Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

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Heschl, S; Hallmann, B; Zilke, T; Gemes, G; Schörghuber, M; Auer-Grumbach, M; Quehenberger, F; Lirk, P; Hogan, Q; Rigaud, M Diabetic neuropathy increases stimulation threshold during popliteal sciatic nerve block
34th Annual ESRA Congress 2015; SEP 2-5, 2015; Ljubljana, SLOVENIA. 2015. [Oral Communication]

Heschl, S; Hallmann, B; Zilke, T; Schörghuber, M; Gemes, G; Auer-Grumbach, M; Quehenberger, F; Lirk, P; Hogan, Q; Rigaud, M Diabetische Neuropathie erhöht den Stimulationsschwellenwert für eine distale Ischiadikusblockade
AIC 2015; NOV 12-14, 2015; Vienna, AUSTRIA. 2015. [Poster]
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Fiorillo, C; Moro, F; Astrea, G; Brisca, G; Battini, R; Auer-Grumbach, M; Santorelli, FM; Bruno, C TRPV4 MUTATIONS IN CHILDREN WITH CONGENITAL DISTAL SPINAL MUSCULAR ATROPHY
J PERIPHER NERV SYST. . 2012; 17: S24-S25.-Meeting of the Italian-Association-for-the-Peripheral-Nervous-System and Pain and Neuroscience Group of the Italian-Society-of-Neurology; APR 12-14, 2012; Pisa, ITALY. [Poster]
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Fiorillo, C; Moro, F; Astrea, G; Battini, R; Gully, C; Olschewski, A; Auer-Grumbach, M; Bruno, C; Santorelli, FM Novel mutation of TRPV4 in congenital distal SMA with vocal cord paralysis
NEUROMUSCULAR DISORD. 2011; 21(9-10):682-682.-16th International Congress of the World-Muscle-Society; OCT 18-22, 2011; Algarve, PORTUGAL. Doi: 10.1016/j.nmd.2011.06.896 [Poster]
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Janssens, K; Rotthier, A; Penno, A; Van Hoof, K; Auer-Grumbach, M; Hornemann, T; Timmerman, V HSAN TYPE I CAUSED BY MUTATIONS IN SPTLC1 AND SPTLC2 IS CONSISTENTLY ASSOCIATED WITH REDUCED SPT ACTIVITY IN VITRO AND FORMATION OF DEOXYSPHINGOID BASES IN VIVO.
J PERIPHER NERV SYST. 2011; 16: S60-S60.
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Auer-Grumbach, M; Fischer, C; Duong, N; Huebner, A; John, E; Wagner, K; Speicher, M; Wehnert, M LMNA p.R644C: Pathogenic mutation of low penetrance, disease modifier or polymorphism?
NEUROMUSCULAR DISORD. 2007; 17(9-10):799-799. Doi: 10.1016/j.nmd.2007.06.129 [Poster]
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Auer-Grumbach, M; John, E; Wallefeld, W; Fischer, C; Speicher, M; Laing, N A novel slow-skeletal myosin (MYH7) mutation in a large Austrian family presenting as late onset distal myopathy
NEUROMUSCULAR DISORD. 2007; 17(9-10):883-884. Doi: 10.1016/j.nmd.2007.06.407 [Poster]
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Gruber-Sedlmayr, U; Mache, Ch; Roedl, S; Auer-Grumbach, M; Quasthoff, S; Brunner-Krainz, M; Plecko, B Chronic inflammatory demyelinating polyradiculoneuropathy in children and adolescents-longterm follow-up in 7 patients.
Neuropediatrics. 37: 174--Jahrestagung der Gesellschaft fuer Neuropaediatrie; 20. -23. Sept. 2006; Mannheim, Deutschland. [Poster]

Laback CH, Rappl T, Quasthoff S, Auer-Grumbach M, Gumpert R, Wittgruber G, Spendel S, Hellbom B, Scharnagl E Treatment of mild carpal tunnel syndrome with the low level laser.
Abstractband2006; (45):-9 th International Congress of the European Society for Laser Aesthetic Surgery - in Association with ESCAD.; Jun 22-24, 2006; Graz, AUSTRIA. [Oral Communication]

Plecko, B; Schara, U; Auer-Grumbach, M; Seifert, T; Bittner, R; Pfleger, A; Zobel, G; Roedl, S; Vincent, A MuSK antibody positive autoimmune myasthenia gravis in a 14 year old boy: difficulties in diagnosis and response to treatment with plasmapheresis and immunosuppression.
Neuropediatrics. 37: 174--Jahrestagung der Gesellschaft Neuropaediatrie; 20. - 23. Sept. 2006; Mannheim, Deutschland. [Oral Communication]

Zgonc, V; Leonardis, L; Auer-Grumbach, M; Strom, TM; Wagenstaller, J; Mauko, B; Pieber, TR; Zidar, J A new type of Hereditary Ulcero-Mutilating Neuropathy in Slovene kinship unlinked to Hereditary Sensory Neuropathy Type 1 and Charcot-Marie-Tooth disease Type 2B loci
NEUROMUSCULAR DISORD. 2006; 16: S132-S133. [Poster]
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Proukakis, C; Crosby, AH; Auer-Grumbach, M; Wagner, K; Reid, E; Patton, MA; Warner, TT Screening of the spastin gene in autosomal dominant hereditary spastic paraplegia reveals seven novel mutations
J NEUROL NEUROSURG PSYCHIAT 2003 74: 406-407.
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Devolder-Irobi, JI; De Vriendt, E; Van Gerwen, V; Auer-Grumbach, M; Plecko, B; Wagner, K; Kennerson, M; Nicholson, G; Zhu, D; Hartung, HP; Timmerman, V; De-Jonghe, P Autosomal dominant juvenile amyotrophic lateral sclerosis (ALS) and distal hereditary motor neuropathy (distal HMN) with pyramidal tract signs
EUR J HUMAN GENET 2002 10: 214-215.
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Verhoeven, K; De Vriendt, E; Van Gerwen, V; Auer-Grumbach, M; Pou-Serradell, A; de Jonghe, P; Timmerman, V Mutation screening of SPTLC1 in patients with hereditary sensory neuropathy type I.
AMER J HUM GENET. 2001; 69 S1(4):601-601.
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Verhoeven, K; De Vriendt, E; De Jonghe, P; Auer-Grumbach, M; Kwon, J; Wagner, K; Hartung, HP; Timmerman, V Ulcero-mutilating peripheral neuropathies: genetic linkage study and mutation analysis of candidate genes.
AMER J HUM GENET 2000 67: 325-325.
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