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

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Publikationen

Suchbegriffe: NEUROPATHY, . Treffer: 158

2018

Alastruey-Izquierdo, A; Cadranel, J; Flick, H; Godet, C; Hennequin, C; Hoenigl, M; Kosmidis, C; Lange, C; Munteanu, O; Page, I; Salzer, HJF; on behalf of CPAnet Treatment of Chronic Pulmonary Aspergillosis: Current Standards and Future Perspectives.
Respiration. 2018; 96(2):159-170
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Löscher, WN; Oberreiter, EM; Erdler, M; Quasthoff, S; Culea, V; Berek, K; Embacher, N; Grinzinger, S; Hess, I; Höger, FS; Horlings, CGC; 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 Multifocal motor neuropathy in Austria: a nationwide survey of clinical features and response to treatment.
J NEUROL. 2018; 265(12): 2834-2840. [OPEN ACCESS]
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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
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Geuens, T; De Winter, V; Rajan, N; Achsel, T; Mateiu, L; Almeida-Souza, L; Asselbergh, B; Bouhy, D; Auer-Grumbach, M; Bagni, C; Timmerman, V Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease.
Acta Neuropathol Commun. 2017; 5(1):5-5 [OPEN ACCESS]
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Hohenberger, GM; Maier, MJ; Grechenig, C; Schwarz, AM; Matzi, V; Weiglein, AH Carpal tunnel release: Safe and simple identification of the flexor retinaculum based on superficial anatomical landmarks.
Clin Anat. 2017; 30(4):512-516
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Maurer-Ertl, W; Pranckh-Matzke, D; Friesenbichler, J; Bratschitsch, G; Holzer, LA; Maier, M; Leithner, A Clinical Results and Serum Metal Ion Concentrations following Ceramic-on-Metal Total Hip Arthroplasty at a Mean Follow-Up of 60 Months.
Biomed Res Int. 2017; 2017(8):3726029-3726029 [OPEN ACCESS]
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Sezer, O; Beksac, M; Hajek, R; Sucak, G; Cagirgan, S; Linkesch, W; Meltem Akay, O; Gülbas, Z; Nahi, H; Plesner, T; Snowden, JA; Timurağaoğlu, A; Dechow, T; Lang, A; Tuğlular, T; Drach, J; Armbrecht, G; Potamianou, A; Couturier, C; Olie, RA; Feys, C; Allietta, N; Terpos, E Effects of single-agent bortezomib as post-transplant consolidation therapy on multiple myeloma-related bone disease: a randomized phase II study.
Br J Haematol. 2017; 178(1):61-71
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Tarmann, L; Wackernagel, W; Ivastinovic, D; Schneider, M; Winkler, P; Langmann, G Tumor parameters predict the risk of side effects after ruthenium-106 plaque brachytherapy of uveal melanomas.
PLoS One. 2017; 12(8): e0183833-e0183833. [OPEN ACCESS]
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2016

Auer-Grumbach, M; Toegel, S; Schabhüttl, M; Weinmann, D; Chiari, C; Bennett, DLH; Beetz, C; Klein, D; Andersen, PM; Böhme, I; Fink-Puches, R; Gonzalez, M; Harms, MB; Motley, W; Reilly, MM; Renner, W; Rudnik-Schöneborn, S; Schlotter-Weigel, B; Themistocleous, AC; Weishaupt, JH; Ludolph, AC; Wieland, T; Tao, F; Abreu, L; Windhager, R; Zitzelsberger, M; Strom, TM; Walther, T; Scherer, SS; Züchner, S; Martini, R; Senderek, J Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies.
Am J Hum Genet. 2016; 99(3):607-623 [OPEN ACCESS]
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Heschl, S; Hallmann, B; Zilke, T; Gemes, G; Schoerghuber, M; Auer-Grumbach, M; Quehenberger, F; Lirk, P; Hogan, Q; Rigaud, M Diabetic neuropathy increases stimulation threshold during popliteal sciatic nerve block.
Br J Anaesth. 2016; 116(4):538-545 [OPEN ACCESS]
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Keeling, IM; Beran, E; Dapunt, OE Kawasaki disease and hepatobiliary involvement: report of two cases.
Ital J Pediatr. 2016; 42(5):27-27 (- Case Report) [OPEN ACCESS]
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Krainz, S; Schneider, MR; Bizjak, B; Wedrich, A Indirect traumatic optic neuropathy after bicycle crash
SPEKTRUM AUGENHEILKD. 2016; 30(3): 142-145. [OPEN ACCESS]
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Lechleitner, M; Abrahamian, H; Francesconi, C; Sturm, W; Köhler, G The diabetic foot].
Wien Klin Wochenschr. 2016; 128 Suppl 2(3):S80-S84
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Radda, S; Bolz, M; Egger, S; Gasser-Steiner, V; Kralinger, M; Mennel, S; Scholda, C; Stolba, U; Wedrich, A; Krepler, K [Diagnosis, treatment and monitoring of diabetic eye control].
Wien Klin Wochenschr. 2016; 128 Suppl 2(4):S97-102
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Weitgasser, R; Abrahamian, H; Clodi, M; Zlamal-Fortunat, S; Hammer, HF Exocrine pancreatic insufficiency and diabetes mellitus].
Wien Klin Wochenschr. 2016; 128 Suppl 2(12):S163-S166
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2015

Herrmann, M; Sullivan, DR; Veillard, AS; McCorquodale, T; Straub, IR; Scott, R; Laakso, M; Topliss, D; Jenkins, AJ; Blankenberg, S; Burton, A; Keech, AC; FIELD Study Investigators Serum 25-hydroxyvitamin D: a predictor of macrovascular and microvascular complications in patients with type 2 diabetes.
Diabetes Care. 2015; 38(3):521-528
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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. [OPEN ACCESS]
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Matthews, L; Enzinger, C; Fazekas, F; Rovira, A; Ciccarelli, O; Dotti, MT; Filippi, M; Frederiksen, JL; Giorgio, A; Küker, W; Lukas, C; Rocca, MA; De Stefano, N; Toosy, A; Yousry, T; Palace, J; MAGNIMS Network MRI in Leber's hereditary optic neuropathy: the relationship to multiple sclerosis.
J Neurol Neurosurg Psychiatry. 2015; 86(5):537-542 [OPEN ACCESS]
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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 (- Case Report)
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Strickland, AV; Schabhüttl, M; Offenbacher, H; Synofzik, M; Hauser, NS; Brunner-Krainz, M; Gruber-Sedlmayr, U; Moore, SA; Windhager, R; Bender, B; Harms, M; Klebe, S; Young, P; Kennerson, M; Garcia, AS; Gonzalez, MA; Züchner, S; Schule, R; Shy, ME; Auer-Grumbach, M Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1.
J Neurol. 2015; 262(9):2124-2134 [OPEN ACCESS]
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2014

Assaf, AT; Jürgens, TP; Benecke, AW; Riecke, B; Blessmann, M; Zrnc, TA; Much, CC; Heiland, M; Friedrich, RE Numb chin syndrome: a rare and often overlooked symptom.
J Oral Facial Pain Headache. 2014; 28(1): 80-90.
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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 (- Case Report)
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Brozkova, DS; Mazanec, R; Bohm, J; Vysata, O; Auer-Grumbach, M; Windpassinger, C; Neupauerova, J; Barankova, L; Nevsimalova, S; Seeman, P Hereditary Ulceromutilating Sensory Neuropathy - Clinical, Electrophysiological and Molecular Genetic Study of Three Families
CESK SLOV NEUROL N. 2014; 77(4): 479-486.
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Fullerton, B; Jeitler, K; Seitz, M; Horvath, K; Berghold, A; Siebenhofer, A Intensive glucose control versus conventional glucose control for type 1 diabetes mellitus.
Cochrane Database Syst Rev. 2014; CD009122-CD009122 [OPEN ACCESS]
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Hammer, HF An update on pancreatic pathophysiology (do we have to rewrite pancreatic pathophysiology?).
Wien Med Wochenschr. 2014; 164(3-4):57-62
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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 [OPEN ACCESS]
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Rahimi Shorin, H; Azizbeig Mohajer, M; Parsa, A; Azhari, A; Assadian, M Femoral Nerve Palsy Following Delayed Reduction of a Dislocated Hip in a 44- Year-old Man.
Iran Red Crescent Med J. 2014; 16(2):e12579-e12579 [OPEN ACCESS]
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Topakian, R; Wimmer, S; Pischinger, B; Pichler, R Hereditary neuropathy with liability to pressure palsies presenting with sciatic neuropathy.
BMJ Case Rep. 2014; 2014(1): (- Case Report) [OPEN ACCESS]
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2013

Auer-Grumbach, M; Bode, H; Pieber, TR; Schabhüttl, M; Fischer, D; Seidl, R; Graf, E; Wieland, T; Schuh, R; Vacariu, G; Grill, F; Timmerman, V; Strom, TM; Hornemann, T Mutations at Ser331 in the HSN type I gene SPTLC1 are associated with a distinct syndromic phenotype.
Eur J Med Genet. 2013; 56(5):266-269 (- Case Report) [OPEN ACCESS]
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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
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Girtler, MT; Krasinski, A; Dejaco, C; Kitzler, HH; Cui, LG; Sherebrin, S; Gardi, L; Chhem, RK; Fenster, A; Romagnoli, C; De Zordo, T Feasibility of 3D ultrasound to evaluate upper extremity nerves.
Ultraschall Med. 2013; 34(4):382-387
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Lechleitner, M; Pils, K; Roller-Wirnsberger, R; Beubler, E; Gasser, R; Mrak, P; Hoppichler, F; Pietschmann, P Diabetes and osteoporosis: pathophysiological interactions and clinical importance for geriatric patients].
Z GERONTOL GERIATRIE. 2013; 46(5): 390-397.
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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. [OPEN ACCESS]
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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
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Kobesova, A; Kolar, P; Mlckova, J; Svehlik, M; Morris, CE; Frank, C; Lepsikova, M; Kozak, J Effect of functional stabilization training on balance and motor patterns in a patient with Charcot-Marie-Tooth disease.
Neuro Endocrinol Lett. 2012; 33(1):3-10
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Leonardis, L; Auer-Grumbach, M; Papić, L; Zidar, J The N355K atlastin 1 mutation is associated with hereditary sensory neuropathy and pyramidal tract features.
Eur J Neurol. 2012; 19(7):992-998
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Stur, M; Egger, S; Haas, A; Kieselbach, G; Mennel, S; Michl, R; Roden, M; Stolba, U; Wedrich, A Diagnosis, therapy and follow up of diabetic eye disease].
Wien Klin Wochenschr. 2012; 124 Suppl 2(12):50-57
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Weitgasser, R; Abrahamian, H; Clodi, M; Fortunat, W; Hammer, H Position paper: Exocrine pancreatic insufficiency and diabetes mellitus].
Wien Klin Wochenschr. 2012; 124 Suppl 2(8):100-103
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Zimon, M; Baets, J; Almeida-Souza, L; De Vriendt, E; Nikodinovic, J; Parman, Y; Battaloglu, E; Matur, Z; Guergueltcheva, V; Tournev, I; Auer-Grumbach, M; De Rijk, P; Petersen, BS; Muller, T; Fransen, E; Van Damme, P; Loscher, WN; Barisic, N; Mitrovic, Z; Previtali, SC; Topaloglu, H; Bernert, G; Beleza-Meireles, A; Todorovic, S; Savic-Pavicevic, D; Ishpekova, B; Lechner, S; Peeters, K; Ooms, T; Hahn, AF; Zuchner, S; Timmerman, V; Van Dijck, P; Rasic, VM; Janecke, AR; De Jonghe, P; Jordanova, A; Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.
NAT GENET. 2012; 44(10): 1080-1083.
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2011

Auer-Grumbach, M; Weger, M; Fink-Puches, R; Papić, L; Fröhlich, E; Auer-Grumbach, P; El Shabrawi-Caelen, L; Schabhüttl, M; Windpassinger, C; Senderek, J; Budka, H; Trajanoski, S; Janecke, AR; Haas, A; Metze, D; Pieber, TR; Guelly, C Fibulin-5 mutations link inherited neuropathies, age-related macular degeneration and hyperelastic skin.
Brain. 2011; 134(Pt 6):1839-1852 [OPEN ACCESS]
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Baets, J; Deconinck, T; De Vriendt, E; Zimon, M; Yperzeele, L; Van Hoorenbeeck, K; Peeters, K; Spiegel, R; Parman, Y; Ceulemans, B; Van Bogaert, P; Pou-Serradell, A; Bernert, G; Dinopoulos, A; Auer-Grumbach, M; Sallinen, SL; Fabrizi, GM; Pauly, F; Van den Bergh, P; Bilir, B; Battaloglu, E; Madrid, RE; Kabzinska, D; Kochanski, A; Topaloglu, H; Miller, G; Jordanova, A; Timmerman, V; De Jonghe, P Genetic spectrum of hereditary neuropathies with onset in the first year of life
BRAIN. 2011; 134: 2664-2676. [OPEN ACCESS]
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Dolderer, JH; Prandl, EC; Kehrer, A; Beham, A; Schaller, HE; Briggs, C; Kelly, JL Solitary Paralysis of the Flexor Pollicis Longus Muscle after Minimally Invasive Elbow Procedures: Anatomical and Clinical Study of the Anterior Interosseous Nerve
PLAST RECONSTR SURG. 2011; 127(3): 1229-1236.
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Finsterer, J; Papic, L; Auer-Grumbach, M Motor neuron, nerve, and neuromuscular junction disease
CURR OPIN NEUROL. 2011; 24(5): 469-474.
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Guelly, C; Zhu, PP; Leonardis, L; Papic, L; Zidar, J; Schabhüttl, M; Strohmaier, H; Weis, J; Strom, TM; Baets, J; Willems, J; De Jonghe, P; Reilly, MM; Fröhlich, E; Hatz, M; Trajanoski, S; Pieber, TR; Janecke, AR; Blackstone, C; Auer-Grumbach, M Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I.
Am J Hum Genet. 2011; 88(1):99-105 [OPEN ACCESS]
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Lee, CK; Gurney, H; Brown, C; Sorio, R; Donadello, N; Tulunay, G; Meier, W; Bacon, M; Maenpaa, J; Petru, E; Reed, N; Gebski, V; Pujade-Lauraine, E; Lord, S; Simes, RJ; Friedlander, M Carboplatin-paclitaxel-induced leukopenia and neuropathy predict progression-free survival in recurrent ovarian cancer.
BRIT J CANCER. 2011; 105(3): 360-365. [OPEN ACCESS]
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Nardone, R; Christova, M; Bratti, A; Lochner, P; Covi, M; Trinka, E; Tezzon, F; Golaszewski, S Corticospinal tract dysfunction in a patient with acute motor axonal neuropathy (AMAN).
Clin Neurol Neurosurg. 2011; 113(9): 779-781. (- Case Report)
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Pansy, J; Lackner, H; Benesch, M; Urban, C Numb chin syndrome in acute lymphoblastic leukemia.
Indian Pediatr. 2011; 48(6): 481-483. [OPEN ACCESS]
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Raju, R; Devi, SK; Mehervani, C; Kumar, AS; Meena, AK; Reddy, PP; Pranay, P; Jain, S; Archelos-Gracia, JJ; Suneetha, S; Suneetha, LM Antibodies to myelin P0 and ceramide perpetuate neuropathy in long standing treated leprosy patients.
Neurochem Res. 2011; 36(5):766-773
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Rotthier, A; Penno, A; Rautenstrauss, B; Auer-Grumbach, M; Stettner, GM; Asselbergh, B; Van Hoof, K; Sticht, H; Levy, N; Timmerman, V; Hornemann, T; Janssens, K Characterization of Two Mutations in the SPTLC1 Subunit of Serine Palmitoyltransferase Associated with Hereditary Sensory and Autonomic Neuropathy Type I
HUM MUTAT. 2011; 32(6): E2211-E2225. [OPEN ACCESS]
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Tanislav, C; Kaps, M; Rolfs, A; Böttcher, T; Lackner, K; Paschke, E; Mascher, H; Laue, M; Blaes, F Frequency of Fabry disease in patients with small-fibre neuropathy of unknown aetiology: a pilot study.
Eur J Neurol. 2011; 18(4):631-636
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