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

Year Number of Results
1990 1
1993 1
1994 3
1996 1
1997 2
1998 2
1999 1
2000 1
2002 4
2003 1
2004 2
2005 4
2006 1
2007 7
2008 7
2009 8
2010 7
2011 11
2012 7
2013 5
2014 8
2015 7
2016 7
2017 4
2018 2
2019 1
2020 1
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Similar Articles for PMID: 20430848

92 results
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Page 1
Clinical and neuroimaging findings of Cree leukodystrophy: a retrospective case series.
Harder S, Gourgaris A, Frangou E, Hopp K, Huntsman R, Lowry N, Seshia S, Lemire E, Robinson C, Tynan J. Harder S, et al. AJNR Am J Neuroradiol. 2010 Sep;31(8):1418-23. doi: 10.3174/ajnr.A2108. Epub 2010 Apr 29. AJNR Am J Neuroradiol. 2010. PMID: 20430848 Free article.
Cree leukoencephalopathy: neuroimaging findings.
Alorainy IA, Patenaude YG, O'Gorman AM, Black DN, Meagher-Villemure K. Alorainy IA, et al. Radiology. 1999 Nov;213(2):400-6. doi: 10.1148/radiology.213.2.r99oc28400. Radiology. 1999. PMID: 10551219
Cree leukoencephalopathy and CACH/VWM disease are allelic at the EIF2B5 locus.
Fogli A, Wong K, Eymard-Pierre E, Wenger J, Bouffard JP, Goldin E, Black DN, Boespflug-Tanguy O, Schiffmann R. Fogli A, et al. Ann Neurol. 2002 Oct;52(4):506-10. doi: 10.1002/ana.10339. Ann Neurol. 2002. PMID: 12325082
Mutations in the genes encoding eukaryotic translation initiation factor 2B in Japanese patients with vanishing white matter disease.
Shimada S, Shimojima K, Sangu N, Hoshino A, Hachiya Y, Ohto T, Hashi Y, Nishida K, Mitani M, Kinjo S, Tsurusaki Y, Matsumoto N, Morimoto M, Yamamoto T. Shimada S, et al. Brain Dev. 2015 Nov;37(10):960-6. doi: 10.1016/j.braindev.2015.03.003. Epub 2015 Apr 3. Brain Dev. 2015. PMID: 25843247
A Japanese girl with an early-infantile onset vanishing white matter disease resembling Cree leukoencephalopathy.
Takano K, Tsuyusaki Y, Sato M, Takagi M, Anzai R, Okuda M, Iai M, Yamashita S, Okabe T, Aida N, Tsurusaki Y, Saitsu H, Matsumoto N, Osaka H. Takano K, et al. Brain Dev. 2015 Jun;37(6):638-42. doi: 10.1016/j.braindev.2014.10.002. Epub 2014 Oct 27. Brain Dev. 2015. PMID: 25457085
Hypomyelination and congenital cataract: neuroimaging features of a novel inherited white matter disorder.
Rossi A, Biancheri R, Zara F, Bruno C, Uziel G, van der Knaap MS, Minetti C, Tortori-Donati P. Rossi A, et al. AJNR Am J Neuroradiol. 2008 Feb;29(2):301-5. doi: 10.3174/ajnr.A0792. Epub 2007 Nov 1. AJNR Am J Neuroradiol. 2008. PMID: 17974614 Free article.
Restricted diffusion in vanishing white matter.
van der Lei HD, Steenweg ME, Bugiani M, Pouwels PJ, Vent IM, Barkhof F, van Wieringen WN, van der Knaap MS. van der Lei HD, et al. Arch Neurol. 2012 Jun;69(6):723-7. doi: 10.1001/archneurol.2011.1658. Arch Neurol. 2012. PMID: 22312162
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation.
Fogli A, Dionisi-Vici C, Deodato F, Bartuli A, Boespflug-Tanguy O, Bertini E. Fogli A, et al. Neurology. 2002 Dec 24;59(12):1966-8. doi: 10.1212/01.wnl.0000041666.76863.47. Neurology. 2002. PMID: 12499492
[Leukoencephalopathy with vanishing white matter: a clinical case of adult onset].
Pato Pato A, Lorenzo González JR, Cimas Hernando I, Rodríguez-Constenla I. Pato Pato A, et al. Neurologia. 2009 Sep;24(7):504-5. Neurologia. 2009. PMID: 21469262 Spanish. No abstract available.
Leucoencephalopathy with vanishing white matter may cause progressive myoclonus epilepsy.
Jansen AC, Andermann E, Niel F, Creveaux I, Boespflug-Tanguy O, Andermann F. Jansen AC, et al. Epilepsia. 2008 May;49(5):910-3. doi: 10.1111/j.1528-1167.2008.01542.x. Epub 2008 Feb 7. Epilepsia. 2008. PMID: 18266750 Free article.
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