Search Results - "Leutmezer, F"

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    Real‐life clinical use of natalizumab and fingolimod in Austria by Guger, M., Enzinger, C., Leutmezer, F., Kraus, J., Kalcher, S., Kvas, E., Berger, T.

    Published in Acta neurologica Scandinavica (01-02-2018)
    “…Objectives To compare the efficacy of natalizumab or fingolimod in a nationwide observational cohort using prospectively collected data. Materials and methods…”
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    Iron Rims in Patients With Multiple Sclerosis as Neurodegenerative Marker? A 7-Tesla Magnetic Resonance Study by 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

    Published in Frontiers in neurology (21-12-2021)
    “…Multiple sclerosis (MS) is a demyelinating and neurodegenerative disease of the central nervous system, characterized by inflammatory-driven demyelination…”
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  3. 3

    Health-related quality of life in multiple sclerosis: temperament outweighs EDSS by Salhofer-Polanyi, S, Friedrich, F, Löffler, S, Rommer, P S, Gleiss, A, Engelmaier, R, Leutmezer, F, Vyssoki, B

    Published in BMC psychiatry (23-05-2018)
    “…The influence of personality on health-related quality of life in patients with multiple sclerosis has been the focus of previous studies showing that…”
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  4. 4

    What to expect after natalizumab cessation in a real-life setting by Salhofer-Polanyi, S., Baumgartner, A., Kraus, J., Maida, E., Schmied, M., Leutmezer, F.

    Published in Acta neurologica Scandinavica (01-08-2014)
    “…Background To minimize the risk of progressive multifocal leucoencephalopathy (PML), treatment with natalizumab is often stopped after 2 years, but evidence…”
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    Disruption of nigrostriatal and cerebellothalamic pathways in dopamine responsive Holmes’ tremor by Seidel, S, Kasprian, G, Leutmezer, F, Prayer, D, Auff, E

    “…Holmes’ tremor is an unusual combination of rest, postural and kinetic tremor of the extremities. Medical treatment of this condition still remains…”
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    Postictal paresis in focal epilepsies: Incidence, duration, and causes a video. EEG monitoring study by GALLMETZER, P, LEUTMEZER, F, SERIES, W, ASSEM-HILGER, E, SPATT, J, BAUMGARTNER, C

    Published in Neurology (22-06-2004)
    “…Although familiar to every neurologist, postictal paresis (PP) has only rarely been analyzed systematically. To describe the frequency and duration of PP in…”
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    Celiac disease with cerebral and peripheral nerve involvement mimicking multiple sclerosis by Finsterer, J, Leutmezer, F

    Published in Journal of medicine and life (15-09-2014)
    “…Due to the similarity in the clinical presentation, morphology, and course, celiac disease (CD) may be mixed up with other immunological disorders, such as…”
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    Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations by STOGMANN, E, LICHTNER, P, ZIMPRICH, F, ZIMPRICH, A, BAUMGARTNER, C, BONELLI, S, ASSEM-HILGER, E, LEUTMEZER, F, SCHMIED, M, HOTZY, C, STROM, T. M, MEITINGER, T

    Published in Neurology (12-12-2006)
    “…We sequenced 61 patients with various idiopathic generalized epilepsy (IGE) syndromes for mutations in the EFHC1 gene. We detected three novel heterozygous…”
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  12. 12

    Autonomic symptoms during epileptic seizures by Baumgartner, Christoph, Lurger, Stefanie, Leutmezer, Fritz

    Published in Epileptic disorders (01-09-2001)
    “…ABSTRACT Autonomic symptoms frequently occur during epileptic seizures either as an accompaniment to other seizure symptoms or as the predominant seizure…”
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    Contribution of spinal cord biopsy to the differential diagnosis of longitudinal extensive transverse myelitis by Ringelstein, M, Aktas, O, Harmel, J, Prayer, D, Jarius, S, Wildemann, B, Hartung, H-P, Salhofer-Polanyi, S, Leutmezer, F, Rommer, P S

    Published in Nervenarzt (01-10-2014)
    “…Neuromyelitis optica spectrum disorders (NMOSD) are characterized by recurrent optic neuritis (ON) and longitudinally extensive transverse myelitis (LETM) as…”
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    A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis by 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. M., Zimprich, A.

    Published in Neurogenetics (01-02-2009)
    “…Neuronal ceroid lipofuscinoses (NCL) are lysosomal storage disorders and constitute the most common group of progressive neurodegenerative diseases in…”
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    Asymmetric ending of secondarily generalized seizures: A lateralizing sign in TLE by LEUTMEZER, F, WÖGINGER, S, ANTONI, E, SEIDL, B, BAUMGARTNER, C

    Published in Neurology (22-10-2002)
    “…The authors investigated whether asymmetric ending of the clonic phase of secondarily generalized tonic clonic seizures (SGTCS) has lateralizing value…”
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    Health-related quality of life (HRQOL), activity of daily living (ADL) and depressive mood disorder in temporal lobe epilepsy patients by Lehrner, J., Kalchmayr, R., Serles, W., Olbrich, A., Pataraia, E., Aull, S., Bacher, J., Leutmezer, F., Gröppel, G., Deecke, L., Baumgartner, C.

    Published in Seizure (London, England) (01-04-1999)
    “…We determined the interrelations of chronological age, age at seizure onset, duration of seizure disorder, cognitive functioning (IQ), scales of activities of…”
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    Ictal urinary urge indicates seizure onset in the nondominant temporal lobe by BAUMGARTNER, C, GRÖPPEL, G, LEUTMEZER, F, AULL-WATSCHINGER, S, PATARAIA, E, FEUCHT, M, TRINKA, E, UNTERBERGER, I, BAUER, G

    Published in Neurology (08-08-2000)
    “…The authors describe six patients with medically refractory temporal lobe epilepsy whose seizures were characterized by an aura of ictal urinary urge. All…”
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    Postictal nose wiping : A lateralizing sign in temporal lobe complex partial seizures by LEUTMEZER, F, SERLES, W, LEHRNER, J, PATARAIA, E, ZEILER, K, BAUMGARTNER, C

    Published in Neurology (01-10-1998)
    “…We report postictal nose wiping as a postictal symptom of localizing and lateralizing significance in focal epilepsy. We reviewed videotapes of 444 focal…”
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    Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes by STOGMANN, E, LICHTNER, P, HATALA, K, STROM, T. M, MEITINGER, T, ZIMPRICH, F, ZIMPRICH, A, BAUMGARTNER, C, SCHMIED, M, HOTZY, C, ASMUS, F, LEUTMEZER, F, BONELLI, S, ASSEM-HILGER, E, VASS, K

    Published in Neurogenetics (01-11-2006)
    “…Mutations in the chloride channel gene CLCN2 have been reported in families with generalized and focal epilepsy syndromes. To evaluate the contribution of…”
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