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Brain & Development|December 12, 2001
Medium-term open label trial of L-carnitine in Rett syndromeC J Ellaway, J Peat, K Williams, et al.Brain & Development|December 12, 2001
Cerebrolysin therapy in Rett syndrome: clinical and EEG mapping studyN Gorbachevskaya, V Bashina, V Gratchev, et al.Brain & Development|December 12, 2001
Disturbance of phasic chin muscle activity during rapid-eye-movement sleepJ Kohyama, J Ohinata, T HasegawaBrain & Development|December 12, 2001
Clinical, neurophysiological and immunological correlations in classical Rett syndromeV V Gratchev, V M Bashina, T P Klushnik, et al.Brain & Development|December 12, 2001
Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndromeI B Van den Veyver, H Y ZoghbiBrain & Development|December 12, 2001
A new assay for the analysis of X-chromosome inactivation in carriers with an X-linked diseaseT KubotaBrain & Development|December 12, 2001
The role of X-chromosome inactivation in the manifestation of Rett syndromeN TakagiBrain & Development|December 12, 2001
FISH analysis of replication and transcription of chromosome X loci: new approach for genetic analysis of Rett syndromeS G Vorsanova, Y B Yurov, A D Kolotii, et al.Brain & Development|December 12, 2001
Spectrum and distribution of MECP2 mutations in 64 Italian Rett syndrome girls: tentative genotype/phenotype correlationL Giunti, S Pelagatti, V Lazzerini, et al.Pageof 483