PuSH - HMGU Publikationen https://push-zb.helmholtz-munich.de PuSH - Publikationen-Server des Helmholtz Zentrums München de-de <![CDATA[Bremer, J.* et al. Mutual reinforcement of lymphotoxin-driven myositis and impaired autophagy in murine muscle. Brain, DOI: 10.1093/brain/awaf260 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75395&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75395&la=de Mon, 13 Oct 2025 00:00:00 +0000 <![CDATA[Erdmann, H.* et al. Repeat-associated ataxias in a German patient cohort analysed by targeted parallel long-read sequencing. Brain 149, 993-1006 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75452&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75452&la=de Fri, 17 Oct 2025 00:00:00 +0000 <![CDATA[Fiorini, C.* et al. Recessive variants in mitochondrial Complex I nuclear subunits are an underrated cause of optic atrophy. Brain:awaf422 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=76031&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=76031&la=de Mon, 17 Nov 2025 00:00:00 +0000 <![CDATA[Jacob, M.* et al. Deciphering DST-associated disorders: Biallelic variants affecting DST-b cause a congenital myopathy. Brain 149, 653-667 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74903&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74903&la=de Tue, 17 Jun 2025 00:00:00 +0000 <![CDATA[Merkevicius, K.* et al. The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency. Brain:awaf430 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=76038&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=76038&la=de Mon, 17 Nov 2025 00:00:00 +0000 <![CDATA[Peymani, F. et al. Pleiotropic effects of MORC2 derive from its epigenetic signature. Brain:awaf159 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74235&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74235&la=de Sun, 11 May 2025 00:00:00 +0000 <![CDATA[Zech, M. et al. Combined genomics and proteomics unveils elusive variants and vast aetiologic heterogeneity in dystonia. Brain 148, 2827-2846 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73367&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73367&la=de Fri, 11 Apr 2025 00:00:00 +0000 <![CDATA[Binks, S.N.M.* et al. Novel risk loci in LGI1-antibody encephalitis: Genome-wide association study discovery and validation cohorts. Brain 148, 737-745 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72164&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72164&la=de Mon, 28 Oct 2024 00:00:00 +0000 <![CDATA[Blickhaeuser, B. et al. Digenic Leigh syndrome on the background of the m.11778G>A Leber hereditary optic neuropathy variant. Brain 147, 1967-1974 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70256&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70256&la=de Tue, 07 May 2024 00:00:00 +0000 <![CDATA[Souza Oliveira, D.* et al. A direct spinal cord-computer interface enables the control of the paralysed hand in spinal cord injury. Brain, DOI: 10.1093/brain/awae088 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70315&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70315&la=de Tue, 14 May 2024 00:00:00 +0000 <![CDATA[Joza, S.* et al. Progression of clinical markers in prodromal Parkinson's disease and dementia with Lewy bodies: a multicentre study. Brain 146, 3258-3272 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67554&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67554&la=de Wed, 08 Mar 2023 00:00:00 +0000 <![CDATA[Nasca, A.* et al. Variants in ATP5F1B are associated with dominantly inherited dystonia. Brain 146, 2730-2738 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67567&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67567&la=de Wed, 08 Mar 2023 00:00:00 +0000 <![CDATA[AlAbdi, L.* et al. Loss-of-function variants in MYCBP2 cause neurobehavioural phenotypes and corpus callosum defects. Brain 146, 1373-1387 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66346&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66346&la=de Wed, 19 Oct 2022 00:00:00 +0000 <![CDATA[Ban, R. et al. The phenotypic spectrum of COX20-associated mitochondrial disorder. Brain 145, e125-e127 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66387&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66387&la=de Fri, 21 Oct 2022 00:00:00 +0000 <![CDATA[Erdmann, H.* et al. Methylation of the 4q35 D4Z4 repeat defines disease status in facioscapulohumeral muscular dystrophy. Brain 146, 1388-1402 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66395&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66395&la=de Fri, 21 Oct 2022 00:00:00 +0000 <![CDATA[Spitzer, H. et al. Interpretable surface-based detection of focal cortical dysplasias: A Multi-centre Epilepsy Lesion Detection study. Brain 145, 3859-3871 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65926&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65926&la=de Mon, 19 Sep 2022 00:00:00 +0000 <![CDATA[Stenton, S. et al. DNAJC30 defect: A frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndrome. Brain 145, 1624-1631 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64376&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64376&la=de Wed, 04 May 2022 00:00:00 +0000 <![CDATA[Sundaram, S.M.* et al. Gene therapy targeting the blood-brain barrier improves neurological symptoms in a model of genetic MCT8 deficiency. Brain 145, 4264-4274 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65910&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65910&la=de Thu, 01 Sep 2022 00:00:00 +0000 <![CDATA[Giesert, F. c-Abl phosphorylation primes PARIS for neurodegeneration. Brain 144, 3555-3557 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63647&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63647&la=de Fri, 10 Dec 2021 00:00:00 +0000 <![CDATA[Invernizzi, F.* et al. Myopathic mitochondrial DNA depletion syndrome associated with biallelic variants in LIG3. Brain 144:e74 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62466&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62466&la=de Tue, 13 Jul 2021 00:00:00 +0000 <![CDATA[Kaiyrzhanov, R.* et al. Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum. Brain 144, e30 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61096&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61096&la=de Mon, 08 Feb 2021 00:00:00 +0000 <![CDATA[Macrini, C.* et al. Features of MOG required for recognition by patients with MOG antibody-associated disorders. Brain 144, 2375-2389 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61553&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61553&la=de Mon, 17 May 2021 00:00:00 +0000 <![CDATA[Mirza-Schreiber, N. et al. Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onset. Brain, DOI: 10.1093/brain/awab360 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63189&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63189&la=de Tue, 23 Nov 2021 00:00:00 +0000 <![CDATA[Monfrini, E.* et al. HOPS-associated neurological disorders (HOPSANDs): Linking endolysosomal dysfunction to the pathogenesis of dystonia. Brain 144, 2610-2615 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61835&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61835&la=de Wed, 16 Jun 2021 00:00:00 +0000 <![CDATA[Neuray, C.* et al. Early-onset phenotype of bi-allelic GRN mutations. Brain 144:e22 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60968&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60968&la=de Tue, 09 Feb 2021 00:00:00 +0000 <![CDATA[Riedhammer, K.M.* et al. De novo stop-loss variants in CLDN11 cause hypomyelinating leukodystrophy. Brain 144, 411-419 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60758&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60758&la=de Wed, 16 Dec 2020 00:00:00 +0000 <![CDATA[Zech, M. et al. MATR3 haploinsufficiency and early-onset neurodegeneration. Brain 144:e72 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62457&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62457&la=de Thu, 22 Jul 2021 00:00:00 +0000 <![CDATA[Mak, C.C.Y.* et al. MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis. Brain 143, 55-68 (2020)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=57633&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=57633&la=de Mon, 27 Jan 2020 00:00:00 +0000 <![CDATA[Zhou, J.* et al. NAD(P)HX dehydratase (NAXD) deficiency: A novel neurodegenerative disorder exacerbated by febrile illnesses (vol 142, pg 50, 2019). Brain 143:e15 (2020)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=58860&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=58860&la=de Wed, 22 Apr 2020 00:00:00 +0000 <![CDATA[Zhou, J.* et al. NAD(P)HX dehydratase (NAXD) deficiency: A novel neurodegenerative disorder exacerbated by febrile illnesses. Brain 143:e8 (2020)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=58861&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=58861&la=de Wed, 22 Apr 2020 00:00:00 +0000 <![CDATA[Esposito, A.* et al. Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course. Brain 142, 3876-3891 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=57270&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=57270&la=de Thu, 14 Nov 2019 00:00:00 +0000 <![CDATA[Forouhideh, Y.* et al. A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification. Brain 142, e4 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55432&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55432&la=de Mon, 25 Feb 2019 00:00:00 +0000 <![CDATA[Van Bergen, N.J.* et al. NAD(P)HX dehydratase (NAXD) deficiency: A novel neurodegenerative disorder exacerbated by febrile illnesses. Brain 142, 50-58 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55083&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55083&la=de Wed, 09 Jan 2019 00:00:00 +0000 <![CDATA[Vaz, F.M.* et al. Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia. Brain 142, 3382-3397 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=57168&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=57168&la=de Thu, 24 Oct 2019 00:00:00 +0000 <![CDATA[Lessel, D.* et al. BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells. Brain 141, 2299-2311 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54173&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54173&la=de Fri, 07 Sep 2018 00:00:00 +0000 <![CDATA[Distelmaier, F.* ; Haack, T.B. ; Wortmann, S.B. ; Mayr, J.A.* & Prokisch, H. Treatable mitochondrial diseases: Cofactor metabolism and beyond. Brain 140:e11 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50883&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50883&la=de Thu, 01 Jun 2017 00:00:00 +0000 <![CDATA[Robak, L.A.* et al. Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease. Brain 140, 3191-3203 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52577&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52577&la=de Fri, 22 Dec 2017 00:00:00 +0000 <![CDATA[Brenner, D.* et al. NEK1 mutations in familial amyotrophic lateral sclerosis. Brain 139:e28 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48054&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48054&la=de Wed, 09 Mar 2016 00:00:00 +0000 <![CDATA[Holzerova, E. et al. Human thioredoxin 2 deficiency impairs mitochondrial redox homeostasis and causes early-onset neurodegeneration. Brain 139, 346-354 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47468&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47468&la=de Thu, 03 Dec 2015 00:00:00 +0000 <![CDATA[Koch, J.* et al. CAD mutations and uridine-responsive epileptic encephalopathy. Brain 140, 279-286 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50472&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50472&la=de Sat, 31 Dec 2016 00:00:00 +0000 <![CDATA[Marroquin, N.* et al. Screening for CHCHD10 mutations in a large cohort of sporadic ALS patients: No evidence for pathogenicity of the p.P34S variant. Brain 139, E8-U10 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46792&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46792&la=de Mon, 14 Sep 2015 00:00:00 +0000 <![CDATA[Müller, S.H.* et al. Genome-wide association study in essential tremor identifies three new loci. Brain 139, 3163-3169 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50157&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50157&la=de Wed, 21 Dec 2016 00:00:00 +0000 <![CDATA[Synofzik, M.* et al. SYNE1 ataxia is a common recessive ataxia with major non-cerebellar features: A large scale multi-centre study. Brain 139, 1378-1393 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48425&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48425&la=de Wed, 20 Apr 2016 00:00:00 +0000 <![CDATA[Oláhová, M.* et al. LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population. Brain 138, 3503-3519 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47230&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47230&la=de Tue, 08 Dec 2015 00:00:00 +0000 <![CDATA[Fischer, D.* et al. A novel missense mutation confirms ATL3 as a gene for hereditary sensory neuropathy type 1. Brain 137:e286 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31204&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31204&la=de Mon, 05 May 2014 00:00:00 +0000 <![CDATA[Haack, T.B. et al. Infantile Leigh-like syndrome caused by SLC19A3 mutations is a treatable disease. Brain 137:e295 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31522&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31522&la=de Mon, 02 Jun 2014 00:00:00 +0000 <![CDATA[Müller, K.* et al. Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease. Brain 137:e309 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31924&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31924&la=de Thu, 14 Aug 2014 00:00:00 +0000 <![CDATA[Synofzik, M.* et al. PNPLA6 mutations cause Boucher-Neuhauser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum. Brain 137, 69-77 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28988&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28988&la=de Mon, 20 Jan 2014 00:00:00 +0000 <![CDATA[Hayflick, S.J.* et al. Beta-propeller protein-associated neurodegeneration: A new X-linked dominant disorder with brain iron accumulation. Brain 136, 1708-1717 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=25745&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=25745&la=de Fri, 12 Jul 2013 00:00:00 +0000 <![CDATA[Stogmann, E.* et al. Autosomal recessive cortical myoclonic tremor and epilepsy: Association with a mutation in the potassium channel associated gene CNTN2. Brain 136, 1155-1160 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24322&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24322&la=de Thu, 09 May 2013 00:00:00 +0000 <![CDATA[Steenweg, M.E.* et al. Leukoencephalopathy with thalamus and brainstem involvement and high lactate 'LTBL' caused by EARS2 mutations. Brain 135, 1387-1394 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7989&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7989&la=de Mon, 23 Jul 2012 00:00:00 +0000 <![CDATA[Gerards, M.* et al. Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: New function for an old gene. Brain 134, 210-219 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5649&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5649&la=de Mon, 16 May 2011 00:00:00 +0000 <![CDATA[Piaton, G.* et al. Class 3 semaphorins influence oligodendrocyte precursor recruitment and remyelination in adult central nervous system. Brain 134, 1156-1167 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6543&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6543&la=de Mon, 19 Sep 2011 00:00:00 +0000 <![CDATA[Rolyan, H.* et al. Telomere shortening reduces Alzheimer's disease amyloid pathology in mice. Brain 134, 2044-2056 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6511&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6511&la=de Thu, 15 Sep 2011 00:00:00 +0000 <![CDATA[de Kovel, C.G.F.* et al. Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies. Brain 133, 23-32 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=234&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=234&la=de Thu, 10 Jun 2010 00:00:00 +0000 <![CDATA[Flinn, L.* et al. Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio). Brain 132, Part 6, 1613-1623 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=747&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=747&la=de Thu, 09 Jul 2009 00:00:00 +0000 <![CDATA[Asmus, F.* et al. Genomic deletion size at the epsilon-sarcoglycan locus determines the clinical phenotype. Brain 130, 2736-2745 (2007)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1793&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1793&la=de Tue, 30 Oct 2007 00:00:00 +0000 <![CDATA[Gempel, K.* et al. The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene. Brain 130, 2037-2044 (2007)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3162&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3162&la=de Thu, 22 Nov 2007 00:00:00 +0000 <![CDATA[Horvath, R.* et al. Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene. Brain 129, 1674-1684 (2006)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4532&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4532&la=de Tue, 01 Aug 2006 00:00:00 +0000 <![CDATA[Berg, D.* et al. Type and frequency of mutations in the LRRK2 gene in familial ans sporadic Parkinson's disease. Brain 128, 3000-3011 (2005)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3522&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3522&la=de Thu, 29 Jun 2006 00:00:00 +0000 <![CDATA[Kamm, C.* ; Illig, T. & Wichmann, H.-E. The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: Data from the EMSA study group. Brain 128, 1855-1860 (2005)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5159&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5159&la=de Sat, 31 Dec 2005 00:00:00 +0000