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Stem cells for amyotrophic lateral sclerosis modeling and therapy: myth or fact?
Cytometry A. 2015 Mar;87(3):197-211. doi: 10.1002/cyto.a.22630. Epub 2015 Feb 2.
Cytometry A. 2015.
PMID: 25645594
Free article.
Review.
Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome.
Melo US, Macedo-Souza LI, Figueiredo T, Muotri AR, Gleeson JG, Coux G, Armas P, Calcaterra NB, Kitajima JP, Amorim S, Olávio TR, Griesi-Oliveira K, Coatti GC, Rocha CR, Martins-Pinheiro M, Menck CF, Zaki MS, Kok F, Zatz M, Santos S.
Melo US, et al. Among authors: olavio tr.
Hum Mol Genet. 2015 Dec 15;24(24):6877-85. doi: 10.1093/hmg/ddv388. Epub 2015 Sep 18.
Hum Mol Genet. 2015.
PMID: 26385635
Free PMC article.
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A novel GFAP mutation in a type II (late-onset) Alexander disease patient.
de Paiva AR, Freua F, Lucato LT, Parmera J, Dória D, Nóbrega PR, Olávio TR, Macedo-Souza LI, Kok F.
de Paiva AR, et al. Among authors: olavio tr.
J Neurol. 2016 Apr;263(4):821-2. doi: 10.1007/s00415-016-8065-8. Epub 2016 Feb 25.
J Neurol. 2016.
PMID: 26914930
No abstract available.
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