Pretraga




Rezultati

Phase III dose-comparison study of glatiramer acetate for multiple sclerosis   [2011]

Comi, Giancarlo; Cohen, Jeffrey A.; Arnold, Douglas L.; Wynn, Daniel; Filippi, Massimo

Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene   [2013]

Lohmann, Katja; ...; Kostic, Vladimir S; ...; (broj, koautora 29)

Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation   [2006]

Hartig, M.B; Hortnagel, K.; Garavaglia, B.; Zorzi, G.; Kmiec, T.; Klopstock, T.; Rostasy, K.; Svetel, Marina ; Kostić, Vladimir ; Schuelke, M.;
Botz, E.; Weindl, A.; Novaković, Ivana  ; Nardocci, N.; Prokisch, H.; Meitinger, T.;

Voxel-based morphometric magnetic resonance imaging (MRI) postprocessing in MRI-negative epilepsies   [2015]

Wang, Irene Z.; Jones, Stephen E.; Jaisani, Zeenat; Najm, Imad M.; Prayson, Richard A.; Burgess, Richard C.; Krishnan, Balu; Ristić, Aleksandar J.  ; Wong, Chong H.; Bingaman, William E.;
Gonzalez-Martinez, Jorge A.; Alexopoulos, Andreas V.;

Intriguing association of Parkinson's disease and epileptic seizures   [2018]

Lukić, Stevo  ; Biševac, Boban; Krstić, Nataša

Role of SC42 mutations in early- and late-onset dopa-responsive parkinsonism   [2002]

Kock, Norman; Muller, B; Vieregge, Peter; Pramstaller, Peter P; Marder, K; Abbruzzese, G; Martinelli, P; Lang, Anthony E; Jacobs, H; Hagenah, Johann M;
Harris, J; Meija-Santana, H; Fahn, S; Hedrich, Katja; Kann, M; Gehlken, U; Culjkovic, Biljana; Schwinger, E; Wszolek, ZK; Zuhlke, C; Klein, Christine;

Brain and cord imaging features in neuromyelitis optica spectrum disorders   [2019]

Cacciaguerra, Laura; Meani, Alessandro; Mesaroš, Šarlota  ; Radaelli, Marta; Palace, Jacqueline; Dujmović-Bašuroski, Irena ; Pagani, Elisabetta; Martinelli, Vittorio; Matthews, Lucy; Drulović, Jelena  ;
Leite, Maria Isabel; Comi, Giancarlo; Filippi, Massimo; Rocca, Maria A.;

Intravenous Thrombolysis 4.5-9 Hours After Stroke Onset: A Cohort Study from the TRISP Collaboration   [2023]

Altersberger, Valerian L.; ...; Jovanović, Dejana R.  ; ...; (broj koautora 42)

The R98Q variation in DJ-1 represents a rare polymorphism   [2004]

Hedrich, Katja; Schafer, N; Hering, R; Hagenah, Johann M; Lanthaler, AJ; Schwinger, E; Kramer, PL; Ozelius, LJ; Bressman, SB; Abbruzzese, G;
Martinelli, P; Kostic, Vladimir S; Pramstaller, Peter P; Vieregge, Peter; Riess, O; Klein, Christine;

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