Pramstaller PP - Search Results

1

Impaired sense of smell and color discrimination in monogenic and idiopathic Parkinson's disease.

Kertelge L, Brüggemann N, Schmidt A, Tadic V, Wisse C, Dankert S, Drude L, van der Vegt J, Siebner H, Pawlack H, Pramstaller PP, Behrens MI, Ramirez A, Reichel D, Buhmann C, Hagenah J, Klein C, Lohmann K, Kasten M. Kertelge L, et al. Among authors: pramstaller pp. Mov Disord. 2010 Nov 15;25(15):2665-9. doi: 10.1002/mds.23272. Mov Disord. 2010. PMID: 20721915

2

Association studies of Parkinson's disease and parkin polymorphisms.

Klein C, Schumacher K, Jacobs H, Hagenah J, Kis B, Garrels J, Schwinger E, Ozelius L, Pramstaller P, Vieregge P, Kramer PL. Klein C, et al. Ann Neurol. 2000 Jul;48(1):126-7. Ann Neurol. 2000. PMID: 10894229 No abstract available.

3

The striatal dopaminergic deficit is dependent on the number of mutant alleles in a family with mutations in the parkin gene: evidence for enzymatic parkin function in humans.

Hilker R, Klein C, Hedrich K, Ozelius LJ, Vieregge P, Herholz K, Pramstaller PP, Heiss WD. Hilker R, et al. Among authors: pramstaller pp. Neurosci Lett. 2002 Apr 19;323(1):50-4. doi: 10.1016/s0304-3940(01)02529-0. Neurosci Lett. 2002. PMID: 11911988

4

Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene.

Pramstaller PP, Kis B, Eskelson C, Hedrich K, Scherer M, Schwinger E, Breakefield XO, Kramer PL, Ozelius LJ, Klein C. Pramstaller PP, et al. Mov Disord. 2002 Mar;17(2):424-6. doi: 10.1002/mds.10071. Mov Disord. 2002. PMID: 11921141 No abstract available.

5

Role of parkin mutations in 111 community-based patients with early-onset parkinsonism.

Kann M, Jacobs H, Mohrmann K, Schumacher K, Hedrich K, Garrels J, Wiegers K, Schwinger E, Pramstaller PP, Breakefield XO, Ozelius LJ, Vieregge P, Klein C. Kann M, et al. Among authors: pramstaller pp. Ann Neurol. 2002 May;51(5):621-5. doi: 10.1002/ana.10179. Ann Neurol. 2002. PMID: 12112109

6

NR4A2 mutations are rare among European patients with familial Parkinson's disease.

Wellenbrock C, Hedrich K, Schäfer N, Kasten M, Jacobs H, Schwinger E, Hagenah J, Pramstaller PP, Vieregge P, Klein C. Wellenbrock C, et al. Among authors: pramstaller pp. Ann Neurol. 2003 Sep;54(3):415. doi: 10.1002/ana.10736. Ann Neurol. 2003. PMID: 12953278 No abstract available.

7

Clinical and genetic features of myoclonus-dystonia in 3 cases: a video presentation.

Kock N, Kasten M, Schüle B, Hedrich K, Wiegers K, Kabakci K, Hagenah J, Pramstaller PP, Nitschke MF, Münchau A, Sperner J, Klein C. Kock N, et al. Among authors: pramstaller pp. Mov Disord. 2004 Feb;19(2):231-4. doi: 10.1002/mds.10635. Mov Disord. 2004. PMID: 14978685

8

Distribution, type, and origin of Parkin mutations: review and case studies.

Hedrich K, Eskelson C, Wilmot B, Marder K, Harris J, Garrels J, Meija-Santana H, Vieregge P, Jacobs H, Bressman SB, Lang AE, Kann M, Abbruzzese G, Martinelli P, Schwinger E, Ozelius LJ, Pramstaller PP, Klein C, Kramer P. Hedrich K, et al. Among authors: pramstaller pp. Mov Disord. 2004 Oct;19(10):1146-57. doi: 10.1002/mds.20234. Mov Disord. 2004. PMID: 15390068 Review.

9

Brain parenchyma sonography detects preclinical parkinsonism.

Walter U, Klein C, Hilker R, Benecke R, Pramstaller PP, Dressler D. Walter U, et al. Among authors: pramstaller pp. Mov Disord. 2004 Dec;19(12):1445-9. doi: 10.1002/mds.20232. Mov Disord. 2004. PMID: 15390070

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: pramstaller pp. Mov Disord. 2005 Sep;20(9):1191-4. doi: 10.1002/mds.20504. Mov Disord. 2005. PMID: 15895422

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