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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. 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
Plasma total prion protein as a potential biomarker for neurodegenerative dementia: diagnostic accuracy in the spectrum of prion diseases.
Llorens F, Villar-Piqué A, Schmitz M, Diaz-Lucena D, Wohlhage M, Hermann P, Goebel S, Schmidt I, Glatzel M, Hauw JJ, Sikorska B, Liberski PP, Riggert J, Ferrer I, Zerr I. Llorens F, et al. Neuropathol Appl Neurobiol. 2020 Apr;46(3):240-254. doi: 10.1111/nan.12573. Epub 2019 Jul 19. Neuropathol Appl Neurobiol. 2020. PMID: 31216593
CSF biomarkers in neurodegenerative and vascular dementias.
Llorens F, Schmitz M, Ferrer I, Zerr I. Llorens F, et al. Prog Neurobiol. 2016 Mar-May;138-140:36-53. doi: 10.1016/j.pneurobio.2016.03.003. Epub 2016 Mar 22. Prog Neurobiol. 2016. PMID: 27016008 Review.
Hereditary Human Prion Diseases: an Update.
Schmitz M, Dittmar K, Llorens F, Gelpi E, Ferrer I, Schulz-Schaeffer WJ, Zerr I. Schmitz M, et al. Among authors: llorens f. Mol Neurobiol. 2017 Aug;54(6):4138-4149. doi: 10.1007/s12035-016-9918-y. Epub 2016 Jun 20. Mol Neurobiol. 2017. PMID: 27324792 Free article. Review.
134 results