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2014 1
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Page 1
Oxytocin and Oxytocin Receptor Gene Regulation in Williams Syndrome: A Systematic Review.
Çalışkan E, Şahin MN, Güldağ MA. Çalışkan E, et al. Yale J Biol Med. 2021 Dec 29;94(4):623-635. eCollection 2021 Dec. Yale J Biol Med. 2021. PMID: 34970101 Free PMC article. Review.
Williams Syndrome (WS) is a rare genetic multisystem disorder that occurs because of a deletion of approximately 25 genes in the 7q11.23 chromosome region. ...
Williams Syndrome (WS) is a rare genetic multisystem disorder that occurs because of a deletion of approximately 25 genes in t
Anxiety Disorders in Williams Syndrome Contrasted with Intellectual Disability and the General Population: A Systematic Review and Meta-Analysis.
Royston R, Howlin P, Waite J, Oliver C. Royston R, et al. J Autism Dev Disord. 2017 Dec;47(12):3765-3777. doi: 10.1007/s10803-016-2909-z. J Autism Dev Disord. 2017. PMID: 27696186 Free PMC article. Review.
Individuals with specific genetic syndromes associated with intellectual disability (ID), such as Williams syndrome (WS), are at increased risk for developing anxiety disorders. ...
Individuals with specific genetic syndromes associated with intellectual disability (ID), such as Williams syndrome (WS), are …
Characteristics of auditory evaluation in Williams syndrome: a systematic review.
Silva LAF, Kim CA, Matas CG. Silva LAF, et al. Codas. 2018 Sep 17;30(5):e20170267. doi: 10.1590/2317-1782/20182017267. Codas. 2018. PMID: 30231111 Free article. Review. English, Portuguese.
PURPOSE: Identify the characteristics of the clinical audiological evaluation of individuals with Williams syndrome by means of a systematic literature review. RESEARCH STRATEGIES: The following research question was initially determined: "What are the characteristi …
PURPOSE: Identify the characteristics of the clinical audiological evaluation of individuals with Williams syndrome by means o …
Neuropsychological Genotype-Phenotype in Patients with Williams Syndrome with Atypical Deletions: A Systematic Review.
Serrano-Juárez CA, Prieto-Corona B, Rodríguez-Camacho M, Sandoval-Lira L, Villalva-Sánchez ÁF, Yáñez-Téllez MG, López MFR. Serrano-Juárez CA, et al. Neuropsychol Rev. 2023 Dec;33(4):891-911. doi: 10.1007/s11065-022-09571-2. Epub 2022 Dec 15. Neuropsychol Rev. 2023. PMID: 36520254 Review.
Williams syndrome (WS) is a neurodevelopmental disorder caused by a microdeletion in the q11.23 region of chromosome 7. ...The objective of this systematic review was to analyze and synthesize the variability of the cognitive and behavioral profile of WS with atypic
Williams syndrome (WS) is a neurodevelopmental disorder caused by a microdeletion in the q11.23 region of chromosome 7. ...The
Mathematical development in Williams syndrome: A systematic review.
Van Herwegen J, Simms V. Van Herwegen J, et al. Res Dev Disabil. 2020 May;100:103609. doi: 10.1016/j.ridd.2020.103609. Epub 2020 Feb 19. Res Dev Disabil. 2020. PMID: 32087508
BACKGROUND: The current systematic review is the first to systematically explore and synthesis research to date on mathematical abilities in Williams syndrome (WS), a rare genetic disorder that results in an uneven cognitive profile. ...
BACKGROUND: The current systematic review is the first to systematically explore and synthesis research to date on mathematical abilities in …
Systematic Review: Emotion Dysregulation in Syndromic Causes of Intellectual and Developmental Disabilities.
Shaffer RC, Reisinger DL, Schmitt LM, Lamy M, Dominick KC, Smith EG, Coffman MC, Esbensen AJ. Shaffer RC, et al. J Am Acad Child Adolesc Psychiatry. 2023 May;62(5):518-557. doi: 10.1016/j.jaac.2022.06.020. Epub 2022 Aug 22. J Am Acad Child Adolesc Psychiatry. 2023. PMID: 36007813 Review.
OBJECTIVE: To summarize the current state of the literature regarding emotion dysregulation (ED) in syndromic intellectual disabilities (S-IDs) in 6 of the most common forms of S-IDs-Down syndrome, fragile X syndrome (FXS), tuberous sclerosis complex, Williams syndrome
OBJECTIVE: To summarize the current state of the literature regarding emotion dysregulation (ED) in syndromic intellectual disabilities (S-I …
Systematic Review and Meta-analysis: Mental Health in Children With Neurogenetic Disorders Associated With Intellectual Disability.
Glasson EJ, Buckley N, Chen W, Leonard H, Epstein A, Skoss R, Jacoby P, Blackmore AM, Bourke J, Downs J. Glasson EJ, et al. J Am Acad Child Adolesc Psychiatry. 2020 Sep;59(9):1036-1048. doi: 10.1016/j.jaac.2020.01.006. Epub 2020 Jan 13. J Am Acad Child Adolesc Psychiatry. 2020. PMID: 31945412 Review.
Ten syndromes were represented, and five were predominant: Down syndrome, 22q11.2 deletion syndrome, fragile X syndrome, Williams syndrome, and Prader-Willi syndrome. The Child Behavior Checklist was the most commonly used assessment tool for psychiatric symptoms. . …
Ten syndromes were represented, and five were predominant: Down syndrome, 22q11.2 deletion syndrome, fragile X syndrome, Williams
Common and distinct neural correlates of facial emotion processing in social anxiety disorder and Williams syndrome: A systematic review and voxel-based meta-analysis of functional resonance imaging studies.
Binelli C, Subirà S, Batalla A, Muñiz A, Sugranyés G, Crippa JA, Farré M, Pérez-Jurado L, Martín-Santos R. Binelli C, et al. Neuropsychologia. 2014 Nov;64:205-17. doi: 10.1016/j.neuropsychologia.2014.08.027. Epub 2014 Sep 4. Neuropsychologia. 2014. PMID: 25194208 Review.
The following search key-words were used: "emotion processing"; "facial emotion"; "social anxiety"; "social phobia"; "Williams syndrome"; "neuroimaging"; "functional magnetic resonance"; "fMRI" and their combinations, as well as terms specifying individual facial em …
The following search key-words were used: "emotion processing"; "facial emotion"; "social anxiety"; "social phobia"; "Williams syn
Ameloblastoma associated with syndromes: A systematic review.
Atarbashi-Moghadam S, Atarbashi-Moghadam F, Sijanivandi S, Mokhtari S. Atarbashi-Moghadam S, et al. J Stomatol Oral Maxillofac Surg. 2020 Apr;121(2):146-149. doi: 10.1016/j.jormas.2019.07.010. Epub 2019 Jul 20. J Stomatol Oral Maxillofac Surg. 2020. PMID: 31336213
Ameloblastoma was reported in association with Gorlin syndrome (6 cases), epidermal nevus syndrome (2 cases), Gardner syndrome (2 cases), Simpson-Golabi-Behmel syndrome (1 case), and Williams syndrome (1 case). The commonest associated syndrome was Gorlin syndrome ( …
Ameloblastoma was reported in association with Gorlin syndrome (6 cases), epidermal nevus syndrome (2 cases), Gardner syndrome (2 cases), Si …
12 results