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Kirschner

Prof. Kirschner

Prof. Dr.
Janbernd Kirschner

Department of Neuropediatrics and Muscle Disorders
Medical Director
Phone: 0049-761-270-43150

www.uniklinik-freiburg.de/kinderklinik

CV

  • 1989-1997 Studies of Medicine, Universities of Freiburg (DEU), Newcastle-upon-Tyne (UK), and Bern (CH)
  • 1997 Dissertation (Dr. med.), University Freiburg
  • 1997-2002 Residency in Pediatrics and Pediatric Neurology, University of Freiburg
  • 2002-2004 DFG Research Fellowship at The Children’s Hospital of Philadelphia, University of Pennsylvania
  • 2004-2017 (Senior) Consultant, Neuropediatrics, Medical Center – University of Freiburg
  • 2017-2019 Interim Medical Director, Department of Neuropediatrics and Muscle Disorders, Medical Center – University of Freiburg
  • 2019-2022 Full Professor (W3) and Medical Director, Department of Neuropediatrics, University Hospital Bonn
  • seit 2022 Full Professor (W3) and Medical Director, Department of Neuropediatrics and Muscle Disorders, Medical Center – University of Freiburg

Focus of research

  • Innovative treatments for neuromuscular diseases
  • Diagnostic approaches for Rare Diseases
  • Real-world evidence for Rare Diseases

Selected publications

  • Friese J, … Kirschner J. Safety Monitoring of Gene Therapy for Spinal Muscular Atrophy with Onasemnogene Abeparvovec -A Single Centre Experience. J Neuromuscul Dis. 2021;8:209-216.
  • Kirschner J, Cathomen T. Gene Therapy for Monogenic Inherited Disorders. Dtsch Arztebl Int. 2020 Dec 21;117(51-52):878-885.
  • Kirschner J, et al. European ad-hoc consensus statement on gene replacement therapy for spinal muscular atrophy. Eur J Paediatr Neurol. 2020;28:38-43.
  • Pechmann A, …, Kirschner J. SMArtCARE - A platform to collect real-life outcome data of patients with spinal muscular atrophy. Orphanet J Rare Dis. 2019 Jan 21:18.
  • Finkel RS, … Kirschner J, … De Vivo DC. Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy. N Engl J Med. 2017;377:1723-1732.

Research methods

  • Innovative treatments for neuromuscular diseases
  • Diagnostic approaches for Rare Diseases
  • Real-world evidence for Rare Diseases