Resultats de la cerca - Azarow, Kenneth

Increased burden of de novo predicted deleterious variants in complex congenital diaphragmatic hernia per 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.

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The association between congenital diaphragmatic hernia and undescended testes per 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

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Variants in GATA4 Are a Rare Cause of Familial and Sporadic Congenital Diaphragmatic Hernia per 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.

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De novo copy number variants are associated with congenital diaphragmatic hernia per 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.

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Whole Exome Sequencing Identifies de Novo Mutations in GATA6 Associated with Congenital Diaphragmatic Hernia per 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.

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The Need for Early Kasai Portoenterostomy: A Western Pediatric Surgery Research Consortium Study per 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

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Guidelines for Opioid Prescribing in Children and Adolescents After Surgery: An Expert Panel Opinion per 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

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Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes per 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.

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De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders per 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

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Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene per 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.

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