Zobrazeno 1 - 10
of 242
pro vyhledávání: '"Fibrodysplasia Ossificans Progressiva (FOP)"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-8 (2023)
Abstract Background Fibrodysplasia ossificans progressiva (FOP) is an ultrarare and disabling genetic disorder of connective tissue characterized by congenital malformation of the great toes, and progressive heterotopic ossification (HO) in soft conn
Externí odkaz:
https://doaj.org/article/1acb140aaffb4553b1b214552f42f364
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-5 (2023)
Abstract Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder associated with increased immune activity and severe, progressive heterotopic ossification. We previously described a cohort of 32 patients with FOP who were either expos
Externí odkaz:
https://doaj.org/article/70cb151f9262437bb90b40fd54b216f2
Publikováno v:
Biomolecules, Vol 14, Iss 3, p 357 (2024)
Background: Inflammation is a major driver of heterotopic ossification (HO), a condition of abnormal bone growth in a site that is not normally mineralized. Purpose of review: This review will examine recent findings on the roles of inflammation and
Externí odkaz:
https://doaj.org/article/e9936f25492d40fcb510e32b61ccdea2
Autor:
Samuel Kou, Sammi Kile, Sai Samhith Kambampati, Evelyn C. Brady, Hayley Wallace, Carlos M. De Sousa, Kin Cheung, Lauren Dickey, Kelly L. Wentworth, Edward C. Hsiao
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background COVID-19, caused by the SARS-CoV-2 virus, is a severe inflammatory condition. Patients with pre-existing conditions including diabetes, hypertension, and cardiovascular disease are at particularly high risk of complications. Fibro
Externí odkaz:
https://doaj.org/article/780dd5b0e3a042889da91f962e023db8
Autor:
上田, 聡司
甲第25499号
医博第5099号
新制||医||1074(附属図書館)
学位規則第4条第1項該当
Doctor of Medical Science
Kyoto University
DFAM
医博第5099号
新制||医||1074(附属図書館)
学位規則第4条第1項該当
Doctor of Medical Science
Kyoto University
DFAM
Externí odkaz:
http://hdl.handle.net/2433/289767
Autor:
Sukhmani Singh, Joseph Kidane, Kelly L. Wentworth, Daria Motamedi, Saam Morshed, Andrew E. Schober, Edward C. Hsiao
Publikováno v:
BMC Musculoskeletal Disorders, Vol 21, Iss 1, Pp 1-8 (2020)
Abstract Background Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare disorder marked by painful, recurrent flare-ups and heterotopic ossification (HO) in soft and connective tissues, which can be idiopathic or provoked by trauma, illness,
Externí odkaz:
https://doaj.org/article/c9d1587c02c74db0b0bb963873eb52f9
Publikováno v:
BMC Musculoskeletal Disorders, Vol 21, Iss 1, Pp 1-8 (2020)
Abstract Background Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare genetic disorder characterized by extraskeletal heterotopic ossification. It is well recognized that FOP can lead to a devastating condition of disability. However, the
Externí odkaz:
https://doaj.org/article/14200dce54e84f7d9d5028aca2e5d915
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/b770f0607bb64987a2cb29c0f3da1b47
Akademický článek
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Autor:
Esmée Botman, Sanne Treurniet, Wouter D. Lubbers, Lothar A. Schwarte, Patrick R. Schober, Louise Sabelis, Edgar J. G. Peters, Annelies van Schie, Ralph de Vries, Zvi Grunwald, Bernard J. Smilde, Jakko A. Nieuwenhuijzen, Marieke Visser, Dimitra Micha, Nathalie Bravenboer, J. Coen Netelenbos, Bernd P. Teunissen, Pim de Graaf, Pieter G. H. M. Raijmakers, Jan Maerten Smit, Elisabeth M. W. Eekhoff
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Fibrodysplasia ossificans progressiva (FOP) is a rare disease in which heterotopic ossification (HO) is formed in muscles, tendons and ligaments. Traumatic events, including surgery, are discouraged as this is known to trigger a flare-up with risk of
Externí odkaz:
https://doaj.org/article/da797b867abd4b51b7ae957eae96ae20