Winkelmann J - Search Results

1

Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease.

Schulte EC, Fukumori A, Mollenhauer B, Hor H, Arzberger T, Perneczky R, Kurz A, Diehl-Schmid J, Hüll M, Lichtner P, Eckstein G, Zimprich A, Haubenberger D, Pirker W, Brücke T, Bereznai B, Molnar MJ, Lorenzo-Betancor O, Pastor P, Peters A, Gieger C, Estivill X, Meitinger T, Kretzschmar HA, Trenkwalder C, Haass C, Winkelmann J. Schulte EC, et al. Among authors: winkelmann j. Eur J Hum Genet. 2015 Oct;23(10):1328-33. doi: 10.1038/ejhg.2014.300. Epub 2015 Jan 21. Eur J Hum Genet. 2015. PMID: 25604855 Free PMC article.

2

Nonmotor fluctuations in patients with Parkinson's disease.

Friess E, Winkelmann J, Trenkwalder C. Friess E, et al. Among authors: winkelmann j. Neurology. 1997 Nov;49(5):1472. doi: 10.1212/wnl.49.5.1472-a. Neurology. 1997. PMID: 9371950 No abstract available.

3

Treatment of restless leg syndrome with pergolide--an open clinical trial.

Winkelmann J, Wetter TC, Stiasny K, Oertel WH, Trenkwalder C. Winkelmann J, et al. Mov Disord. 1998 May;13(3):566-9. doi: 10.1002/mds.870130333. Mov Disord. 1998. PMID: 9613756 Clinical Trial.

4

[Restless leg syndrome].

Winkelmann J, Collado-Seidel V, Trenkwalder C. Winkelmann J, et al. Med Monatsschr Pharm. 1999 Mar;22(3):67-71. Med Monatsschr Pharm. 1999. PMID: 10097580 Review. German. No abstract available.

5

Magnetic resonance imaging findings in corticobasal degeneration.

Winkelmann J, Auer DP, Lechner C, Elbel G, Trenkwalder C. Winkelmann J, et al. Mov Disord. 1999 Jul;14(4):669-73. doi: 10.1002/1531-8257(199907)14:4<669::aid-mds1018>3.0.co;2-y. Mov Disord. 1999. PMID: 10435506

6

Visual hallucinations, white matter lesions and disease severity in Parkinson's disease.

Kraft E, Winkelmann J, Trenkwalder C, Auer DP. Kraft E, et al. Among authors: winkelmann j. Acta Neurol Scand. 1999 Jun;99(6):362-7. doi: 10.1111/j.1600-0404.1999.tb07365.x. Acta Neurol Scand. 1999. PMID: 10577270

7

[Pathophysiology of restless-legs syndrome. Review of current research].

Winkelmann J, Trenkwalder C. Winkelmann J, et al. Nervenarzt. 2001 Feb;72(2):100-7. doi: 10.1007/s001150050721. Nervenarzt. 2001. PMID: 11256143 Review. German.

8

Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome.

Zimprich A, Grabowski M, Asmus F, Naumann M, Berg D, Bertram M, Scheidtmann K, Kern P, Winkelmann J, Müller-Myhsok B, Riedel L, Bauer M, Müller T, Castro M, Meitinger T, Strom TM, Gasser T. Zimprich A, et al. Among authors: winkelmann j. Nat Genet. 2001 Sep;29(1):66-9. doi: 10.1038/ng709. Nat Genet. 2001. PMID: 11528394

9

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. Ann Neurol. 2002 Sep;52(3):297-302. doi: 10.1002/ana.10282. Ann Neurol. 2002. PMID: 12205641

10

Long-term course of restless legs syndrome in dialysis patients after kidney transplantation.

Winkelmann J, Stautner A, Samtleben W, Trenkwalder C. Winkelmann J, et al. Mov Disord. 2002 Sep;17(5):1072-6. doi: 10.1002/mds.10231. Mov Disord. 2002. PMID: 12360562

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