Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sammi Kile"'
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:
Mona Al Mukaddam, Frederick S. Kaplan, Robert J. Pignolo, Michelle Davis, Sammi Kile, Kin Cheung
Publikováno v:
Journal of Rare Diseases Research & Treatment. 6:6-12
Background:Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare disease characterized by malformed great toes and progressive heterotopic ossification (HO) in soft tissues. Current standard-of-care is aimed at palliation of symptoms; there ar
Autor:
Samuel Kou, Kelly L. Wentworth, Edward C. Hsiao, Carlos M De Sousa, Lauren Dickey, Kin Cheung, Hayley Wallace, Sammi Kile, Sai Samhith Kambampati, Evelyn C Brady
Publikováno v:
Research Square
article-version (status) pre
article-version (number) 1
article-version (status) pre
article-version (number) 1
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. Fibrodysplasia
Autor:
Zvi Grunwald, Mona Al Mukaddam, Geneviève Baujat, Sammi Kile, Edward C. Hsiao, Nobuhiko Haga, Adam Sherman, Kin Cheung, Mary Anne Fitzpatrick, Richard Keen, Christiaan Scott, Benjamin Levi, Maja Di Rocco, Robert J. Pignolo, Rolf Morhart, Carmen De Cunto, Keqin Zhang, Elisabeth M.W. Eekhoff, Patricia Delai, F.S. Kaplan
Publikováno v:
Bone, 134:115274. Elsevier Inc.
Pignolo, R J, Cheung, K, Kile, S, Fitzpatrick, M A, De Cunto, C, Al Mukaddam, M, Hsiao, E C, Baujat, G, Delai, P, Eekhoff, E M W, Di Rocco, M, Grunwald, Z, Haga, N, Keen, R, Levi, B, Morhart, R, Scott, C, Sherman, A, Zhang, K & Kaplan, F S 2020, ' Self-reported baseline phenotypes from the International Fibrodysplasia Ossificans Progressiva (FOP) Association Global Registry ', Bone, vol. 134, 115274 . https://doi.org/10.1016/j.bone.2020.115274
Pignolo, R J, Cheung, K, Kile, S, Fitzpatrick, M A, De Cunto, C, Al Mukaddam, M, Hsiao, E C, Baujat, G, Delai, P, Eekhoff, E M W, Di Rocco, M, Grunwald, Z, Haga, N, Keen, R, Levi, B, Morhart, R, Scott, C, Sherman, A, Zhang, K & Kaplan, F S 2020, ' Self-reported baseline phenotypes from the International Fibrodysplasia Ossificans Progressiva (FOP) Association Global Registry ', Bone, vol. 134, 115274 . https://doi.org/10.1016/j.bone.2020.115274
A global, patient-reported registry has been established to characterize the course of disease and track clinical outcomes in patients with fibrodysplasia ossificans progressiva (FOP), an ultra-rare genetic condition of progressive heterotopic ossifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::674f745e782f24f8846b830f283e7dbe
https://research.vumc.nl/en/publications/94538d33-52dc-487a-a047-ebc7e90151e9
https://research.vumc.nl/en/publications/94538d33-52dc-487a-a047-ebc7e90151e9