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1.
Indelicato, E. et al.: Dystonia and mitochondrial disease: The movement disorder connection revisited in 900 genetically diagnosed patients. J. Neurol., DOI: 10.1007/s00415-024-12447-5 (2024)
2.
Sorrentino, U. et al.: CHD8-related disorders redefined: An expanding spectrum of dystonic phenotypes. J. Neurol. 271, 2859-2865 (2024)
3.
Krenn, M.* et al.: The clinical and molecular landscape of congenital myasthenic syndromes in Austria: A nationwide study. J. Neurol. 270, 909-916 (2023)
4.
Krenn, M.* et al.: Next-generation sequencing and comprehensive data reassessment in 263 adult patients with neuromuscular disorders: Insights into the gray zone of molecular diagnoses. J. Neurol., DOI: 10.1007/s00415-023-12101-6 (2023)
5.
Dusl, M.* et al.: Congenital myasthenic syndrome caused by novel COL13A1 mutations. J. Neurol. 266, 1107-1112 (2019)
6.
Jochim, A.* et al.: Treatment of cervical dystonia with abo- and onabotulinumtoxinA: Long-term safety and efficacy in daily clinical practice. J. Neurol. 266, 1879-1886 (2019)
7.
Wang, X.* et al.: Vertigo and dizziness cause considerable more health care resource use and costs: Results from the KORA FF4 study. J. Neurol. 266, 2120-2128 (2019)
8.
Krenn, M.* et al.: Mutations outside the N-terminal part of RBCK1 may cause polyglucosan body myopathy with immunological dysfunction: Expanding the genotype-phenotype spectrum. J. Neurol. 265, 394–401 (2018)
9.
Altmann, J.* et al.: Expanded phenotypic spectrum of the m.8344A>G "MERRF" mutation: Data from the German mitoNET registry. J. Neurol. 263, 961-972 (2016)
10.
Schabhüttl, M.* et al.: Whole-exome sequencing in patients with inherited neuropathies: Outcome and challenges. J. Neurol. 261, 970-982 (2014)
11.
Deschauer, M.* et al.: C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis J. Neurol. 259, 2434-2439 (2012)
12.
Schulte, E.C.* & Winkelmann, J.: When Parkinson's disease patients go to sleep: Specific sleep disturbances related to Parkinson's disease. J. Neurol. 258, Suppl. 2, S328-S335 (2011)
13.
Winkler, J.* et al.: Parkinson's disease risk score: Moving to a premotor diagnosis. J. Neurol. 258, Suppl 2, S311-S315 (2011)
14.
Fernández-Santiago, R.* et al.: Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis. J. Neurol. 256, 1337-1342 (2009)
15.
Lücking, C.B.* et al.: Polymorphisms in the proteasomal subunit alpha4 are not associated with Parkinson's disease. J. Neurol. 255, 441-442 (2008)
16.
Prestel, J.* et al.: Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutation. J. Neurol. 255, 643-648 (2008)
17.
Bax, R. et al.: Amplitude Cycles in the EEG of Premature Infants During Quiet Sleep by Means of "Running" Frequency Analysis. J. Neurol. 239 (Suppl.2), S. 224 (1992)
18.
Eckardt, T. et al.: Simultaneous Changes of the Periodic Breathing Cycles Duration and the EEG Rhythmicity in Preterm Infants. J. Neurol. 239 (Suppl.2), S. 225 (1992)
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