Resultados de procura - Stauber, Tali

Prolonged excretion of type-2 poliovirus from a primary immune deficient patient during the transition to a type-2 poliovirus-free world, Israel, 2016 por Weil, Merav, Shulman, Lester M, Heiman, Sophia, Stauber, Tali, Alfandari, Jacqueline, Weiss, Leah, Silberstein, Ilana, Indenbaum, Viki, Mendelson, Ella, Sofer, Danit

Ligazón do recurso Ligazón do recurso Ligazón do recurso

Reduced Function and Diversity of T Cell Repertoire and Distinct Clinical Course in Patients With IL7RA Mutation por Lev, Atar, Simon, Amos J., Barel, Ortal, Eyal, Eran, Glick-Saar, Efrat, Nayshool, Omri, Birk, Ohad, Stauber, Tali, Hochberg, Amit, Broides, Arnon, Almashanu, Shlomo, Hendel, Ayal, Lee, Yu Nee, Somech, Raz

Ligazón do recurso Ligazón do recurso Ligazón do recurso

First Year of Israeli Newborn Screening for Severe Combined Immunodeficiency—Clinical Achievements and Insights por Rechavi, Erez, Lev, Atar, Simon, Amos J., Stauber, Tali, Daas, Suha, Saraf-Levy, Talia, Broides, Arnon, Nahum, Amit, Marcus, Nufar, Hanna, Suhair, Stepensky, Polina, Toker, Ori, Dalal, Ilan, Etzioni, Amos, Almashanu, Shlomo, Somech, Raz

Ligazón do recurso Ligazón do recurso Ligazón do recurso

Whole exome sequencing in childhood-onset lupus frequently detects single gene etiologies por Tirosh, Irit, Spielman, Shiri, Barel, Ortal, Ram, Reut, Stauber, Tali, Paret, Gideon, Rubinsthein, Marina, Pessach, Itai M., Gerstein, Maya, Anikster, Yair, Shukrun, Rachel, Dagan, Adi, Adler, Katerina, Pode-Shakked, Ben, Volkov, Alexander, Perelman, Marina, Greenberger, Shoshana, Somech, Raz, Lahav, Einat, Majmundar, Amar J., Padeh, Shai, Hildebrandt, Friedhelm, Vivante, Asaf

Ligazón do recurso Ligazón do recurso Ligazón do recurso

Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects por Lev, Atar, Lee, Yu Nee, Sun, Guangping, Hallumi, Enas, Simon, Amos J., Zrihen, Keren S., Levy, Shiran, Beit Halevi, Tal, Papazian, Maria, Shwartz, Neta, Somekh, Ido, Levy-Mendelovich, Sarina, Wolach, Baruch, Gavrieli, Ronit, Vernitsky, Helly, Barel, Ortal, Javasky, Elisheva, Stauber, Tali, Ma, Chi A., Zhang, Yuan, Amariglio, Ninette, Rechavi, Gideon, Hendel, Ayal, Yablonski, Deborah, Milner, Joshua D., Somech, Raz

Ligazón do recurso Ligazón do recurso Ligazón do recurso

Genotype and functional correlates of disease phenotype in deficiency of adenosine deaminase 2 (DADA2) por Lee, Pui Y., Kellner, Erinn S., Huang, Yuelong, Furutani, Elissa, Huang, Zhengping, Bainter, Wayne, Alosaimi, Mohammed F., Stafstrom, Kelsey, Platt, Craig D., Stauber, Tali, Raz, Somech, Tirosh, Irit, Weiss, Aaron, Jordan, Michael B., Krupski, Christa, Eleftheriou, Despina, Brogan, Paul, Sobh, Ali, Baz, Zeina, Lefranc, Gerard, Irani, Carla, Kilic, Sara S., El-Owaidy, Rasha, Lokeshwar, M.R., Pimpale, Pallavi, Khubchandani, Raju, Chambers, Eugene P., Chou, Janet, Geha, Raif S., Nigrovic, Peter A., Zhou, Qing

Ligazón do recurso Ligazón do recurso Ligazón do recurso

CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesis por Somekh, Ido, Thian, Marini, Medgyesi, David, Gülez, Nesrin, Magg, Thomas, Gallón Duque, Alejandro, Stauber, Tali, Lev, Atar, Genel, Ferah, Unal, Ekrem, Simon, Amos J., Lee, Yu Nee, Kalinichenko, Artem, Dmytrus, Jasmin, Kraakman, Michael J., Schiby, Ginette, Rohlfs, Meino, Jacobson, Jeffrey M., Özer, Erdener, Akcal, Ömer, Conca, Raffaele, Patiroglu, Türkan, Karakukcu, Musa, Ozcan, Alper, Shahin, Tala, Appella, Eliana, Tatematsu, Megumi, Martinez-Jaramillo, Catalina, Chinn, Ivan K., Orange, Jordan S., Trujillo-Vargas, Claudia Milena, Franco, José Luis, Hauck, Fabian, Somech, Raz, Klein, Christoph, Boztug, Kaan

Ligazón do recurso Ligazón do recurso Ligazón do recurso