ALLMedicine™ Williams Syndrome Center
Research & Reviews 340 results
https://doi.org/10.1186/s13023-022-02395-6 10.1162/089892900562002 10.1177/088307380201700406 10.1111/j.1467-8721.2007.00484.x 10.1002/ajmg.a.20416 10.1111/j.1467-7687.2007.00626.x 10.3389/fpsyg.2016.01131 10.1016/S1364-6613(00)01501-1 10.1001/archpsyc.65.8.946 10.1038/nature12715 10.1002/cncr.27633.Percutaneous 10.1080/87565641.2003.9651894 10.1162/089892900561959 10.1097/00001756-200207020-00009 10.1080/17470210701855629 10.1016/S0010-0277(03)00049-0 10.1186/s11689-016-9172-7 10.1016/j.cub.2009.08.055 10.1038/ncomms11940 10.1073/pnas.152159999 10.1093/oxfordhb/9780199559053.013.0039 10.1037/0012-1649.34.3.525 10.1016/j.neuropsychologia.2015.09.026 10.1093/cercor/9.5.415 10.1162/jocn.1996.8.6.551 10.1016/j.neuroimage.2011.03.067 10.1007/s00221-011-2579-1 10.1523/jneurosci.18-06-02188.1998 10.1093/scan/nsx119 10.1152/jn.00155.2004 10.1016/j.neuropsychologia.2017.04.028 10.1016/j.tins.2006.06.004 10.1016/j.neuron.2005.10.018 10.1016/j.neuroimage.2007.04.024 10.1097/WCO.0b013e328351823c 10.1097/WNN.0b013e31817720e4 10.1002/ajmg.b.32422 10.1101/2021.03.29.433074 10.2147/PRBM.S63474 10.1016/j.neuropsychologia.2009.12.021 10.1016/j.neuropsychologia.2008.10.023 10.1093/cercor/bhm140 10.1162/089892900562165 10.1162/089892900561977 10.3758/s13415-017-0528-6 10.1503/jpn.140384 10.1162/jocn.2011.21604 10.1523/JNEUROSCI.4268-09.2010 10.1523/JNEUROSCI.5272-03.2004 10.1007/s00018-005-5553-x 10.3389/fpsyg.2015.00760 10.1016/j.neuropsychologia.2009.04.017 10.1038/ng0993-11 10.1207/S15326942DN1602_3 10.1111/1469-7610.00312 10.1016/j.encep.2019.02.001 10.1038/nrn.2016.164 10.1016/j.neuroimage.2012.04.018 10.1016/j.cnr.2006.08.001 10.1016/j.cub.2016.05.072 10.1016/j.neuropsychologia.2007.05.006 10.1016/j.dcn.2018.04.005 10.1093/scan/nsv029 10.1023/B:JADD.0000018078.82542.ab 10.1167/1.3.333 10.1016/S1388-2457(00)00527-7 10.1016/S0925-2312(02)00821-4 10.1016/j.neuroimage.2005.05.032 10.1109/10.623056 10.1006/meth.2001.1238 10.1002/hbm.22567 10.2307/2532216 10.1176/appi.books.9780890425596 10.1111/1469-7610.00312 10.1006/nimg.2002.1212 10.1007/s10803-008-0641-z
Orphanet Journal of Rare Diseases; Gomez A, Lio G et. al.
Jun 23rd, 2022 - Williams syndrome (WS) and Autism Spectrum Disorders (ASD) are neurodevelopmental conditions associated with atypical but opposite face-to-face interactions patterns: WS patients overly stare at others, ASD individuals escape eye contact. Whether ...
https://clinicaltrials.gov/ct2/show/NCT02692846
Jun 16th, 2022 - Williams syndrome (WS) is a multisystem developmental disorder caused by deletion of 26-28 genes, including the elastin gene, located on chromosome 7q11.23. Cardiovascular disease in WS, including obstructive vascular disease and hypertension, and...
https://clinicaltrials.gov/ct2/show/NCT01132885
Jun 16th, 2022 - Williams syndrome (WS) is a rare disorder caused by hemizygous microdeletion of approximately 1.6 megabases on chromosomal band 7q11.23, typically by spontaneous mutation. The disorder is characterized by a collection of unique neuropsychiatric ma...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109668
Journal of Autism and Developmental Disorders; Fisher MH, Kammes RR et. al.
May 17th, 2022 - Adults with Williams syndrome (WS) display hypersocial behaviors and experience social skills deficits. To improve social outcomes, we evaluated the feasibility, acceptability, and preliminary efficacy of an 8-week distance-delivered social skills...
https://doi.org/10.1177/17446295221079583
Journal of Intellectual Disabilities : JOID; Pereira RCM, Apis A et. al.
May 12th, 2022 - This cross-sectional and descriptive study examined the family quality of life (FQoL) among 72 Brazilian families who have children with Williams syndrome, a rare genetic disorder in which most individuals have an intellectual disability, usually ...
Guidelines 1 results
https://doi.org/10.1542/peds.2019-3761
Pediatrics Morris CA, Braddock SR et. al.
Jan 23rd, 2020 - 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...
Clinicaltrials.gov 4 results
https://clinicaltrials.gov/ct2/show/NCT02692846
Jun 16th, 2022 - Williams syndrome (WS) is a multisystem developmental disorder caused by deletion of 26-28 genes, including the elastin gene, located on chromosome 7q11.23. Cardiovascular disease in WS, including obstructive vascular disease and hypertension, and...
https://clinicaltrials.gov/ct2/show/NCT01132885
Jun 16th, 2022 - Williams syndrome (WS) is a rare disorder caused by hemizygous microdeletion of approximately 1.6 megabases on chromosomal band 7q11.23, typically by spontaneous mutation. The disorder is characterized by a collection of unique neuropsychiatric ma...
https://clinicaltrials.gov/ct2/show/NCT04807517
Sep 9th, 2021 - After being informed about the study and potential risks, all patients or their legal guardians giving written informed consent will be screened for study eligibility. Patients who meet the eligibility requirements will participate in a 16-week, f...
https://clinicaltrials.gov/ct2/show/NCT03827525
Oct 18th, 2019 - Most studies agree that anxiety disorders are more frequent in people with intellectual disabilities that in the general population. Williams syndrome (WS) is a rare disease, associated with an anxiety rate 8 times higher than in the general popul...
News 2 results
https://www.mdedge.com/familymedicine/article/76496/pediatrics/socially-vulnerable-need-specific-interventions-stop-abuse
MDedge Psychiatry; Denise Napoli
Jul 22nd, 2013 - Patients with autism, Williams syndrome, and Down syndrome are all socially vulnerable, but in "markedly different" ways. Understanding these differences might help tailor specific interventions to keep these populations safe from abuse and exploi.
https://www.mdedge.com/psychiatry/article/76496/pediatrics/socially-vulnerable-need-specific-interventions-stop-abuse
Denise Napoli
Jul 22nd, 2013 - Patients with autism, Williams syndrome, and Down syndrome are all socially vulnerable, but in "markedly different" ways. Understanding these differences might help tailor specific interventions to keep these populations safe from abuse and exploi.
