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Year Number of Results
1962 1
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1969 2
1971 2
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1975 3
1976 2
1977 1
1979 1
1980 1
1981 2
1983 3
1984 3
1985 37
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1987 54
1988 48
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1990 89
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1992 59
1993 40
1994 37
1995 53
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1997 62
1998 58
1999 59
2000 63
2001 149
2002 90
2003 97
2004 78
2005 138
2006 146
2007 132
2008 128
2009 166
2010 157
2011 204
2012 216
2013 204
2014 227
2015 233
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4,826 results

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Page 1
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), …
Multidisciplinary Management of Rett Syndrome: Twenty Years' Experience.
Vilvarajan S, McDonald M, Douglas L, Newham J, Kirkland R, Tzannes G, Tay D, Christodoulou J, Thompson S, Ellaway C. Vilvarajan S, et al. Genes (Basel). 2023 Aug 11;14(8):1607. doi: 10.3390/genes14081607. Genes (Basel). 2023. PMID: 37628658 Free PMC article. Review.
Rett syndrome, a complex X-linked condition, affecting mainly females, is due to pathogenic variants of the MECP2 gene in most affected individuals. The Rett syndrome Multidisciplinary Management clinic at The Children's Hospital at Westmead, Sydney, A …
Rett syndrome, a complex X-linked condition, affecting mainly females, is due to pathogenic variants of the MECP2 gene in most …
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 …
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.
Gold WA, Percy AK, Neul JL, Cobb SR, Pozzo-Miller L, Issar JK, Ben-Zeev B, Vignoli A, Kaufmann WE. Gold WA, et al. Nat Rev Dis Primers. 2024 Nov 7;10(1):84. doi: 10.1038/s41572-024-00568-0. Nat Rev Dis Primers. 2024. PMID: 39511247 Review.
Rett syndrome (RTT) is a severe, progressive, neurodevelopmental disorder, which affects predominantly females. ...
Rett syndrome (RTT) is a severe, progressive, neurodevelopmental disorder, which affects predominantly females. ...
Rett Syndrome: The Emerging Landscape of Treatment Strategies.
Percy AK, Ananth A, Neul JL. Percy AK, et al. CNS Drugs. 2024 Nov;38(11):851-867. doi: 10.1007/s40263-024-01106-y. Epub 2024 Sep 9. CNS Drugs. 2024. PMID: 39251501 Free PMC article. Review.
Rett syndrome (RTT) has enjoyed remarkable progress in achieving specific therapies. RTT, a unique neurodevelopmental disorder first described in 1966, progressed slowly until the landmark paper of Hagberg and colleagues in 1983. ...This information was essential fo …
Rett syndrome (RTT) has enjoyed remarkable progress in achieving specific therapies. RTT, a unique neurodevelopmental disorder …
Rett Syndrome Spectrum in Monogenic Developmental-Epileptic Encephalopathies and Epilepsies: A Review.
Spagnoli C, Fusco C, Pisani F. Spagnoli C, et al. Genes (Basel). 2021 Jul 28;12(8):1157. doi: 10.3390/genes12081157. Genes (Basel). 2021. PMID: 34440332 Free PMC article. Review.
INTRODUCTION: Progress in the clinical application of next-generation-sequencing-based techniques has resulted in a dramatic increase in the recognized genetic heterogeneity of the Rett syndrome spectrum (RSS). Our awareness of the considerable overlap with pediatri …
INTRODUCTION: Progress in the clinical application of next-generation-sequencing-based techniques has resulted in a dramatic increase in the …
Gene Editing and Rett Syndrome: Does It Make the Cut?
Coorey B, Haase F, Ellaway C, Clarke A, Lisowski L, Gold WA. Coorey B, et al. CRISPR J. 2022 Aug;5(4):490-499. doi: 10.1089/crispr.2022.0020. Epub 2022 Jul 26. CRISPR J. 2022. PMID: 35881862 Review.
Rett syndrome (RTT) is a rare neurogenetic disorder caused by pathogenic variants of the Methyl CpG binding protein 2 (MECP2) gene. ...Advances in understanding RTT has provided insight into the complexity and exquisite control of MECP2 expression, where loss of exp …
Rett syndrome (RTT) is a rare neurogenetic disorder caused by pathogenic variants of the Methyl CpG binding protein 2 (MECP2) …
Rett syndrome.
Segawa M, Nomura Y. Segawa M, et al. Curr Opin Neurol. 2005 Apr;18(2):97-104. doi: 10.1097/01.wco.0000162848.99154.9a. Curr Opin Neurol. 2005. PMID: 15791137 Review.
PURPOSE OF REVIEW: Nearly 70 reports on Rett syndrome were published in 2004. We have selected 51 articles, including clinical reports, on pathophysiology, genotype-phenotype correlation, and clinical and basic molecular biology studies. ...Developmental studies sug …
PURPOSE OF REVIEW: Nearly 70 reports on Rett syndrome were published in 2004. We have selected 51 articles, including clinical …
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 …
4,826 results