10q25.2, . et al. 0 and 8p23.1) in 3 patients born to consanguineous parents - issue: - volume: - pages: .
the sequential appearance of the in vivo deficits in this mouse line. The observed deficits initially concern major parameters (such as body weight), . et al. 0 and are followed by involuntary and sensitive defects (reflexes). Subsequently - issue: - volume: - pages: .
C l a r k e A, . et al. 0 B e n - Z e e v B M a r i F B o s n j a k V M - issue: D j u r i c M - volume: B i s g a a r d A M - pages: V i g n o l i A .
J Neurol Neurosurg Psychiatry. 2009 Dec, . et al. 0 Solé G 10.1136/jnnp.2008.162263 - issue: - volume: - pages: .
Ori, . et al. 0 Alessandra; Villard Mercedes; Armstrong Bela; Vignoli - issue: Alexsandra; Pini - volume: Giorgio; Bisgaard - pages: Milena; Craiu.
Virginie, . et al. 0 Laurent; Peyronnet-Roux 4-difluorobenzamide (ICA73). Immunostaining and mutant mice highlight an important role of Kv7.2-con - issue: - volume: - pages: .
but only a tendency towards reduction. Finally, . et al. 0 we did not found any apoptotic neurons in the pons indicating that LC neurons are not dying but are more likely loosing their catecholaminergic phenotype. In conclusion - issue: - volume: - pages: .
W h a l e n S, . et al. 0 F r e d r i k s e n T D u b o u r g C - issue: V i l l a r d L - volume: G o o s s e n s M - pages: P h i l i p N .
severity of epilepsy, . et al. 0 and type of seizures were collected. Statistical analysis was done using the IBM SPSS Version 21 software associated with a milder Rett phenotype - issue: - volume: - pages: .