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

Year Number of Results
1962 1
1966 1
1968 3
1969 2
1971 2
1972 2
1973 1
1975 3
1976 2
1977 1
1979 1
1980 1
1981 2
1983 3
1984 3
1985 37
1986 51
1987 54
1988 48
1989 41
1990 89
1991 43
1992 59
1993 41
1994 37
1995 53
1996 32
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 203
2012 216
2013 204
2014 227
2015 232
2016 254
2017 231
2018 217
2019 234
2020 226
2021 193
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4,130 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),
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
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 …
Developmental Dynamics of Rett Syndrome.
Feldman D, Banerjee A, Sur M. Feldman D, et al. Neural Plast. 2016;2016:6154080. doi: 10.1155/2016/6154080. Epub 2016 Jan 31. Neural Plast. 2016. PMID: 26942018 Free PMC article. Review.
Rett Syndrome was long considered to be simply a disorder of postnatal development, with phenotypes that manifest only late in development and into adulthood. ...The effects of MeCP2 are mediated by diverse signaling, transcriptional, and epigenetic mechanisms. Atte
Rett Syndrome was long considered to be simply a disorder of postnatal development, with phenotypes that manifest only late in
Rett Syndrome: A Genetic Update and Clinical Review Focusing on Comorbidities.
Gold WA, Krishnarajy R, Ellaway C, Christodoulou J. Gold WA, et al. ACS Chem Neurosci. 2018 Feb 21;9(2):167-176. doi: 10.1021/acschemneuro.7b00346. Epub 2017 Dec 15. ACS Chem Neurosci. 2018. PMID: 29185709 Review.
Rett syndrome (RTT) is a unique neurodevelopmental disorder that primarily affects females resulting in severe cognitive and physical disabilities. ...
Rett syndrome (RTT) is a unique neurodevelopmental disorder that primarily affects females resulting in severe cognitive and p
Treating Rett syndrome: from mouse models to human therapies.
Vashi N, Justice MJ. Vashi N, et al. Mamm Genome. 2019 Jun;30(5-6):90-110. doi: 10.1007/s00335-019-09793-5. Epub 2019 Feb 28. Mamm Genome. 2019. PMID: 30820643 Free PMC article. Review.
Rare diseases are very difficult to study mechanistically and to develop therapies for because of the scarcity of patients. Here, the rare neuro-metabolic disorder Rett syndrome (RTT) is discussed as a prototype for precision medicine, demonstrating how mouse models …
Rare diseases are very difficult to study mechanistically and to develop therapies for because of the scarcity of patients. Here, the rare n …
MeCP2 mutations: progress towards understanding and treating Rett syndrome.
Shah RR, Bird AP. Shah RR, et al. Genome Med. 2017 Feb 17;9(1):17. doi: 10.1186/s13073-017-0411-7. Genome Med. 2017. PMID: 28212680 Free PMC article. Review.
Rett syndrome is a profound neurological disorder caused by mutations in the MECP2 gene, but preclinical research has indicated that it is potentially treatable. ...
Rett syndrome is a profound neurological disorder caused by mutations in the MECP2 gene, but preclinical research has indicate
The psychopharmacology of autism spectrum disorder and Rett syndrome.
Persico AM, Ricciardello A, Cucinotta F. Persico AM, et al. Handb Clin Neurol. 2019;165:391-414. doi: 10.1016/B978-0-444-64012-3.00024-1. Handb Clin Neurol. 2019. PMID: 31727226 Review.
ASD can be idiopathic or syndromic, in the latter case representing one of the many manifestations of a genetic disorder, such as Rett syndrome. Psychopharmacology cannot directly ameliorate core autistic symptoms, but rather aims at treating comorbid disorders, suc …
ASD can be idiopathic or syndromic, in the latter case representing one of the many manifestations of a genetic disorder, such as Rett
[Molecular basis of Rett syndrome: A current look].
Pantaleón F G, Juvier R T. Pantaleón F G, et al. Rev Chil Pediatr. 2015 May-Jun;86(3):142-51. doi: 10.1016/j.rchipe.2015.07.001. Epub 2015 Aug 1. Rev Chil Pediatr. 2015. PMID: 26239053 Free article. Review. Spanish.
Rett syndrome (RS) is a neurodevelopmental disorder that exclusively affects girls, and occurs along with autism. ...With the aim of updating the information about RS, a search was performed in the computer data bases of PubMed, Hinari, SCIELO and Medline, as well a
Rett syndrome (RS) is a neurodevelopmental disorder that exclusively affects girls, and occurs along with autism. ...With the
A Coordinated Attack: Rett Syndrome Therapeutic Development.
Gogliotti RG, Niswender CM. Gogliotti RG, et al. Trends Pharmacol Sci. 2019 Apr;40(4):233-236. doi: 10.1016/j.tips.2019.02.007. Trends Pharmacol Sci. 2019. PMID: 30905360 Free PMC article. Review.
Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the Methyl CpG binding protein 2 (MeCP2) gene. ...
Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the Methyl CpG binding protein 2 (MeCP2) gene. ...
4,130 results