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Page 1
DCTN1 mutations in Perry syndrome.
Farrer MJ, Hulihan MM, Kachergus JM, Dächsel JC, Stoessl AJ, Grantier LL, Calne S, Calne DB, Lechevalier B, Chapon F, Tsuboi Y, Yamada T, Gutmann L, Elibol B, Bhatia KP, Wider C, Vilariño-Güell C, Ross OA, Brown LA, Castanedes-Casey M, Dickson DW, Wszolek ZK. Farrer MJ, et al. Among authors: chapon f. Nat Genet. 2009 Feb;41(2):163-5. doi: 10.1038/ng.293. Epub 2009 Jan 11. Nat Genet. 2009. PMID: 19136952 Free PMC article.
Pallidonigral TDP-43 pathology in Perry syndrome.
Wider C, Dickson DW, Stoessl AJ, Tsuboi Y, Chapon F, Gutmann L, Lechevalier B, Calne DB, Personett DA, Hulihan M, Kachergus J, Rademakers R, Baker MC, Grantier LL, Sujith OK, Brown L, Calne S, Farrer MJ, Wszolek ZK. Wider C, et al. Among authors: chapon f. Parkinsonism Relat Disord. 2009 May;15(4):281-6. doi: 10.1016/j.parkreldis.2008.07.005. Epub 2008 Aug 23. Parkinsonism Relat Disord. 2009. PMID: 18723384 Free PMC article.
[Raeder's syndrome caused by carotid dissection].
Brandel JP, Chapon F, Viader F, Lechevalier B. Brandel JP, et al. Among authors: chapon f. Presse Med. 1987 Mar 28;16(11):541. Presse Med. 1987. PMID: 2951700 French. No abstract available.
[Acquired rubella : encephalitis with exophthalmos].
Lechevalier B, Freymuth P, Chapon F. Lechevalier B, et al. Among authors: chapon f. Nouv Presse Med. 1979 Jan 27;8(5):368-9. Nouv Presse Med. 1979. PMID: 554099 French. No abstract available.
195 results