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PRRT2-related disorders: further PKD and ICCA cases and review of the literature.
Becker F, Schubert J, Striano P, Anttonen AK, Liukkonen E, Gaily E, Gerloff C, Müller S, Heußinger N, Kellinghaus C, Robbiano A, Polvi A, Zittel S, von Oertzen TJ, Rostasy K, Schöls L, Warner T, Münchau A, Lehesjoki AE, Zara F, Lerche H, Weber YG. Becker F, et al. Among authors: munchau a. J Neurol. 2013 May;260(5):1234-44. doi: 10.1007/s00415-012-6777-y. Epub 2013 Jan 9. J Neurol. 2013. PMID: 23299620 Review.
Modulation of motor cortex excitability induced by pinch grip repetition.
Gorsler A, Zittel S, Weiller C, Münchau A, Liepert J. Gorsler A, et al. Among authors: munchau a. J Neural Transm (Vienna). 2004 Aug;111(8):1005-16. doi: 10.1007/s00702-004-0139-6. Epub 2004 Apr 8. J Neural Transm (Vienna). 2004. PMID: 15254789 Clinical Trial.
Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit?
Hedrich K, Hagenah J, Djarmati A, Hiller A, Lohnau T, Lasek K, Grünewald A, Hilker R, Steinlechner S, Boston H, Kock N, Schneider-Gold C, Kress W, Siebner H, Binkofski F, Lencer R, Münchau A, Klein C. Hedrich K, et al. Among authors: munchau a. Arch Neurol. 2006 Jun;63(6):833-8. doi: 10.1001/archneur.63.6.833. Arch Neurol. 2006. PMID: 16769864
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak.
Weber YG, Storch A, Wuttke TV, Brockmann K, Kempfle J, Maljevic S, Margari L, Kamm C, Schneider SA, Huber SM, Pekrun A, Roebling R, Seebohm G, Koka S, Lang C, Kraft E, Blazevic D, Salvo-Vargas A, Fauler M, Mottaghy FM, Münchau A, Edwards MJ, Presicci A, Margari F, Gasser T, Lang F, Bhatia KP, Lehmann-Horn F, Lerche H. Weber YG, et al. Among authors: munchau a. J Clin Invest. 2008 Jun;118(6):2157-68. doi: 10.1172/JCI34438. J Clin Invest. 2008. PMID: 18451999 Free PMC article.
Severe Tangier disease with a novel ABCA1 gene mutation.
Schippling S, Orth M, Beisiegel U, Rosenkranz T, Vogel P, Münchau A, Hagel C, Seedorf U. Schippling S, et al. Among authors: munchau a. Neurology. 2008 Oct 28;71(18):1454-5. doi: 10.1212/01.wnl.0000327870.29639.20. Neurology. 2008. PMID: 18955690 No abstract available.
Sensory afferent inhibition within and between limbs in humans.
Bikmullina R, Bäumer T, Zittel S, Münchau A. Bikmullina R, et al. Among authors: munchau a. Clin Neurophysiol. 2009 Mar;120(3):610-8. doi: 10.1016/j.clinph.2008.12.003. Epub 2009 Jan 10. Clin Neurophysiol. 2009. PMID: 19136299
Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study.
Djarmati A, Schneider SA, Lohmann K, Winkler S, Pawlack H, Hagenah J, Brüggemann N, Zittel S, Fuchs T, Raković A, Schmidt A, Jabusch HC, Wilcox R, Kostić VS, Siebner H, Altenmüller E, Münchau A, Ozelius LJ, Klein C. Djarmati A, et al. Among authors: munchau a. Lancet Neurol. 2009 May;8(5):447-52. doi: 10.1016/S1474-4422(09)70083-3. Epub 2009 Apr 1. Lancet Neurol. 2009. PMID: 19345148
424 results