Sortiert nach Autor

Publikationen - sortiert nach Autor

• Altmann P, Leithner K, Leutmezer F, Monschein T, Ponleitner M, Stattmann M, Rommer P, Zrzavy T, Zulehner G, Berek K, Berger T, Bsteh G (2021) Sexuality and Multiple Sclerosis: Patient and Doctor Perspectives JSM, 18 (4): 743-749
• Altmann P, Leutmezer F, Leithner K, Monschein T, Ponleitner M, Stattmann M, Rommer P, Zrzavy T, Zulehner G, Berek K, Berger T, Bsteh G (2021) Predisposing Factors for Sexual Dysfunction in Multiple Sclerosis Front Neurol, 12: 618370
• 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,

• Milenkovic I, Klotz S, Zulehner G, Sycha T, Wiest G (2019) Slowed vertical saccades as a hallmark of hereditary spastic paraplegia type 7 Ann Clin Transl Neurol, 6 (10): 2127-2132
• 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
• 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

• 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
• 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

• 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

• 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

• Salhofer-Polanyi S, Windt J, Sumper H, Grill H, Essmeister M, Diermayr G, Zebenholzer K, Leutmezer F, Zulehner G, Vass K, Asenbaum-Nan S (2013) Benefits of inpatient multidisciplinary rehabilitation in multiple sclerosis NeuroRehabilitation, 33(2): 285-292