نتائج البحث - Azarow, Kenneth
- يعرض 1 - 10 نتائج من 10
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1
Increased burden of de novo predicted deleterious variants in complex congenital diaphragmatic hernia حسب Yu, Lan, Sawle, Ashley D., Wynn, Julia, Aspelund, Gudrun, Stolar, Charles J., Arkovitz, Marc S., Potoka, Douglas, Azarow, Kenneth S., Mychaliska, George B., Shen, Yufeng, Chung, Wendy K.
منشور في 2015نص -
2
The association between congenital diaphragmatic hernia and undescended testes حسب Azarow, Kenneth S, Cusick, Robert, Wynn, Julia, Chung, Wendy, Mychaliska, George B, Crombleholme, Timothy M, Chung, Dai H, Lim, Foong Yen, Potolka, Douglas, Warner, Brad W, Aspelund, Gundrun, Arkovitz, Marc S
منشور في 2015نص -
3
Variants in GATA4 Are a Rare Cause of Familial and Sporadic Congenital Diaphragmatic Hernia حسب Yu, Lan, Wynn, Julia, Cheung, Yee Him, Shen, Yufeng, Mychaliska, George B., Crombleholme, Timothy M., Azarow, Kenneth S., Lim, Foong Yen, Chung, Dai H., Potoka, Douglas, Warner, Brad W., Bucher, Brian, Stolar, Charles, Aspelund, Gudrun, Arkovitz, Marc S., Chung, Wendy K.
منشور في 2012نص -
4
De novo copy number variants are associated with congenital diaphragmatic hernia حسب Yu, Lan, Wynn, Julia, Ma, Lijiang, Guha, Saurav, Mychaliska, George B., Crombleholme, Timothy M., Azarow, Kenneth S., Lim, Foong Yen, Chung, Dai H., Potoka, Douglas, Warner, Brad W., Bucher, Brian, LeDuc, Charles A., Costa, Katherine, Stolar, Charles, Aspelund, Gudrun, Arkovitz, Marc, Chung, Wendy K.
منشور في 2012نص -
5
Whole Exome Sequencing Identifies de Novo Mutations in GATA6 Associated with Congenital Diaphragmatic Hernia حسب Yu, Lan, Bennett, James T., Wynn, Julia, Carvill, Gemma L., Cheung, Yee Him, Shen, Yufeng, Mychaliska, George B., Azarow, Kenneth S., Crombleholme, Timothy M., Chung, Dai H., Potoka, Douglas, Warner, Brad W., Bucher, Brian, Lim, Foong-Yen, Pietsch, John, Stolar, Charles, Aspelund, Gudrun, Arkovitz, Marc S., Mefford, Heather, Chung, Wendy K.
منشور في 2014نص -
6
The Need for Early Kasai Portoenterostomy: A Western Pediatric Surgery Research Consortium Study حسب Kelley-Quon, Lorraine I., Shue, Eveline, Burke, Rita V., Smith, Caitlin, Kling, Karen, Mahdi, Elaa, Ourshalimian, Shadassa, Fenlon, Michael, Dellinger, Matthew, Shew, Stephen B., Lee, Justin, Padilla, Benjamin, Inge, Thomas, Roach, Jonathan, Marwan, Ahmed I., Russell, Katie W., Ignacio, Romeo, Fialkowski, Elizabeth, Nijagal, Amar, Im, Cecilia, Azarow, Kenneth S., Ostlie, Daniel J., Wang, Kasper
منشور في 2021نص -
7
Guidelines for Opioid Prescribing in Children and Adolescents After Surgery: An Expert Panel Opinion حسب Kelley-Quon, Lorraine I., Kirkpatrick, Matthew G., Ricca, Robert L., Baird, Robert, Harbaugh, Calista M., Brady, Ashley, Garrett, Paula, Wills, Hale, Argo, Jonathan, Diefenbach, Karen A., Henry, Marion C.W., Sola, Juan E., Mahdi, Elaa M., Goldin, Adam B., St Peter, Shawn D., Downard, Cynthia D., Azarow, Kenneth S., Shields, Tracy, Kim, Eugene
منشور في 2021نص -
8
Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes حسب Qiao, Lu, Wynn, Julia, Yu, Lan, Hernan, Rebecca, Zhou, Xueya, Duron, Vincent, Aspelund, Gudrun, Farkouh-Karoleski, Christiana, Zygumunt, Annette, Krishnan, Usha S., Nees, Shannon, Khlevner, Julie, Lim, Foong Yen, Crombleholme, Timothy, Cusick, Robert, Azarow, Kenneth, Danko, Melissa Ellen, Chung, Dai, Warner, Brad W., Mychaliska, George B., Potoka, Douglas, Wagner, Amy J., Soffer, Samuel, Schindel, David, McCulley, David J., Shen, Yufeng, Chung, Wendy K.
منشور في 2020نص -
9
De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders حسب Qi, Hongjian, Yu, Lan, Zhou, Xueya, Wynn, Julia, Zhao, Haoquan, Guo, Yicheng, Zhu, Na, Kitaygorodsky, Alexander, Hernan, Rebecca, Aspelund, Gudrun, Lim, Foong-Yen, Crombleholme, Timothy, Cusick, Robert, Azarow, Kenneth, Danko, Melissa E., Chung, Dai, Warner, Brad W., Mychaliska, George B., Potoka, Douglas, Wagner, Amy J., ElFiky, Mahmoud, Wilson, Jay M., Nickerson, Debbie, Bamshad, Michael, High, Frances A., Longoni, Mauro, Donahoe, Patricia K., Chung, Wendy K., Shen, Yufeng
منشور في 2018نص -
10
Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene حسب Qiao, Lu, Xu, Le, Yu, Lan, Wynn, Julia, Hernan, Rebecca, Zhou, Xueya, Farkouh-Karoleski, Christiana, Krishnan, Usha S., Khlevner, Julie, De, Aliva, Zygmunt, Annette, Crombleholme, Timothy, Lim, Foong-Yen, Needelman, Howard, Cusick, Robert A., Mychaliska, George B., Warner, Brad W., Wagner, Amy J., Danko, Melissa E., Chung, Dai, Potoka, Douglas, Kosiński, Przemyslaw, McCulley, David J., Elfiky, Mahmoud, Azarow, Kenneth, Fialkowski, Elizabeth, Schindel, David, Soffer, Samuel Z., Lyon, Jane B., Zalieckas, Jill M., Vardarajan, Badri N., Aspelund, Gudrun, Duron, Vincent P., High, Frances A., Sun, Xin, Donahoe, Patricia K., Shen, Yufeng, Chung, Wendy K.
منشور في 2021نص