Zobrazeno 1 - 10
of 828
pro vyhledávání: '"Hemophilic arthropathy"'
Autor:
Dong Wang, Wenzhe Chen, Jiali Chen, Du He, Yanli Pan, Pinger Wang, Qinghe Zeng, Mancang Gu, Peijian Tong, Di Chen, Hongting Jin
Publikováno v:
Bioactive Materials, Vol 40, Iss , Pp 47-63 (2024)
In individuals afflicted with hemophilia, characterized by a deficiency of coagulation factor VIII (FVIII), the occurrence of spontaneous recurrent intra-articular hemorrhage precipitates the emergence of hemophilic arthropathy (HA). Although clottin
Externí odkaz:
https://doaj.org/article/0044da476f984a10934c93726ec4836b
Publikováno v:
BMC Musculoskeletal Disorders, Vol 25, Iss 1, Pp 1-6 (2024)
Abstract Crohn’s disease (CD) is an inflammatory bowel disease affecting the digestive tract, the incidence of which is on the rise worldwide. The most common clinical manifestation of hemophilia is arthropathy secondary to recurrent joint effusion
Externí odkaz:
https://doaj.org/article/66e8b0d9fa4149caa29cfbfa62afb187
Publikováno v:
Quality in Sport, Vol 21 (2024)
Hemophilia is a genetically determined bleeding disorder characterized by a tendency for spontaneous bleeding, mainly into the joints, which can lead to arthropathy and significantly reduce the quality of a patient's life. The objective of this paper
Externí odkaz:
https://doaj.org/article/1b75fe011ab941628d39e2a484458c78
Autor:
Oana Viola Badulescu, Dragos-Viorel Scripcariu, Minerva Codruta Badescu, Manuela Ciocoiu, Maria Cristina Vladeanu, Carmen Elena Plesoianu, Andrei Bojan, Dan Iliescu-Halitchi, Razvan Tudor, Bogdan Huzum, Otilia Elena Frasinariu, Iris Bararu-Bojan
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 18, p 9897 (2024)
Hemophilia, which is a rare disease, results from congenital deficiencies of coagulation factors VIII and IX, respectively, leading to spontaneous bleeding into joints, resulting in hemophilic arthropathy (HA). HA involves complex processes, includin
Externí odkaz:
https://doaj.org/article/240275f79b564418ad02c716ab358533
Autor:
Jiali Chen, Qinghe Zeng, Xu Wang, Rui Xu, Weidong Wang, Yuliang Huang, Qi Sun, Wenhua Yuan, Pinger Wang, Di Chen, Peijian Tong, Hongting Jin
Publikováno v:
eLife, Vol 13 (2024)
Recurrent joint bleeding in hemophilia patients frequently causes hemophilic arthropathy (HA). Drastic degradation of cartilage is a major characteristic of HA, but its pathological mechanisms has not yet been clarified. In HA cartilages, we found se
Externí odkaz:
https://doaj.org/article/a5510fb5ce96417ebb45f1787762b026
Publikováno v:
EFORT Open Reviews, Vol 8, Iss 11, Pp 830-840 (2023)
Advanced hemophilic knee arthropathy is a frequent and devastating manifestation of severe hemophilia with significant implications for activities of daily living. Hemophilic arthropathy is caused by repeated bleeding, resulting in joint degeneration
Externí odkaz:
https://doaj.org/article/047de9352e864b4f9a8e9bbf4999334d
Publikováno v:
BMC Musculoskeletal Disorders, Vol 24, Iss 1, Pp 1-7 (2023)
Abstract This report introduces a young adult who has been in bed for more than ten years with end-stage hemophilic arthropathy. He didn’t have access to factor VIII (FVIII) in the early stage of hemophilia due to the high costs of clotting replace
Externí odkaz:
https://doaj.org/article/80bf955219dd4837ba23574712eef5b0
Autor:
Hui‐ming Peng, Chao Jiang, Zhi‐bo Zheng, Xin Chen, Bin Feng, Ji‐liang Zhai, Yan‐yan Bian, Xi‐sheng Weng
Publikováno v:
Orthopaedic Surgery, Vol 15, Iss 6, Pp 1670-1676 (2023)
Objective Although total joint replacement (TJR) procedures are efficacious, perioperative high‐dose factors replacement therapy (FRT) to avoid catastrophic bleeding represents a significant hurdle, particularly for patients with multiple joint aff
Externí odkaz:
https://doaj.org/article/30a0a187c55241b18460af377874fba4
Publikováno v:
Patient Preference and Adherence, Vol Volume 17, Pp 249-257 (2023)
Yan-Qiu Liu,1 Yu-Lin Guo,2 Jia Xu,3 Wen-Jing Geng,1 Zhen-Zhen Li,4 Ming Jia,1 Yu-Dan Liu,1 Hua Zhao1 1College of Nursing, Shanxi University of Chinese Medicine, Jinzhong, Shanxi, People’s Republic of China; 2Department of Rehabilitation, The Second
Externí odkaz:
https://doaj.org/article/f786fad8a30a4a7f94d5f19d5479a470
Publikováno v:
Hematology, Vol 27, Iss 1, Pp 1263-1271 (2022)
ABSTRACTPurpose To explore the value of magnetic resonance imaging (MRI) T2 mapping combined with susceptibility-weighted imaging (SWI) in detecting early cartilage damage and joint bleeding in the hemophilic arthropathy (HA).Methods 147 patients and
Externí odkaz:
https://doaj.org/article/7174a0389c734e6cb5fbd6a7d889e9e6