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Elena Belousova, Vladimir Sukhorukov, Marina Dorofeeva, Lev Shagam and Dmitrii V. Vlodavetz

-015-0359-5. Davydov E.V., Goode D.L., Sirota M., Cooper G.M., Sidow A., Batzoglou S.: Identifying a high fraction of the human genome to be under selective constraint using GERP++ . PLoS Comput. Biol., 2010, 6: e1001025. Della Sala G., Pizzorusso T.: Synaptic plasticity and signaling in Rett syndrome. Dev. Neurobiol., 2014, 74: 178–196. Dolce A., Ben-Zeev B., Naidu S., Kossoff E.H.: Rett syndrome and epilepsy: an update for child neurologists . Pediatr. Neurol., 2013, 48: 337–345. Gadalla K.K., Bailey M.E., Cobb S.R.: MeCP2 and Rett syndrome

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Heinz Gregor Wieser

., 2005, 37: 733–738. El Helou J., Navarro V., Depienne C., Fedirko E., LeGuern E., Baulac M. et al.: K-complex induced seizures in autosomal dominant nocturnal frontal lobe epilepsy . Clin. Neurophysiol., 2008, 119: 2201–2204. Epi4K Consortium; Epilepsy Phenome/Genome Project, Allen A.S., Berkovic S.F., Cossette P., Delanty N., Dlugos D., Eichler E.E., Epstein M.P. et al.: De novo mutations in epileptic encephalopathies . Nature, 2013, 501: 217–221. EPICURE Consortium; EMINet Consortium, Steffens M., Leu C., Ruppert A.K., Zara F., Striano P