Результати пошуку - Khlevner, Julie

Brain–Gut Axis Clinical Implications за авторством Khlevner, Julie, Park, Yeji, Margolis, Kara Gross

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Autoimmune gastrointestinal dysmotility following SARS-CoV-2 infection successfully treated with intravenous immunoglobulin за авторством Montalvo, Mayra, Nallapaneni, Padmini, Hassan, Sara, Nurko, Samuel, Pittock, Sean J., Khlevner, Julie

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Novel candidate genes in esophageal atresia/tracheoesophageal fistula identified by exome sequencing за авторством Wang, Jiayao, Ahimaz, Priyanka R., Hashemifar, Somaye, Khlevner, Julie, Picoraro, Joseph A., Middlesworth, William, Elfiky, Mahmoud M., Que, Jianwen, Shen, Yufeng, Chung, Wendy K.

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Hypomorphic SI genetic variants are associated with childhood chronic loose stools за авторством Chumpitazi, Bruno P., Lewis, Jeffery, Cooper, Derick, D’Amato, Mauro, Lim, Joel, Gupta, Sandeep, Miranda, Adrian, Terry, Natalie, Mehta, Devendra, Scheimann, Ann, O’Gorman, Molly, Tipnis, Neelesh, Davies, Yinka, Friedlander, Joel, Smith, Heather, Punati, Jaya, Khlevner, Julie, Setty, Mala, Di Lorenzo, Carlo

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Identification and validation of candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulas за авторством Zhong, Guojie, Ahimaz, Priyanka, Edwards, Nicole A., Hagen, Jacob J., Faure, Christophe, Lu, Qiao, Kingma, Paul, Middlesworth, William, Khlevner, Julie, El Fiky, Mahmoud, Schindel, David, Fialkowski, Elizabeth, Kashyap, Adhish, Forlenza, Sophia, Kenny, Alan P., Zorn, Aaron M., Shen, Yufeng, Chung, Wendy K.

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Identification and validation of candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulas за авторством Zhong, Guojie, Ahimaz, Priyanka, Edwards, Nicole A., Hagen, Jacob J., Faure, Christophe, Lu, Qiao, Kingma, Paul, Middlesworth, William, Khlevner, Julie, El Fiky, Mahmoud, Schindel, David, Fialkowski, Elizabeth, Kashyap, Adhish, Forlenza, Sophia, Kenny, Alan P., Zorn, Aaron M., Shen, Yufeng, Chung, Wendy K.

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Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes за авторством 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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Proceedings of the 2018 Advances in Motility and in Neurogastroenterology: AIMING for the Future Single Topic Symposium за авторством Ambartsumyan, Lusine, Khlevner, Julie, Nurko, Samuel, Rosen, Rachel, Kaul, Ajay, Pandolfino, John E., Ratcliffe, Elyanne, Yacob, Desale, Li, B U.K., Punati, Jaya, Sood, Manu, Rao, Satish SC, Levitt, Marc A, Cocjin, Jose, Rodriguez, Leonel, Flores, Alejandro, Rosen, John M, Belkind-Gerson, Jaime, Saps, Miguel, Garza, Jose M, Fortunato, John, Schroedl, Rose L, Keefer, Laurie, Friedlander, Joel, Heuckeroth, Robert O., Rao, Meenakshi, El-Chammas, Khalil, Vaz, Karla, Chumpitazi, Bruno P, Sanghavi, Rina, Matta, Sravan, Danialifar, Tanaz, Di Lorenzo, Carlo, Darbari, Anil

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Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene за авторством 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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Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study за авторством Barzaghi, Federica, Hernandez, Laura Cristina Amaya, Neven, Benedicte, Ricci, Silvia, Kucuk, Zeynep Yesim, Bleesing, Jack J., Nademi, Zohreh, Slatter, Mary Anne, Ulloa, Erlinda Rose, Shcherbina, Anna, Roppelt, Anna, Worth, Austen, Silva, Juliana, Aiuti, Alessandro, Murguia-Favela, Luis, Speckmann, Carsten, Carneiro-Sampaio, Magda, Fernandes, Juliana Folloni, Baris, Safa, Ozen, Ahmet, Karakoc-Aydiner, Elif, Kiykim, Ayca, Schulz, Ansgar, Steinmann, Sandra, Notarangelo, Lucia Dora, Gambineri, Eleonora, Lionetti, Paolo, Shearer, William Thomas, Forbes, Lisa R., Martinez, Caridad, Moshous, Despina, Blanche, Stephane, Fisher, Alain, Ruemmele, Frank M., Tissandier, Come, Ouachee-Chardin, Marie, Rieux-Laucat, Frédéric, Cavazzana, Marina, Qasim, Waseem, Lucarelli, Barbarella, Albert, Michael H., Kobayashi, Ichiro, Alonso, Laura, De Heredia, Cristina Diaz, Kanegane, Hirokazu, Lawitschka, Anita, Seo, Jong Jin, Gonzalez-Vicent, Marta, Diaz, Miguel Angel, Goyal, Rakesh Kumar, Sauer, Martin G., Yesilipek, Akif, Kim, Minsoo, Yilmaz-Demirdag, Yesim, Bhatia, Monica, Khlevner, Julie, Richmond Padilla, Erick J., Martino, Silvana, Montin, Davide, Neth, Olaf, Molinos-Quintana, Agueda, Valverde-Fernandez, Justo, Broides, Arnon, Pinsk, Vered, Ballauf, Antje, Haerynck, Filomeen, Bordon, Victoria, Dhooge, Catharina, Garcia-Lloret, Maria Laura, Bredius, Robbert G., Ka1wak, Krzysztof, Haddad, Elie, Seidel, Markus Gerhard, Duckers, Gregor, Pai, Sung-Yun, Dvorak, Christopher C., Ehl, Stephan, Locatelli, Franco, Goldman, Frederick, Gennery, Andrew Richard, Cowan, Mort J., Roncarolo, Maria-Grazia, Bacchetta, Rosa

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