EXPRESSION OF FACTOR VII AND IX ACTIVITIES IN MAMMALIAN CELLS von FREDERICK S. HAGEN, MARGARET Y. INSLEY, CHARLES L. GRAY, SHARON J. BUSHBY, MARK J. MURRAY, KATHLEEN L. BERKNER, RICHARD G. WOODBURY

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Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development von Anderson, Louise V. B., Davison, Keith, Moss, Jennifer A., Young, Carol, Cullen, Michael J., Walsh, John, Johnson, Margaret A., Bashir, Rumaisa, Britton, Stephen, Keers, Sharon, Argov, Zohar, Mahjneh, Ibrahim, Fougerousse, Françoise, Beckmann, Jacques S., Bushby, Kate M. D.

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The TREAT-NMD advisory committee for therapeutics (TACT): an innovative de-risking model to foster orphan drug development von Heslop, Emma, Csimma, Cristina, Straub, Volker, McCall, John, Nagaraju, Kanneboyina, Wagner, Kathryn R, Caizergues, Didier, Korinthenberg, Rudolf, Flanigan, Kevin M, Kaufmann, Petra, McNeil, Elizabeth, Mendell, Jerry, Hesterlee, Sharon, Wells, Dominic J, Bushby, Kate

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Identical Mutation in Patients with Limb Girdle Muscular Dystrophy Type 2B Or Miyoshi Myopathy Suggests a Role for Modifier Gene(s) von Weiler, Tracey, Bashir, Rumaisa, Anderson, Louise V. B., Davison, Keith, Moss, Jennifer A., Britton, Stephen, Nylen, Edward, Keers, Sharon, Vafiadaki, Elizabeth, Greenberg, Cheryl R., Bushby, Kate M. D., Wrogemann, Klaus

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A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B von Bushby, Kate, Bashir, Rumaisa, Britton, Stephen, Strachan, Tom, Keers, Sharon, Vafiadaki, Elizabeth, Lako, Majlinda, Richard, Isabelle, Marchand, Sylvie, Bourg, Nathalie, Argov, Zohar, Sadeh, Menachem, Mahjneh, Ibrahim, Marconi, Giampiero, Passos-Bueno, Maria Rita, Moreira, Eloisa de S, Zatz, Mayana, Beckmann, Jacques S

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Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies) von Anderson, Louise V.B, Harrison, Ruth M, Pogue, Robert, Vafiadaki, Elizabeth, Pollitt, Christine, Davison, Keith, Moss, Jennifer A, Keers, Sharon, Pyle, Angela, Shaw, Pamela J, Mahjneh, Ibrahim, Argov, Zohar, Greenberg, Cheryl R, Wrogemann, Klaus, Bertorini, Tulio, Goebel, Hans H, Beckmann, Jacques S, Bashir, Rumaisa, Bushby, Kate M.D

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Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Clinical and genetic features von Argov, Z, Sadeh, M, Mazor, K, Soffer, D, Kahana, E, Eisenberg, I, Mitrani-Rosenbaum, S, Richard, I, Beckmann, J, Keers, S, Bashir, R, Bushby, K, Rosenmann, H

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Current trends in biobanking for rare diseases: a review [Corrigendum] von Graham, Caroline, Dawkins, Hugh, Baynam, Gareth, Lockmuller, Hanns, Bushby, Kate, Monaco, Lucia, Zatloukal, Kurt, Rubinstein, Yaffa, Mora, Marina, Knoppers, Bartha Maria, Terry, Sharon, Hansson, Mats, Reiss, Olaf, Schaefer, Franz, Carpentieri, David, Taruscio, Domenica, Posada, Manuel, Bellgard, Matthew, Kole, Anna, Molster, Caron, Mascalzoni, Deborah

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Current trends in biobanking for rare diseases: a review von Graham, Caroline E, Molster, Caron, Baynam, Gareth S, Bushby, Kate, Hansson, Mats, Kole, Anna, Mora, Marina, Monaco, Lucia, Bellgard, Matthew, Carpentieri, David, Posada, Manuel, Riess, Olaf, Rubinstein, Yaffa R, Schaefer, Franz, Taruscio, Domenica, Terry, Sharon F, Zatloukal, Kurt, Knoppers, Bartha, Lochmuller, Hanns, Dawkins, Hugh J.S

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Genetic and Physical Mapping at the Limb-Girdle Muscular Dystrophy Locus (LGMD2B) on Chromosome 2p von Bashir, Rumaisa, Keers, Sharon, Strachan, Tom, Passos-Bueno, Rita, Zatz, Mayana, Weissenbach, Jean, Le Paslier, Denis, Meisler, Miriam, Bushby, Kate

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Confirmation of the 2p Locus for the Mild Autosomal Recessive Limb-Girdle Muscular Dystrophy Gene (LGMD2B) in Three Families Allows Refinement of the Candidate Region von Passos-Bueno, M.Rita, Bashir, Ramaisa, Moreira, Eloisa S., Vainzof, Mariz, Marie, Suely K., Vasquez, Luciana, Iughetti, Paula, Bakker, Egbert, Keers, Sharon, Stephenson, Anthea, Strachan, Tom, Mahneh, Ibrahim, Weissenbach, Jean, Bushby, Katharine, Zatz, Mayana

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13th IIS (UK group) symposium von Caddick, Stephen, Stone-Elander, Sharon, Patching, Simon G., Herbert, Richard B., Henderson, Peter J. F., Brough, Adrian R., Middleton, David A., Coumbarides, Gregory S., Eames, Jason, Ghilagaber, Stephanos, Suggate, Michael J., Weerasooriya, Neluka, Spivey, Alan C., Diaper, Chris, Srikaran, Ratnasothy, Jones, Teyrnon, Noban, Catherine, Ellames, George J., Kohler, Andrew, Wadsworth, Harry, Blagbrough, Ian S., Ballinger, James R., Shemilt, Gary, Reid, R Gordon, Wilde, Philip D, Mangion, Andrew, Knight, Julian G., Geach, Neil J., Oldfield, Mark F., Atzrodt, Jens, Loewe, Claudia, Chappelle, Michael R., Hawes, Calvin R., Morgan, Alan D., Rees, Anthony T., Kitson, Sean L., Booth, Helen, Harding, John R., Woodhouse, David P., Bergin, Julie A., Bushby, Nicholas, Killick, David A., King, Clare D., Wilkinson, David J., Hickey, Michael J., Kingston, Lee P., Jones, John R., Lockley, William J.S., Mather, Andrew N., Wilkinson, David J., Hickey, Michael J., Kingston, Lee P., Lockley, William J.S., Mather, Andrew N., McAuley, Barry, Wilkinson, David J., Filer, Crist N., Ullas, Giliyar, Kelly, Terry, Lloyd, Cindy, Potwin, Jeannette, Wright, Christopher, v Adelman, Stuart L., v Adelman, Jane C. Bowden, Nilsson, Göran N., Simonsson, Roger, Wilkinson, David J., Jones, Teyrnon, Spivey, Alan C, Kohler, Andrew, Ellames, George, Cleij, Marcel C., Aigbirhio, Franklin I., Baron, Jean-Claude, Clark, John C., Johnström, Peter, Fryer, Tim D., Richards, Hugh K., Barret, Olivier, Clark, John C., Pickard, John D., Davenport, Anthony P.

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