Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
My NCBI Filters
Results by year

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

Year Number of Results
1950 1
1958 1
1960 1
2000 1
2001 4
2002 4
2004 3
2005 8
2006 8
2007 2
2008 9
2009 15
2010 23
2011 13
2012 13
2013 8
2014 18
2015 14
2016 12
2017 6
2018 9
2019 9
2020 1
Text availability
Article attribute
Article type
Publication date

Similar Articles for PMID: 20581069

164 results
Results by year
Filters applied: . Clear all
Page 1
Cavitating leukoencephalopathy in a child carrying the mitochondrial A8344G mutation.
Biancheri R, Rossi D, Cassandrini D, Rossi A, Bruno C, Santorelli FM. Biancheri R, et al. AJNR Am J Neuroradiol. 2010 Oct;31(9):E78-9. doi: 10.3174/ajnr.A2182. Epub 2010 Jun 25. AJNR Am J Neuroradiol. 2010. PMID: 20581069 Free article. No abstract available.
Leukodystrophies and other genetic metabolic leukoencephalopathies in children and adults.
Kohlschütter A, Bley A, Brockmann K, Gärtner J, Krägeloh-Mann I, Rolfs A, Schöls L. Kohlschütter A, et al. Brain Dev. 2010 Feb;32(2):82-9. doi: 10.1016/j.braindev.2009.03.014. Epub 2009 May 7. Brain Dev. 2010. PMID: 19427149 Review.
Progressive megalencephaly due to specific EIF2Bepsilon mutations in two unrelated families.
Passemard S, Gelot A, Fogli A, N'Guyen S, Barnerias C, Niel F, Doummar D, Arbues AS, Mignot C, de Villemeur TB, Ponsot G, Boespflug-Tanguy O, Rodriguez D. Passemard S, et al. Neurology. 2007 Jul 24;69(4):400-2. doi: 10.1212/01.wnl.0000266388.02772.f8. Neurology. 2007. PMID: 17646634 No abstract available.
Leukoencephalopathies in adulthood.
Tillema JM, Renaud DL. Tillema JM, et al. Semin Neurol. 2012 Feb;32(1):85-94. doi: 10.1055/s-0032-1306391. Epub 2012 Mar 15. Semin Neurol. 2012. PMID: 22422211 Review.
TNFRSF1A R92Q mutation in association with a multiple sclerosis-like demyelinating syndrome.
Hoffmann LA, Lohse P, König FB, Feneberg W, Hohlfeld R, Kümpfel T. Hoffmann LA, et al. Neurology. 2008 Mar 25;70(13 Pt 2):1155-6. doi: 10.1212/01.wnl.0000296279.98236.8a. Epub 2008 Feb 20. Neurology. 2008. PMID: 18287568 No abstract available.
A de novo mutation in the adenosine triphosphatase (ATPase) 8 gene in a patient with mitochondrial disorder.
Mkaouar-Rebai E, Kammoun F, Chamkha I, Kammoun N, Hsairi I, Triki C, Fakhfakh F. Mkaouar-Rebai E, et al. J Child Neurol. 2010 Jun;25(6):770-5. doi: 10.1177/0883073809344351. Epub 2010 Mar 4. J Child Neurol. 2010. PMID: 20207608
Hereditary leukodystrophies without identified mutations.
Robitaille Y. Robitaille Y. J Neurol Sci. 2005 Feb 15;228(2):208-9. doi: 10.1016/j.jns.2004.10.013. Epub 2004 Dec 2. J Neurol Sci. 2005. PMID: 15694209 Review. No abstract available.
Central nervous system involvement in hereditary neuropathy with liability to pressure palsies: description of a large family with this association.
Sanahuja J, Franco E, Rojas-García R, Gallardo E, Combarros O, Begué R, Granés P, Illa I. Sanahuja J, et al. Arch Neurol. 2005 Dec;62(12):1911-4. doi: 10.1001/archneur.62.12.1911. Arch Neurol. 2005. PMID: 16344349
164 results
Jump to page
Feedback