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

Year Number of Results
1989 1
1992 2
1993 3
1994 9
1995 4
1996 4
1997 5
1998 13
1999 11
2000 11
2001 5
2002 5
2003 5
2004 10
2005 10
2006 3
2007 5
2008 5
2009 5
2010 8
2011 2
2012 3
2013 11
2014 6
2015 2
2016 3
2017 9
2018 5
2019 7
2020 4
2021 10
2022 11
2023 2
2024 0

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Similar articles for PMID: 16187142

185 results

Results by year

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Page 1
Genetic prion disease: the EUROCJD experience.
Kovács GG, Puopolo M, Ladogana A, Pocchiari M, Budka H, van Duijn C, Collins SJ, Boyd A, Giulivi A, Coulthart M, Delasnerie-Laupretre N, Brandel JP, Zerr I, Kretzschmar HA, de Pedro-Cuesta J, Calero-Lara M, Glatzel M, Aguzzi A, Bishop M, Knight R, Belay G, Will R, Mitrova E; EUROCJD. Kovács GG, et al. Hum Genet. 2005 Nov;118(2):166-74. doi: 10.1007/s00439-005-0020-1. Epub 2005 Nov 15. Hum Genet. 2005. PMID: 16187142
Mutations of the prion protein gene phenotypic spectrum.
Kovács GG, Trabattoni G, Hainfellner JA, Ironside JW, Knight RS, Budka H. Kovács GG, et al. J Neurol. 2002 Nov;249(11):1567-82. doi: 10.1007/s00415-002-0896-9. J Neurol. 2002. PMID: 12420099
Novel twelve-generation kindred of fatal familial insomnia from germany representing the entire spectrum of disease expression.
Harder A, Jendroska K, Kreuz F, Wirth T, Schafranka C, Karnatz N, Théallier-Janko A, Dreier J, Lohan K, Emmerich D, Cervós-Navarro J, Windl O, Kretzschmar HA, Nürnberg P, Witkowski R. Harder A, et al. Am J Med Genet. 1999 Dec 3;87(4):311-6. doi: 10.1002/(sici)1096-8628(19991203)87:4<311::aid-ajmg6>3.0.co;2-5. Am J Med Genet. 1999. PMID: 10588836
185 results