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

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Publikationen

Suchbegriffe: TYPING, . Treffer: 336

2019

Binder, E; Rohrer, T; Denzer, C; Marg, W; Ohlenschläger, U; Schenk-Huber, H; Schierloh, U; Skopnik, H; Fröhlich-Reiterer, EE; Holl, RW; Prinz, N Screening for coeliac disease in 1624 mainly asymptomatic children with type 1 diabetes: is genotyping for coeliac-specific human leucocyte antigen the right approach?
Arch Dis Child. 2019; 104(4):354-359
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Budde, M; Anderson-Schmidt, H; Gade, K; Reich-Erkelenz, D; Adorjan, K; Kalman, JL; Senner, F; Papiol, S; Andlauer, TFM; Comes, AL; Schulte, EC; Klöhn-Saghatolislam, F; Gryaznova, A; Hake, M; Bartholdi, K; Flatau, L; Reitt, M; Quast, S; Stegmaier, S; Meyers, M; Emons, B; Haußleiter, IS; Juckel, G; Nieratschker, V; Dannlowski, U; Schaupp, SK; Schmauß, M; Zimmermann, J; Reimer, J; Schulz, S; Wiltfang, J; Reininghaus, E; Anghelescu, IG; Arolt, V; Baune, BT; Konrad, C; Thiel, A; Fallgatter, AJ; Figge, C; von Hagen, M; Koller, M; Lang, FU; Wigand, ME; Becker, T; Jäger, M; Dietrich, DE; Stierl, S; Scherk, H; Spitzer, C; Folkerts, H; Witt, SH; Degenhardt, F; Forstner, AJ; Rietschel, M; Nöthen, MM; Falkai, P; Schulze, TG; Heilbronner, U A longitudinal approach to biological psychiatric research: The PsyCourse study.
Am J Med Genet B Neuropsychiatr Genet. 2019; 180(2):89-102
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Gallon, R; Mühlegger, B; Wenzel, SS; Sheth, H; Hayes, C; Aretz, S; Dahan, K; Foulkes, W; Kratz, CP; Ripperger, T; Azizi, AA; Feldman, HB; Chong, AL; Demirsoy, U; Florkin, B; Imschweiler, T; Januszkiewicz-Lewandowska, D; Lobitz, S; Nathrath, M; Pander, HJ; Perez-Alonso, V; Perne, C; Ragab, I; Rosenbaum, T; Rueda, D; Seidel, MG; Suerink, M; Taeubner, J; Zimmermann, SY; Zschocke, J; Borthwick, GM; Burn, J; Jackson, MS; Santibanez-Koref, M; Wimmer, K A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes.
Hum Mutat. 2019;
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Lilly, E; Bunick, CG; Maley, AM; Zhang, S; Spraker, MK; Theos, AJ; Vivar, KL; Seminario-Vidal, L; Bennett, AE; Sidbury, R; Ogawa, Y; Akiyama, M; Binder, B; Hadj-Rabia, S; Morotti, RA; Glusac, EJ; Choate, KA; Richard, G; Milstone, LM More than keratitis, ichthyosis, and deafness: Multisystem effects of lethal GJB2 mutations.
J Am Acad Dermatol. 2019; 80(3):617-625 [OPEN ACCESS]
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Rhodes, CJ; Batai, K; Bleda, M; Haimel, M; Southgate, L; Germain, M; Pauciulo, MW; Hadinnapola, C; Aman, J; Girerd, B; Arora, A; Knight, J; Hanscombe, KB; Karnes, JH; Kaakinen, M; Gall, H; Ulrich, A; Harbaum, L; Cebola, I; Ferrer, J; Lutz, K; Swietlik, EM; Ahmad, F; Amouyel, P; Archer, SL; Argula, R; Austin, ED; Badesch, D; Bakshi, S; Barnett, C; Benza, R; Bhatt, N; Bogaard, HJ; Burger, CD; Chakinala, M; Church, C; Coghlan, JG; Condliffe, R; Corris, PA; Danesino, C; Debette, S; Elliott, CG; Elwing, J; Eyries, M; Fortin, T; Franke, A; Frantz, RP; Frost, A; Garcia, JGN; Ghio, S; Ghofrani, HA; Gibbs, JSR; Harley, J; He, H; Hill, NS; Hirsch, R; Houweling, AC; Howard, LS; Ivy, D; Kiely, DG; Klinger, J; Kovacs, G; Lahm, T; Laudes, M; Machado, RD; MacKenzie Ross, RV; Marsolo, K; Martin, LJ; Moledina, S; Montani, D; Nathan, SD; Newnham, M; Olschewski, A; Olschewski, H; Oudiz, RJ; Ouwehand, WH; Peacock, AJ; Pepke-Zaba, J; Rehman, Z; Robbins, I; Roden, DM; Rosenzweig, EB; Saydain, G; Scelsi, L; Schilz, R; Seeger, W; Shaffer, CM; Simms, RW; Simon, M; Sitbon, O; Suntharalingam, J; Tang, H; Tchourbanov, AY; Thenappan, T; Torres, F; Toshner, MR; Treacy, CM; Vonk Noordegraaf, A; Waisfisz, Q; Walsworth, AK; Walter, RE; Wharton, J; White, RJ; Wilt, J; Wort, SJ; Yung, D; Lawrie, A; Humbert, M; Soubrier, F; Trégouët, DA; Prokopenko, I; Kittles, R; Gräf, S; Nichols, WC; Trembath, RC; Desai, AA; Morrell, NW; Wilkins, MR; UK NIHR BioResource Rare Diseases Consortium; UK PAH Cohort Study Consortium; US PAH Biobank Consortium Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis.
Lancet Respir Med. 2019; 7(3):227-238 [OPEN ACCESS]
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2018

Bis, JC; Jian, X; Kunkle, BW; Chen, Y; Hamilton-Nelson, KL; Bush, WS; Salerno, WJ; Lancour, D; Ma, Y; Renton, AE; Marcora, E; Farrell, JJ; Zhao, Y; Qu, L; Ahmad, S; Amin, N; Amouyel, P; Beecham, GW; Below, JE; Campion, D; Charbonnier, C; Chung, J; Crane, PK; Cruchaga, C; Cupples, LA; Dartigues, JF; Debette, S; Deleuze, JF; Fulton, L; Gabriel, SB; Genin, E; Gibbs, RA; Goate, A; Grenier-Boley, B; Gupta, N; Haines, JL; Havulinna, AS; Helisalmi, S; Hiltunen, M; Howrigan, DP; Ikram, MA; Kaprio, J; Konrad, J; Kuzma, A; Lander, ES; Lathrop, M; Lehtimäki, T; Lin, H; Mattila, K; Mayeux, R; Muzny, DM; Nasser, W; Neale, B; Nho, K; Nicolas, G; Patel, D; Pericak-Vance, MA; Perola, M; Psaty, BM; Quenez, O; Rajabli, F; Redon, R; Reitz, C; Remes, AM; Salomaa, V; Sarnowski, C; Schmidt, H; Schmidt, M; Schmidt, R; Soininen, H; Thornton, TA; Tosto, G; Tzourio, C; van der Lee, SJ; van Duijn, CM; Vardarajan, B; Wang, W; Wijsman, E; Wilson, RK; Witten, D; Worley, KC; Zhang, X; Alzheimer’s Disease Sequencing Project; Bellenguez, C; Lambert, JC; Kurki, MI; Palotie, A; Daly, M; Boerwinkle, E; Lunetta, KL; Destefano, AL; Dupuis, J; Martin, ER; Schellenberg, GD; Seshadri, S; Naj, AC; Fornage, M; Farrer, LA Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation.
Mol Psychiatry. 2018; [OPEN ACCESS]
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Brcic, L; Vlacic, G; Quehenberger, F; Kern, I Reproducibility of Malignant Pleural Mesothelioma Histopathologic Subtyping.
Arch Pathol Lab Med. 2018; 142(6):747-752
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Buder, A; Hochmair, MJ; Schwab, S; Bundalo, T; Schenk, P; Errhalt, P; Mikes, RE; Absenger, G; Patocka, K; Baumgartner, B; Setinek, U; Burghuber, OC; Prosch, H; Pirker, R; Filipits, M Cell-Free Plasma DNA-Guided Treatment With Osimertinib in Patients With Advanced EGFR-Mutated NSCLC.
J THORAC ONCOL. 2018; 13(6): 821-830.
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Enko, D; Harringer, S; Oberkanins, C; Pühringer, H; Halwachs-Baumann, G; Kriegshäuser, G SLCO1B1 c.521T>C Genotyping in the Austrian Population Using 2 Commercial Real-Time Polymerase Chain Reaction Assays: An Implementation Study.
Pharmacology. 2018; 102(1-2): 88-90.
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Enko, D; Wagner, H; Kriegshäuser, G; Brandmayr, W; Halwachs-Baumann, G; Schnedl, WJ; Zelzer, S; Mangge, H; Meinitzer, A Assessment of tryptophan metabolism and signs of depression in individuals with carbohydrate malabsorption.
Psychiatry Res. 2018; 262(1):595-599
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Harripaul, R; Vasli, N; Mikhailov, A; Rafiq, MA; Mittal, K; Windpassinger, C; Sheikh, TI; Noor, A; Mahmood, H; Downey, S; Johnson, M; Vleuten, K; Bell, L; Ilyas, M; Khan, FS; Khan, V; Moradi, M; Ayaz, M; Naeem, F; Heidari, A; Ahmed, I; Ghadami, S; Agha, Z; Zeinali, S; Qamar, R; Mozhdehipanah, H; John, P; Mir, A; Ansar, M; French, L; Ayub, M; Vincent, JB Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families.
Mol Psychiatry. 2018; 23(4):973-984
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Hassan, AM; Mancano, G; Kashofer, K; Fröhlich, EE; Matak, A; Mayerhofer, R; Reichmann, F; Olivares, M; Neyrinck, AM; Delzenne, NM; Claus, SP; Holzer, P High-fat diet induces depression-like behaviour in mice associated with changes in microbiome, neuropeptide Y, and brain metabolome.
Nutr Neurosci. 2018; 1-17
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Heits, N; Brosch, M; Herrmann, A; Behrens, R; Röcken, C; Schrem, H; Kaltenborn, A; Klempnauer, J; Kreipe, HH; Reichert, B; Lenschow, C; Wilms, C; Vogel, T; Wolters, H; Wardelmann, E; Seehofer, D; Buch, S; Zeissig, S; Pannach, S; Raschzok, N; Dietel, M; von Schoenfels, W; Hinz, S; Teufel, A; Evert, M; Franke, A; Becker, T; Braun, F; Hampe, J; Schafmayer, C Evolutionary Distance Predicts Recurrence After Liver Transplantation in Multifocal Hepatocellular Carcinoma.
Transplantation. 2018; 102(10): e424-e430-e424-e430.
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Hofving, T; Arvidsson, Y; Almobarak, B; Inge, L; Pfragner, R; Persson, M; Stenman, G; Johanson, V; Nilsson, O The Neuroendocrine Phenotype, Genomic Profile, and Therapeutic Sensitivity of GEPNET Cell Lines
NEUROENDOCRINOLOGY. 2018; 106: 48-48.-15th Annual ENETS Conference for the Diagnosis and Treatment of Neuroendocrine Tumor Disease; MAR 07-09, 2018; Barcelona, SPAIN. [Oral Communication]
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Hofving, T; Arvidsson, Y; Almobarak, B; Inge, L; Pfragner, R; Persson, M; Stenman, G; Kristiansson, E; Johanson, V; Nilsson, O The neuroendocrine phenotype, genomic profile and therapeutic sensitivity of GEPNET cell lines.
ENDOCR-RELAT CANCER. 2018; 25(3): 367-380. [OPEN ACCESS]
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Kimbacher, C; Paar, C; Freystetter, A; Berg, J Cell Line Controls for the Genotyping of a Spectrum of Human Single Nucleotide Polymorphisms in the Clinical Laboratory
CLIN LAB. 2018; 64(5): 823-834. [OPEN ACCESS]
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Pflanzl-Knizacek, L; Bergmoser, K; Mattersdorfer, K; Schilcher, G; Baumgartner, C Development of a Clinical Decision Support System in Intensive Care.
Stud Health Technol Inform. 2018; 248: 247-254.
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Schöllnast, H Radiological characterization of chronic inflammatory bowel disease].
Radiologe. 2018; 58(4): 312-319.
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Truschnegg, A; Acham, S; Kqiku, L; Jakse, N; Beham, A Ectomesenchymal chondromyxoid tumor: a comprehensive updated review of the literature and case report.
Int J Oral Sci. 2018; 10(1): 4-4. [OPEN ACCESS]
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Vaes, AW; Spruit, MA; Theunis, J; Goswami, N; Vanfleteren, LE; Franssen, FME; Wouters, EFM; De Boever, P Looking into the eye of patients with chronic obstructive pulmonary disease: an opportunity for better microvascular profiling of these complex patients.
Acta Ophthalmol. 2018; 96(6): 539-549.
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Wolfesberger, B; Fuchs-Baumgartinger, A; Greß, V; Hammer, SE; Gradner, G; Knödl, K; Tichy, A; Rütgen, BC; Beham-Schmid, C World Health Organisation Classification of Lymphoid Tumours in Veterinary and Human Medicine: a Comparative Evaluation of Gastrointestinal Lymphomas in 61 Cats.
J COMP PATHOL. 2018; 159(1): 1-10.
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2017

Binder, E; Loinger, M; Mühlbacher, A; Edlinger, M; Steichen, E; Meraner, D; Loacker, L; Weigel, G; Müller, T; Fröhlich-Reiterer, E; Hofer, SE Genotyping of coeliac-specific human leucocyte antigen in children with type 1 diabetes: does this screening method make sense?
Arch Dis Child. 2017; 102(7):603-606
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Egger, J; Gall, M; Tax, A; Ücal, M; Zefferer, U; Li, X; von Campe, G; Schäfer, U; Schmalstieg, D; Chen, X Interactive reconstructions of cranial 3D implants under MeVisLab as an alternative to commercial planning software.
PLoS One. 2017; 12(3):e0172694-e0172694 [OPEN ACCESS]
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Giese, AK; Schirmer, MD; Donahue, KL; Cloonan, L; Irie, R; Winzeck, S; Bouts, MJRJ; McIntosh, EC; Mocking, SJ; Dalca, AV; Sridharan, R; Xu, H; Frid, P; Giralt-Steinhauer, E; Holmegaard, L; Roquer, J; Wasselius, J; Cole, JW; McArdle, PF; Broderick, JP; Jimenez-Conde, J; Jern, C; Kissela, BM; Kleindorfer, DO; Lemmens, R; Lindgren, A; Meschia, JF; Rundek, T; Sacco, RL; Schmidt, R; Sharma, P; Slowik, A; Thijs, V; Woo, D; Worrall, BB; Kittner, SJ; Mitchell, BD; Rosand, J; Golland, P; Wu, O; Rost, NS Design and rationale for examining neuroimaging genetics in ischemic stroke: The MRI-GENIE study.
Neurol Genet. 2017; 3(5):e180-e180 [OPEN ACCESS]
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Hladicz, A; Kittinger, C; Zarfel, G Tigecycline Resistant Klebsiella pneumoniae Isolated from Austrian River Water.
Int J Environ Res Public Health. 2017; 14(10): [OPEN ACCESS]
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Jajić, I; Benčić, A; Siroglavić, M; Zarfel, G; Ružić, B; Pezelj, I; Bedenić, B Klebsiella Pneumoniaeoxa-48 in a Urology Patient: Case Report
Acta Clin Croat. 2017; 56(1):166-171 (- Case Report)
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Kägi, G; Ruge, D; Brugger, F; Katschnig, P; Sauter, R; Fiorio, M; Tinazzi, M; Rothwell, J; Bhatia, KP Endophenotyping in idiopathic adult onset cervical dystonia.
Clin Neurophysiol. 2017; 128(7):1142-1147
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Kessler, HH; Stelzl, E Profile of Roche's cobas® HCV tests.
Expert Rev Mol Diagn. 2017; 17(4):311-319
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Lax, SF Pathology of Endometrial Carcinoma.
Adv Exp Med Biol. 2017; 943(4):75-96
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Lucas, JS; Barbato, A; Collins, SA; Goutaki, M; Behan, L; Caudri, D; Dell, S; Eber, E; Escudier, E; Hirst, RA; Hogg, C; Jorissen, M; Latzin, P; Legendre, M; Leigh, MW; Midulla, F; Nielsen, KG; Omran, H; Papon, JF; Pohunek, P; Redfern, B; Rigau, D; Rindlisbacher, B; Santamaria, F; Shoemark, A; Snijders, D; Tonia, T; Titieni, A; Walker, WT; Werner, C; Bush, A; Kuehni, CE European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia.
Eur Respir J. 2017; 49(1): [OPEN ACCESS]
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Obasi, A; Nwachukwu, S; Ugoji, E; Kohler, C; Göhler, A; Balau, V; Pfeifer, Y; Steinmetz, I Extended-Spectrum β-Lactamase-Producing Klebsiella pneumoniae from Pharmaceutical Wastewaters in South-Western Nigeria.
Microb Drug Resist. 2017; 23(8):1013-1018
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Phuah, CL; Dave, T; Malik, R; Raffeld, MR; Ayres, AM; Goldstein, JN; Viswanathan, A; Greenberg, SM; Jagiella, JM; Hansen, BM; Norrving, B; Jimenez-Conde, J; Roquer, J; Pichler, A; Enzinger, C; Montaner, J; Fernandez-Cadenas, I; Lindgren, A; Slowik, A; Schmidt, R; Biffi, A; Rost, N; Langefeld, CD; Markus, HS; Mitchell, BD; Worrall, BB; Kittner, SJ; Woo, D; Dichgans, M; Rosand, J; Anderson, CD; METASTROKE; NINDS-SiGN Consortium; International Stroke Genetics Consortium Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke.
Brain. 2017; 140(10):2663-2672 [OPEN ACCESS]
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Redin, C; Brand, H; Collins, RL; Kammin, T; Mitchell, E; Hodge, JC; Hanscom, C; Pillalamarri, V; Seabra, CM; Abbott, MA; Abdul-Rahman, OA; Aberg, E; Adley, R; Alcaraz-Estrada, SL; Alkuraya, FS; An, Y; Anderson, MA; Antolik, C; Anyane-Yeboa, K; Atkin, JF; Bartell, T; Bernstein, JA; Beyer, E; Blumenthal, I; Bongers, EM; Brilstra, EH; Brown, CW; Brüggenwirth, HT; Callewaert, B; Chiang, C; Corning, K; Cox, H; Cuppen, E; Currall, BB; Cushing, T; David, D; Deardorff, MA; Dheedene, A; D'Hooghe, M; de Vries, BB; Earl, DL; Ferguson, HL; Fisher, H; FitzPatrick, DR; Gerrol, P; Giachino, D; Glessner, JT; Gliem, T; Grady, M; Graham, BH; Griffis, C; Gripp, KW; Gropman, AL; Hanson-Kahn, A; Harris, DJ; Hayden, MA; Hill, R; Hochstenbach, R; Hoffman, JD; Hopkin, RJ; Hubshman, MW; Innes, AM; Irons, M; Irving, M; Jacobsen, JC; Janssens, S; Jewett, T; Johnson, JP; Jongmans, MC; Kahler, SG; Koolen, DA; Korzelius, J; Kroisel, PM; Lacassie, Y; Lawless, W; Lemyre, E; Leppig, K; Levin, AV; Li, H; Li, H; Liao, EC; Lim, C; Lose, EJ; Lucente, D; Macera, MJ; Manavalan, P; Mandrile, G; Marcelis, CL; Margolin, L; Mason, T; Masser-Frye, D; McClellan, MW; Mendoza, CJ; Menten, B; Middelkamp, S; Mikami, LR; Moe, E; Mohammed, S; Mononen, T; Mortenson, ME; Moya, G; Nieuwint, AW; Ordulu, Z; Parkash, S; Pauker, SP; Pereira, S; Perrin, D; Phelan, K; Aguilar, RE; Poddighe, PJ; Pregno, G; Raskin, S; Reis, L; Rhead, W; Rita, D; Renkens, I; Roelens, F; Ruliera, J; Rump, P; Schilit, SL; Shaheen, R; Sparkes, R; Spiegel, E; Stevens, B; Stone, MR; Tagoe, J; Thakuria, JV; van Bon, BW; van de Kamp, J; van Der Burgt, I; van Essen, T; van Ravenswaaij-Arts, CM; van Roosmalen, MJ; Vergult, S; Volker-Touw, CM; Warburton, DP; Waterman, MJ; Wiley, S; Wilson, A; Yerena-de Vega, MC; Zori, RT; Levy, B; Brunner, HG; de Leeuw, N; Kloosterman, WP; Thorland, EC; Morton, CC; Gusella, JF; Talkowski, ME The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.
Nat Genet. 2017; 49(1):36-45 [OPEN ACCESS]
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Sims, R; van der Lee, SJ; Naj, AC; Bellenguez, C; Badarinarayan, N; Jakobsdottir, J; Kunkle, BW; Boland, A; Raybould, R; Bis, JC; Martin, ER; Grenier-Boley, B; Heilmann-Heimbach, S; Chouraki, V; Kuzma, AB; Sleegers, K; Vronskaya, M; Ruiz, A; Graham, RR; Olaso, R; Hoffmann, P; Grove, ML; Vardarajan, BN; Hiltunen, M; Nöthen, MM; White, CC; Hamilton-Nelson, KL; Epelbaum, J; Maier, W; Choi, SH; Beecham, GW; Dulary, C; Herms, S; Smith, AV; Funk, CC; Derbois, C; Forstner, AJ; Ahmad, S; Li, H; Bacq, D; Harold, D; Satizabal, CL; Valladares, O; Squassina, A; Thomas, R; Brody, JA; Qu, L; Sánchez-Juan, P; Morgan, T; Wolters, FJ; Zhao, Y; Garcia, FS; Denning, N; Fornage, M; Malamon, J; Naranjo, MCD; Majounie, E; Mosley, TH; Dombroski, B; Wallon, D; Lupton, MK; Dupuis, J; Whitehead, P; Fratiglioni, L; Medway, C; Jian, X; Mukherjee, S; Keller, L; Brown, K; Lin, H; Cantwell, LB; Panza, F; McGuinness, B; Moreno-Grau, S; Burgess, JD; Solfrizzi, V; Proitsi, P; Adams, HH; Allen, M; Seripa, D; Pastor, P; Cupples, LA; Price, ND; Hannequin, D; Frank-García, A; Levy, D; Chakrabarty, P; Caffarra, P; Giegling, I; Beiser, AS; Giedraitis, V; Hampel, H; Garcia, ME; Wang, X; Lannfelt, L; Mecocci, P; Eiriksdottir, G; Crane, PK; Pasquier, F; Boccardi, V; Henández, I; Barber, RC; Scherer, M; Tarraga, L; Adams, PM; Leber, M; Chen, Y; Albert, MS; Riedel-Heller, S; Emilsson, V; Beekly, D; Braae, A; Schmidt, R; Blacker, D; Masullo, C; Schmidt, H; Doody, RS; Spalletta, G; Longstreth, WT; Fairchild, TJ; Bossù, P; Lopez, OL; Frosch, MP; Sacchinelli, E; Ghetti, B; Yang, Q; Huebinger, RM; Jessen, F; Li, S; Kamboh, MI; Morris, J; Sotolongo-Grau, O; Katz, MJ; Corcoran, C; Dunstan, M; Braddel, A; Thomas, C; Meggy, A; Marshall, R; Gerrish, A; Chapman, J; Aguilar, M; Taylor, S; Hill, M; Fairén, MD; Hodges, A; Vellas, B; Soininen, H; Kloszewska, I; Daniilidou, M; Uphill, J; Patel, Y; Hughes, JT; Lord, J; Turton, J; Hartmann, AM; Cecchetti, R; Fenoglio, C; Serpente, M; Arcaro, M; Caltagirone, C; Orfei, MD; Ciaramella, A; Pichler, S; Mayhaus, M; Gu, W; Lleó, A; Fortea, J; Blesa, R; Barber, IS; Brookes, K; Cupidi, C; Maletta, RG; Carrell, D; Sorbi, S; Moebus, S; Urbano, M; Pilotto, A; Kornhuber, J; Bosco, P; Todd, S; Craig, D; Johnston, J; Gill, M; Lawlor, B; Lynch, A; Fox, NC; Hardy, J; ARUK Consortium; Albin, RL; Apostolova, LG; Arnold, SE; Asthana, S; Atwood, CS; Baldwin, CT; Barnes, LL; Barral, S; Beach, TG; Becker, JT; Bigio, EH; Bird, TD; Boeve, BF; Bowen, JD; Boxer, A; Burke, JR; Burns, JM; Buxbaum, JD; Cairns, NJ; Cao, C; Carlson, CS; Carlsson, CM; Carney, RM; Carrasquillo, MM; Carroll, SL; Diaz, CC; Chui, HC; Clark, DG; Cribbs, DH; Crocco, EA; DeCarli, C; Dick, M; Duara, R; Evans, DA; Faber, KM; Fallon, KB; Fardo, DW; Farlow, MR; Ferris, S; Foroud, TM; Galasko, DR; Gearing, M; Geschwind, DH; Gilbert, JR; Graff-Radford, NR; Green, RC; Growdon, JH; Hamilton, RL; Harrell, LE; Honig, LS; Huentelman, MJ; Hulette, CM; Hyman, BT; Jarvik, GP; Abner, E; Jin, LW; Jun, G; Karydas, A; Kaye, JA; Kim, R; Kowall, NW; Kramer, JH; LaFerla, FM; Lah, JJ; Leverenz, JB; Levey, AI; Li, G; Lieberman, AP; Lunetta, KL; Lyketsos, CG; Marson, DC; Martiniuk, F; Mash, DC; Masliah, E; McCormick, WC; McCurry, SM; McDavid, AN; McKee, AC; Mesulam, M; Miller, BL; Miller, CA; Miller, JW; Morris, JC; Murrell, JR; Myers, AJ; O'Bryant, S; Olichney, JM; Pankratz, VS; Parisi, JE; Paulson, HL; Perry, W; Peskind, E; Pierce, A; Poon, WW; Potter, H; Quinn, JF; Raj, A; Raskind, M; Reisberg, B; Reitz, C; Ringman, JM; Robe ... Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.
Nat Genet. 2017; 49(9):1373-1384 [OPEN ACCESS]
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Skrabl-Baumgartner, A; Christine Hauer, A; Erwa, W; Jahnel, J HLA genotyping as first-line screening tool for coeliac disease in children with juvenile idiopathic arthritis.
Arch Dis Child. 2017; 102(7):607-611
Web of Science PubMed FullText FullText_MUG

 

Stelzl, E; Appel, HM; Mehta, R; Marins, EG; Berg, J; Paar, C; Zurl, H; Santner, BI; Kessler, HH Evaluation of the new cobas® HCV genotyping test based on real-time PCRs of three different HCV genome regions.
Clin Chem Lab Med. 2017; 55(4):517-521 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Stelzl, E; Haas, B; Bauer, B; Zhang, S; Fiss, EH; Hillman, G; Hamilton, AT; Mehta, R; Heil, ML; Marins, EG; Santner, BI; Kessler, HH First identification of a recombinant form of hepatitis C virus in Austrian patients by full-genome next generation sequencing.
PLoS One. 2017; 12(7):e0181273-e0181273 [OPEN ACCESS]
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Thijs, V; Grittner, U; Fazekas, F; McCabe, DJH; Giese, AK; Kessler, C; Martus, P; Norrving, B; Ringelstein, EB; Schmidt, R; Tanislav, C; Putaala, J; Tatlisumak, T; von Sarnowski, B; Rolfs, A; Enzinger, C; Stroke in Fabry (SIFAP1) Investigators Dolichoectasia and Small Vessel Disease in Young Patients With Transient Ischemic Attack and Stroke.
Stroke. 2017; 48(9):2361-2367
Web of Science PubMed FullText FullText_MUG

 

Ulrich, S; Matzhold, E; Posch, U; Schlenke, P; Helmberg, W HLA-DRB3*02:61Q , a novel HLA-DRB3 allele identified in a volunteer bone marrow donor.
HLA. 2017; 90(3): 186-187.
Web of Science PubMed FullText FullText_MUG

 

Vaes, AW; Spruit, MA; Theunis, J; Goswami, N; Vanfleteren, LE; Franssen, FME; Wouters, EFM; De Boever, P Endothelial function in patients with chronic obstructive pulmonary disease: a systematic review of studies using flow mediated dilatation.
Expert Rev Respir Med. 2017; 11(12):1021-1031
Web of Science PubMed FullText FullText_MUG

 

Wolf, J; Petroff, D; Richter, T; Auth, MKH; Uhlig, HH; Laass, MW; Lauenstein, P; Krahl, A; Händel, N; de Laffolie, J; Hauer, AC; Kehler, T; Flemming, G; Schmidt, F; Rodrigues, A; Hasenclever, D; Mothes, T Validation of Antibody-Based Strategies for Diagnosis of Pediatric Celiac Disease Without Biopsy.
Gastroenterology. 2017; 153(2):410-419 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

2016

Bedenić, B; Firis, N; Elveđi-Gašparović, V; Krilanović, M; Matanović, K; Štimac, I; Luxner, J; Vraneš, J; Meštrović, T; Zarfel, G; Grisold, A Emergence of multidrug-resistant Proteus mirabilis in a long-term care facility in Croatia.
Wien Klin Wochenschr. 2016; 128(11-12):404-413
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Bedenić, B; Sardelić, S; Luxner, J; Bošnjak, Z; Varda-Brkić, D; Lukić-Grlić, A; Mareković, I; Frančula-Zaninović, S; Krilanović, M; Šijak, D; Grisold, A; Zarfel, G Molecular characterization of class b carbapenemases in advanced stage of dissemination and emergence of class d carbapenemases in Enterobacteriaceae from Croatia.
Infect Genet Evol. 2016; 43(3):74-82
Web of Science PubMed FullText FullText_MUG

 

Endris, V; Stenzinger, A; Pfarr, N; Penzel, R; Möbs, M; Lenze, D; Darb-Esfahani, S; Hummel, M; Sabine-Merkelbach-Bruse, M; Jung, A; Lehmann, U; Kreipe, H; Kirchner, T; Büttner, R; Jochum, W; Höfler, G; Dietel, M; Weichert, W; Schirmacher, P NGS-based BRCA1/2 mutation testing of high-grade serous ovarian cancer tissue: results and conclusions of the first international round robin trial.
Virchows Arch. 2016; 468(6):697-705
Web of Science PubMed FullText FullText_MUG

 

Enko, D; Kriegshäuser, G; Stolba, R; Mangge, H; Brandstetter, D; Mayr, N; Forstner, T; Halwachs-Baumann, G Assessment of vitamin D status and serum CrossLaps levels in adults with primary lactose malabsorption.
Eur J Clin Nutr. 2016; 70(9):1000-1003
Web of Science PubMed FullText FullText_MUG

 

Enko, D; Pollheimer, V; Németh, S; Pühringer, H; Stolba, R; Halwachs-Baumann, G; Kriegshäuser, G Lactase Non-Persistence Genotyping: Comparison of Two Real-Time PCR Assays and Assessment of Concomitant Fructose/Sorbitol Malabsorption Rates.
Clin Lab. 2016; 62(4):727-730 [OPEN ACCESS]
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Holtfreter, S; Grumann, D; Balau, V; Barwich, A; Kolata, J; Goehler, A; Weiss, S; Holtfreter, B; Bauerfeind, SS; Döring, P; Friebe, E; Haasler, N; Henselin, K; Kühn, K; Nowotny, S; Radke, D; Schulz, K; Schulz, SR; Trübe, P; Vu, CH; Walther, B; Westphal, S; Cuny, C; Witte, W; Völzke, H; Grabe, HJ; Kocher, T; Steinmetz, I; Bröker, BM Molecular Epidemiology of Staphylococcus aureus in the General Population in Northeast Germany: Results of the Study of Health in Pomerania (SHIP-TREND-0).
J Clin Microbiol. 2016; 54(11):2774-2785 [OPEN ACCESS]
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Juric, MK; Ghimire, S; Ogonek, J; Weissinger, EM; Holler, E; van Rood, JJ; Oudshoorn, M; Dickinson, A; Greinix, HT Milestones of Hematopoietic Stem Cell Transplantation - From First Human Studies to Current Developments
FRONT IMMUNOL. 2016; 7: UNSP 470 [OPEN ACCESS]
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Khan, MA; Mohan, S; Zubair, M; Windpassinger, C Homozygosity mapping identified a novel protein truncating mutation (p.Ser100Leufs*24) of the BBS9 gene in a consanguineous Pakistani family with Bardet Biedl syndrome.
BMC Med Genet. 2016; 17(6): 10-10. [OPEN ACCESS]
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Konstantiniuk, P; Grisold, A; Schramayer, G; Santler, SC; Koter, S; Cohnert, T Impact of Staphylococcus aureus protein A (spa) genetic typing in cases of prosthetic shunt graft infections.
Gefasschirurgie. 2016; 21(Suppl 2):59-62 [OPEN ACCESS]
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