Management of XLP-1 and ITK deficiency: The challenges posed by PID with an unpredictable spectrum of disease manifestations von Shadur, B., Abuzaitoun, O., NaserEddin, A., Even-Or, E., Zaidman, I., Stepensky, P.

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Hepatitis D virus in Victoria 2000-2009 von Shadur, B., MacLachlan, J., Cowie, B.

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Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score von Tesch, Victoria Katharina, Abolhassani, Hassan, Shadur, Bella, Zobel, Joachim, Mareika, Yuliya, Sharapova, Svetlana, Karakoc-Aydiner, Elif, Rivière, Jacques G., Garcia-Prat, Marina, Moes, Nicolette, Haerynck, Filomeen, Gonzales-Granado, Luis I., Santos Pérez, Juan Luis, Mukhina, Anna, Shcherbina, Anna, Aghamohammadi, Asghar, Hammarström, Lennart, Dogu, Figen, Haskologlu, Sule, İkincioğulları, Aydan İ., Köstel Bal, Sevgi, Baris, Safa, Kilic, Sara Sebnem, Karaca, Neslihan Edeer, Kutukculer, Necil, Girschick, Hermann, Kolios, Antonios, Keles, Sevgi, Uygun, Vedat, Stepensky, Polina, Worth, Austen, van Montfrans, Joris M., Peters, Anke M.J., Meyts, Isabelle, Adeli, Mehdi, Marzollo, Antonio, Padem, Nurcicek, Khojah, Amer M., Chavoshzadeh, Zahra, Avbelj Stefanija, Magdalena, Bakhtiar, Shahrzad, Florkin, Benoit, Meeths, Marie, Gamez, Laura, Grimbacher, Bodo, Seppänen, Mikko R.J., Lankester, Arjan, Gennery, Andrew R., Seidel, Markus G.

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Hepatitis D virus in V ictoria 2000–2009 von Shadur, B., MacLachlan, J., Cowie, B.

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Allogeneic hematopoietic stem cell transplantation in leukocyte adhesion deficiency type I and III von Bakhtiar, Shahrzad, Salzmann-Manrique, Emilia, Blok, Henric-Jan, Eikema, Dirk-Jan, Hazelaar, Sheree, Ayas, Mouhab, Toren, Amos, Goldstein, Gal, Moshous, Despina, Locatelli, Franco, Merli, Pietro, Michel, Gerard, Öztürk, Gülyüz, Schulz, Ansgar, Heilmann, Carsten, Ifversen, Marianne, Wynn, Rob F., Aleinikova, Olga, Bertrand, Yves, Tbakhi, Abdelghani, Veys, Paul, Karakukcu, Musa, Kupesiz, Alphan, Ghavamzadeh, Ardeshir, Handgretinger, Rupert, Unal, Emel, Perez-Martinez, Antonio, Gokce, Muge, Porta, Fulvio, Aksu, Tekin, Karasu, Gülsün, Badell, Isabel, Ljungman, Per, Skorobogatova, Elena, Yesilipek, Akif, Zuckerman, Tsila, Bredius, Robbert R.G., Stepensky, Polina, Shadur, Bella, Slatter, Mary, Gennery, Andrew R., Albert, Michael H., Bader, Peter, Lankester, Arjan

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Treatment forms and clinical course of LPS-Responsive beige-like anchor protein deficiency and introduction of the immune deficiency and -dysregulation activity (=IDDA) score von Tesch, VK, Abolhassani, H, Grimbacher, B, Lankaster, A, Gennery, A, Shadur, B, Stepensky, P, Mareika, Y, Sharapova, S, Karakoc-Aydiner, E, Riviere, JG, Garcia-Prat, M, Moes, N, Haerynck, F, Gonzales-Granado, LI, Perez, JLS, Mukhina, A, Aghamohammadi, A, Hammarstrom, L, Dogu, F, Ikinciogullari, AI, Bal, S, Baris, S, Kilic, SS, Karaca, NE, Kutukculer, N, Girschick, H, Kolios, A, Keles, S, Seidel, MG

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Characterization of the Clinical and Immunological Phenotype and Management of 157 Individuals with 56 Distinct Heterozygous NFKB1 Mutations von Lorenzini, T, Fliegauf, M, Klammer, N, Frede, N, Proietti, M, Bulashevska, A, Camacho-Ordonez, N, Varjosalo, M, Kinnunen, M, de Vries, E, van der Meer, JWM, Ameratunga, R, Roifman, CM, Schejter, YD, Kobbe, R, Hautala, T, Atschekzei, F, Schmidt, RE, Schroder, C, Stepensky, P, Shadur, B, Pedroza, LA, van der Flier, M, Martinez-Gallo, M, Gonzalez-Granado, LI, Allende, LM, Shcherbina, A, Kuzmenko, N, Zakharova, V, Neves, JF, Svec, P, Fischer, U, Ip, W, Bartsch, O, Baris, S, Klein, C, Geha, R, Chou, J, Alosaimi, M, Weintraub, L, Boztug, K, Hirschmugl, T, Vilela, MMD, Holzinger, D, Seidl, M, Lougaris, V, Plebani, A, Alsina, L, Piquer-Gibert, M, Deya-Martinez, A, Slade, CA, Aghamohammadi, A, Abolhassani, H, Hammarstrom, L, Kuismin, O, Helminen, M, Allen, HL, Thaventhiran, JE, Freeman, AF, Cook, M, Bakhtiar, S, Christiansen, M, Cunningham-Rundles, C, Patel, NC, Rae, W, Niehues, T, Brauer, N, Syrjanen, J, Seppanen, MRJ, Burns, SO, Tuijnenburg, P, Kuijpers, TW, Warnatz, K, Grimbacher, B

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Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score von Tesch, V.K., Abolhassani, H., Shadur, B., Zobel, J., Mareika, Y., Sharapova, S., Karakoc-Aydiner, E., Riviere, J.G., Garcia-Prat, M., Moes, N., Haerynck, F., Gonzales-Granado, L.I., Perez, J.L.S., Mukhina, A., Shcherbina, A., Aghamohammadi, A., Hammarstrom, L., Dogu, F., Haskologlu, S., Ikinciogullari, A.I., Bal, S.K., Baris, S., Kilic, S.S., Karaca, N.E., Kutukculer, N., Girschick, H., Kolios, A., Keles, S., Uygun, V., Stepensky, P., Worth, A., Montfrans, J.M. van, Peters, A.M.J., Meyts, I., Adeli, M., Marzollo, A., Padem, N., Khojah, A.M., Chavoshzadeh, Z., Stefanija, M.A., Bakhtiar, S., Florkin, B., Meeths, M., Gamez, L., Grimbacher, B., Seppanen, M.R.J., Lankester, A., Gennery, A.R., Seidel, M.G.

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Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations von Lorenzini, T, Fliegauf, M, Klammer, N, Frede, N, Proietti, M, Bulashevska, A, Camacho-Ordonez, N, Varjosalo, M, Kinnunen, M, de Vries, E, van der Meer, JWM, Ameratunga, R, Roifman, CM, Schejter, YD, Kobbe, R, Hautala, T, Atschekzei, F, Schmidt, RE, Schröder, C, Stepensky, P, Shadur, B, Pedroza, LA, van der Flier, M, Martínez-Gallo, M, Gonzalez-Granado, LI, Allende, LM, Shcherbina, A, Kuzmenko, N, Zakharova, V, Neves, JF, Svec, P, Fischer, U, Ip, W, Bartsch, O, Barış, S, Klein, C, Geha, R, Chou, J, Alosaimi, M, Weintraub, L, Boztug, K, Hirschmugl, T, Dos Santos Vilela, MM, Holzinger, D, Seidl, M, Lougaris, V, Plebani, A, Alsina, L, Piquer-Gibert, M, Deyà-Martínez, A, Slade, CA, Aghamohammadi, A, Abolhassani, H, Hammarström, L, Kuismin, O, Helminen, M, Allen, HL, Thaventhiran, JE, Freeman, AF, Cook, M, Bakhtiar, S, Christiansen, M, Cunningham-Rundles, C, Patel, NC, Rae, W, Niehues, T, Brauer, N, Syrjänen, J, Seppänen, MRJ, Burns, SO, Tuijnenburg, P, Kuijpers, TW, NIHR-BioResource – Rare Diseases Consortium, Warnatz, K, Grimbacher, B

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Effects of Recombinant Human Erythropoietin on Renal Function in Chronic Renal Failure Predialysis Patients von Roth, David, Smith, Ronald D., Schulman, Gerald, Steinman, Theodore I., Hatch, Fred E., Rudnick, Michael R., Sloand, James A., Freedman, Barry I., Williams, Winfred W., Shadur, Craig A., Benz, Robert L., Teehan, Brendan P., Revicki, Dennis A., Sarokhan, Brenda J., Abels, Robert I.

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Darwinian selection does not eliminate irrational traders von Biais, Bruno, Shadur, Raphael

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Cyclosporin A spares selectively lymphocytes with donor-specific suppressor characteristics von Hutchinson, I F, Shadur, C A, Duarte, J S, Strom, T B, Tilney, N L

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Managing diversity von Kochan, Thomas A, Tung, Rosalie L, Caligiuri, Paula M, Stroh, Linda K, Lam, Alice, Mamman, Aminu, Nam, Sang H, Paik, Yongsun, Teagarden, Mary B, Tayeb, Monir, Wever, Kirsten S, Yeh, Rhy-song, Amante, Maragtas S.V., Dyer, Lee, Reeves, Todd, Horwitz, Frank M, Bowmaker-Falconer, Angus, Searll, Peter, Lee, Michael Byungnam, Scarpello, Vida, Rockmore, B Wayne, Marginson, Paul, Armstrong, Peter, Edwards, P K, Purcell, John, Negrelli, Serafino, Treu, Tiziano, Shadur, Mark A, Rodwell, John J, Bamber, Greg J

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Immunological properties of subcellular rat lymphocyte preparations. Primary allogeneic stimulation in vitro by fractions containing Ia (RT1-B), but not RT1-A antigens von Kaldany, A, Carpenter, C B, Shadur, C A, George, K, Lundin, 3rd, A P, Suthanthiran, M, Strom, T B

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