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Identification of new molecular alterations in fatal familial insomnia.
Llorens F, Thüne K, Schmitz M, Ansoleaga B, Frau-Méndez MA, Cramm M, Tahir W, Gotzmann N, Berjaoui S, Carmona M, Silva CJ, Fernandez-Vega I, José Zarranz J, Zerr I, Ferrer I. Llorens F, et al. Among authors: schmitz m. Hum Mol Genet. 2016 Jun 15;25(12):2417-2436. doi: 10.1093/hmg/ddw108. Epub 2016 Apr 7. Hum Mol Genet. 2016. PMID: 27056979
Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
Schmitz M, Lüllmann K, Zafar S, Ebert E, Wohlhage M, Oikonomou P, Schlomm M, Mitrova E, Beekes M, Zerr I. Schmitz M, et al. Neurobiol Aging. 2014 May;35(5):1177-88. doi: 10.1016/j.neurobiolaging.2013.11.010. Epub 2013 Nov 16. Neurobiol Aging. 2014. PMID: 24360565
Characteristic CSF prion seeding efficiency in humans with prion diseases.
Cramm M, Schmitz M, Karch A, Zafar S, Varges D, Mitrova E, Schroeder B, Raeber A, Kuhn F, Zerr I. Cramm M, et al. Among authors: schmitz m. Mol Neurobiol. 2015 Feb;51(1):396-405. doi: 10.1007/s12035-014-8709-6. Epub 2014 May 9. Mol Neurobiol. 2015. PMID: 24809690 Free PMC article.
1,397 results