Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Kristin M Conway"'
Autor:
Jonathan Suhl, Kristin M Conway, Anthony Rhoads, Peter H Langlois, Marcia L Feldkamp, Adrian M Michalski, Jacob J Oleson, Alpa Sidhu, Vijaya Kancherla, John Obrycki, Maitreyi Mazumdar, Paul A Romitti, the National Birth Defects Prevention Study
Publikováno v:
Public Health Nutrition, Vol 26, Pp 620-632 (2023)
Abstract Objectives: To explore associations between maternal pre-pregnancy exposure to arsenic in diet and non-cardiac birth defects. Design: This is a population-based, case–control study using maternal responses to a dietary assessment and pu
Externí odkaz:
https://doaj.org/article/1eee39438afa4c65a84f62dad4ac4201
Autor:
Kristin M Conway, Katy Eichinger, Christina Trout, Paul A Romitti, Katherine D Mathews, Shree K Pandya
Publikováno v:
SAGE Open Medicine, Vol 7 (2019)
Purpose: To collect information about the needs of families affected by childhood-onset dystrophinopathies residing in the United States. Methods: Individuals with an eligible dystrophinopathy were identified by the Muscular Dystrophy Surveillance, T
Externí odkaz:
https://doaj.org/article/b0a981e0ed034b70b7ff3f82e9adfcb3
Autor:
Kristin, Palmsten, Jonathan, Suhl, Kristin M, Conway, Elyse O, Kharbanda, Thomas D, Scholz, Elizabeth C, Ailes, Janet D, Cragan, Eirini, Nestoridi, Eleni A, Papadopoulos, Stephen M, Kerr, Sean G, Young, Christine, Olson, Paul A, Romitti
Publikováno v:
Birth Defects Research. 115:88-95
Although results from studies of first-trimester influenza vaccination and congenital heart defects (CHDs) have been reassuring, data are limited for specific CHDs.We assessed associations between reported maternal influenza vaccination, 1 month befo
Autor:
Jonathan, Suhl, Kristin M, Conway, Anthony, Rhoads, Peter H, Langlois, Marcia L, Feldkamp, Adrian M, Michalski, Jacob, Oleson, Alpa, Sidhu, Thomas D, Scholz, Vijaya, Kancherla, John, Obrycki, Maitreyi, Mazumdar, Paul A, Romitti
Publikováno v:
Birth Defects Research. 115:79-87
Arsenic crosses the placenta and accumulates in fetal tissues. In the United States, diet is the predominant route of arsenic exposure, but epidemiologic data are sparse regarding this exposure and development of birth defects. Using data from a larg
Autor:
Paula L. Hedley, Ulrik Lausten-Thomsen, Kristin M. Conway, Klaus Hindsø, Paul A. Romitti, Michael Christiansen
Background and purposeCongenital clubfoot is a common musculoskeletal anomaly, with a suspected multifactorial etiopathogenesis. To begin examining its etiopathogenesis in a nationwide Danish population, liveborn infants with clubfoot were ascertaine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89070c7c1bba6b828e90c26ba7cf2554
https://doi.org/10.1101/2023.05.11.23289837
https://doi.org/10.1101/2023.05.11.23289837
Autor:
Pangaja Paramsothy, Yinding Wang, Bo Cai, Kristin M. Conway, Nicholas E. Johnson, Shree Pandya, Emma Ciafaloni, Katherine D. Mathews, Paul A. Romitti, James F. Howard, Catharine Riley
Publikováno v:
Neuromuscul Disord
Population-based estimates of survival among individuals with Duchenne muscular dystrophy (DMD) living in the United States are lacking. It is also unclear whether the association between glucocorticoid use and all-cause mortality persists in the con
Autor:
Kristin, Palmsten, Jonathan, Suhl, Kristin M, Conway, Elyse O, Kharbanda, Elizabeth C, Ailes, Janet D, Cragan, Eirini, Nestoridi, Eleni A, Papadopoulos, Stephen M, Kerr, Sean G, Young, Frank, DeStefano, Paul A, Romitti
Publikováno v:
Pharmacoepidemiology and Drug Safety. 31:851-862
To assess associations between influenza vaccination during etiologically-relevant windows and selected major structural non-cardiac birth defects.We analyzed data from the National Birth Defects Prevention Study, a multisite, population-based case-c
Autor:
Shiny, Thomas, Kristin M, Conway, Olushola, Fapo, Natalie, Street, Katherine D, Mathews, Joshua R, Mann, Paul A, Romitti, Aida, Soim, Christina, Westfield, Deborah J, Fox, Emma, Ciafaloni
Publikováno v:
Muscle & Nerve. 66:193-197
With current and anticipated disease-modifying treatments, including gene therapy, an early diagnosis for Duchenne muscular dystrophy (DMD) is crucial to assure maximum benefit. In 2009, a study from the Muscular Dystrophy Surveillance, Tracking, and
Autor:
Georgia, Pitsava, Marcia L, Feldkamp, Nathan, Pankratz, John, Lane, Denise M, Kay, Kristin M, Conway, Charlotte, Hobbs, Gary M, Shaw, Jennita, Reefhuis, Mary M, Jenkins, Lynn M, Almli, Cynthia, Moore, Martha, Werler, Marilyn L, Browne, Chris, Cunniff, Andrew F, Olshan, Faith, Pangilinan, Lawrence C, Brody, Robert J, Sicko, Richard H, Finnell, Michael J, Bamshad, Daniel, McGoldrick, Deborah A, Nickerson, James C, Mullikin, Paul A, Romitti, James L, Mills
Publikováno v:
Birth Defects Res
BACKGROUND: Sacral agenesis (SA) consists of partial or complete absence of the caudal end of the spine and often presents with additional birth defects. Several studies have examined gene variants for syndromic forms of SA, but only one has examined