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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Bibliografische gegevens
Hoofdauteurs: Doppler, Edith, Rockenstein, Edward, Ubhi, Kiren, Inglis, Chandra, Mante, Michael, Adame, Anthony, Crews, Leslie, Hitzl, Monika, Moessler, Herbert, Masliah, Eliezer
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2008
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Online toegang: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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