Bauer P - Search Results

1

Mutations in CIZ1 are not a major cause for dystonia in Germany.

Dufke C, Hauser AK, Sturm M, Fluhr S, Wächter T, Leube B, Auburger G, Ott T, Bauer P, Gasser T, Grundmann K. Dufke C, et al. Among authors: bauer p. Mov Disord. 2015 Apr 15;30(5):740-3. doi: 10.1002/mds.26198. Epub 2015 Mar 17. Mov Disord. 2015. PMID: 25778706 No abstract available.

2

Frequency and phenotypic variability of the GAG deletion of the DYT1 gene in an unselected group of patients with dystonia.

Grundmann K, Laubis-Herrmann U, Bauer I, Dressler D, Vollmer-Haase J, Bauer P, Stuhrmann M, Schulte T, Schöls L, Topka H, Riess O. Grundmann K, et al. Among authors: bauer i, bauer p. Arch Neurol. 2003 Sep;60(9):1266-70. doi: 10.1001/archneur.60.9.1266. Arch Neurol. 2003. PMID: 12975293

3

Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystonias.

Grundmann K, Laubis-Herrmann U, Dressler D, Vollmer-Haase J, Bauer P, Stuhrmann M, Schulte T, Schöls L, Topka H, Riess O. Grundmann K, et al. Among authors: bauer p. Mov Disord. 2004 Nov;19(11):1294-7. doi: 10.1002/mds.20128. Mov Disord. 2004. PMID: 15390016

4

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

Grundmann K, Laubis-Herrmann U, Dressler D, Vollmer-Haase J, Bauer P, Stuhrmann M, Schulte T, Schöls L, Topka H, Riess O. Grundmann K, et al. Among authors: bauer p. J Neurol. 2004 Oct;251(10):1232-4. doi: 10.1007/s00415-004-0520-2. J Neurol. 2004. PMID: 15503103

5

Alpha-synuclein and Parkinson's disease: implications from the screening of more than 1,900 patients.

Berg D, Niwar M, Maass S, Zimprich A, Möller JC, Wuellner U, Schmitz-Hübsch T, Klein C, Tan EK, Schöls L, Marsh L, Dawson TM, Janetzky B, Müller T, Woitalla D, Kostic V, Pramstaller PP, Oertel WH, Bauer P, Krueger R, Gasser T, Riess O. Berg D, et al. Among authors: bauer p. Mov Disord. 2005 Sep;20(9):1191-4. doi: 10.1002/mds.20504. Mov Disord. 2005. PMID: 15895422

6

Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause.

Bauer P, Kreuz FR, Bürk K, Saft C, Andrich J, Heilemann H, Riess O, Schöls L. Bauer P, et al. Mov Disord. 2006 Oct;21(10):1734-7. doi: 10.1002/mds.21031. Mov Disord. 2006. PMID: 16830318

7

Mitochondrial translation initiation factor 3 gene polymorphism associated with Parkinson's disease.

Abahuni N, Gispert S, Bauer P, Riess O, Krüger R, Becker T, Auburger G. Abahuni N, et al. Among authors: bauer p. Neurosci Lett. 2007 Mar 6;414(2):126-9. doi: 10.1016/j.neulet.2006.12.053. Epub 2007 Jan 11. Neurosci Lett. 2007. PMID: 17267121

8

Transcranial ultrasound in different monogenetic subtypes of Parkinson's disease.

Schweitzer KJ, Brüssel T, Leitner P, Krüger R, Bauer P, Woitalla D, Tomiuk J, Gasser T, Berg D. Schweitzer KJ, et al. Among authors: bauer p. J Neurol. 2007 May;254(5):613-6. doi: 10.1007/s00415-006-0369-7. Epub 2007 Apr 6. J Neurol. 2007. PMID: 17415511

9

Prevalence of THAP1 sequence variants in German patients with primary dystonia.

Söhn AS, Glöckle N, Doetzer AD, Deuschl G, Felbor U, Topka HR, Schöls L, Riess O, Bauer P, Müller U, Grundmann K. Söhn AS, et al. Among authors: bauer p. Mov Disord. 2010 Sep 15;25(12):1982-6. doi: 10.1002/mds.23207. Mov Disord. 2010. PMID: 20669277

10

Lack of sequence variations in THAP1 gene and THAP1-binding sites in TOR1A promoter of DYT1 patients.

Palada V, Stiern S, Glöckle N, Gómez-Garre P, Carrillo F, Mir P, Szczaluba K, Tinazzi M, Ajena D, Romani M, Valente EM, Müller U, Bauer P, Riess O, Ott T, Grundmann K. Palada V, et al. Among authors: bauer p. Mov Disord. 2012 Jun;27(7):917. doi: 10.1002/mds.24974. Epub 2012 Apr 16. Mov Disord. 2012. PMID: 22508326 No abstract available.

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