Items where Author is "Proukakis, C"

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Article

Kara, E and Tucci, A and Manzoni, C and Lynch, DS and Elpidorou, M and Bettencourt, C and Chelban, V and Manole, A and Hamed, S and Federoff, M and Preza, E and Hughes, D and Pittman, A and Jaunmuktane, Z and Brandner, S and Xiromerisiou, G and Wiethoff, S and Schottlaender, L and Proukakis, C and Morris, HW and Warner, T and Bhatia, KP and Korlipara, P and Singleton, AB and Hardy, J and Wood, NW and Lewis, PA And Houlden, H (2016) Genetic and phenotypic characterisation of complex hereditary spastic paraplegia. BRAIN, 139 (7). pp. 1904-1918.

Kiely, A P and Ling, H and Asi, Y T and Kara, E and Proukakis, C and Schapira, A H and Morris, H R and Lubbe, S and Limousin, P and Lewis, P A and Lees, A J and Quinn, N and Hardy, J and Love, S and Revesz, T and Houlden, H and Holton, J L (2015) Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation. Molecular Neurodegeneration, 10. p. 41.

This list was generated on Tue May 18 07:34:21 2021 BST.