Zobrazeno 1 - 10
of 152
pro vyhledávání: '"L Wentworth"'
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:
Samuel Kou, Carmen De Cunto, Geneviève Baujat, Kelly L. Wentworth, Donna R. Grogan, Matthew A. Brown, Maja Di Rocco, Richard Keen, Mona Al Mukaddam, Kim-Hanh le Quan Sang, Umesh Masharani, Frederick S. Kaplan, Robert J. Pignolo, Edward C. Hsiao
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Abstract Background Genetic contributors to cardiac arrhythmias are often found in cardiovascular conduction pathways and ion channel proteins. Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare disease of massive heterotopic ossification c
Externí odkaz:
https://doaj.org/article/ecf5cd5133884fc7ab8361ac88baf204
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:
Frontiers in Endocrinology, Vol 10 (2020)
The Gs G-protein coupled receptor pathway is a critical regulator of normal bone formation and function. The Gs pathway increases intracellular cAMP levels by ultimately acting on adenylate cyclase. McCune-Albright Syndrome (MAS) and fibrous dysplasi
Externí odkaz:
https://doaj.org/article/34ffbb22da4f4b8092c80d754b5f0bcb
Autor:
Kelly L. Wentworth, Robert L. Lalonde, Jay C. Groppe, Niambi Brewer, Tania Moody, Steven Hansberry, Kimberly E. Taylor, Eileen M. Shore, Frederick S. Kaplan, Robert J. Pignolo, Pamela C. Yelick, Edward C. Hsiao
Publikováno v:
Journal of Bone and Mineral Research. 37:2058-2076
Autor:
E Alcorn, L Wentworth
Publikováno v:
Age and Ageing. 50:i1-i6
Introduction With our ageing population there is increasing number of patients who experience a decline in their mobility either because of their underlying diagnosis or as a consequence of their hospital stay. There are only a limited number of inpa
Autor:
Sukhmani Singh, Saam Morshed, Daria Motamedi, Joseph Kidane, Alexandra Paul, Edward C Hsiao, Kelly L Wentworth
Publikováno v:
The Journal of clinical endocrinology and metabolism. 107(9)
PurposeHeterotopic ossification (HO) is a process by which bone forms abnormally in soft tissues. Known risk factors for developing HO include male sex, spinal cord injury, trauma, and surgery. We investigated additional risk factors in the developme
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
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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
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Publikováno v:
Br J Clin Pharmacol
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease in which heterotopic bone forms in muscle and soft tissue, leading to joint dysfunction and significant disability. FOP is progressive and many patients are wheelchair-bound by the