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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: zerr i. 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
Molecular genetics of human prion diseases in Germany.
Windl O, Giese A, Schulz-Schaeffer W, Zerr I, Skworc K, Arendt S, Oberdieck C, Bodemer M, Poser S, Kretzschmar HA. Windl O, et al. Among authors: zerr i. Hum Genet. 1999 Sep;105(3):244-52. doi: 10.1007/s004399900124. Hum Genet. 1999. PMID: 10987652
Fatal familial insomnia: Clinical features and early identification.
Krasnianski A, Bartl M, Sanchez Juan PJ, Heinemann U, Meissner B, Varges D, Schulze-Sturm U, Kretzschmar HA, Schulz-Schaeffer WJ, Zerr I. Krasnianski A, et al. Among authors: zerr i. Ann Neurol. 2008 May;63(5):658-61. doi: 10.1002/ana.21358. Ann Neurol. 2008. PMID: 18360821
A proposal of new diagnostic pathway for fatal familial insomnia.
Krasnianski A, Sanchez Juan P, Ponto C, Bartl M, Heinemann U, Varges D, Schulz-Schaeffer WJ, Kretzschmar HA, Zerr I. Krasnianski A, et al. Among authors: zerr i. J Neurol Neurosurg Psychiatry. 2014 Jun;85(6):654-9. doi: 10.1136/jnnp-2013-305978. Epub 2013 Nov 18. J Neurol Neurosurg Psychiatry. 2014. PMID: 24249784 Free PMC article.
408 results