Zobrazeno 1 - 10
of 490
pro vyhledávání: '"R Rodney"'
Autor:
Vaibhav Pralhad Lende, Vivekananda, C P S Sravan, P Jain, D Davra, H Chaudhari, R Rodney, V Motukuru, K Sumanth Raj, K R Suresh
Publikováno v:
Indian Journal of Vascular and Endovascular Surgery, Vol 5, Iss 3, Pp 187-190 (2018)
Superior mesenteric artery aneurysm (SMAA) is a rare clinical entity which can present with a wide spectrum of symptoms. It is associated with a high risk of rupture, morbidity, and mortality. Variable clinical manifestations often lead to misdiagnos
Externí odkaz:
https://doaj.org/article/970dceca1b2b4c3fa08b343e4e50780b
Autor:
Alana R. Rodney, Zachary L. Skidmore, Jennifer K. Grenier, Obi L. Griffith, Andrew D. Miller, Shirley Chu, Faraz Ahmed, Jeffrey N. Bryan, Santiago Peralta, Wesley C. Warren
Publikováno v:
Frontiers in Veterinary Science, Vol 10 (2023)
Feline oral squamous cell carcinoma (FOSCC) is a cancer of the squamous cell lining in the oral cavity and represents up to 80% of all oral cancers in cats, with a poor prognosis. We have used whole exome sequencing (WES) and RNA sequencing of the tu
Externí odkaz:
https://doaj.org/article/ebfd0b050cca416e8f39ac5ad5dc3f0a
Autor:
Alana R. Rodney, Reuben M. Buckley, Robert S. Fulton, Catrina Fronick, Todd Richmond, Christopher R. Helps, Peter Pantke, Dianne J. Trent, Karen M. Vernau, John S. Munday, Andrew C. Lewin, Rondo Middleton, Leslie A. Lyons, Wesley C. Warren
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Over 94 million domestic cats are susceptible to cancers and other common and rare diseases. Whole exome sequencing (WES) is a proven strategy to study these disease-causing variants. Presented is a 35.7 Mb exome capture design based on the
Externí odkaz:
https://doaj.org/article/e18ff08359a64385b50b033630e617e2
Autor:
Goldenberg, Aaron J., Lloyd-Puryear, Michele, Brosco, Jeffrey P., Therrell, Bradford, Bush, Lynn, Berry, Susan, Brower, Amy, Bonhomme, Natasha, Bowdish, Bruce, Chrysler, Denise, Clarke, Angus, Crawford, Thomas, Goldman, Edward, Hiner, Sally, Howell, R. Rodney, Orren, David, Wilfond, Benjamin S., Watson, Michael
Publikováno v:
In Genetics in Medicine March 2019 21(3):525-533
Publikováno v:
International Journal of Neonatal Screening, Vol 8, Iss 3, p 41 (2022)
Progress in newborn screening (NBS) has been driven for 60 years by developments in science and technology, growing consumer advocacy, the actions of providers involved in the care of rare disease patients, and by federal and State government funding
Externí odkaz:
https://doaj.org/article/effae7a4000a43fc8f581638bb840b54
Autor:
Jerry Vockley, Annemieke Aartsma‐Rus, Jennifer L. Cohen, Lex M. Cowsert, R. Rodney Howell, Timothy W. Yu, Melissa P. Wasserstein, Thomas Defay
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 193:19-29
Rare genetic disorders affect as many as 3%-5% of all babies born. Approximately 10,000 such disorders have been identified or hypothesized to exist. Treatment is supportive except in a limited number of instances where specific therapies exist. Deve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2821798ccdb5f2a76dc62c5bbda828a
https://doi.org/10.1002/ajmg.c.32017
https://doi.org/10.1002/ajmg.c.32017
Autor:
R. Rodney Howell
Publikováno v:
International Journal of Neonatal Screening, Vol 7, Iss 1, p 3 (2021)
It would be difficult to overestimate the importance of persistent, thoughtful parents and their importance in the development of treatments for their children’s rare disorders. Almost a century ago in Norway, observant parents led a brilliant youn
Externí odkaz:
https://doaj.org/article/500acd9136aa41a6a2c034d6f9ccd093
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Akademický článek
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