Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anmei Qiu"'
Autor:
Zhijia Tan, Hiu Tung Shek, Peikai Chen, Zhongxin Dong, Yapeng Zhou, Shijie Yin, Anmei Qiu, Lina Dong, Bo Gao, Michael Kai Tsun To
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 4, Pp n/a-n/a (2023)
Abstract Background Osteogenesis imperfecta (OI) is a group of rare skeletal dysplasia. Long bone deformity and scoliosis are often associated with progressively deforming types of OI. FKBP65 (encoded by FKBP10, OMIM *607063) plays a crucial role in
Externí odkaz:
https://doaj.org/article/6d2ef864299c4f9a9221c94d5512513e
Autor:
Peikai Chen, Zhijia Tan, Anmei Qiu, Shijie Yin, Yapeng Zhou, Zhongxin Dong, Yan Qiu, Jichun Xu, Kangsen Li, Lina Dong, Hiu Tung Shek, Jingwen Liu, Eric H. K. Yeung, Bo Gao, Kenneth Man Chee Cheung, Michael Kai-Tsun To
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-16 (2022)
Abstract Background Osteogenesis imperfecta (OI) is a rare congenital disorder of the skeletal system, inflicting debilitating physical and psychological distress on patients and caregivers. Over the decades, much effort has been channeled towards un
Externí odkaz:
https://doaj.org/article/b45f7876371f4926abaf01ca67686ae0
Autor:
Peikai Chen, Zhijia Tan, Hiu Tung Shek, Jia-nan Zhang, Yapeng Zhou, Shijie Yin, Zhongxin Dong, Jichun Xu, Anmei Qiu, Lina Dong, Bo Gao, Michael Kai Tsun To
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Osteogenesis imperfecta (OI) is a rare inherited connective tissue dysplasia characterized with skeletal fragility, recurrent fractures and bone deformity, predominantly caused by mutations in the genes COL1A1 or COL1A2 that encode the chains of type
Externí odkaz:
https://doaj.org/article/9b8b669d02684560b0fb8f2daba32957
Publikováno v:
IEEE Transactions on Instrumentation and Measurement. 71:1-10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::459bbb5de721612b69970ac318f6c912
https://doi.org/10.1109/tim.2021.3135546
https://doi.org/10.1109/tim.2021.3135546
Autor:
Zhijia Tan, Hiu Tung Shek, Zhongxin Dong, Lin Feng, Yapeng Zhou, Shijie Yin, Anmei Qiu, Lina Dong, Bo Gao, Peikai Chen, Michael Kai Tsun To
Publikováno v:
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA.
Type V osteogenesis imperfecta (OI) is a form of OI characterized by radial head dislocation (RHD), calcification of interosseous membrane (CIM), and hyperplastic callus (HPC). In this study, we characterized the clinical features of 28 type V OI pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30e1bfcfa1a85902f9647660f3d60b90
https://pubmed.ncbi.nlm.nih.gov/36456709
https://pubmed.ncbi.nlm.nih.gov/36456709