By Authors

Publications - sorted by Authors

• Rath J, Schober B, Zulehner G, Grisold A, Krenn M, Cetin H, Zimprich F (2021) Nerve conduction studies in Guillain-Barré syndrome: Influence of timing and value of repeated measurements J Neurol Sci, 420: 117267
• 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,

• Altmann P, De Simoni D, Kaider A, Ludwig B, Rath J, Leutmezer F, Zimprich F, Hoeftberger R, Lunn M, Heslegrave A, Berger T, Zetterberg H, Rommer P (2020) Increased serum neurofilament light chain concentration indicates poor outcome in Guillain-Barré syndrome J Neuroinflammation, 17 (1)
• Macher S, Zrzavy T, Höftberger R, Altmann P, Pataraia E, Zimprich F, Berger T, Rommer P (2020) Longitudinal measurement of cerebrospinal fluid neurofilament light in anti‐N‐methyl‐D‐aspartate receptor encephalitis Eur J Neurol, 28 (4): 1401-1405
• Tomschik M, Hilger E, Rath J, Mayer E, Fahrner M, Cetin H, Löscher W, Zimprich F (2020) Subgroup stratification and outcome in recently diagnosed generalized myasthenia gravis Neurology, 95 (10): e1426-e1436
• Cetin H, Sun J, Almqvist C, Reichardt B, Tomschik M, Zimprich F, Fang F, Ingre C (2020) No association between proton pump inhibitor use and ALS risk: a nationwide nested case–control study Sci Rep, 10 (1)
• Cetin H, Webster R, Liu W, Nagaishi A, Koneczny I, Zimprich F, Maxwell S, Cossins J, Beeson D, Vincent A (2020) Myasthenia gravis AChR antibodies inhibit function of rapsyn-clustered AChRs J Neurol Neurosurg Psychiatry, 91 (5): 526-532
• 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
• Greisenegger E, Llufriu S, Chamorro A, Cervera A, Jimenez-Escrig A, Rappersberger K, Marik W, Greisenegger S, Stögmann E, Kopp T, Strom T, Henes J, Joutel A, Zimprich A (2020) A NOTCH3 homozygous nonsense mutation in familial Sneddon syndrome with pediatric stroke J Neurol,
• Klotz S, König T, Erdler M, Ulram A, Nguyen A, Ströbel T, Zimprich A, Stögmann E, Regelsberger G, Höftberger R, Budka H, Kovacs G, Gelpi E (2020) Co‐incidental C9orf72 expansion mutation‐related frontotemporal lobar degeneration pathology and sporadic Creutzfeldt−Jakob disease Eur J Neurol,
• 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
• Gerner M, Ziegler L, Schmidt R, Krenn M, Zimprich F, Uyanik‐Ünal K, Konstantopoulou V, Derdak S, Del Favero G, Schwarzinger I, Boztug K, Schmetterer K (2020) The TGF‐b/SOX4 axis and ROS‐driven autophagy co‐mediate CD39 expression in regulatory T‐cells FASEB J, 34 (6): 8367-8384
• 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

• Vilariño-Güell C, Zimprich A, Martinelli-Boneschi F, Herculano B, Wang Z, Matesanz F, Urcelay E, Vandenbroeck K, Leyva L, Gris D, Massaad C, Quandt J, Traboulsee A, Encarnacion M, Bernales C, Follett J, Yee I, Criscuoli M, Deutschländer A, Reinthaler E, Zrzavy T, Mascia E, Zauli A, Esposito F, Alcina A, Izquierdo G, Espino-Paisán L, Mena J, Antigüedad A, Urbaneja-Romero P, Ortega-Pinazo J, Song W, Sadovnick A (2019) Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease PLOS Genet, 15 (6): e1008180
• Krenn M, Tomschik M, Rath J, Cetin H, Grisold A, Zulehner G, Milenkovic I, Stogmann E, Zimprich A, Strom T, Meitinger T, Wagner M, Zimprich F (2019) Genotype‐guided diagnostic reassessment after exome sequencing in neuromuscular disorders: experiences with a two‐step approach Eur J Neurol, 27 (1): 51-61
• Berghuis B, Stapleton C, Sonsma A, Hulst J, de Haan G, Lindhout D, Demurtas R, Krause R, Depondt C, Kunz W, Zara F, Striano P, Craig J, Auce P, Marson A, Stefansson H, O'Brien T, Johnson M, Sills G, Wolking S, Lerche H, Sisodiya S, Sander J, Cavalleri G, Koeleman B, McCormack M, (2019) A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine Epilepsia Open, 4 (1): 102-109
• Lerche H, Berkovic SF, Lowenstein DH; EuroEPINOMICS-CoGIE Consortium; EpiPGX Consortium; Epi4K Consortium/Epilepsy Phenome/Genome Project (2019) Intestinal-Cell Kinase and Juvenile Myoclonic Epilepsy N Engl J Med, 380 (16): e24
• Krenn M, Milenkovic I, Eckstein G, Zimprich F, Meitinger T, Foki T, Wagner M (2019) Adult-onset variant ataxia-telangiectasia diagnosed by exome and cDNA sequencing Neurol Genet, 5 (4): e346
• Krenn M, Ernst M, Tomschik M, Treven M, Wagner M, Westphal D, Meitinger T, Pataraia E, Zimprich F, Aull‐Watschinger S (2019) Phenotypic variability of GABRA1 ‐related epilepsy in monozygotic twins Ann Clin Transl Neurol, 6 (11): 2317-2322
• Stevelink R, Pangilinan F, Jansen F, Braun K, Molloy A, Brody L, Koeleman B (2019) Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy Mol Genet Metab, 21: 100518
• Rath J, Brunner I, Tomschik M, Zulehner G, Hilger E, Krenn M, Paul A, Cetin H, Zimprich F (2019) Frequency and clinical features of treatment-refractory myasthenia gravis J Neurol, 267 (4): 1004-1011

• Löscher W, Oberreiter E, Erdler M, Quasthoff S, Culea V, Berek K, Embacher N, Grinzinger S, Hess I, Höger F, Horlings C, Huemer M, Jecel J, Kleindienst W, Laich E, Müller P, Oel D, Örtl W, Lenzenweger E, Rath J, Stadler K, Stieglbauer K, Thaler-Wolf C, Wanschitz J, Zimprich F, Cetin H, Topakian R (2018) Multifocal motor neuropathy in Austria: a nationwide survey of clinical features and response to treatment J Neurol, 265 (12): 2834-2840
• May P, Girard S, Harrer M, Bobbili D, Schubert J, Wolking S, Becker F, Lachance-Touchette P, Meloche C, Gravel M, Niturad C, Knaus J, De Kovel C, Toliat M, Polvi A, Iacomino M, Guerrero-López R, Baulac S, Marini C, Thiele H, Altmüller J, Jabbari K, Ruppert A, Jurkowski W, Lal D, Rusconi R, Cestèle S, Terragni B, Coombs I, Reid C, Striano P, Caglayan H, Siren A, Everett K, Møller R, Hjalgrim H, Muhle H, Helbig I, Kunz W, Weber Y, Weckhuysen S, Jonghe P, Sisodiya S, Nabbout R, Franceschetti S, Coppola A, Vari M, Kasteleijn-Nolst Trenité D, Baykan B, Ozbek U, Bebek N, Klein K, Rosenow F, Nguyen D, Dubeau F, Carmant L, Lortie A, Desbiens R, Clément J, Cieuta-Walti C, Sills G, Auce P, Francis B, Johnson M, Marson A, Berghuis B, Sander J, Avbersek A, McCormack M, Cavalleri G, Delanty N, Depondt (2018) Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study Lancet Neurol, 17 (8): 699-708
• International League Against Epilepsy Consortium on Complex Epilepsies (2018) Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies Nat Commun, 9 (1)
• 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

• Trimmel K, Sachsenweger J, Lindinger G, Auff E, Zimprich F, Pataraia E (2017) Lateralization of language function in epilepsy patients: A high-density scalp-derived event-related potentials (ERP) study Clin Neurophysiol, 128 (3): 472-479
• Krenn M, Zulehner G, Hotzy C, Rath J, Stogmann E, Wagner M, Haack T, Strom T, Zimprich A, Zimprich F (2017) Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene Eur J Neurol, 24 (5): 741-747
• Pérez-Palma E, Helbig I, Klein K, Anttila V, Horn H, Reinthaler E, Gormley P, Ganna A, Byrnes A, Pernhorst K, Toliat M, Saarentaus E, Howrigan D, Hoffman P, Miquel J, De Ferrari G, Nürnberg P, Lerche H, Zimprich F, Neubauer B, Becker A, Rosenow F, Perucca E, Zara F, Weber Y, Lal D (2017) Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies J Med Genet, 54 (9): 598-606
• Rath J, Mauritz M, Zulehner G, Hilger E, Cetin H, Kasprian G, Auff E, Zimprich F (2017) Iodinated contrast agents in patients with myasthenia gravis: a retrospective cohort study J Neurol, 264 (6): 1209-1217

• 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
• Hilger E, Zimprich F, Pataraia E, Aull-Watschinger S, Jung R, Baumgartner C, Bonelli S (2016) Psychoses in epilepsy: A comparison of postictal and interictal psychoses Epilepsy Behav, 60: 58-62
• Peragallo J, Bitrian E, Kupersmith M, Zimprich F, Whittaker T, Lee M, Bruce B (2016) Relationship Between Age, Gender, and Race in Patients Presenting With Myasthenia Gravis With Only Ocular Manifestations JNO, 36 (1): 29-32
• Lal D, Reinthaler E, Dejanovic B, May P, Thiele H, Lehesjoki A, Schwarz G, Riesch E, Ikram M, Duijn C, Uitterlinden A, Hofman A, Steinböck H, Gruber-Sedlmayr U, Neophytou B, Zara F, Hahn A, Gormley P, Becker F, Weber Y, Cilio M, Kunz W, Krause R, Zimprich F, Lemke J, Nürnberg P, Sander T, Lerche H, Neubauer B, , (2016) Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes PlosOne, 11 (3): e0150426
• Melzer N, Ruck T, Fuhr P, Gold R, Hohlfeld R, Marx A, Melms A, Tackenberg B, Schalke B, Schneider-Gold C, Zimprich F, Meuth S, Wiendl H (2016) Clinical features, pathogenesis, and treatment of myasthenia gravis: a supplement to the Guidelines of the German Neurological Society J Neurol, 263 (8): 1473-1494
• Cetin H, Wöhrer A, Rittelmeyer I, Gencik M, Zulehner G, Zimprich F, Ströbel T, Zimprich A (2016) The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNA Clin Genet, 90 (4): 366-371
• Sadovnick A, Traboulsee A, Bernales C, Ross J, Forwell A, Yee I, Guillot-Noel L, Fontaine B, Cournu-Rebeix I, Alcina A, Fedetz M, Izquierdo G, Matesanz F, Hilven K, Dubois B, Goris A, Astobiza I, Alloza I, Antiguedad A, Vandenbroeck K, Akkad D, Aktas O, Blaschke P, Buttmann M, Chan A, Epplen J, Gerdes L, Kroner A, Kubisch C, Kumpfel T, Lohse P, Rieckmann P, Zettl U, Zipp F, Bertram L, Lill C, Fernandez O, Urbaneja P, Leyva L, Alvarez-Cermeno J, Arroyo R, Garagorri A, Garcia-Martinez A, Villar L, Urcelay E, Malhotra S, Montalban X, Comabella M, Berger T, Fazekas F, Reindl M, Schmied M, Zimprich A, Vilarino-Guell C (2016) Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients G3, 6 (7): 2073-2079

• Grisold A, Weber C, Kiener H, Kovacs GG, Schnider P, Auff E, Zimprich F (2015) Hypereosinophilia and vasculitic neuropathy without lung manifestation. An atypical presentation of Churg-Strauss syndrome Eur J Neurol, 22: 411
• Cetin H, Rath J, Füzi J, Reichardt B, Fülöp G, Koppi S, Erdler M, Ransmayr G, Weber J, Neumann K, Hagmann M, Löscher W, Auff E, Zimprich F (2015) Epidemiology of Amyotrophic Lateral Sclerosis and Effect of Riluzole on Disease Course Neuroepidemiol, 44 (1): 6-15
• Reinthaler E, Dejanovic B, Lal D, Semtner M, Merkler Y, Reinhold A, Pittrich D, Hotzy C, Feucht M, Steinböck H, Gruber-Sedlmayr U, Ronen G, Neophytou B, Geldner J, Haberlandt E, Muhle H, Ikram M, van Duijn C, Uitterlinden A, Hofman A, Altmüller J, Kawalia A, Toliat M, Nürnberg P, Lerche H, Nothnagel M, Thiele H, Sander T, Meier J, Schwarz G, Neubauer B, Zimprich F, (2015) Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes Ann Neurol, 77 (6): 972-986
• Lal D, Ruppert A, Trucks H, Schulz H, de Kovel C, Kasteleijn-Nolst Trenité D, Sonsma A, Koeleman B, Lindhout D, Weber Y, Lerche H, Kapser C, Schankin C, Kunz W, Surges R, Elger C, Gaus V, Schmitz B, Helbig I, Muhle H, Stephani U, Klein K, Rosenow F, Neubauer B, Reinthaler E, Zimprich F, Feucht M, Møller R, Hjalgrim H, De Jonghe P, Suls A, Lieb W, Franke A, Strauch K, Gieger C, Schurmann C, Schminke U, Nürnberg P, Sander T, (2015) Burden Analysis of Rare Microdeletions Suggests a Strong Impact of Neurodevelopmental Genes in Genetic Generalised Epilepsies PLoS Genet, 11 (5): e1005226
• Cetin H, Klickovic U, Rath J, Zulehner G, Füzi J, Reichardt B, Hagmann M, Wanschitz J, Löscher W, Auff E, Zimprich F (2015) Associations between co-medications and survival in ALS—a cohort study from Austria J Neurol, 262 (7): 1698-1705
• Reinthaler E, Dejanovic B, Lal D, Semtner M, Merkler Y, Reinhold A, Pittrich D, Hotzy C, Feucht M, Steinböck H, Gruber-Sedlmayr U, Ronen G, Neophytou B, Geldner J, Haberlandt E, Muhle H, Ikram M, van Duijn C, Uitterlinden A, Hofman A, Altmüller J, Kawalia A, Toliat M, Nürnberg P, Lerche H, Nothnagel M, Thiele H, Sander T, Meier J, Schwarz G, Neubauer B, Zimprich F (2015) Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes Ann Neurol, 77 (6): 972-986

• International League Against Epilepsy Consortium on Complex Epilepsies (2014) Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies Lancet Neurol, 13 (9): 893-903
• Ripke S, Neale B, Corvin A, Walters J, Farh K, Holmans P, Lee P, Bulik-Sullivan B, Collier D, Huang H, Pers T, Agartz I, Agerbo E, Albus M, Alexander M, Amin F, Bacanu S, Begemann M, Belliveau Jr R, Bene J, Bergen S, Bevilacqua E, Bigdeli T, Black D, Bruggeman R, Buccola N, Buckner R, Byerley W, Cahn W, Cai G, Campion D, Cantor R, Carr V, Carrera N, Catts S, Chambert K, Chan R, Chen R, Chen E, Cheng W, Cheung E, Ann Chong S, Robert Cloninger C, Cohen D, Cohen N, Cormican P, Craddock N, Crowley J, Curtis D, Davidson M, Davis K, Degenhardt F, Del Favero J, Demontis D, Dikeos D, Dinan T, Djurovic S, Donohoe G, Drapeau E, Duan J, Dudbridge F, Durmishi N, Eichhammer P, Eriksson J, Escott-Price V, Essioux L, Fanous A, Farrell M, Frank J, Franke L, Freedman R, Freimer N, Friedl M, Friedman J, Fro (2014) Biological insights from 108 schizophrenia-associated genetic loci Nature, 511 (7510): 421-427
• Votinov M, Pripfl J, Windischberger C, Kalcher K, Zimprich A, Zimprich F, Moser E, Lamm C, Sailer U (2014) A Genetic Polymorphism of the Endogenous Opioid Dynorphin Modulates Monetary Reward Anticipation in the Corticostriatal Loop PLoS One, 9 (2): e89954
• Reinthaler EM, Lal D, Lebon S, Hildebrand MS, Dahl HH, Regan BM, Feucht M, Steinböck H, Neophytou B, Ronen GM, Roche L, Gruber-Sedlmayr U, Geldner J, Haberlandt E, Hoffmann P, Herms S, Gieger C, Waldenberger M, Franke A, Wittig M, Schoch S, Becker AJ, Hahn A, Männik K, Toliat MR, Winterer G; The 16p11.2 European Consortium, Lerche H, Nürnberg P, Mefford H, Scheffer IE, Berkovic SF, Beckmann JS; The EPICURE Consortium, The EuroEPINOMICS Consortium, Sander T, Jacquemont S, Reymond A, Zimprich F, Neubauer BA. (2014) 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy Hum Mol Genet,
• Reinthaler E, Lal D, Jurkowski W, Feucht M, Steinböck H, Gruber-Sedlmayr U, Ronen G, Geldner J, Haberlandt E, Neophytou B, Hahn A, Altmüller J, Thiele H, Toliat M, Lerche H, Nürnberg P, Sander T, Neubauer B, Zimprich F (2014) Analysis of ELP4 , SRPX2 , and interacting genes in typical and atypical rolandic epilepsy Epilepsia, 55 (8): e89-e93
• Lal D, Reinthaler E, Schubert J, Muhle H, Riesch E, Kluger G, Jabbari K, Kawalia A, Bäumel C, Holthausen H, Hahn A, Feucht M, Neophytou B, Haberlandt E, Becker F, Altmüller J, Thiele H, Lemke J, Lerche H, Nürnberg P, Sander T, Weber Y, Zimprich F, Neubaue (2014) DEPDC5 mutations in genetic focal epilepsies of childhood Ann Neurol, 75 (5): 788-792

• Zach H, Cetin H, Hilger E, Paul A, Wuschitz B, Jung R, Auff E, Zimprich F (2013) The effect of early prednisolone treatment on the generalization rate in ocular myasthenia gravis Eur J Neurol, 20(4): 708-13
• Hilger E, Zimprich F, Jung R, Pataraia E, Baumgartner C, Bonelli S (2013) Postictal psychosis in temporal lobe epilepsy: a case-control study. Eur J Neurol, 20 (6): 955-61
• Greisenegger EK, Zimprich F, Zimprich A, Gleiss A, Kopp T (2013) Association of the chromosome 11q13.5 variant with atopic dermatitis in Austrian patients Eur J Dermatol, 23(2): 142-145
• Lemke J, Lal D, Reinthaler E, Steiner I, Nothnagel M, Alber M, Geider K, Laube B, Schwake M, Finsterwalder K, Franke A, Schilhabel M, Jähn J, Muhle H, Boor R, Van Paesschen W, Caraballo R, Fejerman N, Weckhuysen S, De Jonghe P, Larsen J, Møller R, Hjalgrim H, Addis L, Tang S, Hughes E, Pal D, Veri K, Vaher U, Talvik T, Dimova P, López R, Serratosa J, Linnankivi T, Lehesjoki A, Ruf S, Wolff M, Buerki S, Wohlrab G, Kroell J, Datta A, Fiedler B, Kurlemann G, Kluger G, Hahn A, Haberlandt D, Kutzer C, Sperner J, Becker F, Weber Y, Feucht M, Steinböck H, Neophythou B, Ronen G, Gruber-Sedlmayr U, Geldner J, Harvey R, Hoffmann P, Herms S, Altmüller J, Toliat M, Thiele H, Nürnberg P, Wilhelm C, Stephani U, Helbig I, Lerche H, Zimprich F, Neubauer B, Biskup S, von Spiczak S (2013) Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes Nat Genet, 45 (9): 1067-1072
• Stogmann E, Zimprich A, Zimprich F (2013) Reply: Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy Brain, 136 (10): e254-e254
• Esko T, Mezzavilla M, Nelis M, Borel C, Debniak T, Jakkula E, Julia A, Karachanak S, Khrunin A, Kisfali P, Krulisova V, Aušrelé Kučinskiené Z, Rehnström K, Traglia M, Nikitina-Zake L, Zimprich F, Antonarakis S, Estivill X, Glavač D, Gut I, Klovins J, Kraw (2013) Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity Eur J Hum Genet, 21 (6): 659-665
• Zach H, Cetin H, Hilger E, Paul A, Wuschitz B, Jung R, Auff E, Zimprich F (2013) The effect of early prednisolone treatment on the generalization rate in ocular myasthenia gravis Eur J Neurol, 20 (4): 708-713
• Lal D, Trucks H, Møller R, Hjalgrim H, Koeleman B, de Kovel C, Visscher F, Weber Y, Lerche H, Becker F, Schankin C, Neubauer B, Surges R, Kunz W, Zimprich F, Franke A, Illig T, Ried J, Leu C, Nürnberg P, Sander T (2013) Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy Epilepsia, 54 (2): 265-271
• Stogmann E, Reinthaler E, ElTawil S, El Etribi M, Hemeda M, El Nahhas N, Gaber A, Fouad A, Edris S, Benet-Pages A, Eck S, Pataraia E, Mei D, Brice A, Lesage S, Guerrini R, Zimprich F, Strom T, Zimprich A (2013) Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2 Brain, 136 (4): 1155-1160
• Hilger E, Zimprich F, Jung R, Pataraia E, Baumgartner C, Bonelli S (2013) Postictal psychosis in temporal lobe epilepsy: a case-control study Eur J Neurol, 20 (6): 955-961
• Kasperaviciute D, Catarino C, Matarin M, Leu C, Novy J, Tostevin A, Leal B, Hessel E, Hallmann K, Hildebrand M, Dahl H, Ryten M, Trabzuni D, Ramasamy A, Alhusaini S, Doherty C, Dorn T, Hansen J, Kramer G, Steinhoff B, Zumsteg D, Duncan S, Kalviainen R, Er (2013) Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A Brain, 136 (10): 3140-3150
• Lal D, Reinthaler E, Altmüller J, Toliat M, Thiele H, Nürnberg P, Lerche H, Hahn A, Møller R, Muhle H, Sander T, Zimprich F, Neubauer B (2013) RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy PLoS One, 8 (9): e73323

• Moser B, Bekos C, Zimprich F, Nickl S, Klepetko W, Ankersmit J (2012) The receptor for advanced glycation endproducts and its ligands in patients with myasthenia gravis Biochem Bioph Res Comm, 420 (1): 96-101
• EPICURE Consortium; EMINet Consortium, Steffens M, Leu C, Ruppert A, Zara F, Striano P, Robbiano A, Capovilla G, Tinuper P, Gambardella A, Bianchi A, La Neve A, Crichiutti G, de Kovel C, Kasteleijn-Nolst Trenite D, de Haan G, Lindhout D, Gaus V, Schmitz B, Janz D, Weber Y, Becker F, Lerche H, Steinhoff B, Kleefuss-Lie A, Kunz W, Surges R, Elger C, Muhle H, von Spiczak S, Ostertag P, Helbig I, Stephani U, Moller R, Hjalgrim H, Dibbens L, Bellows S, Oliver K, Mullen S, Scheffer I, Berkovic S, Everett K, Gardiner M, Marini C, Guerrini R, Lehesjoki A, Siren A, Guipponi M, Malafosse A, Thomas P, Nabbout R, Baulac S, Leguern E, Guerrero R, Serratosa J, Reif P, Rosenow F, Morzinger M, Feucht M, Zimprich F, Kapser C, Schankin C, Suls A, Smets K, De Jonghe P, Jordanova A, Caglayan H, Yapici Z, Yalc (2012) Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 Hum Mol Genet, 21 (24): 5359-5372
• Cetin H, Fülöp G, Zach H, Auff E, Zimprich F (2012) Epidemiology of myasthenia gravis in Austria: rising prevalence in an ageing society Wiener Klinische Wochenschrift, 124 (21-22): 763-768
• 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

• Zimprich A, Benet-Pagès A, Struhal W, Graf E, Eck S, Offman M, Haubenberger D, Spielberger S, Schulte E, Lichtner P, Rossle S, Klopp N, Wolf E, Seppi K, Pirker W, Presslauer S, Mollenhauer B, Katzenschlager R, Foki T, Hotzy C, Reinthaler E, Harutyunyan A, Kralovics R, Peters A, Zimprich F, Brücke T, Poewe W, Auff E, Trenkwalder C, Rost B, Ransmayr G, Winkelmann J, Meitinger T, Strom T (2011) A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease Am J Hum Genet, 89 (1): 168-175

• Greisenegger E, Novak N, Maintz L, Bieber T, Zimprich F, Haubenberger D, Gleiss A, Stingl G, Kopp T, Zimprich A (2010) Analysis of four prevalent filaggrin mutations (R501X, 2282del4, R2447X and S3247X) in Austrian and German patients with atopic dermatitis J Eur Acad Dermatol Venereol, 24 (5): 607-610
• Jamali S, Salzmann A, Perroud N, Ponsole-Lenfant M, Cillario J, Roll P, Roeckel-Trevisiol N, Crespel A, Balzar J, Schlachter K, Gruber-Sedlmayr U, Pataraia E, Baumgartner C, Zimprich A, Zimprich F, Malafosse A, Szepetowski P (2010) Functional Variant in Complement C3 Gene Promoter and Genetic Susceptibility to Temporal Lobe Epilepsy and Febrile Seizures PLoS One, 5 (9): e12740

• Löscher W, Klotz U, Zimprich F, Schmidt D (2009) The clinical impact of pharmacogenetics on the treatment of epilepsy Epilepsia, 50 (1): 1-23
• Helbig I, Mefford H, Sharp A, Guipponi M, Fichera M, Franke A, Muhle H, de Kovel C, Baker C, von Spiczak S, Kron K, Steinich I, Kleefuß-Lie A, Leu C, Gaus V, Schmitz B, Klein K, Reif P, Rosenow F, Weber Y, Lerche H, Zimprich F, Urak L, Fuchs K, Feucht M, Genton P, Thomas P, Visscher F, de Haan G, Møller R, Hjalgrim H, Luciano D, Wittig M, Nothnagel M, Elger C, Nürnberg P, Romano C, Malafosse A, Koeleman B, Lindhout D, Stephani U, Schreiber S, Eichler E, Sander T (2009) 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy Nature Genetics, 41 (2): 160-162
• Ronen G, Meaney B, Dan B, Zimprich F, Stögmann W, Neugebauer W (2009) From Eugenic Euthanasia to Habilitation of ``Disabled'' Children: Andreas Rett's Contribution J. Child Neurol., 24 (1): 115-127
• Pirker S, Gasser E, Czech T, Baumgartner C, Schuh E, Feucht M, Novak K, Zimprich F, Sperk G (2009) Dynamic up-regulation of prodynorphin transcription in temporal lobe epilepsy Hippocampus, 19 (11): 1051-1054
• de Kovel C, Trucks H, Helbig I, Mefford H, Baker C, Leu C, Kluck C, Muhle H, von Spiczak S, Ostertag P, Obermeier T, Kleefuss-Lie A, Hallmann K, Steffens M, Gaus V, Klein K, Hamer H, Rosenow F, Brilstra E, Kasteleijn-Nolst Trenite D, Swinkels M, Weber Y, Unterberger I, Zimprich F, Urak L, Feucht M, Fuchs K, Moller R, Hjalgrim H, De Jonghe P, Suls A, Ruckert I, Wichmann H, Franke A, Schreiber S, Nurnberg P, Elger C, Lerche H, Stephani U, Koeleman B, Lindhout D, Eichler E, Sander T (2009) Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies Brain, 133 (1): 23-32
• Stefansson H, Steinberg S, Petursson H, Gustafsson O, Gudjonsdottir I, Jonsdottir G, Palsson S, Jonsson T, Saemundsdottir J, Bjornsdottir G, Böttcher Y, Thorlacius T, Haubenberger D, Zimprich A, Auff E, Hotzy C, Testa C, Miyatake L, Rosen A, Kristleifsson K, Rye D, Asmus F, Schöls L, Dichgans M, Jakobsson F, Benedikz J, Thorsteinsdottir U, Gulcher J, Kong A, Stefansson K (2009) Variant in the sequence of the LINGO1 gene confers risk of essential tremor Nat Genet, 41 (3): 277-279
• Djamshidian A, Schaefer J, Haubenberger D, Stogmann E, Zimprich F, Auff E, Zimprich A (2009) A novel mutation in the VCP gene (G157R) in a german family with inclusion-body myopathy with paget disease of bone and frontotemporal dementia Muscle Nerve, 39 (3): 389-391
• Schlachter K, Gruber-Sedlmayr U, Stogmann E, Lausecker M, Hotzy C, Balzar J, Schuh E, Baumgartner C, Mueller J, Illig T, Wichmann H, Lichtner P, Meitinger T, Strom T, Zimprich A, Zimprich F (2009) A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures Neurology, 72 (11): 974-978
• Nelis M, Esko T, Mägi R, Zimprich F, Zimprich A, Toncheva D, Karachanak S, Piskáčková T, Balaščák I, Peltonen L, Jakkula E, Rehnström K, Lathrop M, Heath S, Galan P, Schreiber S, Meitinger T, Pfeufer A, Wichmann H, Melegh B, Polgár N, Toniolo D, Gasparini P, D'Adamo P, Klovins J, Nikitina-Zake L, Kučinskas V, Kasnauskienė J, Lubinski J, Debniak T, Limborska S, Khrunin A, Estivill X, Rabionet R, Marsal S, Julià A, Antonarakis S, Deutsch S, Borel C, Attar H, Gagnebin M, Macek M, Krawczak M, Remm M, Metspalu A (2009) Genetic Structure of Europeans: A View from the North–East PLoS One, 4 (5): e5472
• Greisenegger E, Zimprich A, Zimprich F, Stingl G, Kopp T (2009) Analysis of the prodynorphin promoter polymorphism in atopic dermatitis and disease-related pruritus Clin Exp Dermatol, 34 (6): 728-730
• Greisenegger E, Novak N, Maintz L, Bieber T, Zimprich F, Haubenberger D, Gleiss A, Stingl G, Kopp T, Zimprich A (2009) Analysis of four prevalent filaggrin mutations (R501X, 2282del4, R2447X and S3247X) in Austrian and German patients with atopic dermatitis J Eur Acad Dermatol Venereol, 24 (5): 607-610
• Haubenberger D, Hotzy C, Pirker W, Katzenschlager R, Brücke T, Zimprich F, Auff E, Zimprich A (2009) Role of LINGO1 polymorphisms in Parkinson's disease Movement Disorders, : NA-NA
• Zimprich A, Schulte C, Reinthaler E, Haubenberger D, Balzar J, Lichtner P, El Tawil S, Edris S, Foki T, Pirker W, Katzenschlager R, Daniel G, Brücke T, Auff E, Gasser T (2009) PARK11 gene (GIGYF2) variants Asn56Ser and Asn457Thr are not pathogenic for Parkinson's disease Parkinsonism & Related Disorders, 15 (7): 532-534

• 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
• 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
• Lopes Lima J, Mesec A, Wilkinson I, Wiles C, Gilhus N, Zimprich F, Alekseenko Y, Grisold W (2008) Report of the Task Force on pre-graduate education in Europe of the education committee of the European Federation of Neurological Societies Composition of the task force of the education committee on pre-graduate education Eur J Neurol, 15 (12): e103-e109
• Zimprich F, Stogmann E, Bonelli S, Baumgartner C, Mueller JC, Meitinger T, Zimprich A, Strom TM (2008) A functional polymorphism in the SCN1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy Epilepsia, 49 (6): 1108-1109
• 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

• Bonelli S, Lurger S, Zimprich F, Stogmann E, Assem-Hilger E, Baumgartner C (2007) Clinical Seizure Lateralization in Frontal Lobe Epilepsy Epilepsia, 48 (3): 517-523
• Freidl M, Spitzl S, Prause W, Zimprich F, Lehner-Baumgartner E, Baumgartner C, Aigner M (2007) The stigma of mental illness: Anticipation and attitudes among patients with epileptic, dissociative or somatoform pain disorder Int Rev Psychiatry, 19 (2): 123-129
• Langer O, Bauer M, Hammers A, Karch R, Pataraia E, Koepp M, Abrahim A, Luurtsema G, Brunner M, Sunder-Plassmann R, Zimprich F, Joukhadar C, Gentzsch S, Dudczak R, Kletter K, Müller M, Baumgartner C (2007) Pharmacoresistance in Epilepsy: A Pilot PET Study with the P-Glycoprotein SubstrateR-[11C]verapamil Epilepsia, 48 (9): 1774-1784
• Langer O, Bauer M, Hammers A, Karch R, Pataraia E, Koepp M, Abrahim A, Luurtsema G, Brunner M, Sunder-Plassmann R, Zimprich F, Joukhadar C, Gentzsch S, Dudczak R, Kletter K, Müller M, Baumgartner C (2007) Pharmacoresistance in Epilepsy: A Pilot PET Study with the P-Glycoprotein Substrate R -[ 11 C]verapamil Epilepsia, 48 (9): 1774-1784

• 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, 7(4): 265-8
• Stogmann E, Lichtner P, Baumgartner C, Bonelli S, Assem-Hilger E, Leutmezer F, Schmied M, Hotzy C, Strom TM, Meitinger T, Zimprich F, Zimprich A (2006) Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations. Neurology, 67(11): 2029-31.
• Zimprich F, Ronen G, Stogmann W, Baumgartner C, Stogmann E, Rett B, Pappas C, Leppert M, Singh N, Anderson V (2006) Andreas Rett and benign familial neonatal convulsions revisited Neurology, 67 (5): 864-866
• Stogmann E, Zimprich A, Baumgartner C, Gleiss A, Zimprich F (2006) Lack of association between a GABA receptor 1 gene polymorphism and temporal lobe epilepsy Epilepsia,
• 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,
• Stogmann E, Lichtner P, Baumgartner C, Bonelli S, Assem-Hilger E, Leutmezer F, Schmied M, Hotzy C, Strom TM, Meitinger T, Zimprich F, Zimprich A (2006) Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations Neurology,

• Rockman M, Hahn M, Soranzo N, Zimprich F, Goldstein D, Wray G (2005) Ancient and Recent Positive Selection Transformed Opioid cis-Regulation in Humans PLoS Biol., 3 (12): e387
• Haubenberger D, Bittner RE, Rauch-Shorny S, Zimprich F, Mannhalter C, Wagner L, Mineva I, Vass K, Auff E, Zimprich A (2005) Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene Neurology,

• Wiest G, Zimprich F, Prayer D, Czech T, Serles W, Baumgartner C (2004) Vestibular processing in human paramedian precuneus as shown by electrical cortical stimulation. Neurology, 62(3): 473-5
• Zimprich F, Sunder-Plassmann R, Stogmann E, Gleiss A, Dal-Bianco A, Zimprich A, Plumer S, Baumgartner C, Mannhalter C (2004) Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy Neurology,

• Zimprich F, Kress HG, Zeitlhofer J (2003) Malignant hyperthermia Wiener Klinische Wochenschrift, 115(15-16): 556-62

• Djamshidian A, Grassl R, Seltenhammer M, Czech T, Baumgartner C, Schmidbauer M, Ulrich W, Zimprich F (2002) Altered expression of voltage-dependent calcium channel alpha(1) subunits in temporal lobe epilepsy with Ammon's horn sclerosis. Neuroscience, 111(1): 57-9
• Stögmann E, Zimprich A, Baumgartner C, Aull-Watschinger S, Höllt V, Zimprich F (2002) A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy Ann Neurol,

• Kornek B, Storch MK, Bauer J, Djamshidian A, Weissert R, Wallstroem E, Stefferl A, Zimprich F, Olsson T, Linington C, Schmidbauer M, Lassmann H (2001) Distribution of a calcium channel subunit in dystrophic axons in multiple sclerosis and experimental autoimmune encephalomyelitis. Brain, 124(Pt 6): 1114-24
• Ashworth R, Zimprich F, Bolsover SR (2001) Buffering intracellular calcium disrupts motoneuron development in intact zebrafish embryos. Brain Res. Dev. Brain Res., 129(2): 169-79
• Lass H, Sator M, Zimprich F, Lang I, Zeitlhofer J, Huber J (2001) Substantial relief of myopathic disability by progesterone therapy. Acta Obstet Gynecol Scand, 80(10): 972-3

• Zimprich F, Djamshidian A, Hainfellner JA, Budka H, Zeitlhofer J (2000) An autosomal dominant early adult-onset distal muscular dystrophy. Muscle Nerve, 23(12): 1876-9

• Zimprich F, Ashworth R, Bolsover S (1998) Real-time measurements of calcium dynamics in neurons developing in situ within zebrafish embryos. , 436(3): 489-93

• Zimprich F, Bolsover SR (1996) Calcium channels in neuroblastoma cell growth cones. Eur J Neurosci, 8(3): 467-75

• Zimprich F, Torok K, Bolsover SR (1995) Nuclear calmodulin responds rapidly to calcium influx at the plasmalemma. Cell Calcium, 17 (3): 233-8

• Zimprich F, Gailey M, Bolsover SR (1994) Biphasic effect of calcium on neurite outgrowth in neuroblastoma and cerebellar granule cells. Brain Res. Dev. Brain Res., 80(1-2): 7-12

• Piddlesden SJ, Lassmann H, Zimprich F, Morgan BP, Linington C (1993) The demyelinating potential of antibodies to myelin oligodendrocyte glycoprotein is related to their ability to fix complement. Am.J.Pathol., 143 (2): 555-64

• Sieghart W, Fuchs K, Zezula J, Buchstaller A, Zimprich F, Lassmann H (1992) Biochemical, immunological, and pharmacological characterization of GABAA-benzodiazepine receptor subtypes. Adv. Biochem. Psychopharmacol., 47: 155-62

• Lassmann H, Zimprich F, Vass K, Hickey WF (1991) Microglial cells are a component of the perivascular glia limitans. J Neurosci Res, 28 (2): 236-43
• Zimprich F, Zezula J, Sieghart W, Lassmann H (1991) Immunohistochemical localization of the alpha 1, alpha 2 and alpha 3 subunit of the GABAA receptor in the rat brain. Neurosci Lett, 127 (1): 125-8
• Körner H, Schliephake A, Winter J, Zimprich F, Lassmann H, Sedgwick J, Siddell S, Wege H (1991) Nucleocapsid or spike protein-specific CD4+ T lymphocytes protect against coronavirus-induced encephalomyelitis in the absence of CD8+ T cells. J Immunol, 147(7): 2317-23
• Zimprich F, Winter J, Wege H, Lassmann H (1991) Coronavirus induced primary demyelination: indications for the involvement of a humoral immune response. Neuropathol Appl Neurobiol, 17 (6): 469-84

• Lassmann H, Rössler K, Zimprich F, Vass K (1991) Expression of adhesion molecules and histocompatibility antigens at the blood-brain barrier. Brain Pathol, 1 (2): 115-23
• Lassmann H, Zimprich F, Rössler K, Vass K (1991) Inflammation in the nervous system. Basic mechanisms and immunological concepts. Rev Neurol (Paris), 147 (12): 763-81

• Wege H, Winter J, Körner H, Flory E, Zimprich F, Lassmann H (1990) Coronavirus induced demyelinating encephalomyelitis in rats: immunopathological aspects of viral persistency. Adv Exp Med Biol, 276: 637-45