Results 181 to 190 of about 2,462,658 (261)

Optimized clonal isolation and immortalization of Rett syndrome patient fibroblasts for in vitro modeling of MECP2 mutations. [PDF]

Sci Rep
Sarne V, Huber A, Beribisky AV, Hengstschläger M, Laccone F, Steinkellner H.   +5 more
europepmc   +1 more source

Modeling Rett Syndrome Using TALEN-Edited MECP2 Mutant Cynomolgus Monkeys.

Cell, 2017
Yongchang Chen, Juehua Yu, Yuyu Niu, Dongdong Qin, Hailiang Liu, Gang Li, Yingzhou Hu, Jiaojian Wang, Yi Lu, Yu Kang, Yong-chao Jiang, Kunhua Wu, Siguang Li, Jingkuan Wei, Jing He, Junbang Wang, Xiaojing Liu, Yuping Luo, Chenyang Si, Raoxian Bai, Kunshan Zhang, Jie Liu, Shaoyong Huang, Zhenzhen Chen, Shuang Wang, Xiaoying Chen, X. Bao, Qingping Zhang, Fuxing Li, Rui Geng, A. Liang, D. Shen, T. Jiang, Xintian Hu, Yuanye Ma, W. Ji, Y. Sun   +36 more
semanticscholar   +1 more source

EMG findings in the course of vidarabine neuropathy [PDF]

, 1988
Berlit, Peter, Brosi, K., Krause, Klaus-Henning, Scheglmann, K.   +3 more
core  

Enhancing cognitive-motor recovery in Rett syndrome: effects of integrated intervention on neuropsychological and motor outcome. [PDF]

Front Psychol
Fabio RA, Semino M, Perina M.
europepmc   +1 more source

Middle-Aged Women With Rett Syndrome: Longitudinal Profile From the British Isles Rett Syndrome Survey and Suggestions for Care. [PDF]

J Appl Res Intellect Disabil
Hryniewiecka-Jaworska A, Sloper E, Archer H, Clarke AJ.   +3 more
europepmc   +1 more source

Clinical differences in monozygotic twins with Rett syndrome: case report and systematic review. [PDF]

Orphanet J Rare Dis
Boeri S, Piai M, Russo S, Alari V, Cogliati F, Simonetta D, Benke TA, Nobili L, Prato G.   +8 more
europepmc   +1 more source

H/M-ratio in spasticity before and after therapy with vibration impulses [PDF]

, 1988
Krause, Klaus-Henning, Kummer, R. von, Morche, K.   +2 more
core  

Molecular Insights into Neurological Regression with a Focus on Rett Syndrome-A Narrative Review. [PDF]

Int J Mol Sci
Singh J, Santosh P.
europepmc   +1 more source

Noonan Syndrome and Rett Syndrome in An 8-Year-Old Girl With A Tectal Neoplasm. [PDF]

JCEM Case Rep
Shetty N, Brown WD, Massingham L, Rogg J, Quintos JB.   +4 more
europepmc   +1 more source

AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders [PDF]

, 2019
al., et, Constantino, John N., Fassi, Emily, Shinawi, Marwan   +3 more
core   +1 more source