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Ophthalmology|July 6, 2004
Ocular features of the congenital cataracts facial dysmorphism neuropathy syndromeAndrea Müllner-Eidenböck, Elisabeth Moser, Nina Klebermass, et al.BMC Musculoskeletal Disorders|January 18, 2013
A new web-based method for automated analysis of muscle histologyCordula Pertl, Markus Eblenkamp, Anja Pertl, et al.Neurology|September 5, 2014
Long-term follow-up in patients with CCFDN syndromeMaggie C Walter, Günther Bernert, Uta Zimmermann, et al.The Cochrane Database of Systematic Reviews|June 5, 2022
Treatment for inclusion body myositisMichael R Rose, Katherine Jones, Kevin Leong, et al.Journal of Neurology|July 20, 2004
The long-term outcome of anti-Jo-1-positive inflammatory myopathiesMichael Späth, Mira Schröder, Beate Schlotter-Weigel, et al.Orphanet Journal of Rare Diseases|May 6, 2016
Disease burden of spinal muscular atrophy in GermanyConstanze Klug, Olivia Schreiber-Katz, Simone Thiele, et al.Orphanet Journal of Rare Diseases|December 19, 2014
Comparative cost of illness analysis and assessment of health care burden of Duchenne and Becker muscular dystrophies in GermanyOlivia Schreiber-Katz, Constanze Klug, Simone Thiele, et al.Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|May 20, 2020
[Patient registries for rare diseases in Germany: concept paper of the NAMSE strategy group]Holger Storf, Jürgen Stausberg, Gerhard Kindle, et al.Orphanet Journal of Rare Diseases|June 26, 2019
De-duplicating patient records from three independent data sources reveals the incidence of rare neuromuscular disorders in GermanyKirsten König, Astrid Pechmann, Simone Thiele, et al.Der Nervenarzt|November 5, 2017
[Spinal muscular atrophy : Time for newborn screening?]K Vill, A Blaschek, U Schara, et al.Pageof 16