Comparison of elapegademase and pegademase in ADA‐deficient patients and mice von Murguia‐Favela, L., Min, W., Loves, R., Leon‐Ponte, M., Grunebaum, E.

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TAT-mediated intracellular delivery of purine nucleoside phosphorylase corrects its deficiency in mice von Toro, Ana, Grunebaum, Eyal

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Classical Islam: A History, 600 A.D. to 1258 A.D von von Grunebaum, G. E.

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Different Effects Of ADA And PNP Deficiency On Thymocytes Development von Grunebaum, E, Papinazath, T, Somech, R, Roifman, C.M

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Matched unrelated bone marrow transplant for T+ combined immunodeficiency von Roifman, C M, Somech, R, Grunebaum, E

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Rituximab for congenital haemophiliacs with inhibitors: a Canadian experience von CARCAO, M., ST LOUIS, J., POON, M-C., GRUNEBAUM, E., LACROIX, S., STAIN, A. M., BLANCHETTE, V. S., RIVARD, G. E.

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Bone marrow transplantation for cartilage-hair-hypoplasia von GUGGENHEIM, R, SOMECH, R, GRUNEBAUM, E, ATKINSON, A, ROIFMAN, C. M

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The pathogenic role of anti‐thyroglobulin antibody on pregnancy: evidence from an active immunization model in mice von Matalon, Shelly Tartakover, Blank, Miri, Levy, Yair, Carp, Howard J.A., Arad, Ayala, Burek, Lynne, Grunebaum, Eyal, Sherer, Yaniv, Ornoy, Asher, Refetoff, Samuel, Weiss, Roy E., Rose, Noel R., Shoenfeld, Yehuda

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Matched Unrelated Bone Marrow Transplant for Omenn Syndrome von Marcus, N, Nahum, A, Reid, B, Grunebaum, E, Roifman, C

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EdU-Click iT Flow Cytometry Assay As An Alternative To [3H]thymidine For Measuring Proliferation Of Human And Mice T Lymphocytes von Yu, Y, Arora, A, Min, W, Roifman, C.M, Grunebaum, E

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Omenn Syndrome is Associated with Mutations in DNA Ligase IV von Kim, V.H.D, Grunebaum, E, Bates, A, Roifman, C.M

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The role of anti‐endothelial cell antibodies in Kawasaki disease –in vitro and in vivo studies von GRUNEBAUM, E., BLANK, M., COHEN, S., AFEK, A., KOPOLOVIC, J., MERONI, P. L., YOUINOU, P., SHOENFELD, Y.

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Bone Marrow Transplantation for Severe Combined Immune Deficiency von Grunebaum, Eyal, Mazzolari, Evelina, Porta, Fulvio, Dallera, Daniela, Atkinson, Adelle, Reid, Brenda, Notarangelo, Luigi D, Roifman, Chaim M

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Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients von Geier, Christoph B., Ellison, Maryssa, Cruz, Rachel, Pawar, Sumit, Leiss-Piller, Alexander, Zmajkovicova, Katarina, McNulty, Shannon M, Yilmaz, Melis, Evans, Martin Oman, Gordon, Sumai, Ujhazi, Boglarka, Wiest, Ivana, Abolhassani, Hassan, Aghamohammadi, Asghar, Barmettler, Sara, Bhar, Saleh, Bondarenko, Anastasia, Bolyard, Audrey Anna, Buchbinder, David, Cada, Michaela, Cavieres, Mirta, Connelly, James A., Dale, David C., Deordieva, Ekaterina, Dorsey, Morna J., Drysdale, Simon B., Ehl, Stephan, Elfeky, Reem, Fioredda, Francesca, Firkin, Frank, Förster-Waldl, Elizabeth, Geng, Bob, Goda, Vera, Gonzalez-Granado, Luis, Grunebaum, Eyal, Grzesk, Elzbieta, Henrickson, Sarah E., Hilfanova, Anna, Hiwatari, Mitsuteru, Imai, Chihaya, Ip, Winnie, Jyonouchi, Soma, Kanegane, Hirokazu, Kawahara, Yuta, Khojah, Amer M., Kim, Vy Hong-Diep, Kojić, Marina, Kołtan, Sylwia, Krivan, Gergely, Langguth, Daman, Lau, Yu-Lung, Leung, Daniel, Miano, Maurizio, Mersyanova, Irina, Mousallem, Talal, Muskat, Mica, Naoum, Flavio A., Noronha, Suzie A., Ouederni, Monia, Ozono, Shuichi, Richmond, G. Wendell, Sakovich, Inga, Salzer, Ulrich, Schuetz, Catharina, Seeborg, Filiz Odabasi, Sharapova, Svetlana O., Sockel, Katja, Volokha, Alla, von Bonin, Malte, Warnatz, Klaus, Wegehaupt, Oliver, Weinberg, Geoffrey A., Wong, Ke-Juin, Worth, Austen, Yu, Huang, Zharankova, Yulia, Zhao, Xiaodong, Devlin, Lisa, Badarau, Adriana, Csomos, Krisztian, Keszei, Marton, Pereira, Joao, Taveras, Arthur G, Beaussant-Cohen, Sarah L., Ong, Mei-Sing, Shcherbina, Anna, Walter, Jolan E.

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Haemophagocytic lymphohistiocytosis in X‐linked severe combined immunodeficiency von Grunebaum, E., Zhang, J., Dadi, H., Roifman, C. M.

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EdU incorporation is an alternative non-radioactive assay to [ 3H]thymidine uptake for in vitro measurement of mice T-cell proliferations von Yu, Yongmao, Arora, Alka, Min, Weixian, Roifman, Chaim M., Grunebaum, Eyal

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Two novel mutations in a purine nucleoside phosphorylase (PNP)-deficient patient von Dalal, I, Grunebaum, E, Cohen, A, Roifman, CM

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Monogenic Early-Onset Lymphoproliferation and Autoimmunity: The Natural History of STAT3 GOF Syndrome von Leiding, J. W., Vogel, T. P., Santarlas, V. G. J., Mhaskar, R., Smith, M. R., Carisey, A., Vargas-Hernandez, A., Silva-Carmona, M., Heeg, M., Rensing-Ehl, A., Neven, Bénédicte, Hadjadj, Jérôme, Hambleton, S., Leahy, T. R., van Hagen, M., Cunningham-Rundles, C., Dutmer, C. M., Sharapova, S. O., Taskinen, M., Chua, I., Hague, R., Klemann, C., Kostyuchenko, L., Morio, T., Thatayatikom, A., Ozen, A., Scherbina, A., Bauer, C. S., Flanagan, S. E., Gambineri, E., Giovannini-Chami, Lisa, Heimall, J., Sullivan, K. E., Allenspach, E., Romberg, N., Deane, S. G., Prince, B. T., Rose, M., Bohnsack, J., Mousallem, T., Jesudas, R., dos Santos Vilela, M. M., O'Sullivan, M., Schmid, J. P., Průhová, Š., Rees, M., Su, H., Bahna, S., Baris, S., Bartnikas, L. M., Chang Berger, A., Briggs, T. A., Brothers, S., Bundy, V., Chan, A. Y., Chandrakasan, S., Christiansen, M., Cole, T., Cook, M. C., Desai, M. M., Fischer, U., Fulcher, D. A., Gallo, S., Gauthier, A., Gennery, A. R., Marques, J. G., Gottrand, Fréderic, Grimbacher, B., Grunebaum, E., Haapaniemi, E., Hämäläinen, S., Heiskanen, K., Heiskanen-Kosma, T., Hoffman, H. M., Gonzalez-Granado, L. I., Guerreiro, A. L., Kainulainen, L., Kumar, A., Lawrence, M. G., Levin, C., Martelius, T., Neth, O., Olbrich, P., Palma, A., Patel, N. C., Pozos, T., Preece, K., Lugo Reyes, S. O., Russell, M. A., Schejter, Y., Seroogy, C., Sinclair, J., Skevofilax, E., Suan, D., Suegeorgz, D., Szabolcs, P., Velasco, H., Warnatz, K., Walkovich, K., Worth, A.

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Anti-Endothelial Cell Antibodies (AECA) in Systemic Sclerosis - Increased Sensitivity using Different Endothelial Cell Substrates and Association with Other Autoantibodies von Renaudineau, Y., Grunebaum, E., Krause, I., Praprotnik, Sonja, Revelen, R., Youinou, P., Blanks, M., Gilburd, B., Sherer, Y., Luderschmidt, C., Eldor, A., Weksler, B., Gershwin, E. M., Shoenfeld, Y.

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A missense mutation in the SEDL gene results in delayed onset of X linked spondyloepiphyseal dysplasia in a large pedigree von Grunebaum, E, Arpaia, E, MacKenzie, J J, Fitzpatrick, J, Ray, P N, Roifman, C M

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