Zobrazeno 1 - 10
of 130
pro vyhledávání: '"David E, Barton"'
Autor:
Nashwa M. Abdulsalam, Jeanne E. Poole, Elizabeth R. Lyden, Arthur J. Easley, Gregory S. Pavlides, Shane F. Tsai, David E. Barton
Publikováno v:
Journal of Interventional Cardiac Electrophysiology. 65:765-772
Autor:
Ganesh, Gajanan, Yiannis S, Chatzizisis, Edward, O'Leary, Andrew M, Goldsweig, Poonam, Velagapudi, Gregory, Pavlides, David E, Barton
Publikováno v:
The Journal of invasive cardiology. 34(3)
In this era of complex high-risk percutaneous coronary intervention (HR-PCI), mechanical support is being increasingly used. Traditionally, mechanical circulatory support with the Impella CP device requires a large-bore arterial access and an additio
Publikováno v:
Active Photonic Platforms XIII.
Here we present high quality factor (high-Q) metasurfaces as a new platform for continuous, electro-optical reconfigurability. Using full-field simulations, we show how applying a voltage across individual nanoantenna shifts the spectral position of
Autor:
Susan Groarke, Catherine McGorrian, John Hurley, Barbara Moran, Andrew K. Roy, Ivan P. Casserly, Gavin Blake, David E. Barton, Ronan Margey, Richard Tanner, Jacqueline Geraghty, Declan D. Sugrue, Jana Boleckova
Publikováno v:
Irish Journal of Medical Science (1971 -). 189:139-148
There is a paucity of published data on the clinical experience with trans-catheter aortic valve implantation (TAVI) in the Republic of Ireland. We sought to examine the clinical outcomes of patients with medium-term follow-up treated with TAVI at ou
Autor:
Tara Clark, Alana Ward, Terri P. McVeigh, Elizabeth Whitmore, Luke J Kelly, David E. Barton, Sally Ann Lynch, Brendan Mullaney
Publikováno v:
Eur J Hum Genet
Multi-gene testing is useful in genetically heterogeneous conditions, including inherited cardiac pathologies. Increasing the number of genes analysed increases diagnostic yield of variants of certain, likely, or uncertain pathogenicity. Concerns exi
Autor:
Robert Garvin, Daniel R. Anderson, David E. Barton, Michael J. Duryee, Geoffrey M. Thiele, Carlos Hunter
Publikováno v:
Journal of the American College of Cardiology. 79:1755
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-9 (2020)
Scientific Reports
Scientific Reports
ROBO2 gene disruption causes vesicoureteric reflux (VUR) amongst other congenital anomalies. Several VUR patient cohorts have been screened for variants in the ubiquitously expressed transcript, ROBO2b, but, apart from low levels in a few adult tissu
Autor:
Jorge M Dinis, David E Barton, Jamsheed Ghadiri, Deepa Surendar, Kavitha Reddy, Fernando Velasquez, Carol L Chaffee, Mei-Chong Wendy Lee, Helen Gavrilova, Hazel Ozuna, Samuel A Smits, Cleber C Ouverney
Publikováno v:
PLoS ONE, Vol 6, Iss 6, p e21280 (2011)
We have identified an environmental bacterium in the Candidate Division TM7 with ≥98.5% 16S rDNA gene homology to a group of TM7 bacteria associated with the human oral cavity and skin. The environmental TM7 bacterium (referred to as TM7a-like) was
Externí odkaz:
https://doaj.org/article/6247679fe4f04610b3261cffcd2977df
Autor:
Tara Clark, Gillian Edge, Olivia Walsh, David E. Barton, Marija Kostocenko, Melissa Rogers, Barry Linnane, Sally Ann Lynch, Loretta O’Grady, Rebecca Muldowney, Ingrid Borovickova, Alana Ward, Niamh Lang, Erina Sasaki
Publikováno v:
European Journal of Human Genetics
Cystic fibrosis (CF) is the most common life-limiting autosomal recessive disease in the Republic of Ireland (ROI), with a previously quoted incidence of 1 in 1353 and carrier rate of 1 in 19. The National Newborn Screening (NBS) for CF was incorpora
Autor:
Tara Clarke, Marija Kostocenko, Erina Sasaki, Melissa Rogers, Niamh Lang, Alana Ward, Sally Ann Lynch, Rebecca Muldowney, David E. Barton
Publikováno v:
Abstracts.
Background Cystic Fibrosis (CF) is the most common life threatening autosomal recessive multisystem disease in the Republic of Ireland (ROI); with a previously quoted incidence of 1 in 1353 and carrier rate of 1 in 19. Screening for CF was incorporat