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Acta Neuropathologica|June 30, 2019
Evidence for bidirectional and trans-synaptic parasympathetic and sympathetic propagation of alpha-synuclein in ratsNathalie Van Den Berge, Nelson Ferreira, Hjalte Gram, et al.
Molecular Neurobiology|October 30, 2021
A Novel SCA3 Knock-in Mouse Model Mimics the Human SCA3 Disease Phenotype Including Neuropathological, Behavioral, and Transcriptional Abnormalities Especially in OligodendrocytesEva Haas, Rana D Incebacak, Thomas Hentrich, et al.
Frontiers in Neurology|January 11, 2020
Single Molecule Molecular Inversion Probes for High Throughput Germline Screenings in DystoniaMichaela Pogoda, Franz-Joachim Hilke, Ebba Lohmann, et al.
Haematologica|August 28, 2025
Extensive non-clonal CAR T-cell expansion causing fatal hyperinflammatory syndrome with immune effector cell-associated hemophagocytic lymphohistiocytosis, cytokine release syndrome, and neurotoxicity syndromeAndreas Riedel, Anna M P Stanger, Lucca M Kimmich, et al.
Cytotherapy|July 29, 2019
Low mutational load in pediatric medulloblastoma still translates into neoantigens as targets for specific T-cell immunotherapyFranziska Blaeschke, Milan Cedric Paul, Martin Ulrich Schuhmann, et al.
Human Molecular Genetics|November 26, 2015
Mitochondrial defects and neurodegeneration in mice overexpressing wild-type or G399S mutant HtrA2Nicolas Casadei, Poonam Sood, Thomas Ulrich, et al.
Human Molecular Genetics|March 13, 2014
Overexpression of the calpain-specific inhibitor calpastatin reduces human alpha-Synuclein processing, aggregation and synaptic impairment in [A30P]αSyn transgenic miceMeike Diepenbroek, Nicolas Casadei, Hakan Esmer, et al.
Neurogenetics|September 18, 2009
Transgenic overexpression of the alpha-synuclein interacting protein synphilin-1 leads to behavioral and neuropathological alterations in miceSilke Nuber, Thomas Franck, Hartwig Wolburg, et al.
International Journal of Molecular Sciences|October 16, 2024
Compound Heterozygous RYR1 Variants in a Patient with Severe Congenital Myopathy: Case Report and Comparison with Additional Cases of Recessive RYR1-Related MyopathySören Janßen, Leoni S Erbe, Moritz Kneifel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 8, 2024
A Novel PINK1 p.F385S Loss-of-Function Mutation in an Indian Family with Parkinson's DiseaseKaran Sharma, Asha Kishore, Anna Lechado-Terradas, et al.
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