Rett syndrome: clinical and molecular update
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Pediatrics, Perinatology, and Child Health
Reference52 articles.
1. An update on clinically applicable diagnostic criteria in Rett syndrome
2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
3. Rett syndrome: clinical and epidemiological aspects in a Brazilian institution
4. Rett Syndrome - an update
Cited by 42 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. MeCP2 inhibits ischemic neuronal injury by enhancing methylation of the FOXO3a promoter to repress the SPRY2-ZEB1 axis;Experimental & Molecular Medicine;2022-08-01
2. Optimized Administration of the M4 PAM VU0467154 Demonstrates Broad Efficacy, but Limited Effective Concentrations in Mecp2+/– Mice;ACS Chemical Neuroscience;2022-06-07
3. Clinical and Preclinical Evidence for M1 Muscarinic Acetylcholine Receptor Potentiation as a Therapeutic Approach for Rett Syndrome;Neurotherapeutics;2022-06-07
4. What Every Internist-Endocrinologist Should Know about Rare Genetic Syndromes in Order to Prevent Needless Diagnostics, Missed Diagnoses and Medical Complications: Five Years of ‘Internal Medicine for Rare Genetic Syndromes’;Journal of Clinical Medicine;2021-11-22
5. Computational and structural studies of MeCP2 and associated mutants;Journal of Theoretical and Computational Chemistry;2020-07-08
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