy. (8th March 2017)

Authors:
Tacik, P.; Sanchez‐Contreras, M.; DeTure, M.; Murray, M. E.; Rademakers, R.; Ross, O. A.; Wszolek, Z. K.; Parisi, J. E.; Knopman, D. S.; Petersen, R. C.; Dickson, D. W.
Journal:
Neuropathology & applied neurobiology
Issue:
Volume 43:Number 3(2017)
Page Start:
200
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients. (September 2015)

Authors:
Lorenzo‐Betancor, O.; Ogaki, K.; Soto‐Ortolaza, A. I.; Labbe, C.; Walton, R. L.; Strongosky, A. J.; van Gerpen, J. A.; Uitti, R. J.; McLean, P. J.; Springer, W.; Siuda, J.; Opala, G.; Krygowska‐Wajs, A.; Barcikowska, M.; Czyzewski, K.; McCarthy, A.; Lynch, T.; Puschmann, A.; Rektorova, I.; Sanots...
Journal:
European journal of neurology
Issue:
Volume 22:Number 9(2015:Sep.)
Page Start:
1323
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗