Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Ju-Yu Tang"'
Publikováno v:
Journal of Orthopaedic Surgery and Research, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Background The reconstruction of complex wounds of the hand still has challenges in achieving aesthetic, functional and sensory recovery. We presented our experience of using the polyfoliate and chimeric radial collateral artery perforator f
Externí odkaz:
https://doaj.org/article/26d95c683316426cb09c98cc02c1d818
Autor:
Ling-li Peng, Lai-yu Xu, Shi-hui Wang, Wei-hong Huang, Qing-qing Liu, Nv-tong Huang, Pan-feng Wu, Ju-yu Tang
Publikováno v:
JPRAS Open, Vol 37, Iss , Pp 109-120 (2023)
ABSTRACT: Background: In microsurgical tissue transfer, skin flap transplantation is frequently used to heal the surface of a wound. Effective microcirculation surveillance of the skin flap is crucial. However, with traditional monitoring methods—t
Externí odkaz:
https://doaj.org/article/06c5a78f661943a491e4db523f2bf77b
Publikováno v:
Journal of Orthopaedic Surgery and Research, Vol 18, Iss 1, Pp 1-9 (2023)
Abstract Background Traumatic tibial defect complicated with soft tissue defect is a difficult problem in clinic. Vascularized iliac crest bone flap (VIBF) and Ilizarov bone transport are effective methods to treat tibial defects with limited defect
Externí odkaz:
https://doaj.org/article/9cde5cd42f744d4dbffe94e524bb1777
Publikováno v:
Frontiers in Surgery, Vol 10 (2023)
BackgroundLegg–Calvé–Perthes disease (LCPD) is a juvenile form of ischemic femoral head osteonecrosis affecting children. The lack of effective and timely treatment results in severe sequelae in children (especially older ones). Although LCPD ha
Externí odkaz:
https://doaj.org/article/b240deaf8fdc462a9b5eb052c28ece8a
Publikováno v:
Cell Death and Disease, Vol 12, Iss 4, Pp 1-14 (2021)
Abstract Osteoporosis is the most prevailing primary bone disease and a growing health care burden. The aim of this study was to clarify the functional roles and mechanisms of the circ-ITCH regulating osteogenic differentiation of osteoporosis. Circ-
Externí odkaz:
https://doaj.org/article/050486f2ceba459e9edd26ada5e0fee6
Publikováno v:
BMC Surgery, Vol 20, Iss 1, Pp 1-11 (2020)
Abstract The success of free vascularized fibular bone graft (FVFBG) has accelerated the osteo reconstruction which results from trauma, resection of a tumor or an infectious bone segment, or correction of congenital deformity. But the complication b
Externí odkaz:
https://doaj.org/article/d9ba7dd06d614365bf8b86ad3c260129
Autor:
Jie-Yuan Jin, Pan-Feng Wu, Fang-Mei Luo, Bing-Bing Guo, Lei Zeng, Liang-Liang Fan, Ju-Yu Tang, Rong Xiang
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2022)
Background: Preaxial polydactyly (PPD) is one of the most common developmental malformations, with a prevalence of 0.8–1.4% in Asians. PPD is divided into four types, PPD I–IV, and PPD I is the most frequent type. Only six loci (GLI1, GLI3, STKLD
Externí odkaz:
https://doaj.org/article/5bd1882e508d4f69be9747ee1b22d095
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Waardenburg syndrome (WS) is a group of autosomal-dominant hereditary conditions with a global incidence of 1/42,000. WS can be categorized into at least four types: WS1–4, and these are characterized by heterochromia iridis, white forelock, promin
Externí odkaz:
https://doaj.org/article/b60310122d81427ebdd381655d3562f1
Autor:
Jie-Yuan Jin, Pan-Feng Wu, Ji-Qiang He, Liang-Liang Fan, Zhuang-Zhuang Yuan, Xiao-Yang Pang, Ju-Yu Tang, Li-Yang Zhang
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Background: Hereditary sensory and autonomic neuropathies (HSANs) are a rare and severe group of sensory axonal neuropathies. HSANs have been classified into eight groups based on mode of inheritance, clinical features, and the involved genes. HSAN-V
Externí odkaz:
https://doaj.org/article/c92236053e754c8aa267b372a61884e2
Autor:
Shuai Guo, Xue-Feng Fan, Jie-Yuan Jin, Liang-Liang Fan, Lei Zeng, Zheng-Bing Zhou, Rong Xiang, Ju-Yu Tang
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-6 (2018)
Abstract Background Chiari malformation type II (CM-II) is mainly characterized by elongation and descent of the cerebellum through the foramen magnum into the spinal canal. Moreover, CM-II is uniquely associated with myelomeningocele. Sprengel’s d
Externí odkaz:
https://doaj.org/article/26c21bbdbdb5424eb7a0c9638e9dbd95