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Year | Number of Results |
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2008 | 1 |
2011 | 1 |
2012 | 3 |
2024 | 0 |
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Page 1
Autosomal dominant dopa-responsive parkinsonism in a multigenerational Swiss family.
Parkinsonism Relat Disord. 2008 Aug;14(6):465-70. doi: 10.1016/j.parkreldis.2007.11.013. Epub 2008 Mar 14.
Parkinsonism Relat Disord. 2008.
PMID: 18342564
A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease.
Zimprich A, Benet-Pagès A, Struhal W, Graf E, Eck SH, Offman MN, Haubenberger D, Spielberger S, Schulte EC, Lichtner P, Rossle SC, Klopp N, Wolf E, Seppi K, Pirker W, Presslauer S, Mollenhauer B, Katzenschlager R, Foki T, Hotzy C, Reinthaler E, Harutyunyan A, Kralovics R, Peters A, Zimprich F, Brücke T, Poewe W, Auff E, Trenkwalder C, Rost B, Ransmayr G, Winkelmann J, Meitinger T, Strom TM.
Zimprich A, et al.
Am J Hum Genet. 2011 Jul 15;89(1):168-75. doi: 10.1016/j.ajhg.2011.06.008.
Am J Hum Genet. 2011.
PMID: 21763483
Free PMC article.
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VPS35 mutation in Japanese patients with typical Parkinson's disease.
Ando M, Funayama M, Li Y, Kashihara K, Murakami Y, Ishizu N, Toyoda C, Noguchi K, Hashimoto T, Nakano N, Sasaki R, Kokubo Y, Kuzuhara S, Ogaki K, Yamashita C, Yoshino H, Hatano T, Tomiyama H, Hattori N.
Ando M, et al.
Mov Disord. 2012 Sep 15;27(11):1413-7. doi: 10.1002/mds.25145. Epub 2012 Sep 18.
Mov Disord. 2012.
PMID: 22991136
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Identification of VPS35 mutations replicated in French families with Parkinson disease.
Lesage S, Condroyer C, Klebe S, Honoré A, Tison F, Brefel-Courbon C, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group.
Lesage S, et al.
Neurology. 2012 May 1;78(18):1449-50. doi: 10.1212/WNL.0b013e318253d5f2. Epub 2012 Apr 18.
Neurology. 2012.
PMID: 22517097
No abstract available.
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Frequency of the D620N mutation in VPS35 in Parkinson disease.
Kumar KR, Weissbach A, Heldmann M, Kasten M, Tunc S, Sue CM, Svetel M, Kostić VS, Segura-Aguilar J, Ramirez A, Simon DK, Vieregge P, Münte TF, Hagenah J, Klein C, Lohmann K.
Kumar KR, et al.
Arch Neurol. 2012 Oct;69(10):1360-4. doi: 10.1001/archneurol.2011.3367.
Arch Neurol. 2012.
PMID: 22801713
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