Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Publikationen
Suchbegriffe: POLYNEUROPATHY, . Treffer: 19
2022
Zeitelhofer, M; Hochmeister, S; Adzemovic, MZ
Editorial: Neuropathology of Autoimmune Inflammatory Demyelination Disorders
FRONT NEUROL. 2022; 13: 925216
Doi: 10.3389/fneur.2022.925216
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2021
Hatzl, S; Posch, F; Rezai, A; Gornicec, M; Beham-Schmid, C; Magnes, T; Wangner, S; Deutsch, A; Greinix, H; Uhl, B; Prochazka, KT; Egle, A; Greil, R; Melchardt, T; Linkesch, W; Schulz, E; Neumeister, P
Vinorelbine as substitute for vincristine in patients with diffuse large B cell lymphoma and vincristine-induced neuropathy.
Support Care Cancer. 2021; 29(9):5197-5207
Doi: 10.1007/s00520-021-06059-2
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2020
Auer-Grumbach, M; Rettl, R; Ablasser, K; Agis, H; Beetz, C; Duca, F; Gattermeier, M; Glaser, F; Hacker, M; Kain, R; Kaufmann, B; Kovacs, GG; Lampl, C; Ljevakovic, N; Nagele, J; Pölzl, G; Quasthoff, S; Raimann, B; Rauschka, H; Reiter, C; Skrahina, V; Schuhfried, O; Sunder-Plassmann, R; Verheyen, ND; Wanschitz, J; Weber, T; Windhager, R; Wurm, R; Zimprich, F; Löscher, WN; Bonderman, D
Hereditary ATTR Amyloidosis in Austria: Prevalence and Epidemiological Hot Spots.
J Clin Med. 2020; 9(7):
Doi: 10.3390/jcm9072234
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2019
Finsterwalder, S; Wuehr, M; Gesierich, B; Dietze, A; Konieczny, MJ; Schmidt, R; Schniepp, R; Duering, M
Minor gait impairment despite white matter damage in pure small vessel disease.
Ann Clin Transl Neurol. 2019; 6(10): 2026-2036.
Doi: 10.1002/acn3.50891
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2017
Finsterer, J; Wanschitz, J; Quasthoff, S; Iglseder, S; Löscher, W; Grisold, W
Causally treatable, hereditary neuropathies in Fabry's disease, transthyretin-related familial amyloidosis, and Pompe's disease.
Acta Neurol Scand. 2017; 136(6):558-569
Doi: 10.1111/ane.12758
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2015
Karall, D; Brunner-Krainz, M; Kogelnig, K; Konstantopoulou, V; Maier, EM; Möslinger, D; Plecko, B; Sperl, W; Volkmar, B; Scholl-Bürgi, S
Clinical outcome, biochemical and therapeutic follow-up in 14 Austrian patients with Long-Chain 3-Hydroxy Acyl CoA Dehydrogenase Deficiency (LCHADD).
Orphanet J Rare Dis. 2015; 10(1): 21-21.
Doi: 10.1186/s13023-015-0236-7
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Roos, A; Weis, J; Korinthenberg, R; Fehrenbach, H; Häusler, M; Züchner, S; Mache, C; Hubmann, H; Auer-Grumbach, M; Senderek, J
Inverted formin 2-related Charcot-Marie-Tooth disease: extension of the mutational spectrum and pathological findings in Schwann cells and axons.
J Peripher Nerv Syst. 2015; 20(1):52-59
Doi: 10.1111/jns.12106
(- Case Report)
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2014
Böck, K; Pschaid, C; Topakian, R; Stieglbauer, K; Doppler, S; von Oertzen, JT; Pichler, R
Mononeuritis multiplex: association with infectious condition and familial background in a tropical environment: a case report.
Wien Klin Wochenschr. 2014; 126 Suppl 1(4):S42-S45
Doi: 10.1007/s00508-014-0504-x
(- Case Report)
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Ludwig, H; Kasparu, H; Leitgeb, C; Rauch, E; Linkesch, W; Zojer, N; Greil, R; Seebacher, A; Pour, L; Weißmann, A; Adam, Z
Bendamustine-bortezomib-dexamethasone is an active and well-tolerated regimen in patients with relapsed or refractory multiple myeloma.
Blood. 2014; 123(7):985-991
Doi: 10.1182/blood-2013-08-521468
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2013
Franz, C; Hoffmann, K; Hinz, U; Singer, R; Hund, E; Gotthardt, DN; Ganten, T; Kristen, AV; Hegenbart, U; Schönland, S; Hinderhofer, K; Büchler, MW; Schemmer, P
Modified body mass index and time interval between diagnosis and operation affect survival after liver transplantation for hereditary amyloidosis: a single-center analysis.
Clin Transplant. 2013; 27 Suppl 25(1):40-48
Doi: 10.1111/ctr.12193
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Maio, P; Bento, D; Vieira, R; Afonso, A; Sachse, F; Kutzner, H;
Non Hodgkin T cell lymphoma: an atypical clinical presentation.
AN BRASIL DERMATOL. 2013; 88(2): 264-267.
Doi: 10.1590/S0365-05962013000200016
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2012
Finsterer, J; Löscher, W; Quasthoff, S; Wanschitz, J; Auer-Grumbach, M; Stevanin, G
Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance.
J Neurol Sci. 2012; 318(1-2):1-18
Doi: 10.1016/j.jns.2012.03.025
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2007
Archelos, JJ
Treatment options in painful diabetic polyneuropathy
Wien Klin Wochenschr. 2007; 119(7-8):205-216
Doi: 10.1007/s00508-007-0795-2
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2005
Singer, R; Mehrabi, A; Schemmer, P; Kashfi, A; Hegenbart, U; Goldschmidt, H; Schönland, S; Kristen, A; Dengler, T; Müller-Schilling, M; Sauer, P; Dogan, A; Hund, E; Helmke, B; Schnabel, P; Altland, K; Linke, R; Friess, H; Schmidt, J; Büchler, MW; Kraus, TW
Indications for liver transplantation in patients with amyloidosis: a single-center experience with 11 cases.
Transplantation. 2005; 80(1 Suppl):S156-S159
Doi: 10.1097/01.tp.0000186910.09213.bf
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2001
Quasthoff, S; Hartung, HP
Nerve growth factor (NGF) in treatment of diabetic polyneuropathy. One hope less?
NERVENARZT 2001 72: 456-459.
Doi: 10.1007/s001150050780
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Reindl, M; Knipping, G; Wicher, I; Dilitz, E; Egg, R; Deisenhammer, F; Berger, T
Increased intrathecal production of apolipoprotein D in multiple sclerosis.
J Neuroimmunol. 2001; 119(2):327-332
Doi: 10.1016%2FS0165-5728%2801%2900378-2
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2000
Kiefer, R; Dangond, F; Mueller, M; Toyka, KV; Hafler, DA; Hartung, HP
Enhanced B7 costimulatory molecule expression in inflammatory human sural nerve biopsies.
J Neurol Neurosurg Psychiatry. 2000; 69(3):362-368
Doi: 10.1136/jnnp.69.3.362
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1998
Stangel, M; Hartung, HP; Marx, P; Gold, R
Intravenous immunoglobulin treatment of neurological autoimmune diseases.
J Neurol Sci. 1998; 153(2):203-214
Doi: 10.1016/S0022-510X(97)00292-X
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1990
Fuchs, D; Möller, AA; Reibnegger, G; Stöckle, E; Werner, ER; Wachter, H
Decreased serum tryptophan in patients with HIV-1 infection correlates with increased serum neopterin and with neurologic/psychiatric symptoms.
J Acquir Immune Defic Syndr. 1990; 3(9):873-876
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