Publications - sorted by Authors
Medical NeuroScience Cluster Publications by Baumgartner, Anna, Dr.med.univ.
2017 Original Articles
- Rommer P, Zschocke J, Fowler B, Födinger M, Konstantopoulou V, Möslinger D, Stögmann E, Suess E, Baumgartner M, Auff E, Sunder-Plassmann G (2017) Manifestations of neurological symptoms and thromboembolism in adults with MTHFR-deficiency J Neurol Sci, 383: 123-127
- Salhofer-Polanyi S, Cetin H, Leutmezer F, Baumgartner A, Blechinger S, Dal-Bianco A, Altmann P, Bajer-Kornek B, Rommer P, Guger M, Leitner-Bohn D, Reichardt B, Alasti F, Temsch W, Stamm T (2017) Epidemiology of Multiple Sclerosis in Austria Neuroepidemiol, 49 (1-2): 40-44
2015 Original Articles
- Walleczek NK, Rauschka H, Bsteh G, Birkl CB, Khalil M, Fuchs S, Enzinger C, Fazekas F, Eggers C, Leutmezer F, Salhofer-Polanyi S, Baumgartner A, Blechinger S, Koppi S, Sellner J, Kraus J, Assar H, Gugger M, Ehling R, Moser H, Raber B, Liendl H, Parigger S, Mayr M, Hiller MS, Meister B, Morgenstern G, Spiess HK, Kempf I, Cisar A, Bachler H, Lehninger R, Berger T, Kristoferitsch W, Aboulenein-Djamshidian F (2015) Month-of-birth-effect in multiple sclerosis in Austria Mult Scler, 21: 102-103
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
2012 Original Articles
- Hilger E, Reinthaler E, Stogmann E, Hotzy C, Pataraia E, Baumgartner C, Zimprich A, Zimprich F (2012) Lack of association between ABCC2 gene variants and treatment response in epilepsy Pharmacogenomics, 13 (2): 185-190
2008 Original Articles
- Stogmann E, El Tawil S, Wagenstaller J, Gaber A, Edris S, Abdelhady A, Assem-Hilger E, Leutmezer F, Bonelli S, Baumgartner C, Zimprich F, Strom T, Zimprich A (2008) A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis Neurogenetics, 10 (1): 73-77
- Stogmann E, El Tawil S, Wagenstaller J, Gaber A, Edris S, Abdelhady A, Assem-Hilger E, Leutmezer F, Bonelli S, Baumgartner C, Zimprich F, Strom T, Zimprich A (2008) A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis Neurogenetics, 10 (1): 73-77
- Beisteiner R, Drabeck K, Foki T, Geißler A, Gartus A, Lehner-Baumgartner E, Baumgartner C (2008) Does clinical memory fMRI provide a comprehensive map of medial temporal lobe structures? Exp. Neurol., 213 (1): 154-162