Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Chronic arthropathy"'
Publikováno v:
IDCases, Vol 23, Iss , Pp e01030- (2021)
A 68-year-old woman with a medical history significant for psoriatic arthritis was found to have an enlarged, painful lump on her left hip 15 months after intramedullary rod placement for a left subtrochanteric femur fracture sustained in a fall. His
Externí odkaz:
https://doaj.org/article/11bc178cdfdb4eedb70c13fe272fea13
Akademický článek
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Autor:
Erik Berntorp, Wolfgang Miesbach
Publikováno v:
Thrombosis Research. 199:67-74
Introduction There is limited awareness of von Willebrand disease (VWD), leading to challenges in both diagnosis and defining the optimal treatment approach for these patients. Patients with VWD are typically treated on-demand, with short-term prophy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67b6f3499247968ad88644ee77ef77b8
https://doi.org/10.1016/j.thromres.2020.12.030
https://doi.org/10.1016/j.thromres.2020.12.030
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 134, Iss 3-4, Pp 143-150 (2006)
Introduction: Patients having severe hemophilia (levels of deficient factor below 1%) frequently suffer from disabling chronic arthropathy. An adequate substitution treatment using the coagulation factor VIII or IX concentrates renders an elective su
Externí odkaz:
https://doaj.org/article/a42e5a34f1df4b9eb11a800c236c66e9
Autor:
Alin Pȋnzariu, Maria Vladeanu, Oana Viola Badulescu, Iris Bararu-Bojan, Carmen Ungureanu, Manuela Ciocoiu, Paul Dan Sirbu, Elena Cojocaru, Nina Filip
Publikováno v:
Exp Ther Med
Hemophilia is a hereditary coagulopathy caused by factor VIII (hemophilia type A) or by coagulation factor IX (hemophilia type B) dysfunction, characterized by an increased bleeding predisposition, which is either spontaneous or secondary to minimal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::921f217d45093dbe263d88d0a327ba9e
https://doi.org/10.3892/etm.2021.10427
https://doi.org/10.3892/etm.2021.10427
Publikováno v:
IDCases
IDCases, Vol 23, Iss, Pp e01030-(2021)
IDCases, Vol 23, Iss, Pp e01030-(2021)
A 68-year-old woman with a medical history significant for psoriatic arthritis was found to have an enlarged, painful lump on her left hip 15 months after intramedullary rod placement for a left subtrochanteric femur fracture sustained in a fall. His
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ce7d3fc3309ffe4344fb8337d2e4fb5
http://europepmc.org/articles/PMC7770526
http://europepmc.org/articles/PMC7770526
Publikováno v:
Cartilage
Objective Osteoarthritis (OA) is a chronic arthropathy that frequently occurs in the middle-aged and elderly population. The aim of this study was to investigate the molecular mechanism of OA based on autophagy theory. Design We downloaded the gene e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::728acb1de82c1fcedde3604371ec53ef
https://europepmc.org/articles/PMC8804715/
https://europepmc.org/articles/PMC8804715/
Publikováno v:
Cochrane Database Syst Rev
This is a protocol for a Cochrane Review (intervention). The objectives are as follows: To assess the efficacy and safety of surgery for chronic arthropathy in people with haemophilia A or B.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47f9000d457ded80035869532b6081e7
https://europepmc.org/articles/PMC7387860/
https://europepmc.org/articles/PMC7387860/
Autor:
Amy L. Dunn, Surbhi Saini
Publikováno v:
Pediatric Bleeding Disorders ISBN: 9783030316600
Hemophilia A is the most common X-linked bleeding disorder, occurring in approximately 1 in 5000 males across all races and ethnicities. A congenital deficiency or absence of coagulation factor VIII leaves these patients prone to excessive and prolon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0deafd430f3b09ecb0dfb62fc209c8be
https://doi.org/10.1007/978-3-030-31661-7_1
https://doi.org/10.1007/978-3-030-31661-7_1
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Background. Hemophilia is a rare disorder characterized by spontaneous bleeding, with pain being a critical aspect. However, a systematic assessment of hemophilia-related pain in Portugal has never been conducted. Objective. To understand the pain ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd36fb7927d09808c74c0ca284b2c85d