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Brain & Development|December 12, 2001
Genetic evidence for noradrenergic control of long-term memory consolidationK Kobayashi, T KobayashiBrain & Development|December 12, 2001
Mind and brain in Rett disorderA M Kerr, P Belichenko, T Woodcock, et al.Brain & Development|December 12, 2001
Neuroimaging studies in Rett syndromeS Naidu, W E Kaufmann, M T Abrams, et al.Brain & Development|December 12, 2001
Reduced expression of neuropeptides can be related to respiratory disturbances in Rett syndromeY Saito, M Ito, Y Ozawa, et al.Brain & Development|December 12, 2001
R133C and R168X mutations in Japanese Rett syndrome patients: a caution for misdiagnosisK Amano, Y Nomura, M Segawa, et al.Brain & Development|December 12, 2001
Multicolor fluorescent in situ hybridization on post-mortem brain in schizophrenia as an approach for identification of low-level chromosomal aneuploidy in neuropsychiatric diseasesY B Yurov, V M Vostrikov, S G Vorsanova, et al.Brain & Development|December 12, 2001
Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndromeY B Yurov, S G Vorsanova, A D Kolotii, et al.Brain & Development|December 12, 2001
A 77-year-old woman and a preserved speech variant among the Danish Rett patients with mutations in MECP2J B Nielsen, K Ravn, M SchwartzBrain & Development|May 17, 2002
The C677T mutation in the methylenetetrahydrofolate reductase gene contributes to hyperhomocysteinemia in patients taking anticonvulsantsHiroaki Ono, Akiko Sakamoto, Nobuyuki Mizoguchi, et al.Pageof 479