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Year | Number of Results |
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2009 | 2 |
2010 | 1 |
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Page 1
Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study.
J Huntingtons Dis. 2018;7(3):209-222. doi: 10.3233/JHD-170263.
J Huntingtons Dis. 2018.
PMID: 30103338
Estimating premorbid IQ in the prodromal phase of a neurodegenerative disease.
Carlozzi NE, Stout JC, Mills JA, Duff K, Beglinger LJ, Aylward EH, Whitlock KB, Solomon AC, Queller S, Langbehn DR, Johnson SA, Paulsen JS; Predict-Hd Investigators Of The Huntington Study Group.
Carlozzi NE, et al.
Clin Neuropsychol. 2011 Jul;25(5):757-77. doi: 10.1080/13854046.2011.577811.
Clin Neuropsychol. 2011.
PMID: 21660882
Free PMC article.
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Challenges assessing clinical endpoints in early Huntington disease.
Paulsen JS, Wang C, Duff K, Barker R, Nance M, Beglinger L, Moser D, Williams JK, Simpson S, Langbehn D, van Kammen DP; PREDICT-HD Investigators of the Huntington Study Group.
Paulsen JS, et al.
Mov Disord. 2010 Nov 15;25(15):2595-603. doi: 10.1002/mds.23337.
Mov Disord. 2010.
PMID: 20623772
Free PMC article.
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Discrepancies in reporting the CAG repeat lengths for Huntington's disease.
Quarrell OW, Handley O, O'Donovan K, Dumoulin C, Ramos-Arroyo M, Biunno I, Bauer P, Kline M, Landwehrmeyer GB; European Huntington’s Disease Network.
Quarrell OW, et al.
Eur J Hum Genet. 2012 Jan;20(1):20-6. doi: 10.1038/ejhg.2011.136. Epub 2011 Aug 3.
Eur J Hum Genet. 2012.
PMID: 21811303
Free PMC article.
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Motor abnormalities in premanifest persons with Huntington's disease: the PREDICT-HD study.
Biglan KM, Ross CA, Langbehn DR, Aylward EH, Stout JC, Queller S, Carlozzi NE, Duff K, Beglinger LJ, Paulsen JS; PREDICT-HD Investigators of the Huntington Study Group.
Biglan KM, et al.
Mov Disord. 2009 Sep 15;24(12):1763-72. doi: 10.1002/mds.22601.
Mov Disord. 2009.
PMID: 19562761
Free PMC article.
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Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease.
Aziz NA, Jurgens CK, Landwehrmeyer GB; EHDN Registry Study Group; van Roon-Mom WM, van Ommen GJ, Stijnen T, Roos RA.
Aziz NA, et al.
Neurology. 2009 Oct 20;73(16):1280-5. doi: 10.1212/WNL.0b013e3181bd1121. Epub 2009 Sep 23.
Neurology. 2009.
PMID: 19776381
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NMDA receptor gene variations as modifiers in Huntington disease: a replication study.
Saft C, Epplen JT, Wieczorek S, Landwehrmeyer GB, Roos RA, de Yebenes JG, Dose M, Tabrizi SJ, Craufurd D; REGISTRY Investigators of the European Huntington's Disease Network; Arning L.
Saft C, et al.
PLoS Curr. 2011 Oct 4;3:RRN1247. doi: 10.1371/currents.RRN1247.
PLoS Curr. 2011.
PMID: 21989477
Free PMC article.
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