76TiP Fecal microbiota transplantation to improve efficacy of immune checkpoint inhibitors in metastatic lung cancer by Massalha, I., Segal, A., Moskovitz, M.T., Yakobson, A., Zabit, R., Stemmer, S.M., Shalata, W., Dudnik, Y., Markel, G., Geva-Zatorsky, N., Meirovitz, A.

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133TiP Neoadjuvant osimertinib followed by sequential definitive radiotherapy and/or surgery in stage III EGFR-mutant NSCLC: An open-label, single-arm, phase II study by Kian, W., Peled, N., Roisman, L.C., Levison, E., Dudnik, J., Chernomordikov, E., Dudnik, E., Keren-Rosenberg, S., Tsuriel, S., Hannes, V., Hershkovitz, D., Lichtenberg, R., Granot, I., Krayim, B., Shalata, W., Allen, A.M., Blumenfeld, P., Lavrenkov, K.

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EP08.02-060 How Do Oncologists Treat Patients With EGFR Exon-20 Mutant NSCLC Outside of Clinical Trials? Updated Analysis From the European EXOTIC Registry by Mountzios, G., Planchard, D., Metro, G., Tsiouda, D., Prelaj, A., Lampaki, S., Shalata, W., Riudavets, M., Christopoulos, P., Girard, N., Albarran, V., Garcia Campelo, R., Samitas, K., Banna, G., Boukovinas, I., Agbarya, A., Koumarianou, A., Perdikouri, E.-I., Kosmidis, P., Reck, M., Lo Russo, G.

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Mechanisms Linking Nonalcoholic Fatty Liver Disease with Coronary Artery Disease by Nseir, W., Shalata, A., Marmor, A., Assy, N.

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Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders by Kaiyrzhanov, Rauan, Rad, Aboulfazl, Lin, Sheng-Jia, Bertoli-Avella, Aida, Kallemeijn, Wouter W, Godwin, Annie, Zaki, Maha S, Huang, Kevin, Lau, Tracy, Petree, Cassidy, Efthymiou, Stephanie, Karimiani, Ehsan Ghayoor, Hempel, Maja, Normand, Elizabeth A, Rudnik-Schöneborn, Sabine, Schatz, Ulrich A, Baggelaar, Marc P, Ilyas, Muhammad, Sultan, Tipu, Alvi, Javeria Raza, Ganieva, Manizha, Fowler, Ben, Aanicai, Ruxandra, Tayfun, Gulsen Akay, Al Saman, Abdulaziz, Alswaid, Abdulrahman, Amiri, Nafise, Asilova, Nilufar, Shotelersuk, Vorasuk, Yeetong, Patra, Azam, Matloob, Babaei, Meisam, Monajemi, Gholamreza Bahrami, Mohammadi, Pouria, Samie, Saeed, Banu, Selina Husna, Pinto Basto, Jorge, Kortüm, Fanny, Bauer, Mislen, Bauer, Peter, Beetz, Christian, Garshasbi, Masoud, Issa, Awatif Hameed, Eyaid, Wafaa, Ahmed, Hind, Hashemi, Narges, Hassanpour, Kazem, Herman, Isabella, Ibrohimov, Sherozjon, Abdul-Majeed, Ban A, Imdad, Maria, Isrofilov, Maksudjon, Kaiyal, Qassem, Khan, Suliman, Kirmse, Brian, Koster, Janet, Lourenço, Charles Marques, Mitani, Tadahiro, Moldovan, Oana, Murphy, David, Najafi, Maryam, Pehlivan, Davut, Rocha, Maria Eugenia, Salpietro, Vincenzo, Schmidts, Miriam, Shalata, Adel, Mahroum, Mohammad, Talbeya, Jawabreh Kassem, Taylor, Robert W, Vazquez, Dayana, Vetro, Annalisa, Waterham, Hans R, Zaman, Mashaya, Schrader, Tina A, Chung, Wendy K, Guerrini, Renzo, Lupski, James R, Gleeson, Joseph, Suri, Mohnish, Jamshidi, Yalda, Bhatia, Kailash P, Vona, Barbara, Schrader, Michael, Severino, Mariasavina, Guille, Matthew, Tate, Edward W, Varshney, Gaurav K, Houlden, Henry, Maroofian, Reza

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Early metabolic defects in Arab subjects with strong family history of Type 2 diabetes by Shalata, A., Jazmawi, W., Aslan, O., Badarni, K., Dabbah, K., Sawaed, S., Castel, O. Cohen, Borochowitz, Z. U., Karkabi, K., DeFronzo, R., Abdul-Ghani, M.

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