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Results by year

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

Year Number of Results
1983 1
1988 1
1991 1
1994 1
1997 1
1998 1
2000 1
2005 1
2006 1
2007 2
2008 2
2010 2
2011 1
2013 1
2014 2
2016 3
2017 2
2018 1
2019 1
2024 0

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PubMed for id: 343184

24 results

Results by year

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Page 1
SYNE1 mutations in autosomal recessive cerebellar ataxia.
Noreau A, Bourassa CV, Szuto A, Levert A, Dobrzeniecka S, Gauthier J, Forlani S, Durr A, Anheim M, Stevanin G, Brice A, Bouchard JP, Dion PA, Dupré N, Rouleau GA. Noreau A, et al. JAMA Neurol. 2013 Oct;70(10):1296-31. doi: 10.1001/jamaneurol.2013.3268. JAMA Neurol. 2013. PMID: 23959263
PLA2G6 mutation underlies infantile neuroaxonal dystrophy.
Khateeb S, Flusser H, Ofir R, Shelef I, Narkis G, Vardi G, Shorer Z, Levy R, Galil A, Elbedour K, Birk OS. Khateeb S, et al. Am J Hum Genet. 2006 Nov;79(5):942-8. doi: 10.1086/508572. Epub 2006 Sep 19. Am J Hum Genet. 2006. PMID: 17033970 Free PMC article.
Neuroimaging in mitochondrial disorders.
Mascalchi M, Montomoli M, Guerrini R. Mascalchi M, et al. Essays Biochem. 2018 Jul 20;62(3):409-421. doi: 10.1042/EBC20170109. Print 2018 Jul 20. Essays Biochem. 2018. PMID: 30030366 Review.
24 results