Klein, Andrea

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2019

Hafner, Patricia; Bonati, Ulrike; Klein, Andrea; Rubino, Daniela; Gocheva, Vanya; Schmidt, Simone; Schroeder, Jonas; Bernert, Günther; Laugel, Vincent; Steinlin, Maja; Capone, Andrea; Gloor, Monika; Bieri, Oliver; Hemkens, Lars G; Speich, Benjamin; Zumbrunn, Thomas; Gueven, Nuri; Fischer, Dirk (2019). Effect of Combination l-Citrulline and Metformin Treatment on Motor Function in Patients With Duchenne Muscular Dystrophy: A Randomized Clinical Trial. JAMA Network Open, 2(10), e1914171. American Medical Association 10.1001/jamanetworkopen.2019.14171

Papuc, Sorina M; Abela, Lucia; Steindl, Katharina; Begemann, Anaïs; Simmons, Thomas L; Schmitt, Bernhard; Zweier, Markus; Oneda, Beatrice; Socher, Eileen; Crowther, Lisa M; Wohlrab, Gabriele; Gogoll, Laura; Poms, Martin; Seiler, Michelle; Papik, Michael; Baldinger, Rosa; Baumer, Alessandra; Asadollahi, Reza; Kroell-Seger, Judith; Schmid, Regula; ... (2019). The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study. European journal of human genetics, 27(3), pp. 408-421. Nature Publishing Group 10.1038/s41431-018-0299-8

Nagy, S.; Schmidt, S.; Hafner, P.; Klein, Andrea; Rubino-Nacht, D.; Gocheva, V.; Bieri, O.; Vuillerot, C.; Bonati, U.; Fischer, D. (2019). Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy. Journal of visualized experiments, 143(143) MYJoVE Corporation 10.3791/58784

Sharkia, R.; Wierenga, K. J.; Kessel, A.; Azem, A.; Bertini, E.; Carrozzo, R.; Torraco, A.; Goffrini, P.; Ceccatelli Berti, C.; McCormick, M. E.; Plecko, B.; Klein, Andrea; Abela, L.; Hengel, H.; Schols, L.; Shalev, S.; Khayat, M.; Mahajnah, M.; Spiegel, R. (2019). Clinical, radiological, and genetic characteristics of 16 patients with ACO2 gene defects: Delineation of an emerging neurometabolic syndrome. Journal of inherited metabolic diseases, 42(2), pp. 264-275. Wiley 10.1002/jimd.12022

2018

Ivanyuk, Anton; García Segarra, Nuria; Buclin, Thierry; Klein, Andrea; Jacquier, David; Newman, Christopher J; Blötzer, Clemens Florian (2018). Myoglobinuria in two patients with Duchenne muscular dystrophy after treatment with zoledronate: a case-report and call for caution. Neuromuscular disorders, 28(10), pp. 865-867. Elsevier 10.1016/j.nmd.2018.08.004

Schmidt, Simone; Hafner, Patricia; Klein, Andrea; Rubino-Nacht, Daniela; Gocheva, Vanya; Schroeder, Jonas; Naduvilekoot Devasia, Arjith; Zuesli, Stephanie; Bernert, Guenther; Laugel, Vincent; Bloetzer, Clemens; Steinlin, Maja; Capone, Andrea; Gloor, Monika; Tobler, Patrick; Haas, Tanja; Bieri, Oliver; Zumbrunn, Thomas; Fischer, Dirk and Bonati, Ulrike (2018). Timed function tests, motor function measure, and quantitative thigh muscle MRI in ambulant children with Duchenne muscular dystrophy: A cross-sectional analysis. Neuromuscular disorders, 28(1), pp. 16-23. Elsevier 10.1016/j.nmd.2017.10.003

2017

Hennes, Eva-Maria; Baumann, Matthias; Schanda, Kathrin; Anlar, Banu; Bajer-Kornek, Barbara; Blaschek, Astrid; Brantner-Inthaler, Sigrid; Diepold, Katharina; Eisenkölbl, Astrid; Gotwald, Thaddäus; Kuchukhidze, Georgi; Gruber-Sedlmayr, Ursula; Häusler, Martin; Höftberger, Romana; Karenfort, Michael; Klein, Andrea; Koch, Johannes; Kraus, Verena; Lechner, Christian; Leiz, Steffen; ... (2017). Prognostic relevance of MOG antibodies in children with an acquired demyelinating syndrome. Neurology, 89(9), pp. 900-908. Lippincott Williams & Wilkins 10.1212/WNL.0000000000004312

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