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41.
Salminen, A.V. et al.: Reply to: Safety of dopamine agonists for treating restless legs syndrome. Mov. Disord. 34, 150-151 (2019)
42.
Riedhammer, K.M.* ; Leszinski, G.S.* ; Andres, S. ; Strobl-Wildemann, G.* & Wagner, M.: First replication that biallelic variants in FITM2 cause a complex deafness-dystonia syndrome. Mov. Disord. 33, 1665-1666 (2018)
43.
Winkelmann, J. et al.: Treatment of restless legs syndrome: Evidence-based review and implications for clinical practice (Revised 2017)§. Mov. Disord. 33, 1077-1091 (2018)
44.
Meles, S.K.* et al.: FDG PET, dopamine transporter SPECT, and olfaction: Combining biomarkers in REM sleep behavior disorder. Mov. Disord. 32, 1482-1486 (2017)
45.
Trenkwalder, C.* et al.: Ferric carboxymaltose in patients with restless legs syndrome and nonanemic iron deficiency: A randomized trial. Mov. Disord. 32, 1478-1482 (2017)
46.
Vill, K.* et al.: A homozygous splice variant in AP4S1 mimicking neurodegeneration with brain iron accumulation. Mov. Disord. 32, 797-799 (2017)
47.
Zech, M. et al.: KMT2B rare missense variants in generalized dystonia. Mov. Disord. 32, 1087-1091 (2017)
48.
Jochim, A.* ; Zech, M. ; Gora-Stahlberg, G.* ; Winkelmann, J. & Haslinger, B.*: The clinical phenotype of early-onset isolated dystonia caused by recessive COL6A3 mutations (DYT27). Mov. Disord. 31, 747-750 (2016)
49.
Zech, M. et al.: Clinical exome sequencing in early-onset generalized dystonia and large-scale resequencing follow-up. Mov. Disord. 32, 549-559 (2016)
50.
Nalls, M.A.* et al.: Genetic risk and age in Parkinson's disease: Continuum not stratum. Mov. Disord. 30, 850-854 (2015)
51.
Witoelar, A.W.* et al.: Genome wide pleiotropic study in 144,701 subjects reveals shared genetic variants between Parkinson's disease and immune-mediated diseases. Mov. Disord. 30, S412 (2015)
52.
Zech, M. ; Castrop, F.* ; Haslinger, B.* & Winkelmann, J.: Reply to letter: Novel compound heterozygous mutations in PRKRA cause pure dystonia. Mov. Disord. 30, 878–879 (2015)
53.
Zech, M. et al.: TOR1A, THAP1, and GNAL mutational screening in Austrian patients with primary isolated dystonia. Mov. Disord. 30, 1853–1854 (2015)
54.
Zech, M. et al.: Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls. Mov. Disord. 29, 143-147 (2014)
55.
Zech, M. et al.: DYT16 revisited: Exome sequencing identifies PRKRA mutations in a European dystonia family. Mov. Disord. 29, 1504-1510 (2014)
56.
Brockmann, K.* et al.: SNCA: Major genetic modifier of age at onset of Parkinson's disease. Mov. Disord. 28, 1217-1221 (2013)
57.
Hopfner, F. et al.: The role of SCARB2 as susceptibility factor in Parkinson's disease. Mov. Disord. 28, 538-540 (2013)
58.
Schulte, E.C. et al.: Mitochondrial membrane protein associated neurodegeneration: A novel variant of neurodegeneration with brain iron accumulation. Mov. Disord. 28, 224-227 (2013)
59.
Fulda, S. ; Beitinger, M.E. ; Reppermund, S. ; Winkelmann, J. & Wetter, T.C.: Short-term attention and verbal fluency is decreased in restless legs syndrome patients. Mov. Disord. 25, 2641-2648 (2010)
60.
Kowarik, M.C.* et al.: Myoclonus-dystonia in 18p deletion syndrome. Mov. Disord. 26, 560-561 (2010)
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