Inhaltsbereich
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Institution: Department of Neurology
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Department of Neurology | Division of Neuropathology and Neurochemistry
- Rath J, Zulehner G, Schober B, Grisold A, Krenn M, Cetin H, Zimprich F (2021) Cerebrospinal fluid analysis in Guillain–Barré syndrome: value of albumin quotients J Neurol,
- Dal-Bianco A, Grabner G, Kronnerwetter C, Weber M, Kornek B, Kasprian G, Berger T, Leutmezer F, Rommer P, Trattnig S, Lassmann H, Hametner S (2021) Long-term evolution of multiple sclerosis iron rim lesions in 7 T MRI Brain, 144(3): 833-847
- Zrzavy T, Schwaiger C, Wimmer I, Berger T, Bauer J, Butovsky O, Schwab J, Lassmann H, Höftberger R (2021) Acute and non-resolving inflammation associate with oxidative injury after human spinal cord injury Brain, 144(1): 144-161
- Wimmer I, Scharler C, Kadowaki T, Hillebrand S, Scheiber‐Mojdehkar B, Ueda S, Bradl M, Berger T, Lassmann H, Hametner S (2021) Iron accumulation in the choroid plexus, ependymal cells and CNS parenchyma in a rat strain with low‐grade haemolysis of fragile macrocytic red blood cells Brain Pathol, 31(2): 333-345
| Weblink | - Zrzavy T, Wimmer I, Rommer P, Berger T (2020) Immunology of COVID‐19 and disease‐modifying therapies: the good, the bad and the unknown Eur J Neurol,
- Hafner J, Zadrazil M, Grisold A, Ricken G, Krenn M, Kitzmantl D, Pollreisz A, Gleiss A, Schmidt-Erfurth U (2020) Retinal and Corneal Neurodegeneration and Their Association with Systemic Signs of Peripheral Neuropathy in Type 2 Diabetes Am J Ophthalmol, 209: 197-205
- Gasser M, Boonsimma P, Netbaramee W, Wechapinan T, Srichomthomg C, Ittiwut C, Krenn M, Zimprich F, Milenkovic I, Abicht A, Biskup S, Roser T, Shotelersuk V, Tacke M, Kuersten M, Wagner M, Borggraefe I, Suphapeetiporn K, von Stülpnagel C (2020) ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatment response J Clin Neurosci, 72: 31-38
- Krenn M, Wagner M, Hotzy C, Graf E, Weber S, Brunet T, Lorenz-Depiereux B, Kasprian G, Aull-Watschinger S, Pataraia E, Stogmann E, Zimprich A, Strom T, Meitinger T, Zimprich F (2020) Diagnostic exome sequencing in non-acquired focal epilepsies highlights a major role of GATOR1 complex genes J Med Genet, 57 (9): 624-633
- Wolking S, Moreau C, Nies A, Schaeffeler E, McCormack M, Auce P, Avbersek A, Becker F, Krenn M, Møller R, Nikanorova M, Weber Y, Weckhuysen S, Cavalleri G, Delanty N, Depondt C, Johnson M, Koeleman B, Kunz W, Marson A, Sander J, Sills G, Striano P, Zara F, Zimprich F, Schwab M, Krause R, Sisodiya S, Cossette P, Girard S, Lerche H, (2020) Testing association of rare genetic variants with resistance to three common antiseizure medications Epilepsia, 61 (4): 657-666
- Wolking S, Schulz H, Nies A, McCormack M, Schaeffeler E, Auce P, Avbersek A, Becker F, Klein K, Krenn M, Møller R, Nikanorova M, Weckhuysen S, Consortium E, Cavalleri G, Delanty N, Depondt C, Johnson M, Koeleman B, Kunz W, Marson A, Sander J, Sills G, Striano P, Zara F, Zimprich F, Weber Y, Krause R, Sisodiya S, Schwab M, Sander T, Lerche H (2020) Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study Pharmacogenomics, 21 (5): 325-335
- Boonsimma P, Michael Gasser M, Netbaramee W, Wechapinan T, Srichomthong C, Ittiwut C, Wagner M, Krenn M, Zimprich F, Abicht A, Biskup S, Roser T, Borggraefe I, Suphapeetiporn K, Shotelersuk V (2020) Mutational and phenotypic expansion of ATP1A3-related disorders: Report of nine cases Gene, 749: 144709
- Schijven D, Stevelink R, McCormack M, van Rheenen W, Luykx J, Koeleman B, Veldink J (2020) Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy Neurobiol Aging, 92: 153.e1-153.e5
- Krenn M, Grisold A, Wohlfarth P, Rath J, Cetin H, Koneczny I, Zimprich F (2020) Pathomechanisms and Clinical Implications of Myasthenic Syndromes Exacerbated and Induced by Medical Treatments Front Mol Neurosci, 13
- Zech M, Jech R, Boesch S, Škorvánek M, Weber S, Wagner M, Zhao C, Jochim A, Necpál J, Dincer Y, Vill K, Distelmaier F, Stoklosa M, Krenn M, Grunwald S, Bock-Bierbaum T, Fečíková A, Havránková P, Roth J, Příhodová I, Adamovičová M, Ulmanová O, Bechyně K, Danhofer P, Veselý B, Haň V, Pavelekova P, Gdovinová Z, Mantel T, Meindl T, Sitzberger A, Schröder S, Blaschek A, Roser T, Bonfert M, Haberlandt E, Plecko B, Leineweber B, Berweck S, Herberhold T, Langguth B, Švantnerová J, Minár M, Ramos-Rivera G, Wojcik M, Pajusalu S, Õunap K, Schatz U, Pölsler L, Milenkovic I, Laccone F, Pilshofer V, Colombo R, Patzer S, Iuso A, Vera J, Troncoso M, Fang F, Prokisch H, Wilbert F, Eckenweiler M, Graf E, Westphal D, Riedhammer K, Brunet T, Alhaddad B, Berutti R, Strom T, Hecht M, Baumann M, Wolf M, Telegraf (2020) Monogenic variants in dystonia: an exome-wide sequencing study Lancet Neurol, 19 (11): 908-918
- Beltrán E+, Paunovic M+, Gebert D, Cesur E, Jeitler M, Höftberger R, Malotka J, Mader S, Kawakami N, Meinl E, Bradl M*, Dornmair K*, Lassmann H* + sharing co-first; *sharing senior authorship (2021) Archeological neuroimmunology: resurrection of a pathogenic immune response from a historical case sheds light on human autoimmune encephalomyelitis and multiple sclerosis Acta Neuropathol, 141(1): 67-83