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Doppler, K.* et al.: Association between probable REM sleep behavior disorder and increased dermal alpha-synuclein deposition in Parkinson's disease. Parkinsonism Relat. Disord. 99, 58-61 (2022)
Dzinovic, I. et al.: Genetic overlap between dystonia and other neurologic disorders: A study of 1,100 exomes. Parkinsonism Relat. Disord. 102, 1-6 (2022)
Dzinovic, I. ; Winkelmann, J. & Zech, M.: Genetic intersection between dystonia and neurodevelopmental disorders: Insights from genomic sequencing. Parkinsonism Relat. Disord. 102, 131-140 (2022)
Garavaglia, B.* et al.: AOPEP variants as a novel cause of recessive dystonia: Generalized dystonia and dystonia-parkinsonism. Parkinsonism Relat. Disord. 97, 52-56 (2022)
Škorvánek, M.* et al.: WARS2 mutations cause dopa-responsive early-onset parkinsonism and progressive myoclonus ataxia. Parkinsonism Relat. Disord. 94, 54-61 (2022)
Straccia, G.* et al.: ACTB gene mutation in combined Dystonia-Deafness syndrome with parkinsonism: Expanding the phenotype and highlighting the long-term GPi DBS outcome. Parkinsonism Relat. Disord. 104, 3-6 (2022)
Svorenova, T.* et al.: Dystonia as a prominent feature of TCF20-associated neurodevelopmental disorder: Expanding the phenotype. Parkinsonism Relat. Disord. 102, 89-91 (2022)
Amprosi, M.* et al.: The rare and the common: An Austrian DRPLA family harboring the European haplotype. Parkinsonism Relat. Disord. 87, 119-121 (2021)
Doppler, K.* et al.: Consistent skin alpha-synuclein positivity in REM sleep behavior disorder-A two center two-to-four-year follow-up study. Parkinsonism Relat. Disord. 86, 108-113 (2021)
Dzinovic, I. et al.: Dystonia as a prominent presenting feature in developmental and epileptic encephalopathies: A case series. Parkinsonism Relat. Disord. 90, 73-78 (2021)
Pavelekova, P.* et al.: Atypical presentations of DYT1 dystonia with acute craniocervical onset. Parkinsonism Relat. Disord. 83, 54-55 (2021)
Zech, M. et al.: Clinically relevant copy-number variants in exome sequencing data of patients with dystonia. Parkinsonism Relat. Disord. 84, 129-134 (2021)
Hopfner, F.* et al.: Private variants in PRKN are associated with late-onset Parkinson's disease. Parkinsonism Relat. Disord. 75, 24-26 (2020)
Necpál, J.* et al.: Severe paroxysmal dyskinesias without epilepsy in a RHOBTB2 mutation carrier. Parkinsonism Relat. Disord. 77, 87-88 (2020)
Zech, M. et al.: Recessive null-allele variants in MAG associated with spastic ataxia, nystagmus, neuropathy, and dystonia. Parkinsonism Relat. Disord. 77, 70-75 (2020)
Becker, A.* ; Faßbender, K.* ; Oertel, W.H. & Unger, M.M.*: A punch in the gut - Intestinal inflammation links environmental factors to neurodegeneration in Parkinson's disease. Parkinsonism Relat. Disord. 60, 43-45 (2019)
Chou, K.L.* et al.: The spectrum of "off" in Parkinson's disease: What have we learned over 40 years? Parkinsonism Relat. Disord. 51, 9-16 (2018)
Jochim, A.* et al.: Microstructural white matter abnormalities in patients with COL6A3 mutations (DYT27 dystonia). Parkinsonism Relat. Disord. 46, 74-78 (2018)
Ouled Amar Bencheikh, B.* et al.: LRRK2 protective haplotype and full sequencing study in REM sleep behavior disorder. Parkinsonism Relat. Disord. 52, 98-101 (2018)
Aridon, P.* et al.: A TRAPPC6B splicing variant associates to restless legs syndrome. Parkinsonism Relat. Disord. 31, 135-138 (2016)