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

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Publikationen

Suchbegriffe: HEARING LOSS, . Treffer: 34

2019

Taheri-Kharameh, Z; Poorolajal, J; Bashirian, S; Heydari Moghadam, R; Parham, M; Barati, M; Rásky, É Risk factors for falls in Iranian older adults: a case-control study.
Int J Inj Contr Saf Promot. 2019; 26(4):354-359
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2017

Moser, S; Luxenberger, W; Freidl, W [Perception of hearing problems in the older population].
HNO. 2017; 65(8):671-679 [OPEN ACCESS]
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Moser, S; Luxenberger, W; Freidl, W The Influence of Social Support and Coping on Quality of Life Among Elderly With Age-Related Hearing Loss.
Am J Audiol. 2017; 26(2):170-179
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Seifert-Held, T; Langner-Wegscheider, BJ; Komposch, M; Simschitz, P; Franta, C; Teuchner, B; Offenbacher, H; Otto, F; Sellner, J; Rauschka, H; Fazekas, F Susac's syndrome: clinical course and epidemiology in a Central European population.
Int J Neurosci. 2017; 127(9):776-780
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Wolf, A; Frohne, A; Allen, M; Parzefall, T; Koenighofer, M; Schreiner, MM; Schoefer, C; Frei, K; Lucas, T A Novel Mutation in SLC26A4 Causes Nonsyndromic Autosomal Recessive Hearing Impairment.
Otol Neurotol. 2017; 38(2):173-179
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2016

Tatlisumak, T; Putaala, J; Innilä, M; Enzinger, C; Metso, TM; Curtze, S; von Sarnowski, B; Amaral-Silva, A; Jungehulsing, GJ; Tanislav, C; Thijs, V; Rolfs, A; Norrving, B; Fazekas, F; Suomalainen, A; Kolodny, EH Frequency of MELAS main mutation in a phenotype-targeted young ischemic stroke patient population.
J Neurol. 2016; 263(2):257-262 [OPEN ACCESS]
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Weinstein, BE; Sirow, LW; Moser, S Relating Hearing Aid Use to Social and Emotional Loneliness in Older Adults.
Am J Audiol. 2016; 25(1):54-61
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2013

Braun, EM; Stanzenberger, H; Nemetz, U; Luxenberger, W; Lackner, A; Bachna-Rotter, S; Tomazic, PV; Hammer, GP; Ropposch, T; Walch, C Sudden unilateral hearing loss as first sign of cerebral sinus venous thrombosis? A 3-year retrospective analysis.
Otol Neurotol. 2013; 34(4):657-661
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Muhn, F; Klopocki, E; Graul-Neumann, L; Uhrig, S; Colley, A; Castori, M; Lankes, E; Henn, W; Gruber-Sedlmayr, U; Seifert, W; Horn, D Novel mutations of the PRKAR1A gene in patients with acrodysostosis.
Clin Genet. 2013; 84(6):531-538
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2012

Huppke, P; Brendel, C; Kalscheuer, V; Korenke, GC; Marquardt, I; Freisinger, P; Christodoulou, J; Hillebrand, M; Pitelet, G; Wilson, C; Gruber-Sedlmayr, U; Ullmann, R; Haas, S; Elpeleg, O; Nürnberg, G; Nürnberg, P; Dad, S; Mller, LB; Kaler, SG; Gärtner, J Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.
AM J HUM GENET. 2012; 90(1): 61-68. [OPEN ACCESS]
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Kau, T; Veraguth, D; Schiegl, H; Scheer, I; Boltshauser, E Chudley-McCullough syndrome: case report and review of the neuroimaging spectrum.
Neuropediatrics. 2012; 43(1): 44-47. (- Case Report)
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2010

Zimon, M; Baets, J; Auer-Grumbach, M; Berciano, J; Garcia, A; Lopez-Laso, E; Merlini, L; Hilton-Jones, D; McEntagart, M; Crosby, AH; Barisic, N; Boltshauser, E; Shaw, CE; Landoure, G; Ludlow, CL; Gaudet, R; Houlden, H; Reilly, MM; Fischbeck, KH; Sumner, CJ; Timmerman, V; Jordanova, A; De Jonghe, P Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies.
BRAIN. 2010; 133(Pt 6): 1798-1809. [OPEN ACCESS]
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2009

Lackner, A; Acham, A; Alborno, T; Moser, M; Engele, H; Raggam, RB; Halwachs-Baumann, G; Kapitan, M; Walch, C Effect on hearing of ganciclovir therapy for asymptomatic congenital cytomegalovirus infection: four to 10 year follow up.
J Laryngol Otol. 2009; 123(4): 391-396.
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Mlynski, R; Goldberg, E; Ebmeyer, J; Scheich, M; Gattenloehner, S; Schwager, K; Hagen, R; Shehata-Dieler, W Histologic and morphologic evaluation of explanted bone anchors from bone-anchored hearing aids.
Eur Arch Otorhinolaryngol. 2009; 266(5):745-752
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2007

Lackner, H; Moser, A; Sovinz, P; Benesch, M; Schwinger, W; Urban, C Long-term care of young adults surviving childhood cancer - where do we go?
Wien Klin Wochenschr. 2007; 119(11-12): 361-364.
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2006

Hofmann, G; Bauernhofer, T; Krippl, P; Lang-Loidolt, D; Horn, S; Goessler, W; Schippinger, W; Ploner, F; Stoeger, H; Samonigg, H Plasmapheresis reverses all side-effects of a cisplatin overdose--a case report and treatment recommendation.
BMC Cancer. 2006; 6(2):1-1 (- Case Report) [OPEN ACCESS]
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Kos, MI; Feigl, G; Anderhuber, F; Wall, C; Fasel, JH; Guyot, JP Transcanal approach to the singular nerve.
OTOL NEUROTOL. 2006; 27(4): 542-546. [Oral Communication]
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Todt, I; Hennies, HC; Küster, W; Smolle, J; Rademacher, G; Mutze, S; Basta, D; Eisenschenk, A; Ernst, A Neurotological and neuroanatomical changes in the connexin-26-related HID/KID syndrome.
Audiol Neurootol. 2006; 11(4):242-248 (- Case Report)
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2005

Janecke, AR; Hennies, HC; Günther, B; Gansl, G; Smolle, J; Messmer, EM; Utermann, G; Rittinger, O GJB2 mutations in keratitis-ichthyosis-deafness syndrome including its fatal form.
Am J Med Genet A. 2005; 133(2):128-131 (- Case Report)
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2004

Formann, E; Stauber, R; Denk, DM; Jessner, W; Zollner, G; Munda-Steindl, P; Gangl, A; Ferenci, P Sudden hearing loss in patients with chronic hepatitis C treated with pegylated interferon/ribavirin.
AMER J GASTROENTEROL. 2004; 99(5): 873-877.
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2003

Petek, E; Windpassinger, C; Mach, M; Rauter, L; Scherer, SW; Wagner, K; Kroisel, PM Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: confirmation and refinement of the DFNA25 locus.
AM J MED GENET PART A. 2003; 117A(2): 122-126. (- Case Report)
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2001

Acham, A; Walch, C Mondini dysplasia without functional impairment in the framework of a CHARGE association
LARYNGO RHINO OTOL. 2001; 80(7): 381-384. (- Case Report)
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Benesch, M; Lackner, H; Schagerl, S; Gallistl, S; Frey, EM; Urban, C Tumor- and treatment-related side effects after multimodal therapy of childhood intracranial germ cell tumors.
Acta Paediatr. 2001; 90(3):264-270
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2000

Lackner, H; Benesch, M; Schagerl, S; Kerbl, R; Schwinger, W; Urban, C Prospective evaluation of late effects after childhood cancer therapy with a follow-up over 9 years.
Eur J Pediatr. 2000; 159(10):750-758
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Penkner, K; Köle, W; Kainz, J; Schied, G; Lorenzoni, M The function of tensor veli palatini muscles in patients with aural symptoms and temporomandibular disorder. An EMG study.
J Oral Rehabil. 2000; 27(4):344-348
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Walch, C; Anderhuber, W; Köle, W; Berghold, A Bilateral sensorineural hearing disorders in children: etiology of deafness and evaluation of hearing tests.
Int J Pediatr Otorhinolaryngol. 2000; 53(1):31-38
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Walch, C; Moser, M; Anderhuber, W; Köle, W 91 dB hearing loss--the threshold for cochlear implant?
HNO. 2000; 48(11):828-831
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1996

Anderhuber, W; Beham, A; Walch, C; Stammberger, H Choristoma of the middle ear.
Eur Arch Otorhinolaryngol. 1996; 253(3):182-184 (- Case Report)
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Offenbacher, H; Fazekas, F; Schmidt, R; Kapeller, P; Fazekas, G Superficial siderosis of the central nervous system: MRI findings and clinical significance.
Neuroradiology. 1996; 38 Suppl 1(4):S51-S56
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1995

Nauck, M; Winkler, K; Siekmeier, R; Marangos, N; Richter, B; März, W; Wieland, H Pseudo-pseudohypertriglyceridemia: a case of increased free glycerol without evidence for glycerol kinase deficiency.
Clin Chem. 1995; 41(4):619-620 [OPEN ACCESS]
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1991

Friedrich, G; Ott, E Prospective randomized study on the comparative effect between 10% HES 200/0.5 and 6% HES 200/0.5 in patients with hearing loss
Laryngorhinootologie. 1991; 70(12): 670-674.
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1990

Jellinger, K; Paulus, W; Grisold, W; Paschke, E New phenotype of adult alpha-L-iduronidase deficiency (mucopolysaccharidosis I) masquerading as Friedreich's ataxia with cardiopathy.
CLIN NEUROPATHOL. 1990; 9(4): 163-169. (- Case Report)
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1985

Friedrich, G Etiology and pathogenesis of sudden deafness
Laryngol Rhinol Otol (Stuttg). 1985; 64(2):62-66
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1980

Moser, M; Jakse, R; Friedrich, G The assessment results of patients with neurootological symptoms (author's transl)
HNO. 1980; 28(6):177-182
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