Rett Syndrome

Citations 1-6 of 6 total displayed.

Most recent content (7 Apr 2009):

ARTICLES
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome

B. Ben Zeev, A. Bebbington, G. Ho, H. Leonard, N. de Klerk, E. Gak, M. Vecksler, and J. Christodoulou
Neurology 2009; 72: 1242-1247. [Abstract] [Full text] [PDF]  

Past content (since Nov 2004):

EDITORIALS
Will my Rett syndrome patient walk, talk, and use her hands?

Yuzhi Zhang and Berge A. Minassian
Neurology 2008; 70: 1302-1303. [Full text] [PDF]  

ARTICLES
Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome

J. L. Neul, P. Fang, J. Barrish, J. Lane, E. B. Caeg, E. O. Smith, H. Zoghbi, A. Percy, and D. G. Glaze
Neurology 2008; 70: 1313-1321. [Abstract] [Full text] [PDF]  

ARTICLES
Investigating genotype–phenotype relationships in Rett syndrome using an international data set

A. Bebbington, A. Anderson, D. Ravine, S. Fyfe, M. Pineda, N. de Klerk, B. Ben-Zeev, N. Yatawara, A. Percy, W. E. Kaufmann, and H. Leonard
Neurology 2008; 70: 868-875. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
A novel familial MECP2 mutation in a young boy: Clinical and molecular findings

P. Ventura, R. Galluzzi, S. M. Bacca, R. Giorda, and A. Massagli
Neurology 2006; 67: 867-868. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Early-onset encephalopathy and cortical myoclonus in a boy with MECP2 gene mutation

V. Leuzzi, M. L. Di Sabato, M. Zollino, M. L. Montanaro, and S. Seri
Neurology 2004; 63: 1968-1970. [Abstract] [Full text] [PDF]