Rissling I - Search Results

1

Daytime sleep latency in medication-matched Parkinsonian patients with and without sudden onset of sleep.

Möller JC, Rethfeldt M, Körner Y, Stiasny-Kolster K, Cassel W, Meindorfner C, Rissling I, Krüger HP, Oertel WH. Möller JC, et al. Among authors: rissling i. Mov Disord. 2005 Dec;20(12):1620-2. doi: 10.1002/mds.20630. Mov Disord. 2005. PMID: 16078226

2

Dopamine receptor gene polymorphisms in Parkinson's disease patients reporting "sleep attacks".

Rissling I, Geller F, Bandmann O, Stiasny-Kolster K, Körner Y, Meindorfner C, Krüger HP, Oertel WH, Möller JC. Rissling I, et al. Mov Disord. 2004 Nov;19(11):1279-84. doi: 10.1002/mds.20245. Mov Disord. 2004. PMID: 15390060

3

Preprohypocretin polymorphisms in Parkinson disease patients reporting "sleep attacks".

Rissling I, Körner Y, Geller F, Stiasny-Kolster K, Oertel WH, Möller JC. Rissling I, et al. Sleep. 2005 Jul;28(7):871-5. doi: 10.1093/sleep/28.7.871. Sleep. 2005. PMID: 16124668

4

Daytime sleepiness and the COMT val158met polymorphism in patients with Parkinson disease.

Rissling I, Frauscher B, Kronenberg F, Tafti M, Stiasny-Kolster K, Robyr AC, Körner Y, Oertel WH, Poewe W, Högl B, Möller JC. Rissling I, et al. Sleep. 2006 Jan;29(1):108-11. Sleep. 2006. PMID: 16453988

5

The PLA2G6 gene in early-onset Parkinson's disease.

Kauther KM, Höft C, Rissling I, Oertel WH, Möller JC. Kauther KM, et al. Among authors: rissling i. Mov Disord. 2011 Nov;26(13):2415-7. doi: 10.1002/mds.23851. Epub 2011 Aug 2. Mov Disord. 2011. PMID: 21812034

6

Enhancing recognition of early Parkinsonism in the community.

Höglinger GU, Rissling I, Metz A, Ries V, Heinermann A, Prinz H, Spieker S, Deuschl G, Baum E, Oertel WH. Höglinger GU, et al. Among authors: rissling i. Mov Disord. 2004 May;19(5):505-12. doi: 10.1002/mds.20033. Mov Disord. 2004. PMID: 15133813

7

Haplotype analysis of the engrailed-2 gene in young-onset Parkinson's disease.

Rissling I, Strauch K, Höft C, Oertel WH, Möller JC. Rissling I, et al. Neurodegener Dis. 2009;6(3):102-5. doi: 10.1159/000207796. Epub 2009 Mar 6. Neurodegener Dis. 2009. PMID: 19270442

8

The prevalence of the G2019S and R1441C/G/H mutations in LRRK2 in German patients with Parkinson's disease.

Möller JC, Rissling I, Mylius V, Höft C, Eggert KM, Oertel WH. Möller JC, et al. Among authors: rissling i. Eur J Neurol. 2008 Jul;15(7):743-5. doi: 10.1111/j.1468-1331.2008.02154.x. Epub 2008 May 15. Eur J Neurol. 2008. PMID: 18484993

9

Prevalence of the H1069Q mutation in ATP7B in discordant pairs with early-onset Parkinson's disease.

Möller JC, Leinweber B, Rissling I, Oertel WH, Bandmann O, Schmidt HH. Möller JC, et al. Among authors: rissling i. Mov Disord. 2006 Oct;21(10):1789-90. doi: 10.1002/mds.21066. Mov Disord. 2006. PMID: 16941464 No abstract available.

10

The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients.

Metzger S, Walter C, Riess O, Roos RA, Nielsen JE, Craufurd D; REGISTRY Investigators of the European Huntington’s Disease Network; Nguyen HP. Metzger S, et al. PLoS One. 2013 Jul 22;8(7):e68951. doi: 10.1371/journal.pone.0068951. Print 2013. PLoS One. 2013. PMID: 23894380 Free PMC article.

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