Kathrin Grundmann und Zitiert - Info zur Person

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Compound Heterozygous DARS2 Mutations as a Mimic of ...John Wiley

movementdisorders.onlinelibrary.wiley.com

von MG Pauly · · Zitiert von: 2 — Kathrin Grundmann-Hauser has nothing to report. Frauke Hinrichs has nothing to report. Katja Lohmann received research funding from the German ...

Dynamic nuclear envelope phenotype in rats ...The Company of Biologists

journals.biologists.com

von L Yu-Taeger · · Zitiert von: 3 — Kathrin Grundmann-Hauser. Kathrin Grundmann-Hauser *. 1. Institute for Medical Genetics and Applied Genomics, University of Tuebingen. ,. , von L Yu-Taeger · · Zitiert von: 3 — Kathrin Grundmann-Hauser. Kathrin Grundmann-Hauser *. 1. Institute for Medical Genetics and Applied Genomics, University of Tuebingen. ,. ,

Review New genetic insights highlight 'old' ideas on motor ...ScienceDirect.com

www.sciencedirect.com

von RE Goodchild · · Zitiert von: 65 — ... in dystonia. Author links open overlay panel. Rose E. Goodchild 1 , Kathrin Grundmann 2 , Antonio Pisani Show more. Add to Mendeley. Share. Cite. https ... von RE Goodchild · · Zitiert von: 65 — ... in dystonia. Author links open overlay panel. Rose E. Goodchild 1 , Kathrin Grundmann 2 , Antonio Pisani Show more. Add to Mendeley. Share. Cite. https ...

Compound Heterozygous DARS2 Mutations as a Mimic ...Universität zu Lübeck

research.uni-luebeck.de

von MG Pauly · · Zitiert von: 2 — Compound Heterozygous DARS2 Mutations as a Mimic of Hereditary Spastic Paraplegia. Martje G. Pauly, Yorck Hellenbroich, Kathrin Grundmann-Hauser, Frauke ...

The evolution of dystonia-like movements in TOR1A rats ...Goethe-Universität Frankfurt

publikationen.ub.uni-frankfurt.de

von S Knorr · · Zitiert von: 17 — ... Kathrin Grundmann-Hauser, Thomas Ott, Aet O'Leary, Andreas Reif, Philip Tovote, Jens Volkmann, Chi Wang Ip. TOR1A is the most common inherited form of ...

Needs and Requirements of Modern Biobanks on the ...CORE

core.ac.uk

von E Lohmann · · Zitiert von: 6 — Kathrin Grundmann kathrin.grundmann@ med.uni-tuebingen.de. Specialty section: This article was submitted to. Movement Disorders, a section of ...

Mutation at the SCA17 locus is not a common cause of ...Springer

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von K Grundmann · · Zitiert von: 4 — Kathrin Grundmann M. D., Peter Bauer & Olaf Riess. Authors. Kathrin Grundmann M. D.. View author publications. You can also search for this author in PubMed ... von K Grundmann · · Zitiert von: 4 — Kathrin Grundmann M. D., Peter Bauer & Olaf Riess. Authors. Kathrin Grundmann M. D.. View author publications. You can also search for this author in PubMed ...