Zobrazeno 1 - 10
of 193
pro vyhledávání: '"Carolyn Sue"'
Autor:
Michal Lubomski, Carolyn Sue, Ryan Davis, Eloise Watson, Christina Liang, Kate Ahmad, Fabienne Edema-Hildebrand, Laura I Rudaks
Publikováno v:
BMJ Neurology Open, Vol 3, Iss Suppl 1 (2021)
Externí odkaz:
https://doaj.org/article/fab1953d30754b2b8b1d4f7bafca63a5
Autor:
Carolyn Sue, Martin B Delatycki, Kim Dalziel, Anneke C Grobler, Phillipa J Lamont, Sarah C Milne, Louise A Corben, Melissa Roberts, David Szmulewicz, J Burns, Shannon Williams, Jillian Chua, Christina Liang, Alison C Grootendorst, Libby Massey, Desiree LaGrappe, Liz Willis, Aleka Freijah, Paul Gerken
Publikováno v:
BMJ Open, Vol 10, Iss 12 (2020)
Introduction Emerging evidence indicates that rehabilitation can improve ataxia, mobility and independence in everyday activities in individuals with hereditary cerebellar ataxia. However, with the rarity of the genetic ataxias and known recruitment
Externí odkaz:
https://doaj.org/article/6d36daf8604945028a0b9e26f0015e26
Publikováno v:
Orphanet Journal of Rare Diseases. 18
Background and objectives Mitochondrial diseases present as multi-system disorders requiring a comprehensive multidisciplinary approach. The data on healthcare resource utilization associated with mitochondrial diseases and the clinical drivers of th
Publikováno v:
The Nurse Practitioner. 47:40-47
The prevalence of hypertension in Black women (57.6%) is among the highest in the world. Many of those who identify as Black do not readily adhere to prescribed antihypertensive medications nor persist with long-term therapy. This qualitative study d
Autor:
Dorien Imberechts, Inge Kinnart, Fieke Wauters, Joanne Terbeek, Liselot Manders, Keimpe Wierda, Kristel Eggermont, Rodrigo Furtado Madeiro, Carolyn Sue, Catherine Verfaillie, Wim Vandenberghe
Loss-of-function mutations in the PRKN, PINK1 and PARK7 genes (encoding parkin, PINK1 and DJ-1, respectively) cause autosomal recessive forms of Parkinson's disease. PINK1 and parkin jointly mediate selective autophagy of damaged mitochondria (mitoph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba46f47cfe94b10086f13b030807ce97
https://lirias.kuleuven.be/handle/20.500.12942/703539
https://lirias.kuleuven.be/handle/20.500.12942/703539
Akademický článek
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Autor:
Jeffrey B. Ratliff, Sara M. Schaefer, Shilpa Chitnis, Jeffrey W. Cooney, Christopher W. Hess, Njideka Okubadejo, Ali Shalash, Elena Moro, Carolyn Sue, Sanjay Pandey, Pramod K. Pal, Laurice Yang
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 37(8)
Autor:
David T. Miller, Kristy Lee, Noura S. Abul-Husn, Laura M. Amendola, Kyle Brothers, Wendy K. Chung, Michael H. Gollob, Adam S. Gordon, Steven M. Harrison, Ray E. Hershberger, Teri E. Klein, Carolyn Sue Richards, Douglas R. Stewart, Christa Lese Martin
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 24(7)
Autor:
Cox, Carolyn Sue
Publikováno v:
free to MU campus, to others for purchase.
Thesis (Ph. D.)--University of Missouri-Columbia, 2000.
Typescript. Vita. Includes bibliographical references (leaves [74]-79). Also available on the Internet.
Typescript. Vita. Includes bibliographical references (leaves [74]-79). Also available on the Internet.
Externí odkaz:
http://wwwlib.umi.com/cr/mo/fullcit?p9974617
Autor:
Barbara A. Koenig, Katie Bergstrom, Ellen Wright Clayton, Yaping Yang, Carolyn Sue Richards, Levi A. Garraway, Sawona Biswas, Kevin M. Bowling, Kathryn M. Porter, Susan M. Hiatt, Tia L. Kauffman, Natasha T. Strande, Holly K. Tabor, Susan M. Wolf, Laura M. Amendola, Katrina A.B. Goddard, Gregory M. Cooper, Gail P. Jarvik, Jonathan S. Berg, Laura K. Conlin, Matthew C. Dulik, Robert C. Green, Danielle R. Azzariti, Wendy K. Chung, Leslie G. Biesecker, Seema M. Jamal, Benjamin S. Wilfond, Arezou A. Ghazani, Heidi L. Rehm, Katie L. Lewis
Publikováno v:
Molecular Genetics & Genomic Medicine
Background Clinical genome and exome sequencing (CGES) is primarily used to address specific clinical concerns by detecting risk of future disease, clarifying diagnosis, or directing treatment. Additionally, CGES makes possible the disclosure of auto