PuSH - HMGU Publikationen https://push-zb.helmholtz-munich.de PuSH - Publikationen-Server des Helmholtz Zentrums München de-de <![CDATA[Baumeister, S. et al. Physical activity and Parkinson's disease: A two-sample Mendelian randomisation study. J. Neurol. Neurosurg. Psychiatr. 92, 334-335 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60474&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60474&la=de Tue, 09 Feb 2021 00:00:00 +0000 <![CDATA[Müller, K.* et al. Comprehensive analysis of the mutation spectrum in 301 German ALS families. J. Neurol. Neurosurg. Psychiatr. 89, 817-827 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53741&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53741&la=de Tue, 03 Jul 2018 00:00:00 +0000 <![CDATA[Obayashi, M.* et al. Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion. J. Neurol. Neurosurg. Psychiatr. 86, 986-995 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42907&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42907&la=de Sun, 07 Dec 2014 00:00:00 +0000 <![CDATA[Synofzik, M.* ; Kernstock, C.* ; Haack, T.B. & Schöls, L.* Ataxia meets chorioretinal dystrophy and hypogonadism: Boucher-Neuhäuser syndrome due to PNPLA6 mutations. J. Neurol. Neurosurg. Psychiatr. 86, 580-581 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31240&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31240&la=de Fri, 09 May 2014 00:00:00 +0000 <![CDATA[Klebe, S.* et al. The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism. J. Neurol. Neurosurg. Psychiatr. 84, 666-673 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=25494&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=25494&la=de Thu, 04 Jul 2013 00:00:00 +0000 <![CDATA[Horvath, R.* et al. Leigh syndrome caused by mutations in the flavoprotein (Fp) subunit of succinate dehydrogenase (SDHA). J. Neurol. Neurosurg. Psychiatr. 77, 74-76 (2006)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5126&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5126&la=de Sun, 31 Dec 2006 00:00:00 +0000