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

Year Number of Results
1980 1
1988 2
1989 5
1990 1
1991 2
1992 4
1993 1
1995 1
1996 2
1997 2
1999 3
2001 1
2003 1
2005 2
2006 1
2007 1
2008 4
2009 4
2010 2
2011 4
2012 7
2013 5
2014 6
2015 5
2016 4
2017 2
2018 1
2024 0

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69 results

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Page 1
Von Hippel-Lindau disease: gene to bedside.
Sims KB. Sims KB. Curr Opin Neurol. 2001 Dec;14(6):695-703. doi: 10.1097/00019052-200112000-00004. Curr Opin Neurol. 2001. PMID: 11723376 Review.
Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage.
Smith KR, Damiano J, Franceschetti S, Carpenter S, Canafoglia L, Morbin M, Rossi G, Pareyson D, Mole SE, Staropoli JF, Sims KB, Lewis J, Lin WL, Dickson DW, Dahl HH, Bahlo M, Berkovic SF. Smith KR, et al. Among authors: sims kb. Am J Hum Genet. 2012 Jun 8;90(6):1102-7. doi: 10.1016/j.ajhg.2012.04.021. Epub 2012 May 17. Am J Hum Genet. 2012. PMID: 22608501 Free PMC article.
Mutations in the Norrie disease gene.
Schuback DE, Chen ZY, Craig IW, Breakefield XO, Sims KB. Schuback DE, et al. Among authors: sims kb. Hum Mutat. 1995;5(4):285-92. doi: 10.1002/humu.1380050403. Hum Mutat. 1995. PMID: 7627181
Targeted exome sequencing of suspected mitochondrial disorders.
Lieber DS, Calvo SE, Shanahan K, Slate NG, Liu S, Hershman SG, Gold NB, Chapman BA, Thorburn DR, Berry GT, Schmahmann JD, Borowsky ML, Mueller DM, Sims KB, Mootha VK. Lieber DS, et al. Among authors: sims kb. Neurology. 2013 May 7;80(19):1762-70. doi: 10.1212/WNL.0b013e3182918c40. Epub 2013 Apr 17. Neurology. 2013. PMID: 23596069 Free PMC article.
69 results