Improvement of the Rett Syndrome Phenotype in a Mecp2 Mouse Model Upon Treatment with Levodopa and a Dopa-Decarboxylase Inhibitor-Reference-Cited by-同舟云学术

Improvement of the Rett Syndrome Phenotype in a Mecp2 Mouse Model Upon Treatment with Levodopa and a Dopa-Decarboxylase Inhibitor

Published:2014-06-11 Issue:12 Volume:39 Page:2846-2856
ISSN:0893-133X
Container-title:Neuropsychopharmacology
language:en
Short-container-title:Neuropsychopharmacol

Author:

Szczesna Karolina,de la Caridad Olga,Petazzi Paolo,Soler Marta,Roa Laura,Saez Mauricio A,Fourcade Stéphane,Pujol Aurora,Artuch-Iriberri Rafael,Molero-Luis Marta,Vidal August,Huertas Dori,Esteller Manel

Publisher

Springer Science and Business Media LLC

Subject

Psychiatry and Mental health,Pharmacology

Link

http://www.nature.com/articles/npp2014136.pdf

Reference55 articles.

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2. Armstrong D, Dunn JK, Antalffy B, Trivedi R (1995). Selective dendritic alterations in the cortex of Rett syndrome. J Neuropathol Exp Neurol 54: 195–201.

3. Armstrong D (1995). The neuropathology of Rett syndrome—overview 1994. Neuropediatrics 26: 100–104.

4. Bauman ML, Kemper TL, Arin DM (1995). Pervasive neuroanatomic abnormalities of the brain in three cases of Rett's syndrome. Neurology 45: 1581–1586.

5. Betarbet R, Turner R, Chockkan V, DeLong MR, Allers KA, Waltersm J et al (1997). Dopaminergic neurons intrinsic to the primate striatum. J Neurosci 17: 6761–6768.

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