Nikolaos Venizelos

Nikolaos Venizelos

Orebro University - Örebro / Sweden
Medical and Health Sciences / Neuroscience
AD Scientific Index ID: 1096049
Örebro universitet
person_outline Nikolaos Venizelos's MOST POPULAR ARTICLES
1-) Excessive production of amyloid beta-protein by peripheral cells of symptomatic and presymptomatic patients carrying the Swedish familial Alzheimer disease mutation.M Citron, C Vigo-Pelfrey, DB Teplow, C Miller, D Schenk, J Johnston, ...Proceedings of the National Academy of Sciences 91 (25), 11993-11997, 19944691994
2-) Increased β‐amyloid release and levels of amyloid precursor protein (APP) in fibroblast cell lines from family members with the Swedish Alzheimer\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\'s disease APP670/671 mutationJA Johnston, RF Cowburn, S Norgren, B Wiehager, N Venizelos, ...FEBS letters 354 (3), 274-278, 19941651994
3-) Long-chain 3-hydroxyacyl–coenzyme A dehydrogenase deficiency with the G1528C mutation: Clinical presentation of thirteen patientsT Tyni, A Palotie, L Viinikka, L Valanne, MK Salo, U von Döbeln, ...The Journal of pediatrics 130 (1), 67-76, 19971501997
4-) Probing the lithium-response pathway in hiPSCs implicates the phosphoregulatory set-point for a cytoskeletal modulator in bipolar pathogenesisBTD Tobe, AM Crain, AM Winquist, B Calabrese, H Makihara, W Zhao, ...Proceedings of the National Academy of Sciences 114 (22), E4462-E4471, 20171432017
5-) N‐acetylaspartic aciduria due to aspartoacylase deficiency — a new aetiology of childhood leukodystrophyL Hagenfeldt, I Bollgren, N VenizelosJournal of inherited metabolic disease 10 (2), 135-141, 19871321987