Trenkwalder C - Search Results

1

The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval.

Zimprich A, Müller-Myhsok B, Farrer M, Leitner P, Sharma M, Hulihan M, Lockhart P, Strongosky A, Kachergus J, Calne DB, Stoessl J, Uitti RJ, Pfeiffer RF, Trenkwalder C, Homann N, Ott E, Wenzel K, Asmus F, Hardy J, Wszolek Z, Gasser T. Zimprich A, et al. Among authors: trenkwalder c. Am J Hum Genet. 2004 Jan;74(1):11-9. doi: 10.1086/380647. Epub 2003 Dec 19. Am J Hum Genet. 2004. PMID: 14691730 Free PMC article.

2

Apomorphine test for dopaminergic responsiveness in patients with previously untreated Parkinson's disease.

Gasser T, Schwarz J, Arnold G, Trenkwalder C, Oertel WH. Gasser T, et al. Among authors: trenkwalder c. Arch Neurol. 1992 Nov;49(11):1131-4. doi: 10.1001/archneur.1992.00530350045017. Arch Neurol. 1992. PMID: 1444878

3

123I-iodobenzamide-SPECT predicts dopaminergic responsiveness in patients with de novo parkinsonism.

Schwarz J, Tatsch K, Arnold G, Gasser T, Trenkwalder C, Kirsch CM, Oertel WH. Schwarz J, et al. Among authors: trenkwalder c. Neurology. 1992 Mar;42(3 Pt 1):556-61. doi: 10.1212/wnl.42.3.556. Neurology. 1992. PMID: 1549216

4

Clinical symptoms and possible anticipation in a large kindred of familial restless legs syndrome.

Trenkwalder C, Seidel VC, Gasser T, Oertel WH. Trenkwalder C, et al. Mov Disord. 1996 Jul;11(4):389-94. doi: 10.1002/mds.870110407. Mov Disord. 1996. PMID: 8813218

5

Striatal dopamine transporter binding assessed by [I-123]IPT and single photon emission computed tomography in patients with early Parkinson's disease: implications for a preclinical diagnosis.

Schwarz J, Linke R, Kerner M, Mozley PD, Trenkwalder C, Gasser T, Tatsch K. Schwarz J, et al. Among authors: trenkwalder c. Arch Neurol. 2000 Feb;57(2):205-8. doi: 10.1001/archneur.57.2.205. Arch Neurol. 2000. PMID: 10681078 Clinical Trial.

6

Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families.

Winkelmann J, Muller-Myhsok B, Wittchen HU, Hock B, Prager M, Pfister H, Strohle A, Eisensehr I, Dichgans M, Gasser T, Trenkwalder C. Winkelmann J, et al. Among authors: trenkwalder c. Ann Neurol. 2002 Sep;52(3):297-302. doi: 10.1002/ana.10282. Ann Neurol. 2002. PMID: 12205641

7

Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease.

Zimprich A, Asmus F, Leitner P, Castro M, Bereznai B, Homann N, Ott E, Rutgers AW, Wieditz G, Trenkwalder C, Gasser T. Zimprich A, et al. Among authors: trenkwalder c. Neurogenetics. 2003 Aug;4(4):219-20. doi: 10.1007/s10048-003-0156-x. Epub 2003 Jun 25. Neurogenetics. 2003. PMID: 12827450 No abstract available.

8

Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.

Winkelmann J, Lichtner P, Pütz B, Trenkwalder C, Hauk S, Meitinger T, Strom T, Muller-Myhsok B. Winkelmann J, et al. Among authors: trenkwalder c. Mov Disord. 2006 Jan;21(1):28-33. doi: 10.1002/mds.20627. Mov Disord. 2006. PMID: 16124010

9

RLS3: fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity.

Liebetanz KM, Winkelmann J, Trenkwalder C, Pütz B, Dichgans M, Gasser T, Müller-Myhsok B. Liebetanz KM, et al. Among authors: trenkwalder c. Neurology. 2006 Jul 25;67(2):320-1. doi: 10.1212/01.wnl.0000224886.65213.b5. Neurology. 2006. PMID: 16864828

10

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.

Winkelmann J, Schormair B, Lichtner P, Ripke S, Xiong L, Jalilzadeh S, Fulda S, Pütz B, Eckstein G, Hauk S, Trenkwalder C, Zimprich A, Stiasny-Kolster K, Oertel W, Bachmann CG, Paulus W, Peglau I, Eisensehr I, Montplaisir J, Turecki G, Rouleau G, Gieger C, Illig T, Wichmann HE, Holsboer F, Müller-Myhsok B, Meitinger T. Winkelmann J, et al. Among authors: trenkwalder c. Nat Genet. 2007 Aug;39(8):1000-6. doi: 10.1038/ng2099. Epub 2007 Jul 18. Nat Genet. 2007. PMID: 17637780

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