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Kirschner, Janbernd; Bernert, Günther; v. der Hagen, Maja; Hahn, Andreas; Johannsen, Jessika; Klein, Andrea; Müller-Felber, Wolfgang; Ziegler, Andreas; Schara, Ulrike (2020). Gene therapy for spinal muscular atrophy with onasemnogene abeparvovec. Statement of the German Speaking Society of Neuropediatrics. Monatsschrift Kinderheilkunde, 168(10), pp. 938-941. Springer-Verlag 10.1007/s00112-020-00944-6
Nagy, Magdolna; Mastenbroek, Tom G; Mattheij, Nadine J A; de Witt, Susanne; Clemetson, Kenneth John; Kirschner, Janbernd; Schulz, Ansgar S; Vraetz, Thomas; Speckmann, Carsten; Braun, Attila; Cosemans, Judith M E M; Zieger, Barbara; Heemskerk, Johan W M (2018). Variable impairment of platelet functions in patients with severe, genetically linked immune deficiencies. Haematologica - the hematology journal, 103(3), pp. 540-549. Ferrata-Storti Foundation 10.3324/haematol.2017.176974
Rudnik-Schöneborn, Sabine; Senderek, Jan; Jen, Joanna C; Houge, Gunnar; Seeman, Pavel; Puchmajerová, Alena; Graul-Neumann, Luitgard; Seidel, Ulrich; Korinthenberg, Rudolf; Kirschner, Janbernd; Seeger, Jürgen; Ryan, Monique M; Muntoni, Francesco; Steinlin, Maja; Sztriha, Laszlo; Colomer, Jaume; Hübner, Christoph; Brockmann, Knut; Van Maldergem, Lionel; Schiff, Manuel; ... (2013). Pontocerebellar hypoplasia type 1: clinical spectrum and relevance of EXOSC3 mutations. Neurology, 80(5), pp. 438-46. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1212/WNL.0b013e31827f0f66
