Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Laura Groves"'
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 14, Iss 1, Pp 1-13 (2022)
Abstract Background Anxiety symptomatology is common in individuals with intellectual disability (ID). Symptomatology includes both traditional Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) anxiety disorders and autism sp
Externí odkaz:
https://doaj.org/article/4d0e316f83cd4262a53bea8e377e41c6
Autor:
Laura Groves, Joanna Moss, Hayley Crawford, Lisa Nelson, Chris Stinton, Gursharan Singla, Chris Oliver
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 11, Iss 1, Pp 1-9 (2019)
Abstract Background Depressive symptomology and low affect are comparatively common in individuals with genetic disorders such as Cornelia de Lange syndrome. However, lifespan trajectories and associated person characteristics have not been examined.
Externí odkaz:
https://doaj.org/article/b66da9775b6546d0a0efc435d19a783b
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 9, Iss 1, Pp 1-12 (2017)
Abstract Background The aim of this study was to examine executive functioning in adolescents and adults with Cornelia de Lange syndrome (CdLS) to identify a syndrome and age-related profile of cognitive impairment. Methods Participants were 24 indiv
Externí odkaz:
https://doaj.org/article/c339982c44e44529a562a9acd90bf12f
Autor:
Chris Oliver, Laura Groves, Blake D. Hansen, Masoud Salehi, Shaydah Kheradmand, Cheri S. Carrico, Patti Caudill, Mark Mattingly, Dale Dorsett, Stephenson Chea, Vijay Pratap Singh, Ian D. Krantz, Sylvia Huisman, Matthew A. Deardorff, Antonie D. Kline
Publikováno v:
American Journal of Medical Genetics Part A. 188:1005-1014
Cornelia de Lange syndrome (CdLS) is a spectrum disorder due to variants in genes of the cohesin protein complex. The following abstracts are from the Cornelia de Lange Syndrome Scientific and Educational Symposium held virtually in October 2020. Asp
Autor:
Hayley Crawford, Chris Oliver, Laura Groves, Louise Bradley, Kayla Smith, Abigail Hogan, Derek Renshaw, Jane Waite, Jane Roberts
Publikováno v:
Psychiatry Research. :115278
Autor:
Chris Oliver, Joanna Moss, Laura Groves, Sotaro Kita, Effie Pearson, Lisa Nelson, Eva Nielsen
Publikováno v:
Journal of Intellectual Disability Research. 65:601-607
Background: Cornelia de Lange syndrsome (CdLS) is a rare genetic syndrome with notable impaired expressive communication characterised by reduced spoken language. We examined gesture use to refine the description of expressive communication impairmen
Autor:
Chris Oliver, Katherine Ellis, Georgie Agar, Stacey Bissell, Justin Cheuk Yin Chung, Hayley Crawford, Effie Pearson, Kelly Wade, Jane Waite, Debbie Allen, Lucy Deeprose, Georgina Edwards, Lauren Jenner, Breanne Kearney, Lauren Shelley, Kayla Smith, Hayley Trower, Dawn Adams, Louise Daniel, Laura Groves, Mary Heald, Jo Moss, Caroline Richards, Rachel Royston, Joanne Tarver, Alice Welham, Lucy Wilde, Kate Woodcock
Publikováno v:
Contemporary Issues in Evaluating Treatment Outcomes in Neurodevelopmental Disorders ISBN: 9780323988834
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e952a66a49a0eadef58ad1adc3963576
https://doi.org/10.1016/bs.irrdd.2022.05.004
https://doi.org/10.1016/bs.irrdd.2022.05.004
Autor:
Chris Oliver, Anna Cereda, Julia O'Connor, Claudia Rigamonti, Ingrid D. C. van Balkom, Whitney Guthrie, David R. FitzPatrick, Paul A. Mulder, Angell Shi, Sylvia A. Huisman, Stacey L. Ishman, Matthew A. Deardorff, Lynne M. Kerr, Sigrid Piening, Joseph P. McCleery, Valérie Cormier-Daire, Peter M. Gillett, David Axtell, Antonella Costantino, Egbert J.W. Redeker, Carol J. Potter, Alex V. Levin, Angelo Selicorni, Raoul C.M. Hennekam, Natalie Blagowidow, Marco A. Grados, Mary Levis, Feliciano J. Ramos, Frank J. Kaiser, Zeynep Tümer, Joanna Moss, Juan Pié, Gerritjan Koekkoek, Laura Groves, Milena Mariani, Paola Francesca Ajmone, Amy Metrena, Ana L. Quaglio, Anne Marie Bisgaard, Leonie A. Menke, Jolanta Wierzba, Antonie D. Kline, David M. Richman
Publikováno v:
Kline, A D, Moss, J F, Selicorni, A, Bisgaard, A-M, Deardorff, M A, Gillett, P M, Ishman, S L, Kerr, L M, Levin, A V, Mulder, P A, Ramos, F J, Wierzba, J, Ajmone, P F, Axtell, D, Blagowidow, N, Cereda, A, Costantino, A, Cormier-Daire, V, FitzPatrick, D, Grados, M, Groves, L, Guthrie, W, Huisman, S, Kaiser, F J, Koekkoek, G, Levis, M, Mariani, M, McCleery, J P, Menke, L A, Metrena, A, O'Connor, J, Oliver, C, Pie, J, Piening, S, Potter, C J, Quaglio, A L, Redeker, E, Richman, D, Rigamonti, C, Shi, A, Tumer, Z, Van Balkom, I D C & Hennekam, R C 2018, ' Diagnosis and management of Cornelia de Lange syndrome : first international consensus statement ', Nature Reviews Genetics, vol. 19, no. 10, pp. 649-666 . https://doi.org/10.1038/s41576-018-0031-0
Nature Reviews. Genetics
Kline, A D, Moss, J F, Selicorni, A, Bisgaard, A-M, Deardorff, M A, Gillett, P M, Ishman, S L, Kerr, L M, Levin, A V, Mulder, P A, Ramos, F J, Wierzba, J, Ajmone, P F, Axtell, D, Blagowidow, N, Cereda, A, Costantino, A, Cormier-Daire, V, FitzPatrick, D, Grados, M, Groves, L, Guthrie, W, Huisman, S, Kaiser, F J, Koekkoek, G, Levis, M, Mariani, M, McCleery, J P, Menke, L A, Metrena, A, O'Connor, J, Oliver, C, Pie, J, Piening, S, Potter, C J, Quaglio, A L, Redeker, E, Richman, D, Rigamonti, C, Shi, A, Tümer, Z, Van Balkom, I D C & Hennekam, R C 2018, ' Diagnosis and management of Cornelia de Lange syndrome : first international consensus statement ', Nature Reviews. Genetics, vol. 19, pp. 649-666 . https://doi.org/10.1038/s41576-018-0031-0
Nature Reviews. Genetics
Kline, A D, Moss, J F, Selicorni, A, Bisgaard, A-M, Deardorff, M A, Gillett, P M, Ishman, S L, Kerr, L M, Levin, A V, Mulder, P A, Ramos, F J, Wierzba, J, Ajmone, P F, Axtell, D, Blagowidow, N, Cereda, A, Costantino, A, Cormier-Daire, V, FitzPatrick, D, Grados, M, Groves, L, Guthrie, W, Huisman, S, Kaiser, F J, Koekkoek, G, Levis, M, Mariani, M, McCleery, J P, Menke, L A, Metrena, A, O'Connor, J, Oliver, C, Pie, J, Piening, S, Potter, C J, Quaglio, A L, Redeker, E, Richman, D, Rigamonti, C, Shi, A, Tümer, Z, Van Balkom, I D C & Hennekam, R C 2018, ' Diagnosis and management of Cornelia de Lange syndrome : first international consensus statement ', Nature Reviews. Genetics, vol. 19, pp. 649-666 . https://doi.org/10.1038/s41576-018-0031-0
Cornelia de Lange syndrome (CdLS) is an archetypical genetic syndrome that is characterized by intellectual disability, well-defined facial features, upper limb anomalies and atypical growth, among numerous other signs and symptoms. It is caused by v
Autor:
Alexej Abyzov, Kevin Cameron Allan, Anahita Amiri, Heather M. Brown, Anne L. Calof, Qiang Chang, Kimberly M. Christian, Benjamin L.L. Clayton, Francesca Cucinotta, Alissa M. D'Gama, Mathew Sean Elitt, L. Fernandez, R. Holly Fitch, Jeffrey A. Golden, Laura Groves, R.J. Hagerman, Eric Jaffe, B.L. Johnson-Kerner, Alexandre Jourdon, Arthur D. Lander, M.J. Leigh, Youngshin Lim, A.H. Mahnke, Jessica Mariani, Guo-li Ming, R.C. Miranda, S.M. Mooney, Jeffrey L. Neul, Zachary Scott Nevin, Lee Niswander, Christopher Oliver, Antonio M. Persico, Sofia A. Pezoa, Christina Pyrgaki, Lawrence T. Reiter, Arianna Ricciardello, Edward Rubenstein, Mustafa Sahin, Rosaysela Santos, Soraya Scuderi, E.H. Sherr, Hongjun Song, Siddharth Srivastava, Paul J. Tesar, Laura Turriziani, Flora M. Vaccarino, Christopher A. Walsh, Feinan Wu, Eunice Y. Yuen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::647b4f4ae80f0afd2ea6367a538313df
https://doi.org/10.1016/b978-0-12-814409-1.01002-8
https://doi.org/10.1016/b978-0-12-814409-1.01002-8