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

Year Number of Results
1946 3
1949 1
1950 1
1952 1
1961 1
1964 1
1972 1
1976 1
1981 1
1982 2
1983 1
1984 1
1986 2
1987 5
1988 4
1989 11
1990 17
1991 17
1992 36
1993 63
1994 45
1995 44
1996 53
1997 63
1998 68
1999 60
2000 51
2001 67
2002 51
2003 55
2004 66
2005 87
2006 61
2007 75
2008 83
2009 73
2010 98
2011 88
2012 83
2013 93
2014 91
2015 109
2016 89
2017 83
2018 90
2019 108
2020 79
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2,006 results
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Page 1
Angelman Syndrome: Identification and Management.
Bonello D, Camilleri F, Calleja-Agius J. Bonello D, et al. Neonatal Netw. 2017 May 1;36(3):142-151. doi: 10.1891/0730-0832.36.3.142. Neonatal Netw. 2017. PMID: 28494826 Review.
Angelman syndrome (AS) is a neurobehavioral and genetically determined condition, which affects approximately 1 in 15,000 individuals. ...
Angelman syndrome (AS) is a neurobehavioral and genetically determined condition, which affects approximately 1 in 15,000 individuals
Angelman syndrome - insights into a rare neurogenetic disorder.
Buiting K, Williams C, Horsthemke B. Buiting K, et al. Nat Rev Neurol. 2016 Oct;12(10):584-93. doi: 10.1038/nrneurol.2016.133. Epub 2016 Sep 12. Nat Rev Neurol. 2016. PMID: 27615419 Review.
Angelman syndrome results from loss of function of the imprinted UBE3A (ubiquitin-protein ligase E3A) gene on chromosome 15q11.2-q13. ...Clinical diagnosis of Angelman syndrome in infants and young children is sometimes difficult, but can be verified by genetic test
Angelman syndrome results from loss of function of the imprinted UBE3A (ubiquitin-protein ligase E3A) gene on chromosome 15q11.2-q13.
Angelman syndrome: Current and emerging therapies in 2016.
Tan WH, Bird LM. Tan WH, et al. Am J Med Genet C Semin Med Genet. 2016 Dec;172(4):384-401. doi: 10.1002/ajmg.c.31536. Epub 2016 Nov 8. Am J Med Genet C Semin Med Genet. 2016. PMID: 27860204 Review.
Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by a loss of the maternally-inherited UBE3A; the paternal UBE3A is silenced in neurons by a mechanism involving an antisense transcript (UBE3A-AS) at the unmethylated paternal locus. ...
Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by a loss of the maternally-inherited UBE3A; the paternal UBE3A
Communication in Angelman syndrome: a scoping review.
Pearson E, Wilde L, Heald M, Royston R, Oliver C. Pearson E, et al. Dev Med Child Neurol. 2019 Nov;61(11):1266-1274. doi: 10.1111/dmcn.14257. Epub 2019 May 10. Dev Med Child Neurol. 2019. PMID: 31074506 Review.
AIM: A scoping review was conducted to examine and evaluate empirical data on the communication profile of Angelman syndrome beyond the described dissociation between receptive language and speech. METHOD: Three databases (PsycINFO, Embase, and Web of Science) were searche …
AIM: A scoping review was conducted to examine and evaluate empirical data on the communication profile of Angelman syndrome beyond t …
Neurologic manifestations of Angelman syndrome.
Thibert RL, Larson AM, Hsieh DT, Raby AR, Thiele EA. Thibert RL, et al. Pediatr Neurol. 2013 Apr;48(4):271-9. doi: 10.1016/j.pediatrneurol.2012.09.015. Pediatr Neurol. 2013. PMID: 23498559 Review.
Angelman syndrome is a neurogenetic disorder characterized by the loss or reduction of the ubiquitin-protein ligase E3A enzyme. ...We focus on a comprehensive whole-child approach to the diagnosis and long-term clinical care of individuals with Angelman syndrome....
Angelman syndrome is a neurogenetic disorder characterized by the loss or reduction of the ubiquitin-protein ligase E3A enzyme. ...We
Myoclonus in Angelman syndrome.
Pollack SF, Grocott OR, Parkin KA, Larson AM, Thibert RL. Pollack SF, et al. Epilepsy Behav. 2018 May;82:170-174. doi: 10.1016/j.yebeh.2018.02.006. Epub 2018 Mar 17. Epilepsy Behav. 2018. PMID: 29555100
Angelman syndrome (AS) is a neurogenetic imprinting disorder caused by loss of the maternally inherited Ube3a gene and is characterized by generalized epilepsy, limited expressive speech, sleep dysfunction, and movement disorders. ...The medical records of 200 individuals
Angelman syndrome (AS) is a neurogenetic imprinting disorder caused by loss of the maternally inherited Ube3a gene and is characteriz
Angelman syndrome.
Kyllerman M. Kyllerman M. Handb Clin Neurol. 2013;111:287-90. doi: 10.1016/B978-0-444-52891-9.00032-4. Handb Clin Neurol. 2013. PMID: 23622177 Review.
Angelman syndrome combines severe mental retardation, epilepsy, ataxia, speech impairment, and unique behavior with happy demeanor, laughing, short attention span, hyperactivity, and sleep disturbance. ...
Angelman syndrome combines severe mental retardation, epilepsy, ataxia, speech impairment, and unique behavior with happy demeanor, l
Angelman Syndrome.
Madaan M, Mendez MD. Madaan M, et al. 2020 Aug 15. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan–. StatPearls. 2020 Jan–. PMID: 32809705 Free Books & Documents. Review.
In 1965 Harry Angelman, British pediatrician, described the "Puppet Children," later being renamed Angelman syndrome (AS). Angelman described three children who had similar symptoms of learning disability, minimal or absent speech, ataxic and jerky movements, …
In 1965 Harry Angelman, British pediatrician, described the "Puppet Children," later being renamed Angelman syndrome (AS). …
Language, neurodevelopment, and behavior in Angelman syndrome: a case report.
Teodoro ATH, Chaves DY, Crenitte PAP, Hage SRV, Lamônica DAC. Teodoro ATH, et al. Codas. 2019 Aug 22;31(4):e20180177. doi: 10.1590/2317-1782/20182018177. Codas. 2019. PMID: 31460569 Free article. English, Portuguese.
PURPOSE: This study aimed to present findings on language, behavior, and neurodevelopment in a girl diagnosed with Angelman Syndrome, evaluated when she was three and eight years old. ...
PURPOSE: This study aimed to present findings on language, behavior, and neurodevelopment in a girl diagnosed with Angelman Syndrome, …
Behavioral Evaluation of Angelman Syndrome Mice at Older Ages.
Dutta R, Crawley JN. Dutta R, et al. Neuroscience. 2020 Oct 1;445:163-171. doi: 10.1016/j.neuroscience.2019.10.027. Epub 2019 Nov 12. Neuroscience. 2020. PMID: 31730795 Free PMC article.
Angelman syndrome is a neurodevelopmental disorder presenting with severe deficits in motor, speech, and cognitive abilities. The primary genetic cause of Angelman syndrome is a maternally transmitted mutation in the Ube3a gene, which has been successfully modeled i
Angelman syndrome is a neurodevelopmental disorder presenting with severe deficits in motor, speech, and cognitive abilities. The pri
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