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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 1
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1997 2
1998 3
1999 4
2000 4
2001 2
2002 3
2003 5
2004 9
2005 8
2006 6
2007 3
2008 2
2009 3
2010 4
2011 2
2012 2
2013 3
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Similar articles for PMID: 15806397

108 results

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Page 1
Ancestral origins of the prion protein gene D178N mutation in the Basque Country.
Rodríguez-Martínez AB, Barreau C, Coupry I, Yagüe J, Sánchez-Valle R, Galdós-Alcelay L, Ibáñez A, Digón A, Fernández-Manchola I, Goizet C, Castro A, Cuevas N, Alvarez-Alvarez M, de Pancorbo MM, Arveiler B, Zarranz JJ. Rodríguez-Martínez AB, et al. Hum Genet. 2005 Jun;117(1):61-9. doi: 10.1007/s00439-005-1277-0. Epub 2005 Apr 2. Hum Genet. 2005. PMID: 15806397
Phenotypic variability in familial prion diseases due to the D178N mutation.
Zarranz JJ, Digon A, Atarés B, Rodríguez-Martínez AB, Arce A, Carrera N, Fernández-Manchola I, Fernández-Martínez M, Fernández-Maiztegui C, Forcadas I, Galdos L, Gómez-Esteban JC, Ibáñez A, Lezcano E, López de Munain A, Martí-Massó JF, Mendibe MM, Urtasun M, Uterga JM, Saracibar N, Velasco F, de Pancorbo MM. Zarranz JJ, et al. J Neurol Neurosurg Psychiatry. 2005 Nov;76(11):1491-6. doi: 10.1136/jnnp.2004.056606. J Neurol Neurosurg Psychiatry. 2005. PMID: 16227536 Free PMC article.
Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
Schmitz M, Lüllmann K, Zafar S, Ebert E, Wohlhage M, Oikonomou P, Schlomm M, Mitrova E, Beekes M, Zerr I. Schmitz M, et al. Neurobiol Aging. 2014 May;35(5):1177-88. doi: 10.1016/j.neurobiolaging.2013.11.010. Epub 2013 Nov 16. Neurobiol Aging. 2014. PMID: 24360565
108 results