Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Meghan S Candee"'
Autor:
Margaret M Cortese, Anita K Kambhampati, Jennifer E Schuster, Zaid Alhinai, Gary R Nelson, Gloria J Guzman Perez-Carrillo, Arastoo Vossough, Michael A Smit, Robert C McKinstry, Timothy Zinkus, Kevin R Moore, Jeffrey M Rogg, Meghan S Candee, James J Sejvar, Sarah E Hopkins
Publikováno v:
PLoS ONE, Vol 15, Iss 2, p e0228671 (2020)
BACKGROUND:Acute flaccid myelitis (AFM) is a severe illness similar to paralytic poliomyelitis. It is unclear how frequently AFM occurred in U.S. children after poliovirus elimination. In 2014, an AFM cluster was identified in Colorado, prompting pas
Externí odkaz:
https://doaj.org/article/2fc6cf9f034b42b7adc86a27c86541bd
Autor:
Sue L. Jaspersen, Deborah A. Bruns, Meghan S. Candee, Agatino Battaglia, John C. Carey, Kristen P. Fishler
Publikováno v:
American journal of medical genetics. Part AREFERENCES.
Changes in medical intervention over the last decade have improved outcomes for individuals with trisomy 18, the second most common human aneuploidy syndrome at birth. As children with trisomy 18 live longer, a shared concern of medical experts and p
Publikováno v:
Neurology. 96:911-914
Hundreds of distinct epilepsy-causing genes have been identified.1 The vitamin B6-dependent epilepsies are a heterogeneous group of genetic disorders due to incomplete formation, transport, or inactivation of pyridoxal 5′-phosphate (PLP).2 The ALDH
Autor:
Shannon Babineau, Rebecca Barmherzig, Frank R. Berenson, Jennifer Bickel, Heidi K. Blume, Andrea Brand, Dawn C. Buse, Meghan S. Candee, Madeline Chadehumbe, Carrie O. Dougherty, Jessica R. Gautreaux, Amy A. Gelfand, Trevor Gerson, Jack Gladstein, Kaitlin Greene, Amanda Hall, Andrew D. Hershey, Jennifer Hranilovich, Samantha Lee Irwin, Marielle Kabbouche, Dina Karvounides, Sita Kedia, Shirley Kessel, Ana Marissa Lagman-Bartolome, Maya Marzouk, Rachel Neely, Hope O’Brien, Serena L. Orr, Ann Pakalnis, Irene Patniyot, Carlyn Patterson Gentile, Nicholas Pietris, Scott Powers, Sharoon Qaiser, William Qubty, Reena Rastogi, Ana Recober, Elizabeth K. Rende, Alexandra C. Ross, Elizabeth Seng, Christina L. Szperka, Scott B. Turner, Juliana VanderPluym, M. Cristina Victorio, Maggie Waung, Kevin Weber, Marcy Yonker, William Young, Jason L. Ziplow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4da5a7f055538cbd825351e38531314
https://doi.org/10.1016/b978-0-323-83005-8.09991-2
https://doi.org/10.1016/b978-0-323-83005-8.09991-2
Autor:
Brooke Rhead, Xiaorong Shao, Jennifer S. Graves, Tanuja Chitnis, Amy T. Waldman, Timothy Lotze, Teri Schreiner, Anita Belman, Lauren Krupp, Benjamin M. Greenberg, Bianca Weinstock–Guttman, Gregory Aaen, Jan M. Tillema, Moses Rodriguez, Janace Hart, Stacy Caillier, Jayne Ness, Yolanda Harris, Jennifer Rubin, Meghan S. Candee, Mark Gorman, Leslie Benson, Soe Mar, Ilana Kahn, John Rose, T. Charles Casper, Hong Quach, Diana Quach, Catherine Schaefer, Emmanuelle Waubant, Lisa F. Barcellos, the US Network of Pediatric MS Centers
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 6, Pp 1053-1061 (2019)
Abstract Objective Onset of multiple sclerosis (MS) occurs in childhood for approximately 5% of cases (pediatric MS, or ped‐MS). Epigenetic influences are strongly implicated in MS pathogenesis in adults, including the contribution from microRNAs (
Externí odkaz:
https://doaj.org/article/7e4b193be7ec429facf7230a6a5acd9e