Bauer P - Search Results

1

SCA3: neurological features, pathogenesis and animal models.

Riess O, Rüb U, Pastore A, Bauer P, Schöls L. Riess O, et al. Among authors: bauer p. Cerebellum. 2008;7(2):125-37. doi: 10.1007/s12311-008-0013-4. Cerebellum. 2008. PMID: 18418689 Review.

2

Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17).

Rolfs A, Koeppen AH, Bauer I, Bauer P, Buhlmann S, Topka H, Schöls L, Riess O. Rolfs A, et al. Among authors: bauer i, bauer p. Ann Neurol. 2003 Sep;54(3):367-75. doi: 10.1002/ana.10676. Ann Neurol. 2003. PMID: 12953269

3

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

4

Screening for mutations of the ferritin light and heavy genes in Parkinson's disease patients with hyperechogenicity of the substantia nigra.

Felletschin B, Bauer P, Walter U, Behnke S, Spiegel J, Csoti I, Sommer U, Zeiler B, Becker G, Riess O, Berg D. Felletschin B, et al. Among authors: bauer p. Neurosci Lett. 2003 Nov 27;352(1):53-6. doi: 10.1016/j.neulet.2003.08.026. Neurosci Lett. 2003. PMID: 14615048

5

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.

Schöls L, Bauer P, Schmidt T, Schulte T, Riess O. Schöls L, et al. Among authors: bauer p. Lancet Neurol. 2004 May;3(5):291-304. doi: 10.1016/S1474-4422(04)00737-9. Lancet Neurol. 2004. PMID: 15099544 Review.

6

Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7).

Hering R, Strauss KM, Tao X, Bauer A, Woitalla D, Mietz EM, Petrovic S, Bauer P, Schaible W, Müller T, Schöls L, Klein C, Berg D, Meyer PT, Schulz JB, Wollnik B, Tong L, Krüger R, Riess O. Hering R, et al. Among authors: bauer p, bauer a. Hum Mutat. 2004 Oct;24(4):321-9. doi: 10.1002/humu.20089. Hum Mutat. 2004. PMID: 15365989

7

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

8

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

9

B-raf and Ha-ras mutations in chemically induced mouse liver tumors.

Jaworski M, Buchmann A, Bauer P, Riess O, Schwarz M. Jaworski M, et al. Among authors: bauer p. Oncogene. 2005 Feb 10;24(7):1290-5. doi: 10.1038/sj.onc.1208265. Oncogene. 2005. PMID: 15592514

10

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

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