Author/Creator: Prokisch, H - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Prokisch, H

1. 408 Hyperkinetic and hypokinetic movement disorders – in pediatric clinical practice. (11th October 2021)

Authors:: Barišić, N; Lehman, I; Bunoza, B; Chudy, D; Duranović, V; Jernej, B; Ahting, U; Haack, T; Prokisch, H; Willemsen, M
Journal:: Archives of disease in childhood
Issue:: Volume 106(2021)Supplement 2
Page Start:: A171
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2. Defective NDUFA9 as a novel cause of neonatally fatal complex I disease. Issue 1 (23rd November 2011)

Authors:: van den Bosch, B J C; Gerards, M; Sluiter, W; Stegmann, A P A; Jongen, E L C; Hellebrekers, D M E I; Oegema, R; Lambrichs, E H; Prokisch, H; Danhauser, K; Schoonderwoerd, K; de Coo, I F M; Smeets, H J M
Journal:: Journal of medical genetics
Issue:: Volume 49:Issue 1(2012)
Page Start:: 10
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

3. Leigh syndrome caused by mutations in the flavoprotein (Fp) subunit of succinate dehydrogenase (SDHA). Issue 1 (16th December 2005)

Authors:: Horváth, R; Abicht, A; Holinski-Feder, E; Laner, A; Gempel, K; Prokisch, H; Lochmüller, H; Klopstock, T; Jaksch, M
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 77:Issue 1(2006)
Page Start:: 74
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗