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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 2
1994 1
1995 1
1996 1
1997 1
1999 3
2000 4
2001 2
2002 1
2003 4
2004 3
2005 1
2006 2
2007 3
2008 13
2009 7
2010 6
2011 1
2012 4
2013 7
2014 7
2015 8
2016 5
2017 6
2018 4
2019 1
2020 0
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Article type
Publication date

Similar Articles for PMID: 20522570

95 results
Results by year
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Page 1
Developmental differences of the major forebrain commissures in lissencephalies.
Kara S, Jissendi-Tchofo P, Barkovich AJ. Kara S, et al. AJNR Am J Neuroradiol. 2010 Oct;31(9):1602-7. doi: 10.3174/ajnr.A2133. Epub 2010 Jun 3. AJNR Am J Neuroradiol. 2010. PMID: 20522570 Free PMC article.
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.
Expanding the spectrum of human ganglionic eminence region anomalies on fetal magnetic resonance imaging.
Righini A, Cesaretti C, Conte G, Parazzini C, Frassoni C, Bulfamante G, Avagliano L, Inverardi F, Izzo G, Rustico M. Righini A, et al. Neuroradiology. 2016 Mar;58(3):293-300. doi: 10.1007/s00234-015-1622-5. Epub 2015 Nov 25. Neuroradiology. 2016. PMID: 26608601
Apparent atypical callosal dysgenesis: analysis of MR findings in six cases and their relationship to holoprosencephaly.
Barkovich AJ. Barkovich AJ. AJNR Am J Neuroradiol. 1990 Mar-Apr;11(2):333-9. AJNR Am J Neuroradiol. 1990. PMID: 1690501
The corpus callosum, the other great forebrain commissures, and the septum pellucidum: anatomy, development, and malformation.
Raybaud C. Raybaud C. Neuroradiology. 2010 Jun;52(6):447-77. doi: 10.1007/s00234-010-0696-3. Epub 2010 Apr 27. Neuroradiology. 2010. PMID: 20422408
[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.
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
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
Anomalies of the corpus callosum: an MR analysis of the phenotypic spectrum of associated malformations.
Hetts SW, Sherr EH, Chao S, Gobuty S, Barkovich AJ. Hetts SW, et al. AJR Am J Roentgenol. 2006 Nov;187(5):1343-8. doi: 10.2214/AJR.05.0146. AJR Am J Roentgenol. 2006. PMID: 17056927
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
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