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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 5
1988 10
1989 5
1990 8
1991 6
1992 13
1993 7
1994 5
1995 5
1996 2
1997 12
1998 11
1999 11
2000 13
2001 36
2002 19
2003 26
2004 10
2005 31
2006 35
2007 18
2008 25
2009 33
2010 23
2011 37
2012 35
2013 41
2014 42
2015 37
2016 36
2017 35
2018 35
2019 40
2020 31
2021 38
2022 27
2023 30
2024 7

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757 results

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Page 1
Global prevalence of Rett syndrome: systematic review and meta-analysis.
Petriti U, Dudman DC, Scosyrev E, Lopez-Leon S. Petriti U, et al. Syst Rev. 2023 Jan 16;12(1):5. doi: 10.1186/s13643-023-02169-6. Syst Rev. 2023. PMID: 36642718 Free PMC article. Review.
BACKGROUND: Rett syndrome is a rare, severe neurodevelopmental disorder. Almost all cases occur in girls, in association with spontaneous (non-inherited) mutations involving the methyl-CpG-binding protein 2 gene located on the X chromosome. Diagnostic criteria for t …
BACKGROUND: Rett syndrome is a rare, severe neurodevelopmental disorder. Almost all cases occur in girls, in association with …
Rett syndrome and MeCP2.
Liyanage VR, Rastegar M. Liyanage VR, et al. Neuromolecular Med. 2014 Jun;16(2):231-64. doi: 10.1007/s12017-014-8295-9. Epub 2014 Mar 11. Neuromolecular Med. 2014. PMID: 24615633 Free PMC article. Review.
Rett syndrome (RTT) is a severe and progressive neurological disorder, which mainly affects young females. ...Despite significant progress in MeCP2 research over the last few decades, there is still a knowledge gap between the in vitro and in vivo research findings …
Rett syndrome (RTT) is a severe and progressive neurological disorder, which mainly affects young females. ...Despite signific …
Rett syndrome: a neurological disorder with metabolic components.
Kyle SM, Vashi N, Justice MJ. Kyle SM, et al. Open Biol. 2018 Feb;8(2):170216. doi: 10.1098/rsob.170216. Open Biol. 2018. PMID: 29445033 Free PMC article. Review.
Rett syndrome (RTT) is a neurological disorder caused by mutations in the X-linked gene methyl-CpG-binding protein 2 (MECP2), a ubiquitously expressed transcriptional regulator. ...Ultimately, we conclude that a thorough knowledge of MeCP2's varied functional target …
Rett syndrome (RTT) is a neurological disorder caused by mutations in the X-linked gene methyl-CpG-binding protein 2 (MECP2), …
Trofinetide: First Approval.
Keam SJ. Keam SJ. Drugs. 2023 Jun;83(9):819-824. doi: 10.1007/s40265-023-01883-8. Drugs. 2023. PMID: 37191913 Review.
Trofinetide was approved in March 2023 in the USA for the treatment of Rett syndrome in adult and pediatric patients 2 years of age and older. This article summarizes the milestones in the development of trofinetide leading to this first approval for Rett …
Trofinetide was approved in March 2023 in the USA for the treatment of Rett syndrome in adult and pediatric patients 2 years o …
MECP2-Related Disorders in Males.
Pascual-Alonso A, Martínez-Monseny AF, Xiol C, Armstrong J. Pascual-Alonso A, et al. Int J Mol Sci. 2021 Sep 4;22(17):9610. doi: 10.3390/ijms22179610. Int J Mol Sci. 2021. PMID: 34502518 Free PMC article. Review.
Methyl CpG binding protein 2 (MECP2) is located at Xq28 and is a multifunctional gene with ubiquitous expression. Loss-of-function mutations in MECP2 are associated with Rett syndrome (RTT), which is a well-characterized disorder that affects mainly females. ...Conv …
Methyl CpG binding protein 2 (MECP2) is located at Xq28 and is a multifunctional gene with ubiquitous expression. Loss-of-function mutations …
Genetic Landscape of Rett Syndrome Spectrum: Improvements and Challenges.
Vidal S, Xiol C, Pascual-Alonso A, O'Callaghan M, Pineda M, Armstrong J. Vidal S, et al. Int J Mol Sci. 2019 Aug 12;20(16):3925. doi: 10.3390/ijms20163925. Int J Mol Sci. 2019. PMID: 31409060 Free PMC article. Review.
Rett syndrome (RTT) is an early-onset neurodevelopmental disorder that primarily affects females, resulting in severe cognitive and physical disabilities, and is one of the most prevalent causes of intellectual disability in females. More than fifty years after the …
Rett syndrome (RTT) is an early-onset neurodevelopmental disorder that primarily affects females, resulting in severe cognitiv …
State-of-the-art therapies for Rett syndrome.
Panayotis N, Ehinger Y, Felix MS, Roux JC. Panayotis N, et al. Dev Med Child Neurol. 2023 Feb;65(2):162-170. doi: 10.1111/dmcn.15383. Epub 2022 Sep 3. Dev Med Child Neurol. 2023. PMID: 36056801 Free PMC article. Review.
Rett syndrome (RTT) is an X-linked neurogenetic disorder caused by mutations of the MECP2 (methyl-CpG-binding protein 2) gene. ...
Rett syndrome (RTT) is an X-linked neurogenetic disorder caused by mutations of the MECP2 (methyl-CpG-binding protein 2) gene. …
Towards a better diagnosis and treatment of Rett syndrome: a model synaptic disorder.
Banerjee A, Miller MT, Li K, Sur M, Kaufmann WE. Banerjee A, et al. Brain. 2019 Feb 1;142(2):239-248. doi: 10.1093/brain/awy323. Brain. 2019. PMID: 30649225 Free PMC article. Review.
With the recent 50th anniversary of the first publication on Rett syndrome, and the almost 20 years since the first report on the link between Rett syndrome and MECP2 mutations, it is important to reflect on the tremendous advances in our understanding …
With the recent 50th anniversary of the first publication on Rett syndrome, and the almost 20 years since the first report on …
Advances in understanding of Rett syndrome and MECP2 duplication syndrome: prospects for future therapies.
Sandweiss AJ, Brandt VL, Zoghbi HY. Sandweiss AJ, et al. Lancet Neurol. 2020 Aug;19(8):689-698. doi: 10.1016/S1474-4422(20)30217-9. Lancet Neurol. 2020. PMID: 32702338 Review.
The X-linked gene encoding MECP2 is involved in two severe and complex neurodevelopmental disorders. Loss of function of the MeCP2 protein underlies Rett syndrome, whereas duplications of the MECP2 locus cause MECP2 duplication syndrome. ...
The X-linked gene encoding MECP2 is involved in two severe and complex neurodevelopmental disorders. Loss of function of the MeCP2 protein u …
Role of DNA Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease.
Pejhan S, Rastegar M. Pejhan S, et al. Biomolecules. 2021 Jan 8;11(1):75. doi: 10.3390/biom11010075. Biomolecules. 2021. PMID: 33429932 Free PMC article. Review.
Rett Syndrome (RTT) is a severe, rare, and progressive developmental disorder with patients displaying neurological regression and autism spectrum features. ...
Rett Syndrome (RTT) is a severe, rare, and progressive developmental disorder with patients displaying neurological regression …
757 results