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

Year Number of Results
1951 2
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1953 9
1954 2
1955 3
1957 2
1958 2
1959 1
1960 4
1961 3
1962 2
1963 5
1964 3
1965 2
1966 10
1967 3
1968 7
1969 5
1970 3
1971 5
1972 4
1973 2
1974 2
1975 5
1976 7
1977 2
1978 1
1979 5
1980 3
1981 2
1982 1
1983 4
1984 3
1985 41
1986 59
1987 63
1988 59
1989 51
1990 96
1991 48
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1993 44
1994 45
1995 58
1996 40
1997 67
1998 60
1999 71
2000 75
2001 154
2002 95
2003 104
2004 81
2005 144
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2009 171
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The following term was not found in PubMed: santitharangkun
Page 1
Showing results for rett santitharangkun
Search for Srett Santitharangkun instead (3 results)
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 first p …
Rett syndrome (RTT) is an early-onset neurodevelopmental disorder that primarily affects females, resulting in severe cognitive and p …
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 and their imp …
With the recent 50th anniversary of the first publication on Rett syndrome, and the almost 20 years since the first report on the lin …
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, Australia, was …
Rett syndrome, a complex X-linked condition, affecting mainly females, is due to pathogenic variants of the MECP2 gene in most affect …
[Rett syndrome].
van Urk PR, van den Berg MP, van Royen BJ, Smeets EE, Curfs LM. van Urk PR, et al. Ned Tijdschr Geneeskd. 2014;158(3):A6686. Ned Tijdschr Geneeskd. 2014. PMID: 24423488 Dutch.
BACKGROUND: Rett syndrome is caused by mutations in the X-linked MECP2 gene, encoding MeCP2 protein. ...CONCLUSION: Rett syndrome is a severe neurological developmental disorder that occurs almost exclusively in females and for which there is still no causal treatme …
BACKGROUND: Rett syndrome is caused by mutations in the X-linked MECP2 gene, encoding MeCP2 protein. ...CONCLUSION: Rett syndr …
Oral Manifestations of Rett Syndrome-A Systematic Review.
Mahdi SS, Jafri HA, Allana R, Amenta F, Khawaja M, Qasim SSB. Mahdi SS, et al. Int J Environ Res Public Health. 2021 Jan 28;18(3):1162. doi: 10.3390/ijerph18031162. Int J Environ Res Public Health. 2021. PMID: 33525609 Free PMC article. Review.
This systematic review was carried out to identify the dental manifestation of Rett syndrome and to shed light on treatment options available for oral health problems associated with Rett syndrome. A systematic literature search was conducted on the PubMed, Scopus, …
This systematic review was carried out to identify the dental manifestation of Rett syndrome and to shed light on treatment options a …
Rett and Rett-related disorders: Common mechanisms for shared symptoms?
D'Mello SR. D'Mello SR. Exp Biol Med (Maywood). 2023 Nov;248(22):2095-2108. doi: 10.1177/15353702231209419. Epub 2023 Dec 6. Exp Biol Med (Maywood). 2023. PMID: 38057990 Review.
Rett syndrome is a neurodevelopmental disorder caused by loss-of-function mutations in the methyl-CpG binding protein-2 (MeCP2) gene that is characterized by epilepsy, intellectual disability, autistic features, speech deficits, and sleep and breathing abnormalities. ...Lo …
Rett syndrome is a neurodevelopmental disorder caused by loss-of-function mutations in the methyl-CpG binding protein-2 (MeCP2) gene …
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 suggest an …
PURPOSE OF REVIEW: Nearly 70 reports on Rett syndrome were published in 2004. We have selected 51 articles, including clinical report …
Rett syndrome.
Ben Zeev Ghidoni B. Ben Zeev Ghidoni B. Child Adolesc Psychiatr Clin N Am. 2007 Jul;16(3):723-43. doi: 10.1016/j.chc.2007.03.004. Child Adolesc Psychiatr Clin N Am. 2007. PMID: 17562589 Review.
Rett syndrome (RS) is an X-linked neurodevelopmental disorder and the second most common cause of genetic mental retardation in females. ...
Rett syndrome (RS) is an X-linked neurodevelopmental disorder and the second most common cause of genetic mental retardation in femal …
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. Attempts to …
Rett Syndrome was long considered to be simply a disorder of postnatal development, with phenotypes that manifest only late in develo …
[Rett Syndrome: an updated view].
Arancibia T, Pardo R, Barrientos P. Arancibia T, et al. Andes Pediatr. 2023 Jan;94(1):94-103. doi: 10.32641/andespediatr.v94i1.4014. Andes Pediatr. 2023. PMID: 37906876 Free article. Spanish.
Rett syndrome (RS) is a rare neurodevelopmental disorder first described in 1966. ...
Rett syndrome (RS) is a rare neurodevelopmental disorder first described in 1966. ...
5,144 results