PuSH - HMGU Publikationen https://push-zb.helmholtz-munich.de PuSH - Publikationen-Server des Helmholtz Zentrums München de-de <![CDATA[Zhu, G.* et al. Autoinflammatory encephalopathy due to PTPN1 haploinsufficiency: A case series. Lancet Neurol. 24, 218-229 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73444&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73444&la=de Tue, 15 Apr 2025 00:00:00 +0000 <![CDATA[GBD 2021 Stroke Risk Factor Collaborators (Breitner-Busch, S.) Global, regional, and national burden of stroke and its risk factors, 1990-2021: A systematic analysis for the Global Burden of Disease Study 2021. Lancet Neurol. 23, 973-1003 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72330&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72330&la=de Mon, 25 Nov 2024 00:00:00 +0000 <![CDATA[Morenas-Rodríguez, E.* et al. Soluble TREM2 in CSF and its association with other biomarkers and cognition in autosomal-dominant Alzheimer's disease: A longitudinal observational study. Lancet Neurol. 21, 329-341 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64613&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64613&la=de Thu, 21 Apr 2022 00:00:00 +0000 <![CDATA[Miglis, M.G.* et al. Biomarkers of conversion to α-synucleinopathy in isolated rapid-eye-movement sleep behaviour disorder. Lancet Neurol. 20, 671-684 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62815&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62815&la=de Thu, 09 Sep 2021 00:00:00 +0000 <![CDATA[Zech, M. et al. Monogenic variants in dystonia: An exome-wide sequencing study. Lancet Neurol. 19, 908-918 (2020)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60563&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60563&la=de Tue, 01 Dec 2020 00:00:00 +0000 <![CDATA[Pottier, C.* et al. Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: A genome-wide association study. Lancet Neurol. 17, 548-558 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53888&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53888&la=de Wed, 18 Jul 2018 00:00:00 +0000 <![CDATA[Trenkwalder, C.* et al. Comorbidities, treatment, and pathophysiology in restless legs syndrome. Lancet Neurol. 17, 994-1005 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54393&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54393&la=de Tue, 02 Oct 2018 00:00:00 +0000 <![CDATA[Moss, D.J.H.* et al. Identification of genetic variants associated with Huntington's disease progression: A genome-wide association study. Lancet Neurol. 16, 701-711 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61156&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61156&la=de Thu, 04 Feb 2021 00:00:00 +0000 <![CDATA[Schormair, B. et al. Identification of novel risk loci for restless legs syndrome: A meta-analysis of genome-wide association studies in individuals of European ancestry: A meta-analysis. Lancet Neurol. 16, 898–907 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52064&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52064&la=de Wed, 11 Oct 2017 00:00:00 +0000 <![CDATA[Mok, K.Y.* et al. Deletions at 22q11.2 in idiopathic Parkinson's disease: A combined analysis of genome-wide association data. Lancet Neurol. 15, 585-596 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48428&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48428&la=de Wed, 04 May 2016 00:00:00 +0000 <![CDATA[International Stroke Genetics Consortium (Pulit, S.L.* ; McArdle, P.F.* ; Wong, Q.* ; Malik, R.* ; Gieger, C. ; Meisinger, C. ; Müller-Nurasyid, M. ; Peters, A. ; Strauch, K. ; Waldenberger, M. ; Rosand, J.*) Loci associated with ischaemic stroke and its subtypes (SiGN): A genome-wide association study. Lancet Neurol. 15, 174-184 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47856&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47856&la=de Thu, 11 Feb 2016 00:00:00 +0000 <![CDATA[Jansen, I.E.* et al. CHCHD2 and Parkinson's disease. Lancet Neurol. 14, 678-679 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=45663&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=45663&la=de Fri, 03 Jul 2015 00:00:00 +0000 <![CDATA[International League Against Epilepsy Consortium on Complex Epilepsies (Gieger, C. ; Grallert, H. ; Heinrich, J. ; Holle, R. ; Leidl, R. ; Meisinger, C. ; Peters, A. ; Strauch, K.) Genetic determinants of common epilepsies: A meta-analysis of genome-wide association studies. Lancet Neurol. 13, 893-903 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=32445&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=32445&la=de Mon, 06 Oct 2014 00:00:00 +0000 <![CDATA[Trenkwalder, C.* et al. Prolonged release oxycodone-naloxone for treatment of severe restless legs syndrome after failure of previous treatment: A double-blind, randomised, placebo-controlled trial with an open-label extension. Lancet Neurol. 12, 1141-1150 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28035&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28035&la=de Thu, 31 Oct 2013 00:00:00 +0000 <![CDATA[Kretzschmar, H.* & Illig, T. Are further genetic factors associated with the risk of developing variant Creutzfeldt-Jakob disease? Lancet Neurol. 8, 25-26 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1254&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1254&la=de Thu, 09 Jul 2009 00:00:00 +0000