PuSH - HMGU Publikationen https://push-zb.helmholtz-munich.de PuSH - Publikationen-Server des Helmholtz Zentrums München de-de <![CDATA[Dzinovic, I. et al. Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variant. Neurogenetics 22, 137-141 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61438&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61438&la=de Mon, 26 Apr 2021 00:00:00 +0000 <![CDATA[Dzinovic, I. et al. Correction to: Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variant. Neurogenetics, DOI: 10.1007/s10048-021-00641-w (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63725&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63725&la=de Fri, 10 Dec 2021 00:00:00 +0000 <![CDATA[Amprosi, M.* et al. Familial writer's cramp: A clinical clue for inherited coenzyme Q10 deficiency. Neurogenetics 22, 81–86 (2020)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=59973&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=59973&la=de Thu, 22 Oct 2020 00:00:00 +0000 <![CDATA[Spiegler, S.* et al. First large genomic inversion in familial cerebral cavernous malformation identified by whole genome sequencing. Neurogenetics 19, 55–59 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52500&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52500&la=de Wed, 13 Dec 2017 00:00:00 +0000 <![CDATA[Carecchio, M.* et al. Rare causes of early-onset dystonia-parkinsonism with cognitive impairment: A de novo PSEN-1 mutation. Neurogenetics 18, 175-178 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51541&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51541&la=de Tue, 01 Aug 2017 00:00:00 +0000 <![CDATA[Glasgow, R.I.C.* et al. Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits. Neurogenetics 18, 1-9 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52264&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52264&la=de Sun, 05 Nov 2017 00:00:00 +0000 <![CDATA[Zech, M. et al. Molecular diversity of combined and complex dystonia: Insights from diagnostic exome sequencing. Neurogenetics 18, 195–205 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51768&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51768&la=de Fri, 15 Sep 2017 00:00:00 +0000 <![CDATA[Baertling, F.* et al. MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalities. Neurogenetics 16, 237-240 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44015&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44015&la=de Sun, 05 Apr 2015 00:00:00 +0000 <![CDATA[Distelmaier, F.* et al. MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic cardiomyopathy. Neurogenetics 16, 319-323 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44083&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44083&la=de Thu, 02 Apr 2015 00:00:00 +0000 <![CDATA[Schulte, E.C. et al. Rare variants in LRRK1 and Parkinson's disease. Neurogenetics 15, 49-57 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28394&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28394&la=de Fri, 22 Nov 2013 00:00:00 +0000 <![CDATA[Schmied, M.C.* et al. Replication study of Multiple Sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients. Neurogenetics 13, 181-187 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8018&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8018&la=de Mon, 23 Jul 2012 00:00:00 +0000 <![CDATA[Schulte, E.C. et al. Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease. Neurogenetics 13, 281-285 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8573&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8573&la=de Fri, 21 Sep 2012 00:00:00 +0000 <![CDATA[Soehn, A.S.* et al. Periphilin is a novel interactor of synphilin-1, a protein implicated in Parkinson's disease. Neurogenetics 11, 203-215 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1601&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1601&la=de Thu, 31 Dec 2009 00:00:00 +0000 <![CDATA[Stogmann, E.* et al. A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis. Neurogenetics 10, 73-77 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3528&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3528&la=de Wed, 31 Dec 2008 00:00:00 +0000 <![CDATA[Kemlink, D. et al. Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13. Neurogenetics 9, 75-82 (2008)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=383&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=383&la=de Tue, 21 Oct 2008 00:00:00 +0000 <![CDATA[Stogmann, E.* et al. Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes. Neurogenetics 7, 265-268 (2006)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3226&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3226&la=de Sun, 31 Dec 2006 00:00:00 +0000 <![CDATA[Asmus, F.* et al. Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome. Neurogenetics 6, 55-56 (2005)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23508&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23508&la=de Sat, 31 Dec 2005 00:00:00 +0000