Zobrazeno 1 - 10
of 231
pro vyhledávání: '"A M Gow"'
Publikováno v:
Psychiatry Research. 272:756-764
Several studies suggest that anxiety disorders (AD) involve dysregulation of the autonomic nervous system (ANS) and hypothalamic-pituitary (HPA) axis. However, it is unknown if alterations in these biological systems are premorbid markers of AD risk
Publikováno v:
B101. NEW BIOLOGICAL TREATMENTS FOR ASTHMA.
Autor:
Julia Cadrin-Tourigny, Dan M. Roden, Valentina Kutyifa, Henry J. Duff, Robert M. Gow, Marco V Perez, Eric Vittinghoff, Wataru Shimizu, Birgit Stallmeyer, Linda M. Knight, Lia Crotti, Michael H. Gollob, Silvia G. Priori, Rafik Tadros, Juan Pablo Kaski, Gregory M. Marcus, S. Yukiko Asaki, Thomas M. Roston, Sharmila Udupa, Takeshi Aiba, Deni Kukavica, Peter J. Schwartz, Nikhil Chavali, M. Benjamin Shoemaker, Carla Spazzolini, Christopher S. Simpson, Fabrizio Drago, Yanushi D. Wijeyeratne, J. Martijn Bos, Sven Dittmann, John R. Giudicessi, Eric Schulze-Bahr, Peter S. Fischbach, Anwar Baban, Keiko Shimamoto, Arthur A. M. Wilde, Jonathan R. Skinner, Jason D. Roberts, Brynn E. Dechert, Peter F. Aziz, Andrew P. Landstrom, Andrea Mazzanti, Elijah R. Behr, Jacob Tfelt-Hansen, Dominic Abrams, Elizabeth S. Kaufman, Izabela Tuleta, Alison Muir, Maisoon D. Yousif, Lorne J. Gula, Michael J. Ackerman, Wojciech Zareba, Imane El Hajjaji, Christopher L. Johnsrude, Melvin M. Scheinman, Susan P. Etheridge, Peter Leong-Sit, Luciana Marcondes, Andrew D. Krahn
Publikováno v:
Circulation, 141(6), 429-439. Lippincott Williams and Wilkins
Circulation
Circulation, vol 141, iss 6
Circulation
Circulation, vol 141, iss 6
Background: Insight into type 5 long QT syndrome (LQT5) has been limited to case reports and small family series. Improved understanding of the clinical phenotype and genetic features associated with rare KCNE1 variants implicated in LQT5 was sought
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab3907edbe9d06026c9633e48586a1d3
https://pure.amc.nl/en/publications/an-international-multicenter-evaluation-of-type-5-long-qt-syndrome-a-low-penetrant-primary-arrhythmic-condition(487076db-6fe4-48b5-af1d-11c5d8806d23).html
https://pure.amc.nl/en/publications/an-international-multicenter-evaluation-of-type-5-long-qt-syndrome-a-low-penetrant-primary-arrhythmic-condition(487076db-6fe4-48b5-af1d-11c5d8806d23).html
Autor:
A M Gow, Maya Ramagopal, Pamela Ohman-Strickland, Barry Weinberger, Elizabeth Yen, Robert Laumbach, Anna M. Vetrano
Publikováno v:
Journal of Neonatal-Perinatal Medicine. 11:399-407
Background Tracheal aspirate is the conventional method to measure biomarkers of inflammation and oxidation from premature infants on mechanical ventilation at risk for bronchopulmonary dysplasia (BPD), but this method is invasive. Exhaled breath con
Autor:
Stephanie E Hesselson, Pär Matsson, James E Shima, Hisayo Fukushima, Sook Wah Yee, Yuya Kobayashi, Jason M Gow, Connie Ha, Benjamin Ma, Annie Poon, Susan J Johns, Doug Stryke, Richard A Castro, Harunobu Tahara, Ji Ha Choi, Ligong Chen, Nicolas Picard, Elin Sjödin, Maarke J E Roelofs, Thomas E Ferrin, Richard Myers, Deanna L Kroetz, Pui-Yan Kwok, Kathleen M Giacomini
Publikováno v:
PLoS ONE, Vol 4, Iss 9, p e6942 (2009)
Membrane transporters play crucial roles in the cellular uptake and efflux of an array of small molecules including nutrients, environmental toxins, and many clinically used drugs. We hypothesized that common genetic variation in the proximal promote
Externí odkaz:
https://doaj.org/article/09fb7e921026438cb6a8f93630163930
Publikováno v:
Medical Journal of Australia. 207:107-110
Autor:
Robert M. Gow, Jennifer Ham, Bhavika J Patel, Margaret Sampson, Patricia E. Longmuir, Makenzie Weekes
Publikováno v:
Cardiology in the young. 28(5)
Potentially fatal arrhythmias add to the mental health challenges of adolescence. This systematic review sought to summarise current knowledge regarding the mental health of adolescents and pre-adolescents diagnosed with inherited arrhythmia syndrome
Autor:
Gail E. Graham, David A. Dyment, Chandree L. Beaulieu, Sara L. Sawyer, Mark A. Tarnopolsky, Jane Green, Patrick Frosk, Julie Richer, Victoria Mok Siu, Constantin Polychronakos, Jacques L. Michaud, Francois P. Bernier, Mark E. Samuels, A.M. Innes, Ordan J. Lehmann, Michael T. Geraghty, Taila Hartley, Dennis E. Bulman, Jacek Majewski, Gabriella Horvath, Guy A. Rouleau, Geneviève Bernard, Sarah M. Nikkel, Farah R. Zahir, Aneal Khan, Amanda C. Smith, H M Bedford, Elise Héon, Johnny Deladoëy, Robert M. Gow, L S Penney, Kym M. Boycott, William T. Gibson, Oksana Suchowersky, Bridget A. Fernandez, Roberto Mendoza-Londono, Jeremy Schwartzentruber, Brenda Gerull, Raymond H. Kim, Robert K. Koenekoop, Bernard Brais, Grace Yoon, David Chitayat, Nada Jabado, J. Warman Chardon
Publikováno v:
Clinical Genetics
An accurate diagnosis is an integral component of patient care for children with rare genetic disease. Recent advances in sequencing, in particular whole-exome sequencing (WES), are identifying the genetic basis of disease for 25-40% of patients. The
Publikováno v:
NeoReviews. 17:e481-e483
Twelve hours after birth, an otherwise healthy newborn infant is noted to have an irregular pulse during routine examination in the well-child unit. The infant was born at term after an uncomplicated pregnancy and vaginal delivery. An electrocardiogr
Autor:
Sabina Buntich, Amber Umble-Romero, Wei-Jian Pan, L Som, Jason M. Gow, C D Krill, Yu Sun, Samantha P. Prokop, Kathleen Köck, Alexander Colbert, Yu Zhang, Wayne Tsuji, Jennifer E. Towne, T J Goletz, M W Trimble, William A. Rees, John P. Gibbs, Michelle Horner, J C O'Neill, Kathryn J. Newhall
Publikováno v:
British Journal of Pharmacology. 172:159-172
Background and Purpose AMG 139 is a human anti-IL-23 antibody currently in a phase II trial for treating Crohn's disease. To support its clinical development in humans, in vitro assays and in vivo studies were conducted in cynomolgus monkeys to deter