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

Year Number of Results
1979 1
1983 1
1984 3
1985 1
1986 2
1987 4
1988 2
1989 2
1990 4
1991 1
1992 1
1993 9
1994 4
1995 13
1996 18
1997 20
1998 13
1999 22
2000 10
2001 25
2002 25
2003 21
2004 19
2005 33
2006 21
2007 48
2008 33
2009 34
2010 41
2011 39
2012 31
2013 42
2014 38
2015 44
2016 28
2017 28
2018 31
2019 23
2020 39
2021 40
2022 27
2023 23
2024 8

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779 results

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Page 1
Williams syndrome.
Kozel BA, Barak B, Kim CA, Mervis CB, Osborne LR, Porter M, Pober BR. Kozel BA, et al. Nat Rev Dis Primers. 2021 Jun 17;7(1):42. doi: 10.1038/s41572-021-00276-z. Nat Rev Dis Primers. 2021. PMID: 34140529 Free PMC article. Review.
Williams syndrome (WS) is a relatively rare microdeletion disorder that occurs in as many as 1:7,500 individuals. ...
Williams syndrome (WS) is a relatively rare microdeletion disorder that occurs in as many as 1:7,500 individuals. ...
Williams-Beuren syndrome.
Pober BR. Pober BR. N Engl J Med. 2010 Jan 21;362(3):239-52. doi: 10.1056/NEJMra0903074. N Engl J Med. 2010. PMID: 20089974 Review. No abstract available.
Health Care Supervision for Children With Williams Syndrome.
Morris CA, Braddock SR; COUNCIL ON GENETICS. Morris CA, et al. Pediatrics. 2020 Feb;145(2):e20193761. doi: 10.1542/peds.2019-3761. Epub 2020 Jan 21. Pediatrics. 2020. PMID: 31964759 Review.
This set of recommendations is designed to assist the pediatrician in caring for children with Williams syndrome (WS) who were diagnosed by using clinical features and with chromosome 7 microdeletion confirmed by fluorescence in situ hybridization, chromosome microa …
This set of recommendations is designed to assist the pediatrician in caring for children with Williams syndrome (WS) who were …
Williams syndrome.
[No authors listed] [No authors listed] Nat Rev Dis Primers. 2021 Jun 17;7(1):43. doi: 10.1038/s41572-021-00283-0. Nat Rev Dis Primers. 2021. PMID: 34140526 No abstract available.
Metabolic and autoimmune syndromes.
Nannini V. Nannini V. Atlas Oral Maxillofac Surg Clin North Am. 2014 Sep;22(2):123-34. doi: 10.1016/j.cxom.2014.05.005. Atlas Oral Maxillofac Surg Clin North Am. 2014. PMID: 25171994 Review. No abstract available.
Ocular features in Williams-Beuren syndrome: a review of the literature.
Nassisi M, Mainetti C, Aretti A, Sperti A, Nicotra V, Rinaldi B, Natacci F, Bedeschi MF, Viola F. Nassisi M, et al. Curr Opin Ophthalmol. 2023 Nov 1;34(6):514-521. doi: 10.1097/ICU.0000000000000990. Epub 2023 Aug 17. Curr Opin Ophthalmol. 2023. PMID: 37589562 Review.
Functional Neurological Symptom Disorder in Williams Syndrome: Case Series and Review of Relevant Literature.
Thom RP, Balaj K, Keary CJ, Pober BR, McDougle CJ. Thom RP, et al. J Acad Consult Liaison Psychiatry. 2022 Mar-Apr;63(2):170-179. doi: 10.1016/j.jaclp.2021.09.007. Epub 2021 Oct 5. J Acad Consult Liaison Psychiatry. 2022. PMID: 34619410 Review.
BACKGROUND: Williams syndrome (WS) is a neurodevelopmental disorder associated with several medical and psychiatric comorbidities. ...
BACKGROUND: Williams syndrome (WS) is a neurodevelopmental disorder associated with several medical and psychiatric comorbidit …
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 …
Repetitive Thoughts and Repetitive Behaviors in Williams Syndrome.
Huston JC, Thom RP, Ravichandran CT, Mullett JE, Moran C, Waxler JL, Pober BR, McDougle CJ. Huston JC, et al. J Autism Dev Disord. 2022 Feb;52(2):852-862. doi: 10.1007/s10803-021-04979-w. Epub 2021 Apr 10. J Autism Dev Disord. 2022. PMID: 33837487
The purpose of the study was to characterize repetitive phenomena in Williams syndrome (WS). The parents of 60 subjects with WS completed the Yale-Brown Obsessive Compulsive Scale (Y-BOCS) or Children's Y-BOCS, the Yale Global Tic Severity Scale, the Stereotyped Beh …
The purpose of the study was to characterize repetitive phenomena in Williams syndrome (WS). The parents of 60 subjects with W …
Understanding Number Line Estimation in Williams Syndrome and Down Syndrome.
Simms V, Karmiloff-Smith A, Ranzato E, Van Herwegen J. Simms V, et al. J Autism Dev Disord. 2020 Feb;50(2):583-591. doi: 10.1007/s10803-019-04268-7. J Autism Dev Disord. 2020. PMID: 31705420 Free PMC article.
Previous studies suggest that tasks dependent on the mental number line may be difficult for Williams Syndrome (WS) and Down Syndrome (DS) groups. However, few have directly assessed number line estimation in these groups. ...
Previous studies suggest that tasks dependent on the mental number line may be difficult for Williams Syndrome (WS) and Down S …
779 results