Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Xin Cynthia Ye"'
Autor:
Antoine Morin Coulombe, Faisal Abdullah Alsadoun, Xin (Cynthia) Ye, Maryam Soleimani, Lucia Nappi, Bernhard J. Eigl, Kim N. Chi, Christian K. Kollmannsberger
Publikováno v:
Journal of Clinical Oncology. 41:646-646
646 Background: Currently available first-line treatment regimens for mRCC include pembrolizumab-axitinib (ICI-TKI) and ipilimumab-nivolumab (ICI-ICI). Although both regimens are superior to sunitinib, direct comparisons between ICI-ICI and ICI-TKI a
Autor:
Colin J. D. Ross, Xiaohua Han, Andrew D. Paterson, Casper Shyr, Care Rare Canada, Michelle Higginson, Victor Pegado, Cheryl Y. Gregory-Evans, Xin (Cynthia) Ye, Wyeth W. Wasserman, Nicole M. Roslin, Deborah Giaschi, Millan S. Patel, Oriol Fornes, Phillip A. Richmond, Christopher J. Lyons
Publikováno v:
Journal of Medical Genetics
Strabismus is a common condition, affecting 1-4% of individuals. Isolated strabismus has been studied in families with Mendelian inheritance patterns. Despite the identification of multiple loci via linkage analyses, no specific genes have been ident
Autor:
Jan M. Friedman, Xin Cynthia Ye, Wyeth W. Wasserman, Causes Study, Robin van der Lee, Anna Lehman
Publikováno v:
Pediatric Neurology. 100:87-91
Purpose Intellectual disability (ID) results from a heterogeneous group of disorders and affects 1% to 2% of children. ID frequently occurs in association with other clinical features such as seizures or malformations. We suspected that strabismus mi
Autor:
Xin (Cynthia) Ye, Roslin, Nicole M., Paterson, Andrew D., Lyons, Christopher J., Pegado, Victor, Richmond, Phillip, Shyr, Casper, Fornes, Oriol, XiaoHua Han, Higginson, Michelle, Ross, Colin J., Giaschi, Deborah, Gregory-Evans, Cheryl, Patel, Millan S., Wasserman, Wyeth W.
Publikováno v:
Journal of Medical Genetics; Jan2022, Vol. 59 Issue 1, p46-55, 10p
Publikováno v:
Gene. 697
Strabismus refers to the misalignment of the eyes and occurs in 2-4% of individuals. The low-resolution label "strabismus" covers a range of heterogeneous defects, which makes it challenging to unravel this condition. Consequently a coherent understa
Autor:
Michael G. Hanna, Andreas Slørdahl, Ulla Werlauff, Christian Krarup, Hilary Vallance, Michael T. Gabbett, Francesco Muntoni, Lin Hua Zhang, Emma Matthews, Mark R. Davis, Louise Hartley, Magnhild Rasmussen, Emily C. Oates, Eveline Blom, Roope Männikkö, Caroline Sewry, Lucy Feng, Xin Cynthia Ye, Nigel G. Laing, Clara D.M. van Karnebeek, Glenda Hendson, Hanne Halvorsen, Maria Sframeli, Mena Abdelsayed, Suzanne M E Lewis, Peter C. Ruben, Anna Sarkozy, Michael G. Thor, Nanna Witting, John Vissing, Rahul Phadke, Irina Zaharieva, Gianina Ravenscroft, Jennifer E. Morgan, Martin Ballegaard, Nicoline Løkken, L. D'Argenzio, Erik-Jan Kamsteeg, K. Suetterlin, Matthew Pitt
Publikováno v:
Brain, 139, 674-91
Brain, 139, Pt 3, pp. 674-91
Brain, 139(3), 674-691. Oxford University Press
Brain, 139, Pt 3, pp. 674-91
Brain, 139(3), 674-691. Oxford University Press
Contains fulltext : 167925.pdf (Publisher’s version ) (Open Access) See Cannon (doi:10.1093/brain/awv400) for a scientific commentary on this article.Congenital myopathies are a clinically and genetically heterogeneous group of muscle disorders cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f40fb4f604936d9d0dd7f3afb8358e98
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/167925
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/167925
Autor:
Puya Seid-Karbasi, Tuhina Imam, Cheryl E Lee, Xin Cynthia Ye, Bobby Gu, Balraj Sharma, Isaiah Ng, Gurinder Johal, Adam Herman, Shirley Yu Chen, Wyeth W. Wasserman
Publikováno v:
JMIR Research Protocols, Vol 2, Iss 2, p e25 (2013)
JMIR Research Protocols
JMIR Research Protocols
BackgroundThe Portal for Families Overcoming Neurodevelopmental Disorders (PFOND) provides a structured Internet interface for the sharing of information with individuals struggling with the consequences of rare developmental disorders. Large disease