Inhaltsbereich
Medical NeuroScience Cluster Publications by
Schmied Christiane, Ao.Univ.-Prof. Dr.med.univ. :
2021 2018 2016 2014 2013 2012 2006
2021 Original Articles
- Dal-Bianco A, Schranzer R, Grabner G, Lanzinger M, Kolbrink S, Pusswald G, Altmann P, Ponleitner M, Weber M, Kornek B, Zebenholzer K, Schmied C, Berger T, Lassmann H, Trattnig S, Hametner S, Leutmezer F, Rommer P (2021) Iron Rims in Patients With Multiple Sclerosis as Neurodegenerative Marker? A 7-Tesla Magnetic Resonance Study Front Neurol, 12: 632749
2018 Original Articles
- Reinthaler E, Graf E, Zrzavy T, Wieland T, Hotzy C, Kopecky C, Pferschy S, Schmied C, Leutmezer F, Keilani M, Lill C, Hoffjan S, Epplen J, Zettl U, Hecker M, Deutschländer A, Meuth S, Ahram M, Mustafa B, El-Khateeb M, Vilariño-Güell C, Sadovnick A, Zimprich F, Tomkinson B, Strom T, Kristoferitsch W, Lassmann H, Zimprich A (2018) TPP2 mutation associated with sterile brain inflammation mimicking MS Neurol Genet, 4 (6): e285
- Zrzavy T, Kovacs-Nagy R, Reinthaler E, Deutschländer A, Schmied C, Kornek B, Leutmezer F, Zimprich A (2018) A rare P2RX7 variant in a Hungarian family with Multiple Sclerosis Mult Scler Relat Disord.,
2016 Original Articles
- Reinthaler EM, Graf E, Zrzavy T, Wieland T, Hotzy C, Kopecky CM, Schmied C, Leutmezer FH, Keilani MY, Lill CM, Hoffjan S, Epplen JT, Zettl UK, Hecker M, Deutschlaender A, Ahram M, Mustafa B, El-Khateeb M, Vilarino-Guell C, Sadovnick DA, Zimprich F, Tomkinson B, Strom TM, Kristoferitsch W, Lassmann H, Zimprich A (2016) Mutations in the gene tripeptidyl peptidase II (TPP2) and multiple sclerosis Mult Scler, 22: 849
2014 Original Articles
- Salhofer-Polanyi S, Baumgartner A, Kraus J, Maida E, Schmied M, Leutmezer F, (2014) What to expect after natalizumab cessation in a real-life setting Acta Neurol Scand, 130 (2): 97-102
2013 Original Articles
- Reinthaler E, Machetanz G, Hotzy C, Reindl M, Fazekas F, Kristoferitsch W, Berger T, Schmied C, Zimprich A (2013) No evidence for a role of rare CYP27B1 variants in Austrian multiple sclerosis patients Mult Scler, 20 (3): 391-392
2012 Original Articles
- Schmied M, Zehetmayer S, Reindl M, Ehling R, Bajer-Kornek B, Leutmezer F, Zebenholzer K, Hotzy C, Lichtner P, Meitinger T, Wichmann H, Illig T, Gieger C, Huber K, Khalil M, Fuchs S, Schmidt H, Auff E, Kristoferitsch W, Fazekas F, Berger T, Vass K, Zimprich A (2012) Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients Neurogenetics, 13 (2): 181-187
2006 Original Articles
- Stogmann E, Lichtner P, Baumgartner C, Schmied M, Hotzy C, Asmus F, Leutmezer F, Bonelli S, Assem-Hilger E, Vass K, Hatala K, Strom TM, Meitinger T, Zimprich F, Zimprich A (2006) Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes Neurogenetics,