THREE-DIMENSIONAL VOLUMETRICS FOR TRACKING VESTIBULAR SCHWANNOMA GROWTH IN NEUROFIBROMATOSIS TYPE II von Harris, Gordon J., Plotkin, Scott R., MacCollin, Mia, Bhat, Shubha, Urban, Trinity, Lev, Michael H., Slattery, William H.

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Survey of Somatic Mutations in Tuberous Sclerosis Complex (TSC) Hamartomas Suggests Different Genetic Mechanisms for Pathogenesis of TSC Lesions von Niida, Yo, Stemmer-Rachamimov, Anat O., Logrip, Marian, Tapon, Dagmar, Perez, Ronald, Kwiatkowski, David J., Sims, Katherine, MacCollin, Mia, Louis, David N., Ramesh, Vijaya

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Modeling NF2 with human arachnoidal and meningioma cell culture systems: NF2 silencing reflects the benign character of tumor growth von James, Marianne F, Lelke, Johanna M, MacCollin, Mia, Plotkin, Scott R, Stemmer-Rachamimov, Anat O, Ramesh, Vijaya, Gusella, James F

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Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation von Legius, Eric, Messiaen, Ludwine, Wolkenstein, Pierre, Pancza, Patrice, Avery, Robert A., Berman, Yemima, Blakeley, Jaishri, Babovic-Vuksanovic, Dusica, Cunha, Karin Soares, Ferner, Rosalie, Fisher, Michael J., Friedman, Jan M., Gutmann, David H., Kehrer-Sawatzki, Hildegard, Korf, Bruce R., Mautner, Victor-Felix, Peltonen, Sirkku, Rauen, Katherine A., Riccardi, Vincent, Schorry, Elizabeth, Stemmer-Rachamimov, Anat, Stevenson, David A., Tadini, Gianluca, Ullrich, Nicole J., Viskochil, David, Wimmer, Katharina, Yohay, Kaleb, Gomes, Alicia, Jordan, Justin T., Mautner, Victor, Merker, Vanessa L., Smith, Miriam J., Stevenson, David, Anten, Monique, Aylsworth, Arthur, Baralle, Diana, Barbarot, Sebastien, Barker, Fred, Ben-Shachar, Shay, Bergner, Amanda, Bessis, Didier, Blanco, Ignacio, Cassiman, Catherine, Ciavarelli, Patricia, Clementi, Maurizio, Frébourg, Thierry, Giovannini, Marco, Halliday, Dorothy, Hammond, Chris, Hanemann, C.O., Hanson, Helen, Heiberg, Arvid, Joly, Pascal, Kalamarides, Michel, Karajannis, Matthias, Kroshinsky, Daniela, Larralde, Margarita, Lázaro, Conxi, Le, Lu, Link, Michael, Listernick, Robert, MacCollin, Mia, Mallucci, Conor, Moertel, Christopher, Mueller, Amy, Ngeow, Joanne, Oostenbrink, Rianne, Packer, Roger, Papi, Laura, Parry, Allyson, Peltonen, Juha, Pichard, Dominique, Poppe, Bruce, Rezende, Nilton, Rodrigues, Luiz Oswaldo, Rosser, Tena, Ruggieri, Martino, Serra, Eduard, Steinke-Lange, Verena, Stivaros, Stavros Michael, Taylor, Amy, Toelen, Jaan, Tonsgard, James, Trevisson, Eva, Upadhyaya, Meena, Varan, Ali, Wilson, Meredith, Wu, Hao, Zadeh, Gelareh, Huson, Susan M., Evans, D. Gareth, Plotkin, Scott R.

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Dopa-responsive hypersomnia and mixed movement disorder due to sepiapterin reductase deficiency von FRIEDMAN, Jennifer, HYLAND, Keith, BLAU, Nenad, MACCOLLIN, Mia

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Comparative pathology of nerve sheath tumors in mouse models and humans von Stemmer-Rachamimov, Anat O, Louis, David N, Nielsen, Gunnlaugur P, Antonescu, Cristina R, Borowsky, Alexander D, Bronson, Roderick T, Burns, Dennis K, Cervera, Pascale, McLaughlin, Margaret E, Reifenberger, Guido, Schmale, Michael C, MacCollin, Mia, Chao, Richard C, Cichowski, Karen, Kalamarides, Michel, Messerli, Shanta M, McClatchey, Andrea I, Niwa-Kawakita, Michiko, Ratner, Nancy, Reilly, Karlyne M, Zhu, Yuan, Giovannini, Marco

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Molecular Analysis of the NF2 Tumor-Suppressor Gene in Schwannomatosis von Jacoby, Lee B., Jones, Deborah, Davis, Kevin, Kronn, David, Short, M. Priscilla, Gusella, James, MacCollin, Mia

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Merlin: the neurofibromatosis 2 tumor suppressor von Gusella, James F., Ramesh, Vijaya, MacCollin, Mia, Jacoby, Lee B.

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Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation von Plotkin, Scott R., Messiaen, Ludwine, Legius, Eric, Pancza, Patrice, Avery, Robert A., Blakeley, Jaishri O., Babovic-Vuksanovic, Dusica, Ferner, Rosalie, Fisher, Michael J., Friedman, Jan M., Giovannini, Marco, Gutmann, David H., Hanemann, Clemens Oliver, Kalamarides, Michel, Kehrer-Sawatzki, Hildegard, Korf, Bruce R., Mautner, Victor-Felix, MacCollin, Mia, Papi, Laura, Rauen, Katherine A., Riccardi, Vincent, Schorry, Elizabeth, Smith, Miriam J., Stemmer-Rachamimov, Anat, Stevenson, David A., Ullrich, Nicole J., Viskochil, David, Wimmer, Katharina, Yohay, Kaleb, Huson, Susan M., Wolkenstein, Pierre, Evans, Dafydd Gareth

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The Neurofibromatosis Type 2 Gene Product, merlin, Reverses the F-Actin Cytoskeletal Defects in Primary Human Schwannoma Cells von Bashour, Anne-Marie, Meng, J.-J., Ip, Wallace, MacCollin, Mia, Ratner, Nancy

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A negative feedback signaling network underlies oncogene-induced senescence von Courtois-Cox, Stéphanie, Genther Williams, Sybil M., Reczek, Elizabeth E., Johnson, Bryan W., McGillicuddy, Lauren T., Johannessen, Cory M., Hollstein, Pablo E., MacCollin, Mia, Cichowski, Karen

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Diagnostic criteria for schwannomatosis von MACCOLLIN, M, CHIOCCA, E. A, SANG, C. N, STEMMER-RACHAMIMOV, A, ROACH, E. S, EVANS, D. G, FRIEDMAN, J. M, HORVIT, R, JARAMILLO, D, LEV, M, MAUTNER, V. F, NIIMURA, M, PLOTKIN, S. R

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Exon scanning for mutation of the NF2 gene in schwannomas von Jacoby, Lee B., MacCollin, Mia, Louls, David N., Mohney, Trina, Rublo, Mari-Paz, Pulaski, Karen, Trofatter, James A., Kley, Nikolai, Seizinger, Bernd, Ramesh, Vijaya, Gusella, James F.

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Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas von RUBIO, M.-P, CORREA, K. M, RAMESH, V, MACCOLLIN, M. M, JACOBY, L. B, VON DEIMLING, A, GUSELLA, J. F, LOUIS, D. N

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Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation von Plotkin, Scott R, Messiaen, Ludwine, Legius, Eric, Pancza, Patrice, Avery, Robert A, Blakeley, Jaishri O, Babovic-Vuksanovic, Dusica, Ferner, Rosalie, Fisher, Michael J, Friedman, Jan M, Giovannini, Marco, Gutmann, David H, Hanemann, Clemens Oliver, Kalamarides, Michel, Kehrer-Sawatzki, Hildegard, Korf, Bruce R, Mautner, Victor-Felix, MacCollin, Mia, Papi, Laura, Rauen, Katherine A, Riccardi, Vincent, Schorry, Elizabeth, Smith, Miriam J, Stemmer-Rachamimov, Anat, Stevenson, David A, Ullrich, Nicole J, Viskochil, David, Wimmer, Katharina, Yohay, Kaleb, Huson, Susan M, Wolkenstein, Pierre, Evans, D. Gareth

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Mutational spectrum of the NF2 gene: a meta-analysis of 12 years of research and diagnostic laboratory findings von Ahronowitz, Iris, Xin, Winnie, Kiely, Rosemary, Sims, Katherine, MacCollin, Mia, Nunes, Fabio P.

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Characterization and Expression of the Human A2a Adenosine Receptor Gene von Peterfreund, Robert A., MacCollin, Mia, Gusella, James, Fink, J. Stephen

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Immunohistochemical Analysis Supports a Role for INI1/SMARCB1 in Hereditary Forms of Schwannomas, but Not in Solitary, Sporadic Schwannomas von Patil, Sushama, Perry, Arie, MacCollin, Mia, Dong, Shumin, Betensky, Rebecca A., Yeh, Tu-Hsueh, Gutmann, David H., Stemmer-Rachamimov, Anat O.

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Temporal Control of Rac in Schwann Cell-Axon Interaction Is Disrupted in NF2-Mutant Schwannoma Cells von Nakai, Yoko, Zheng, Yi, MacCollin, Mia, Ratner, Nancy

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Dopa-responsive hypersomnia and mixed movement disorder due to sepiapterin reductase deficiency von Friedman, Jennifer, Hyland, Keith, Blau, Nenad, MacCollin, Mia

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