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Neurofilaments in the diagnosis of motoneuron diseases: a prospective study on 455 patients.
Steinacker P, Feneberg E, Weishaupt J, Brettschneider J, Tumani H, Andersen PM, von Arnim CA, Böhm S, Kassubek J, Kubisch C, Lulé D, Müller HP, Muche R, Pinkhardt E, Oeckl P, Rosenbohm A, Anderl-Straub S, Volk AE, Weydt P, Ludolph AC, Otto M. Steinacker P, et al. Among authors: muller hp. J Neurol Neurosurg Psychiatry. 2016 Jan;87(1):12-20. doi: 10.1136/jnnp-2015-311387. Epub 2015 Aug 21. J Neurol Neurosurg Psychiatry. 2016. PMID: 26296871
Open magnetic and electric graphic analysis.
Müller HP, DeCesaris I, DeMelis M, Marzetti L, Pasquarelli A, Erné SN, Ludolph AC, Kassubek J. Müller HP, et al. IEEE Eng Med Biol Mag. 2005 May-Jun;24(3):109-16. doi: 10.1109/memb.2005.1436468. IEEE Eng Med Biol Mag. 2005. PMID: 15971849
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons.
Braunstein KE, Eschbach J, Ròna-Vörös K, Soylu R, Mikrouli E, Larmet Y, René F, Gonzalez De Aguilar JL, Loeffler JP, Müller HP, Bucher S, Kaulisch T, Niessen HG, Tillmanns J, Fischer K, Schwalenstöcker B, Kassubek J, Pichler B, Stiller D, Petersen A, Ludolph AC, Dupuis L. Braunstein KE, et al. Among authors: muller hp. Hum Mol Genet. 2010 Nov 15;19(22):4385-98. doi: 10.1093/hmg/ddq361. Epub 2010 Aug 31. Hum Mol Genet. 2010. PMID: 20807776 Free PMC article.
369 results