Immunization against Marek's disease: influence of strain of chickens, maternal antibody, and type of vaccine von Spencer, J.L, Gavora, J.S, Grunder, A.A, Robertson, A, Speckmann, G.W

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Studies on genetic and vaccination-induced resistance of chickens to lymphoid tumor transplants. 1. Marek's disease tumor transplant (JMV) von Spencer, J L, Gavora, J S, Hare, W C, Grunder, A A, Robertson, A, Speckmann, G W

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Studies on Genetic and Vaccination-Induced Resistance of Chickens to Lymphoid Tumor Transplants 2. Transmissible Lymphoid Tumor of Olson von Spencer, J. L., Gavora, J. S., Grunder, A. A., Robertson, A., Speckmann, G. W.

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An investigation of the etiology of Brucella abortus singleton reactors von Dukes, T W, Nielsen, K H, Eaglesome, M D, Speckmann, G W, Corner, A H

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Attenuated Marek's disease herpesvirus: Protection conferred on strains of chickens varying in genetic resistance von Spencer, J.L, Grunder, A.A, Robertson, A, Speckmann, G.W

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An assessment of effects of vaccination on genetic resistance to Marek's disease von Gavora, J S, Grunder, A A, Spencer, J L, Gowe, R S, Robertson, A, Speckmann, G W

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Osteolytic Osteosarcoma in a German Shepherd Bitch von Bundza, A., Greig, A. S., Speckmann, G. W.

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Resistance of strains of chickens to Marek's disease von Grunder, A.A, Jeffers, T.K, Spencer, J.L, Robertson, A, Speckmann, G.W

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Der Wärmehaushalt Landwirtschaftlicher Nutztiere (Thermoregulation in Farm Animals) von Speckmann, G. W. O.

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Case report: osteolytic osteosarcoma in a German Shepherd bitch von Bundza, A, Greig, A S, Speckmann, G W

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Genetic and vaccination-induced resistance of chickens to lymphoid tumor transplants, 1: Marek's disease tumor transplant (JMV) [Herpesvirus induced tumors] von Spencer, J. L., Gavora, J. S., Hare, W. C. D., Grunder, A. A., Robertson, A., Speckmann, G. W.

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Rubella vaccine–induced granulomas are a novel phenotype with incomplete penetrance of genetic defects in cytotoxicity von Groß, Miriam, Speckmann, Carsten, May, Annette, Gajardo-Carrasco, Tania, Wustrau, Katharina, Maier, Sarah Lena, Panning, Marcus, Huzly, Daniela, Agaimy, Abbas, Bryceson, Yenan T., Choo, Sharon, Chow, C.W., Dückers, Gregor, Fasth, Anders, Fraitag, Sylvie, Gräwe, Katja, Haxelmans, Sabine, Holzinger, Dirk, Hudowenz, Ole, Hübschen, Judith M., Khurana, Claudia, Kienle, Korbinian, Klifa, Roman, Korn, Klaus, Kutzner, Heinz, Lämmermann, Tim, Ledig, Svea, Lipsker, Dan, Meeths, Marie, Naumann-Bartsch, Nora, Rascon, Jelena, Schänzer, Anne, Seidl, Maximilian, Tesi, Bianca, Vauloup-Fellous, Christelle, Vollmer-Kary, Beate, Warnatz, Klaus, Wehr, Claudia, Neven, Bénédicte, Vargas, Pablo, Sepulveda, Fernando E., Lehmberg, Kai, Schmitt-Graeff, Annette, Ehl, Stephan

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The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis von Bode, Sebastian Fn, Ammann, Sandra, Al-Herz, Waleed, Bataneant, Mihaela, Dvorak, Christopher C, Gehring, Stephan, Gennery, Andrew, Gilmour, Kimberly C, Gonzalez-Granado, Luis I, Groß-Wieltsch, Ute, Ifversen, Marianne, Lingman-Framme, Jenny, Matthes-Martin, Susanne, Mesters, Rolf, Meyts, Isabelle, van Montfrans, Joris M, Pachlopnik Schmid, Jana, Pai, Sung-Yun, Soler-Palacin, Pere, Schuermann, Uta, Schuster, Volker, Seidel, Markus G, Speckmann, Carsten, Stepensky, Polina, Sykora, Karl-Walter, Tesi, Bianca, Vraetz, Thomas, Waruiru, Catherine, Bryceson, Yenan T, Moshous, Despina, Lehmberg, Kai, Jordan, Michael B, Ehl, Stephan

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Variable impairment of platelet functions in patients with severe, genetically linked immune deficiencies von Nagy, Magdolna, Mastenbroek, Tom G, Mattheij, Nadine J A, de Witt, Susanne, Clemetson, Kenneth J, Kirschner, Janbernd, Schulz, Ansgar S, Vraetz, Thomas, Speckmann, Carsten, Braun, Attila, Cosemans, Judith M E M, Zieger, Barbara, Heemskerk, Johan W M

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Mosaic Drawings and Cartograms von Cano, R. G., Buchin, K., Castermans, T., Pieterse, A., Sonke, W., Speckmann, B.

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Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases von ROHR, Jan, BEUTEL, Karin, WOESSMANN, Wilhelm, GROLL, Andreas H, STRAHM, Brigitte, PAGEL, Julia, SPECKMANN, Carsten, JANKA, Gritta, GRIFFITHS, Gillian, SCHWARZ, Klaus, ZUR STADT, Udo, EHL, Stephan, MAUL-PAVICIC, Andrea, VRAETZ, Thomas, THIEL, Jens, WARNATZ, Klaus, BONDZIO, Ilka, GROSS-WIELTSCH, Ute, SCHÜNDELN, Michael, SCHÜTZ, Barbara

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The BEACH protein LRBA is required for hair bundle maintenance in cochlear hair cells and for hearing von Vogl, Christian, Butola, Tanvi, Haag, Natja, Hausrat, Torben J, Leitner, Michael G, Moutschen, Michel, Lefèbvre, Philippe P, Speckmann, Carsten, Garrett, Lillian, Becker, Lore, Fuchs, Helmut, Hrabe de Angelis, Martin, Nietzsche, Sandor, Kessels, Michael M, Oliver, Dominik, Kneussel, Matthias, Kilimann, Manfred W, Strenzke, Nicola

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International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome von Dimitrova, Dimana, Nademi, Zohreh, Maccari, Maria Elena, Ehl, Stephan, Uzel, Gulbu, Tomoda, Takahiro, Okano, Tsubasa, Imai, Kohsuke, Carpenter, Benjamin, Ip, Winnie, Rao, Kanchan, Worth, Austen J.J., Laberko, Alexandra, Mukhina, Anna, Néven, Bénédicte, Moshous, Despina, Speckmann, Carsten, Warnatz, Klaus, Wehr, Claudia, Abolhassani, Hassan, Aghamohammadi, Asghar, Bleesing, Jacob J., Dara, Jasmeen, Dvorak, Christopher C., Ghosh, Sujal, Kang, Hyoung Jin, Markelj, Gašper, Modi, Arunkumar, Bayer, Diana K., Notarangelo, Luigi D., Schulz, Ansgar, Garcia-Prat, Marina, Soler-Palacín, Pere, Karakükcü, Musa, Yilmaz, Ebru, Gambineri, Eleonora, Menconi, Mariacristina, Masmas, Tania N., Holm, Mette, Bonfim, Carmem, Prando, Carolina, Hughes, Stephen, Jolles, Stephen, Morris, Emma C., Kapoor, Neena, Koltan, Sylwia, Paneesha, Shankara, Steward, Colin, Wynn, Robert, Duffner, Ulrich, Gennery, Andrew R., Lankester, Arjan C., Slatter, Mary, Kanakry, Jennifer A.

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RNA editing (R/G site) and flip–flop splicing of the AMPA receptor subunit GluR2 in nervous tissue of epilepsy patients von Vollmar, W, Gloger, J, Berger, E, Kortenbruck, G, Köhling, R, Speckmann, E.-J, Musshoff, U

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PGM3 Mutations Cause a Congenital Disorder of Glycosylation with Severe Immunodeficiency and Skeletal Dysplasia von Stray-Pedersen, Asbjørg, Backe, Paul H., Sorte, Hanne S., Mørkrid, Lars, Chokshi, Niti Y., Erichsen, Hans Christian, Gambin, Tomasz, Elgstøen, Katja B.P., Bjørås, Magnar, Wlodarski, Marcin W., Krüger, Marcus, Jhangiani, Shalini N., Muzny, Donna M., Patel, Ankita, Raymond, Kimiyo M., Sasa, Ghadir S., Krance, Robert A., Martinez, Caridad A., Abraham, Shirley M., Speckmann, Carsten, Ehl, Stephan, Hall, Patricia, Forbes, Lisa R., Merckoll, Else, Westvik, Jostein, Nishimura, Gen, Rustad, Cecilie F., Abrahamsen, Tore G., Rønnestad, Arild, Osnes, Liv T., Egeland, Torstein, Rødningen, Olaug K., Beck, Christine R., Boerwinkle, Eric A., Gibbs, Richard A., Lupski, James R., Orange, Jordan S., Lausch, Ekkehart, Hanson, I. Celine

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