Zobrazeno 1 - 10
of 395
pro vyhledávání: '"K. Percy"'
Autor:
K. Percy, C. Ouimet, S. Ward, M. Santana Quintero, C. Cancino, L. Wong, B. Marcus, S. Whittaker, M. Boussalh
Publikováno v:
ISPRS Annals of the Photogrammetry, Remote Sensing and Spatial Information Sciences, Vol II-5/W3, Pp 229-234 (2015)
As it is broadly understood, recording serves as a basis for the diagnosis, treatment and preservation of historic places and contributes to record our built cultural heritage for posterity. This work is not a stand-alone practice but a part of the o
Externí odkaz:
https://doaj.org/article/be8714c03eab43aabb3b477cf3930477
Publikováno v:
ISPRS Annals of the Photogrammetry, Remote Sensing and Spatial Information Sciences, Vol II-5/W3, Pp 235-241 (2015)
This contribution summarizes the collaboration between Carleton Immersive Media Studio (CIMS) and Heritage Standing in the use of digital technologies to document the Beinn Bhreagh Hall historic site (house and immediate surroundings) in Baddeck, Nov
Externí odkaz:
https://doaj.org/article/1d9ccadda3f943b288aaf36d223efe80
Publikováno v:
Annals of the Child Neurology Society, Vol 2, Iss 3, Pp 189-205 (2024)
Abstract Understanding clinical features and disease progression of Rett syndrome (RTT) and establishing clinical trial readiness was enhanced by the RTT Natural History Study (NHS). The NHS benefited from two key developments: one, the Orphan Drug A
Externí odkaz:
https://doaj.org/article/1619a1ca66504a88bc0626eed04de483
Autor:
Walter E. Kaufmann, Alan K. Percy, Jeffrey L. Neul, Jenny Downs, Helen Leonard, Paige Nues, Girish D. Sharma, Theresa E. Bartolotta, Gillian S. Townend, Leopold M. G. Curfs, Orietta Mariotti, Claude Buda, Heather M. O’Leary, Lindsay M. Oberman, Vanessa Vogel-Farley, Katherine V. Barnes, Christopher U. Missling
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-14 (2024)
Abstract Background Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder associated with multiple neurologic impairments. Previous studies have shown challenges to the quality of life of individuals with RTT and their caregivers. Howe
Externí odkaz:
https://doaj.org/article/9f2f215cd3a24fd58dac55f46755ce60
Autor:
Damian May, Kalé Kponee-Shovein, Jeffrey L. Neul, Alan K. Percy, Malena Mahendran, Nathaniel Downes, Grace Chen, Talissa Watson, Dominique C. Pichard, Melissa Kennedy, Patrick Lefebvre
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 16, Iss 1, Pp 1-12 (2024)
Abstract Background With the advent of the first targeted therapy for Rett Syndrome (RTT), a comprehensive assessment of the journey of RTT is needed to elucidate on present unmet needs in this population. This study characterized females with RTT in
Externí odkaz:
https://doaj.org/article/85d4f235fe314dd9b90f1126e2424377
Autor:
K. Percy, C. Hanley, M. Santana Quintero, S. Fai, C. Ouimet, C. Cancino, L. Rainer, L. Villacorta-Santamato
Publikováno v:
ISPRS Annals of the Photogrammetry, Remote Sensing and Spatial Information Sciences, Vol II-5/W1, Pp 235-240 (2013)
According to UNESCO "Earthen architecture is one of the most original and powerful expressions of our ability to create a built environment with readily available resources. It includes a great variety of structures, ranging from mosques, palaces and
Externí odkaz:
https://doaj.org/article/bbdb79d25af74882bb9a0174091a49f2
Autor:
Z. Ekim, M. Santana Quintero, K. Percy, S. Ward, S. Fai, J. Gregg, C. Ouimet, C. Cancino, M. Boussalh
Publikováno v:
The International Archives of the Photogrammetry, Remote Sensing and Spatial Information Sciences, Vol XL-5-W2, Pp 243-248 (2013)
Heritage recording serves as a basis for methodologies regarding diagnosis, treatment and preservation of historic places and contributes to make posterity records of our built cultural heritage. This work is not a stand-alone practice, but a part o
Externí odkaz:
https://doaj.org/article/10b441598bfe44a2bf81aee85b540856
Autor:
Jeffrey L. Neul, Timothy A. Benke, Eric D. Marsh, Bernhard Suter, Lori Silveira, Cary Fu, Sarika U. Peters, Alan K. Percy, for the Rett syndrome Natural History Study Group
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 15, Iss 1, Pp 1-17 (2023)
Abstract Objective Recent advances in the understanding of neurodevelopmental disorders such as Rett syndrome (RTT) have enabled the discovery of novel therapeutic approaches that require formal clinical evaluation of efficacy. Clinical trial success
Externí odkaz:
https://doaj.org/article/46dabe3f9d4f4458ad61f971214298e1
Autor:
Jeffrey L. Neul, Tim A. Benke, Eric D. Marsh, Jane B. Lane, David N. Lieberman, Steven A. Skinner, Daniel G. Glaze, Bernhard Suter, Peter T. Heydemann, Arthur A. Beisang, Shannon M. Standridge, Robin C. C. Ryther, Richard H. Haas, Lloyd J. Edwards, Amitha Ananth, Alan K. Percy
Publikováno v:
Annals of the Child Neurology Society, Vol 1, Iss 3, Pp 228-238 (2023)
Abstract Objective We aimed to determine the longitudinal distribution of hand function skills in individuals with classic Rett syndrome (RTT), an X‐linked dominant neurodevelopmental disorder, and correlate with MECP2 variants. Method We conducted
Externí odkaz:
https://doaj.org/article/a0d6b9c130ce49d09ab69e1545e711bb
Autor:
Melissa Kennedy, Larry Glass, Daniel G. Glaze, Steve Kaminsky, Alan K. Percy, Jeffrey L. Neul, Nancy E. Jones, Daniela Tropea, Joseph P. Horrigan, Paige Nues, Kathie M. Bishop, James M. Youakim
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2024)
Rett syndrome (RTT) is rare neurodevelopmental disorder caused by mutations in the MECP2 gene that encodes methyl-CpG-binding protein 2 (MeCP2), a DNA-binding protein with roles in epigenetic regulation of gene expression. Functional loss of MeCP2 re
Externí odkaz:
https://doaj.org/article/b550d1b8d2c644c1ba103860350a3bb0