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Results by year

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

Year Number of Results
1976 1
1983 1
1988 1
1989 1
1990 1
1991 2
1992 3
1993 1
1994 1
1995 1
1996 1
1997 1
1999 1
2000 4
2001 2
2002 2
2003 5
2004 2
2005 2
2006 2
2007 4
2008 14
2009 7
2010 5
2011 1
2012 1
2013 5
2014 6
2015 7
2016 4
2017 6
2018 3
2020 5
2021 1
2024 0

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Similar articles for PMID: 20522570

92 results

Results by year

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Page 1
Midbrain-hindbrain involvement in lissencephalies.
Jissendi-Tchofo P, Kara S, Barkovich AJ. Jissendi-Tchofo P, et al. Neurology. 2009 Feb 3;72(5):410-8. doi: 10.1212/01.wnl.0000333256.74903.94. Epub 2008 Nov 19. Neurology. 2009. PMID: 19020296 Free PMC article.
Overlapping cortical malformations and mutations in TUBB2B and TUBA1A.
Cushion TD, Dobyns WB, Mullins JG, Stoodley N, Chung SK, Fry AE, Hehr U, Gunny R, Aylsworth AS, Prabhakar P, Uyanik G, Rankin J, Rees MI, Pilz DT. Cushion TD, et al. Brain. 2013 Feb;136(Pt 2):536-48. doi: 10.1093/brain/aws338. Epub 2013 Jan 29. Brain. 2013. PMID: 23361065
[Genetic and clinical aspects of lissencephaly].
Verloes A, Elmaleh M, Gonzales M, Laquerrière A, Gressens P. Verloes A, et al. Rev Neurol (Paris). 2007 May;163(5):533-47. doi: 10.1016/s0035-3787(07)90460-9. Rev Neurol (Paris). 2007. PMID: 17571022 Review. French.
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations.
Bahi-Buisson N, Poirier K, Boddaert N, Saillour Y, Castelnau L, Philip N, Buyse G, Villard L, Joriot S, Marret S, Bourgeois M, Van Esch H, Lagae L, Amiel J, Hertz-Pannier L, Roubertie A, Rivier F, Pinard JM, Beldjord C, Chelly J. Bahi-Buisson N, et al. J Med Genet. 2008 Oct;45(10):647-53. doi: 10.1136/jmg.2008.058073. Epub 2008 Aug 26. J Med Genet. 2008. PMID: 18728072
Commissural malformations: beyond the corpus callosum.
Smith T, Tekes A, Boltshauser E, Huisman TA. Smith T, et al. J Neuroradiol. 2008 Dec;35(5):301-3. doi: 10.1016/j.neurad.2008.06.002. Epub 2008 Aug 8. J Neuroradiol. 2008. PMID: 18692242
92 results