Bauer P - Search Results

1

Genetic variability in the dopamine system (dopamine receptor D4, catechol-O-methyltransferase) modulates neurophysiological responses to gains and losses.

Marco-Pallarés J, Cucurell D, Cunillera T, Krämer UM, Càmara E, Nager W, Bauer P, Schüle R, Schöls L, Münte TF, Rodriguez-Fornells A. Marco-Pallarés J, et al. Among authors: bauer p. Biol Psychiatry. 2009 Jul 15;66(2):154-61. doi: 10.1016/j.biopsych.2009.01.006. Epub 2009 Feb 28. Biol Psychiatry. 2009. PMID: 19251248

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

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.

5

Spectrin mutations in spinocerebellar ataxia (SCA).

Bauer P, Schöls L, Riess O. Bauer P, et al. Bioessays. 2006 Aug;28(8):785-7. doi: 10.1002/bies.20443. Bioessays. 2006. PMID: 16927298 Review.

6

Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia.

Hehr U, Bauer P, Winner B, Schule R, Olmez A, Koehler W, Uyanik G, Engel A, Lenz D, Seibel A, Hehr A, Ploetz S, Gamez J, Rolfs A, Weis J, Ringer TM, Bonin M, Schuierer G, Marienhagen J, Bogdahn U, Weber BH, Topaloglu H, Schols L, Riess O, Winkler J. Hehr U, et al. Among authors: bauer p. Ann Neurol. 2007 Dec;62(6):656-65. doi: 10.1002/ana.21310. Ann Neurol. 2007. PMID: 18067136

7

The impact of catechol-O-methyltransferase and dopamine D4 receptor genotypes on neurophysiological markers of performance monitoring.

Krämer UM, Cunillera T, Càmara E, Marco-Pallarés J, Cucurell D, Nager W, Bauer P, Schüle R, Schöls L, Rodriguez-Fornells A, Münte TF. Krämer UM, et al. Among authors: bauer p. J Neurosci. 2007 Dec 19;27(51):14190-8. doi: 10.1523/JNEUROSCI.4229-07.2007. J Neurosci. 2007. PMID: 18094258 Free PMC article.

8

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.

9

Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridization.

Bauer P, Winner B, Schüle R, Bauer C, Häfele V, Hehr U, Bonin M, Walter M, Karle K, Ringer TM, Riess O, Winkler J, Schöls L. Bauer P, et al. Among authors: bauer c. Neurogenetics. 2009 Feb;10(1):43-8. doi: 10.1007/s10048-008-0144-2. Epub 2008 Sep 12. Neurogenetics. 2009. PMID: 18787847

10

The effects of COMT (Val108/158Met) and DRD4 (SNP -521) dopamine genotypes on brain activations related to valence and magnitude of rewards.

Camara E, Krämer UM, Cunillera T, Marco-Pallarés J, Cucurell D, Nager W, Mestres-Missé A, Bauer P, Schüle R, Schöls L, Tempelmann C, Rodriguez-Fornells A, Münte TF. Camara E, et al. Among authors: bauer p. Cereb Cortex. 2010 Aug;20(8):1985-96. doi: 10.1093/cercor/bhp263. Epub 2009 Dec 27. Cereb Cortex. 2010. PMID: 20038544

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