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Scientific Reports|December 3, 2015
Conserved targeting information in mammalian and fungal peroxisomal tail-anchored proteinsJudith Buentzel, Fabio Vilardi, Amelie Lotz-Havla, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|June 23, 2026
Serum neurofilament light chain in paediatric patients treated with natalizumab for highly active multiple sclerosisBrenda Huppke, Marie-Christine Reinert, Wiebke Stark, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 21, 2006
Treatment of epilepsy in Rett syndromePeter Huppke, Karola Köhler, Knut Brockmann, et al.Journal of Structural Biology|July 12, 2011
The unusual extended C-terminal helix of the peroxisomal α/β-hydrolase Lpx1 is involved in dimer contacts but dispensable for dimerizationSven Thoms, Julia Hofhuis, Christian Thöing, et al.Human Mutation|December 25, 2007
Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiencyLars Schlotawa, Robert Steinfeld, Kurt von Figura, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|July 6, 2013
Pediatric onset multiple sclerosis: McDonald criteria 2010 and the contribution of spinal cord MRIHannah-Maria Hummel, Wolfgang Brück, Steffi Dreha-Kulaczewski, et al.Plos One|December 27, 2014
Characterization of the MeCP2R168X knockin mouse model for Rett syndromeEike Wegener, Cornelia Brendel, Andre Fischer, et al.Archives of Neurology|December 10, 2008
Natalizumab use in pediatric multiple sclerosisPeter Huppke, Wiebke Stark, Claudia Zürcher, et al.American Journal of Medical Genetics. Part A|June 24, 2004
Mutation analysis of the M6b gene in patients with Pelizaeus-Merzbacher-like syndromeMarco Henneke, Lars-Erik Wehner, Hans Christian Hennies, et al.Pediatric Neurology|December 12, 2022
Association of Overweight and Obesity With Bell Palsy in ChildrenVivian Breitling, Andreas Leha, Stina Schiller, et al.Pageof 17