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Avenali, M; Toffoli, M; Mullin, S; McNeil, A; Hughes, DA; Mehta, A; Blandini, F; (2019) Evolution of prodromal parkinsonian features in a cohort of GBA mutation-positive individuals: a 6-year longitudinal study. Journal of Neurology, Neurosurgery & Psychiatry 10.1136/jnnp-2019-320394. (In press). Green open access


Blandini, F; Cilia, R; Cerri, S; Pezzoli, G; Schapira, AHV; Mullin, S; Lanciego, JL; (2019) Glucocerebrosidase mutations and synucleinopathies: Toward a model of precision medicine. Movement Disorders , 34 (1) pp. 9-21. 10.1002/mds.27583.

Brown, R; Ginsberg, L; (2019) POEMS syndrome: clinical update. Journal of Neurology , 266 (1) pp. 268-277. 10.1007/s00415-018-9110-6. Green open access


Leija-Salazar, M; Sedlazeck, FJ; Toffoli, M; Mullin, S; Mokretar, K; Athanasopoulou, M; Donald, A; ... Proukakis, C; + view all (2019) Evaluation of the detection of GBA missense mutations and other variants using the Oxford Nanopore MinION. Molecular Genetics & Genomic Medicine 10.1002/mgg3.564. (In press). Green open access


Mullin, S; Beavan, M; Bestwick, J; McNeill, A; Proukakis, C; Cox, T; Hughes, D; ... Schapira, AHV; + view all (2019) Evolution and clustering of prodromal parkinsonian features in GBA1 carriers. Movement Disorders , 34 (9) pp. 1365-1373. 10.1002/mds.27775. Green open access

This list was generated on Sun Feb 2 21:59:14 2020 GMT.