PuSH - HMGU Publikationen https://push-zb.helmholtz-munich.de PuSH - Publikationen-Server des Helmholtz Zentrums München de-de <![CDATA[Al-Azzani, M.* et al. A novel α-synuclein K58N missense variant in a patient with Parkinson's disease. Mov. Disord., DOI: 10.1002/mds.70030 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75463&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75463&la=de Thu, 13 Nov 2025 00:00:00 +0000 <![CDATA[Harrer, P. et al. Expanding the allelic and clinical heterogeneity of movement disorders linked to defects of mitochondrial adenosine triphosphate synthase. Mov. Disord. 40, 1388-1400 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74199&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74199&la=de Sun, 11 May 2025 00:00:00 +0000 <![CDATA[Heger, L.M.* et al. Patient-derived neurons exhibit α-synuclein pathology and previously unrecognized major histocompatibility complex class I elevation in mitochondrial membrane protein-associated neurodegeneration. Mov. Disord., DOI: 10.1002/mds.70029 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75564&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75564&la=de Tue, 04 Nov 2025 00:00:00 +0000 <![CDATA[Keritam, O.* et al. Rediscovery of the tubulin β-4A p.Arg2Gly variant in whispering dysphonia: A report from Austria. Mov. Disord. 40, 1725-1726 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74801&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74801&la=de Wed, 28 May 2025 00:00:00 +0000 <![CDATA[Krenn, M.* & Zech, M. Reduced penetrance in interferonopathy-Aasociated dystonia: Hope for clues to mechanism? Mov. Disord., DOI: 10.1002/mds.30205 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74127&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74127&la=de Sat, 10 May 2025 00:00:00 +0000 <![CDATA[Sorrentino, U. et al. Integrating long-read nanopore sequencing for precision resolution of genomic variants in dystonia. Mov. Disord., DOI: 10.1002/mds.70072 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75682&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75682&la=de Thu, 06 Nov 2025 00:00:00 +0000 <![CDATA[Travaglini, L.* et al. Biallelic variants in SLC27A3 cause a complex form of neurodegeneration with brain iron accumulation. Mov. Disord., DOI: 10.1002/mds.70079 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75718&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75718&la=de Mon, 03 Nov 2025 00:00:00 +0000 <![CDATA[Wirth, T.* ; Kumar, K.R.* & Zech, M. Long-read sequencing: The third generation of diagnostic testing for dystonia. Mov. Disord. 40, 1009-1019 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74166&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74166&la=de Sat, 10 May 2025 00:00:00 +0000 <![CDATA[Calakos, N.* & Zech, M. Emerging molecular-genetic families in dystonia: Endosome-autophagosome-lysosome and integrated stress response pathways. Mov. Disord., DOI: 10.1002/mds.30037 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72170&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72170&la=de Tue, 29 Oct 2024 00:00:00 +0000 <![CDATA[Castellotti, B.* et al. Paroxysmal non-kinesigenic dyskinesias associated with biallelic POLG variants: A case report. Mov. Disord., DOI: 10.1002/mds.30029 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72017&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72017&la=de Wed, 16 Oct 2024 00:00:00 +0000 <![CDATA[Indelicato, E. et al. Genome aggregation database version 4-new challenges of variant analysis in movement disorders. Mov. Disord., DOI: 10.1002/mds.29797 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70297&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70297&la=de Mon, 13 May 2024 00:00:00 +0000 <![CDATA[Indelicato, E. ; Boesch, S.* & Zech, M. Heterogeneous phenotypic evolution in ANO3-related dystonia due to the recurrent p.Glu510Lys variant. Mov. Disord. 39, 631-632 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70402&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70402&la=de Thu, 23 May 2024 00:00:00 +0000 <![CDATA[Indelicato, E. et al. Genome aggregation database version 4-allele frequency changes and impact on variant interpretation in dystonia. Mov. Disord., DOI: 10.1002/mds.30066 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72464&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72464&la=de Fri, 22 Nov 2024 00:00:00 +0000 <![CDATA[Laabs, B.H.* et al. Genetic risk factors in isolated dystonia escape genome-wide association studies. Mov. Disord. 39, 2110-2116 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71730&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71730&la=de Mon, 28 Oct 2024 00:00:00 +0000 <![CDATA[Prokisch, H. & Zech, M. Proteomic profiling in dystonia: The next frontier for pathophysiology research and biomarker exploration. Mov. Disord., DOI: 10.1002/mds.29964 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71460&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71460&la=de Mon, 30 Sep 2024 00:00:00 +0000 <![CDATA[Svec, M.* ; Mantel, T.* ; Zech, M. & Haslinger, B.* Reply to: "Clinical and molecular profiling in GNAO1 permits phenotype-genotype correlation". Mov. Disord. 39, 2124-2125 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72388&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72388&la=de Wed, 27 Nov 2024 00:00:00 +0000 <![CDATA[Zorzi, G.* et al. Potassium channel subunit Kir4.1 mutated in paroxysmal kinesigenic dyskinesia: Screening of an Italian cohort. Mov. Disord., DOI: 10.1002/mds.30008 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71553&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71553&la=de Wed, 09 Oct 2024 00:00:00 +0000 <![CDATA[Harrer, P. et al. Epigenetic association analyses and risk prediction of RLS. Mov. Disord. 38, 1410-1418 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67914&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67914&la=de Fri, 06 Oct 2023 00:00:00 +0000 <![CDATA[Harrer, P. et al. Dystonia linked to EIF4A2 haploinsufficiency: A disorder of protein translation dysfunction. Mov. Disord. 38, 1914-1924 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68072&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68072&la=de Fri, 06 Oct 2023 00:00:00 +0000 <![CDATA[Indelicato, E.* ; Boesch, S.* & Zech, M. Reply to: "Early onset nonprogressive generalized dystonia is caused by biallelic SHQ1 variants". Mov. Disord. 38, 1119-1120 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68082&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68082&la=de Fri, 06 Oct 2023 00:00:00 +0000 <![CDATA[Indelicato, E. et al. Dystonia in ATP synthase defects: Reconnecting mitochondria and dopamine. Mov. Disord. 39, 29-35 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68778&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68778&la=de Tue, 28 Nov 2023 00:00:00 +0000 <![CDATA[Kuzkina, A.* et al. Dermal real-time quaking-induced conversion is a sensitive marker to confirm isolated rapid eye movement sleep behavior disorder as an early α-synucleinopathy. Mov. Disord. 38, 1077-1082 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67421&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67421&la=de Mon, 13 Feb 2023 00:00:00 +0000 <![CDATA[Sugier, P.E.* et al. Investigation of shared genetic risk factors between parkinson's disease and cancers. Mov. Disord. 38, 604-615 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67472&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67472&la=de Thu, 23 Feb 2023 00:00:00 +0000 <![CDATA[Vollstedt, E.J.* et al. Embracing monogenic Parkinson's disease: The MJFF global genetic PD cohort. Mov. Disord. 38, 286-303 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67406&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67406&la=de Fri, 08 Mar 2024 00:00:00 +0000 <![CDATA[Di Fonzo, A.* & Zech, M. Nuclear pore complex dysfunction in dystonia pathogenesis: Nucleoporins in the spotlight. Mov. Disord. 38, 23-24 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66860&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66860&la=de Fri, 09 Dec 2022 00:00:00 +0000 <![CDATA[Domenighetti, C.* et al. Dairy intake and Parkinson's disease: A mendelian randomization study. Mov. Disord. 37, 857-864 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64000&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64000&la=de Tue, 08 Feb 2022 00:00:00 +0000 <![CDATA[Domenighetti, C.* et al. The interaction between HLA-DRB1 and smoking in Parkinson's disease revisited. Mov. Disord. 37, 1929-1937 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65646&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65646&la=de Mon, 31 Oct 2022 00:00:00 +0000 <![CDATA[Hopfner, F.* et al. Common variants near ZIC1 and ZIC4 in autopsy-confirmed multiple system atrophy. Mov. Disord. 37, 2110-2121 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65996&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65996&la=de Thu, 17 Nov 2022 00:00:00 +0000 <![CDATA[Indelicato, E.* et al. Confirmation of a causal role for SHQ1 variants in early infantile-onset recessive dystonia. Mov. Disord., DOI: 10.1002/mds.29281 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66827&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66827&la=de Thu, 08 Dec 2022 00:00:00 +0000 <![CDATA[Krenn, M.* ; Sommer, R.* ; Sycha, T.* & Zech, M. GNAO1 haploinsufficiency associated with a mild delayed-onset dystonia phenotype. Mov. Disord. 37, 2464-2466 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66512&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66512&la=de Fri, 25 Nov 2022 00:00:00 +0000 <![CDATA[Neilson, D.E.* et al. A novel variant of ATP5MC3 associated with both dystonia and spastic paraplegia. Mov. Disord. 37, 375-383 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63280&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63280&la=de Wed, 03 Nov 2021 00:00:00 +0000 <![CDATA[Škorvánek, M.* et al. Adult-onset neurodegeneration in nucleotide excision repair disorders: More common than expected. Mov. Disord. 37, 2323-2324 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66432&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66432&la=de Fri, 21 Oct 2022 00:00:00 +0000 <![CDATA[Straka, I.* ; Švantnerová, J.* ; Minár, M.* ; Stanková, S.* & Zech, M. Neurodevelopmental gene-related dystonia-parkinsonism with onset in adults: A case with NAA15 variant. Mov. Disord. 37, 1955-1957 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65543&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65543&la=de Mon, 11 Jul 2022 00:00:00 +0000 <![CDATA[Straka, I.* ; Švantnerová, J.* & Zech, M. Reply to letter: Neurodevelopmental gene-related dystonia: A pediatric case with NAA15 variant. Mov. Disord. 37:2322 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66671&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66671&la=de Tue, 06 Dec 2022 00:00:00 +0000 <![CDATA[Janzen, A.* et al. Rapid eye movement sleep behavior disorder: Abnormal cardiac image and progressive abnormal metabolic brain pattern. Mov. Disord., DOI: 10.1002/mds.28859 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63560&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63560&la=de Fri, 03 Dec 2021 00:00:00 +0000 <![CDATA[Kogan, R.V.* et al. Four‐year follow‐up of [18F]fluorodeoxyglucose positron emission tomography–based Parkinson disease–related pattern expression in 20 patients with isolated rapid eye movement sleep behavior disorder shows prodromal progression. Mov. Disord. 36, 230-235 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60053&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60053&la=de Thu, 29 Oct 2020 00:00:00 +0000 <![CDATA[Maass, F.* et al. Cerebrospinal fluid iron-ferritin ratio as a potential progression marker for parkinson's disease. Mov. Disord. 36, 2967-2969 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63120&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63120&la=de Fri, 12 Nov 2021 00:00:00 +0000 <![CDATA[Ostrozovičová, M.* et al. A recurrent VPS16 p.Arg187* nonsense variant in early-onset generalized dystonia. Mov. Disord. 36, 1984-1985 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62107&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62107&la=de Mon, 28 Jun 2021 00:00:00 +0000 <![CDATA[Salminen, A.V. et al. Consensus guidelines on rodent models of restless legs syndrome. Mov. Disord. 36, 558-569 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60898&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60898&la=de Thu, 07 Jan 2021 00:00:00 +0000 <![CDATA[Shadrin, A.A.* et al. Shared genetics of multiple system atrophy and inflammatory bowel disease. Mov. Disord. 36, 449-459 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60409&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60409&la=de Fri, 04 Dec 2020 00:00:00 +0000 <![CDATA[Winter, B.* et al. NR4A2 and dystonia with dopa responsiveness. Mov. Disord. 36, 2203-2204 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62310&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62310&la=de Mon, 12 Jul 2021 00:00:00 +0000 <![CDATA[Zech, M. et al. Scoring algorithm-based genomic testing in dystonia: A prospective validation study. Mov. Disord. 36, 959-1964 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61940&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61940&la=de Tue, 15 Jun 2021 00:00:00 +0000 <![CDATA[Zech, M. et al. A neurodevelopmental disorder with dystonia and chorea resulting from clustering CAMK4 variants. Mov. Disord. 36, 520-521 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60644&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60644&la=de Tue, 09 Feb 2021 00:00:00 +0000 <![CDATA[Zech, M. et al. Biallelic AOPEP loss-of-function variants cause progressive dystonia with prominent limb involvement. Mov. Disord., DOI: 10.1002/mds.28804 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63184&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63184&la=de Tue, 23 Nov 2021 00:00:00 +0000 <![CDATA[Hopfner, F.* et al. Rare variants in specific lysosomal genes are associated with Parkinson's disease. Mov. Disord. 35, 1245-1248 (2020)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=58806&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=58806&la=de Thu, 16 Apr 2020 00:00:00 +0000 <![CDATA[Kishore, A.* et al. Understanding the role of genetic variability in LRRK2 in Indian population. Mov. Disord. 34, 496-505 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54856&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54856&la=de Wed, 12 Dec 2018 00:00:00 +0000 <![CDATA[Kübler, D.* et al. Widespread microglial activation in multiple system atrophy. Mov. Disord. 34, 564-568 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55516&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55516&la=de Wed, 13 Mar 2019 00:00:00 +0000 <![CDATA[Salminen, A.V. et al. Reply to: A note on rotigotine for restless legs syndrome after renal transplantation. Mov. Disord. 34, 152-153 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55246&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55246&la=de Mon, 25 Feb 2019 00:00:00 +0000 <![CDATA[Salminen, A.V. et al. Reply to: Safety of dopamine agonists for treating restless legs syndrome. Mov. Disord. 34, 150-151 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55247&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55247&la=de Mon, 25 Feb 2019 00:00:00 +0000 <![CDATA[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)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54513&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54513&la=de Wed, 24 Oct 2018 00:00:00 +0000 <![CDATA[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)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54361&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54361&la=de Wed, 26 Sep 2018 00:00:00 +0000 <![CDATA[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)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52167&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52167&la=de Sun, 22 Oct 2017 00:00:00 +0000 <![CDATA[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)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51480&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51480&la=de Thu, 13 Jul 2017 00:00:00 +0000 <![CDATA[Vill, K.* et al. A homozygous splice variant in AP4S1 mimicking neurodegeneration with brain iron accumulation. Mov. Disord. 32, 797-799 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50511&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50511&la=de Tue, 21 Mar 2017 00:00:00 +0000 <![CDATA[Zech, M. et al. KMT2B rare missense variants in generalized dystonia. Mov. Disord. 32, 1087-1091 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51147&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51147&la=de Mon, 10 Jul 2017 00:00:00 +0000 <![CDATA[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)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47654&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47654&la=de Thu, 31 Dec 2015 00:00:00 +0000 <![CDATA[Zech, M. et al. Clinical exome sequencing in early-onset generalized dystonia and large-scale resequencing follow-up. Mov. Disord. 32, 549-559 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49563&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49563&la=de Fri, 07 Oct 2016 00:00:00 +0000 <![CDATA[Nalls, M.A.* et al. Genetic risk and age in Parkinson's disease: Continuum not stratum. Mov. Disord. 30, 850-854 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=45139&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=45139&la=de Fri, 12 Jun 2015 00:00:00 +0000 <![CDATA[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)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46439&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46439&la=de Fri, 31 Jul 2015 00:00:00 +0000 <![CDATA[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)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44556&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44556&la=de Thu, 30 Apr 2015 00:00:00 +0000 <![CDATA[Zech, M. et al. TOR1A, THAP1, and GNAL mutational screening in Austrian patients with primary isolated dystonia. Mov. Disord. 30, 1853–1854 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47357&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47357&la=de Mon, 23 Nov 2015 00:00:00 +0000 <![CDATA[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)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28100&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28100&la=de Wed, 06 Nov 2013 00:00:00 +0000 <![CDATA[Zech, M. et al. DYT16 revisited: Exome sequencing identifies PRKRA mutations in a European dystonia family. Mov. Disord. 29, 1504-1510 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31965&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31965&la=de Sat, 23 Aug 2014 00:00:00 +0000 <![CDATA[Brockmann, K.* et al. SNCA: Major genetic modifier of age at onset of Parkinson's disease. Mov. Disord. 28, 1217-1221 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=26094&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=26094&la=de Tue, 30 Jul 2013 00:00:00 +0000 <![CDATA[Hopfner, F. et al. The role of SCARB2 as susceptibility factor in Parkinson's disease. Mov. Disord. 28, 538-540 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24326&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24326&la=de Thu, 09 May 2013 00:00:00 +0000 <![CDATA[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)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23617&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23617&la=de Thu, 28 Mar 2013 00:00:00 +0000 <![CDATA[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)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3840&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3840&la=de Fri, 03 Dec 2010 00:00:00 +0000 <![CDATA[Kowarik, M.C.* et al. Myoclonus-dystonia in 18p deletion syndrome. Mov. Disord. 26, 560-561 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3998&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3998&la=de Fri, 31 Dec 2010 00:00:00 +0000 <![CDATA[Lyoo, C.H.* et al. Anticholinergic-responsive gait freezing in a patient with pantothenate kinase-associated neurodegeneration. Mov. Disord. 23, 283-284 (2008)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3101&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3101&la=de Wed, 30 Jan 2008 00:00:00 +0000 <![CDATA[Winkelmann, J. et al. Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome. Mov. Disord. 23, 350-358 (2008)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3390&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3390&la=de Mon, 28 Apr 2008 00:00:00 +0000 <![CDATA[Baier, P.C.* ; Ondo, W.G.* & Winkelmann, J. Animal studies in restless legs syndrome. Mov. Disord. 22, (Suppl.18), 459-465 (2007)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=800&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=800&la=de Mon, 31 Dec 2007 00:00:00 +0000 <![CDATA[García-Borreguero, D.* et al. Augmentation as a treatment complication of restless legs syndrome: Concept and management. Mov. Disord. 22, (Suppl.18), 476-484 (2007)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=801&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=801&la=de Mon, 31 Dec 2007 00:00:00 +0000 <![CDATA[Haubenberger, D.* et al. A novel LRRK2 mutation in an Austrian cohort of patients with Parkinson's disease. Mov. Disord. 22, 1640-1643 (2007)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2123&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2123&la=de Wed, 15 Aug 2007 00:00:00 +0000 <![CDATA[Kemlink, D. et al. Family-based association study of the restless legs syndrome loci 2 and 3 in a European population. Mov. Disord. 22, 207-212 (2007)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=595&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=595&la=de Thu, 22 Nov 2007 00:00:00 +0000 <![CDATA[Winkelmann, J. et al. Genetics of restless legs syndrome (RLS: State-of-the-art and future directions). Mov. Disord. 22, (Suppl.18), 449-458 (2007)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3475&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3475&la=de Mon, 31 Dec 2007 00:00:00 +0000 <![CDATA[Vogl, F.D.* et al. Restless legs syndrome: Epidemiological and clinicogenetic study in a South tyrolean population isolate. Mov. Disord. 21, 1189-1195 (2006)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4983&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4983&la=de Thu, 21 Sep 2006 00:00:00 +0000 <![CDATA[Winkelmann, J. et al. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome. Mov. Disord. 21, 28-33 (2006)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3976&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3976&la=de Wed, 02 Aug 2006 00:00:00 +0000 <![CDATA[Antonini, A.* et al. Genetic, clinical and imaging characterization of one patient with late-onset, slowly progressive, pantothenate kinase-associated neurodegeneration. Mov. Disord. 21, 417-425 (2005)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4530&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4530&la=de Thu, 27 Jul 2006 00:00:00 +0000