Showing results (1-10 of 35) with videos related to
Sort By:
Pageof 4
Biochimica Et Biophysica Acta|May 27, 2008
Caenorhabditis elegans as a model for lysosomal storage disordersGert de Voer, Dorien Peters, Peter E M TaschnerBiochimica Et Biophysica Acta|October 20, 2006
Characterizing pathogenic processes in Batten disease: use of small eukaryotic model systemsSeasson N Phillips, Neda Muzaffar, Sandra Codlin, et al.Journal of Comparative Effectiveness Research|May 19, 2018
Healthcare utilization and costs of multiple sclerosis patients in the Netherlands: a healthcare claims database studyServaas Buijs, Marieke Krol, Gert de VoerPatient Preference and Adherence|July 27, 2017
Patient adherence to subcutaneous IFN beta-1a injections using the RebiSmart® injection device: a retrospective real-world study among Dutch and German patients with multiple sclerosisMarieke Krol, Gert de Voer, Ulrike OsowskiMolecular Biology of the Cell|July 11, 2008
Drosophila Sec16 mediates the biogenesis of tER sites upstream of Sar1 through an arginine-rich motifViorica Ivan, Gert de Voer, Despina Xanthakis, et al.Human Mutation|February 11, 2011
Describing structural changes by extending HGVS sequence variation nomenclaturePeter E M Taschner, Johan T den DunnenHuman Mutation|December 28, 2016
Synonymous Somatic Variants in Human Cancer Are Not Infamous: A Plea for Full Disclosure in Databases and PublicationsThierry Soussi, Peter E M Taschner, Yardena SamuelsHuman Mutation|April 15, 2014
Recommendations for analyzing and reporting TP53 gene variants in the high-throughput sequencing eraThierry Soussi, Bernard Leroy, Peter E M TaschnerEneurologicalsci|June 23, 2022
The longitudinal relationship between fatigue, depression, anxiety, disability, and adherence with cognitive status in patients with early multiple sclerosis treated with interferon beta-1aHanne van Ballegooijen, Karin van der Hiele, Christian Enzinger, et al.BMC Medical Genetics|November 18, 2005
The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiencyJean-Pierre Bayley, Peter Devilee, Peter E M TaschnerPageof 4