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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2010 | 1 |
2014 | 1 |
2015 | 3 |
2024 | 0 |
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4 results
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Page 1
Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA).
Ann Neurol. 2010 Nov;68(5):611-8. doi: 10.1002/ana.22122.
Ann Neurol. 2010.
PMID: 20853438
Free PMC article.
Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis.
Zaki MS, Selim L, Mansour L, Mahmoud IG, Fenstermaker AG, Gabriel SB, Gleeson JG.
Zaki MS, et al.
Clin Genet. 2015 Jul;88(1):95-7. doi: 10.1111/cge.12516. Epub 2014 Dec 11.
Clin Genet. 2015.
PMID: 25496456
No abstract available.
Item in Clipboard
Fatty acid 2-hydroxylase deficiency: clinical features and brain iron accumulation.
Pedroso JL, Handfas BW, Abrahão A, Kok F, Barsottini OG, Oliveira AS.
Pedroso JL, et al.
Neurology. 2015 Mar 3;84(9):960-1. doi: 10.1212/WNL.0000000000001316.
Neurology. 2015.
PMID: 25732363
No abstract available.
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Novel FA2H mutation in a girl with familial spastic paraplegia.
Aguirre-Rodríguez FJ, Lucenilla MI, Alvarez-Cubero MJ, Mata C, Entrala-Bernal C, Fernandez-Rosado F.
Aguirre-Rodríguez FJ, et al.
J Neurol Sci. 2015 Oct 15;357(1-2):332-4. doi: 10.1016/j.jns.2015.07.042. Epub 2015 Aug 29.
J Neurol Sci. 2015.
PMID: 26344562
No abstract available.
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