Pramstaller PP - Search Results

1

Restless legs syndrome: epidemiological and clinicogenetic study in a South Tyrolean population isolate.

Vogl FD, Pichler I, Adel S, Pinggera GK, Bracco S, De Grandi A, Volpato CB, Aridon P, Mayer T, Meitinger T, Klein C, Casari G, Pramstaller PP. Vogl FD, et al. Among authors: pramstaller pp. Mov Disord. 2006 Aug;21(8):1189-95. doi: 10.1002/mds.20922. Mov Disord. 2006. PMID: 16685686

2

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.

3

Mode of inheritance and susceptibility locus for restless legs syndrome, on chromosome 12q.

Kock N, Culjkovic B, Maniak S, Schilling K, Müller B, Zühlke C, Ozelius L, Klein C, Pramstaller PP, Kramer PL. Kock N, et al. Among authors: pramstaller pp. Am J Hum Genet. 2002 Jul;71(1):205-8; author reply 208. doi: 10.1086/341097. Am J Hum Genet. 2002. PMID: 12068378 Free PMC article. No abstract available.

4

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

5

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.

6

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

7

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

8

Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease?

Hedrich K, Pramstaller PP, Stübke K, Hiller A, Kabakci K, Purmann S, Kasten M, Scaglione C, Schwinger E, Volkmann J, Kostic V, Vieregge P, Martinelli P, Abbruzzese G, Klein C, Zühlke C. Hedrich K, et al. Among authors: pramstaller pp. Mov Disord. 2005 Aug;20(8):1060-2. doi: 10.1002/mds.20512. Mov Disord. 2005. PMID: 15929093

9

Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers.

Pramstaller PP, Schlossmacher MG, Jacques TS, Scaravilli F, Eskelson C, Pepivani I, Hedrich K, Adel S, Gonzales-McNeal M, Hilker R, Kramer PL, Klein C. Pramstaller PP, et al. Ann Neurol. 2005 Sep;58(3):411-22. doi: 10.1002/ana.20587. Ann Neurol. 2005. PMID: 16130111

10

Co-occurrence of restless legs syndrome and Parkin mutations in two families.

Adel S, Djarmati A, Kabakci K, Pichler I, Eskelson C, Lohnau T, Kock N, Hagenah J, Hedrich K, Schwinger E, Kramer PL, Pramstaller PP, Klein C. Adel S, et al. Among authors: pramstaller pp. Mov Disord. 2006 Feb;21(2):258-63. doi: 10.1002/mds.20690. Mov Disord. 2006. PMID: 16161156

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