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Progressive supranuclear palsy
Citations 11-20 of 34 total displayed.
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Past content
(since Jan 2001):
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- CLINICAL/SCIENTIFIC NOTES
LRRK2 mutations on Crete: R1441H associated with PD evolving to PSP
- Cleanthe Spanaki, Helen Latsoudis, and Andreas Plaitakis
Neurology 2006; 67: 1518-1519.
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- ARTICLES
New and reliable MRI diagnosis for progressive supranuclear palsy
- H. Oba, A. Yagishita, H. Terada, A. J. Barkovich, K. Kutomi, T. Yamauchi, S. Furui, T. Shimizu, M. Uchigata, K. Matsumura, M. Sonoo, M. Sakai, K. Takada, A. Harasawa, K. Takeshita, H. Kohtake, H. Tanaka, and S. Suzuki
Neurology 2005; 64: 2050-2055.
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- BRIEF COMMUNICATIONS
"Applause sign" helps to discriminate PSP from FTD and PD
- B. Dubois, A. Slachevsky, B. Pillon, R. Beato, J. M. Villalponda, and I. Litvan
Neurology 2005; 64: 2132-2133.
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- ARTICLES
Quantitative MRI measurement of superior cerebellar peduncle in progressive supranuclear palsy
- D. C. Paviour, S. L. Price, J. M. Stevens, A. J. Lees, and N. C. Fox
Neurology 2005; 64: 675-679.
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Young onset limb spasticity with PSP-like brain and spinal cord NFT-tau pathology
- S. Papapetropoulos, T. Scaravilli, H. Morris, S. F. An, D. C. Henderson, N. P. Quinn, F. Scaravilli, and K. P. Bhatia
Neurology 2005; 64: 731-733.
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- ARTICLES
Limb apraxia in corticobasal degeneration and progressive supranuclear palsy
- Paola Soliveri, Sylvie Piacentini, and Floriano Girotti
Neurology 2005; 64: 448-453.
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- ARTICLES
Sonographic discrimination of corticobasal degeneration vs progressive supranuclear palsy
- U. Walter, D. Dressler, A. Wolters, T. Probst, A. Grossmann, and R. Benecke
Neurology 2004; 63: 504-509.
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Syndrome resembling PSP after surgical repair of ascending aorta dissection or aneurysm
- Bahram Mokri, J. Eric Ahlskog, Jimmy R. Fulgham, and Joseph Y. Matsumoto
Neurology 2004; 62: 971-973.
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- BRIEF COMMUNICATIONS
Strong association of the Saitohin gene Q7 variant with progressive supranuclear palsy
- R. de Silva, A. Hope, A. Pittman, M.E. Weale, H.R. Morris, N.W. Wood, and A.J. Lees
Neurology 2003; 61: 407-409.
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- BRIEF COMMUNICATIONS
Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP
- H.R. Morris, Y. Osaki, J. Holton, A.J. Lees, N.W. Wood, T. Revesz, and N. Quinn
Neurology 2003; 61: 102-104.
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