Neurotrophic effects of Cerebrolysin in the Mecp2(308/Y) transgenic model of Rett Syndrome

Rett syndrome is a childhood neurodevelopmental disorder caused by mutations in the gene encoding for methyl CpG binding protein (MeCP2). Neuropathological studies in patients with Rett syndrome and in MeCP2 mutant models have shown reduced dendritic arborization and abnormal neuronal packing. We ha...

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Detalhes bibliográficos
Main Authors: Doppler, Edith, Rockenstein, Edward, Ubhi, Kiren, Inglis, Chandra, Mante, Michael, Adame, Anthony, Crews, Leslie, Hitzl, Monika, Moessler, Herbert, Masliah, Eliezer
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2732193/
https://ncbi.nlm.nih.gov/pubmed/18600331
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00401-008-0407-x
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