Showing 1 - 5 results of 5 for search 'Proukakis, C', query time: 0.02s
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Selective vulnerability in α-synucleinopathies. by Alegre-Abarrategui, J, Brimblecombe, K, Roberts, R, Velentza-Almpani, E, Tilley, B, Bengoa-Vergniory, N, Proukakis, C
Published 2019Journal article -
2
Human GM3 synthase deficiency: Autosomal recessive infantile onset symptomatic epilepsy syndrome. by Priestman, D, Neville, D, Reinkensmeier, G, Simpson, M, Proukakis, C, Patton, M, Dwek, R, Butters, T, Platt, F, Crosby, A
Published 2004Conference item -
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Human GM3 synthase deficiency: A novel form of hereditary childhood epilepsy by Priestman, D, Neville, D, Reinkensmeier, G, Simpson, M, Proukakis, C, Patten, M, Dwek, R, Butters, T, Platt, F, Crosby, A
Published 2005Conference item -
4
Visual short-term memory deficits associated with GBA mutation and Parkinson's disease. by Zokaei, N, McNeill, A, Proukakis, C, Beavan, M, Jarman, P, Korlipara, P, Hughes, D, Mehta, A, Hu, M, Schapira, A, Husain, M
Published 2014Journal article -
5
Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase. by Simpson, M, Cross, H, Proukakis, C, Priestman, D, Neville, D, Reinkensmeier, G, Wang, H, Wiznitzer, M, Gurtz, K, Verganelaki, A, Pryde, A, Patton, M, Dwek, R, Butters, T, Platt, F, Crosby, A
Published 2004Journal article