P57 IGHMBP2 mutations cause recessive axonal neuropathy: Genetic and functional characterisation in seven families von Cottenie, E, Kochanski, A, Jordanova, A, Baets, J, Rasic, V. Milic, Quinlivan, R, Lunn, M, Hanna, M.G, Zuchner, S, Harms, M, Choi, B, Reilly, M.M, Houlden, H

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P56 Whole-exome sequencing in patients with sensory and motor inherited neuropathies von Horga, A, Cottenie, E, Liu, Y-T, Pandraud, A, Rossor, A.M, Pitceathly, R.D.S, Laurá, M, Hanna, M.G, Houlden, H, Reilly, M.M

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P41 Genetic analysis of FIG4 in patients with CMT von Cottenie, E, Laurá, M, Hanna, M, Dick, D, Blake, J, Houlden, H, Reilly, M.M

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P50 Genetic dysfunction of MT-ATP6 can cause axonal Charcot-Marie-Tooth disease von Pitceathly, R.D.S, Murphy, S.M, Cottenie, E, Chalasani, A, Sweeney, M.G, Woodward, C, Mudanohwo, E.E, Hargreaves, I, Heales, S, Holton, J.L, Houlden, H, Lunn, M.P, Rahman, S, Reilly, M.M, Hanna, M.G

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Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth disease von Pitceathly, Robert D S, Murphy, Sinéad M, Cottenie, Ellen, Chalasani, Annapurna, Sweeney, Mary G, Woodward, Cathy, Mudanohwo, Ese E, Hargreaves, Iain, Heales, Simon, Land, John, Holton, Janice L, Houlden, Henry, Blake, Julian, Champion, Michael, Flinter, Frances, Robb, Stephanie A, Page, Rupert, Rose, Michael, Palace, Jacqueline, Crowe, Carol, Longman, Cheryl, Lunn, Michael P, Rahman, Shamima, Reilly, Mary M, Hanna, Michael G

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Genetic and functional investigation of inherited neuropathies von Cottenie, E

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Cryptic Amyloidogenic Elements in the 3' UTRs of Neurofilament Genes Trigger Axonal Neuropathy von Rebelo, AP, Abrams, AJ, Cottenie, E, Horga, A, Gonzalez, M, Bis, DM, Sanchez-Mejias, A, Pinto, M, Buglo, E, Markel, K, Prince, J, Laura, M, Houlden, H, Blake, J, Woodward, C, Sweeney, MG, Holton, JL, Hanna, M, Dallman, JE, Auer-Grumbach, M, Reilly, MM, Zuchner, S

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Mutations in gamma adducin are associated with inherited cerebral palsy von Kruer, MC, Jepperson, T, Dutta, S, Steiner, RD, Cottenie, E, Sanford, L, Merkens, M, Russman, BS, Blasco, PA, Fan, G, Pollock, J, Green, S, Woltjer, RL, Mooney, C, Kretzschmar, D, Paisán-Ruiz, C, Houlden, H

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Truncating and missense mutations in IGHMBP2 cause Charcot-Marie Tooth disease type 2 von Cottenie, E, Kochanski, A, Jordanova, A, Bansagi, B, Zimon, M, Horga, A, Jaunmuktane, Z, Saveri, P, Rasic, VM, Baets, J, Bartsakoulia, M, Ploski, R, Teterycz, P, Nikolic, M, Quinlivan, R, Laura, M, Sweeney, MG, Taroni, F, Lunn, MP, Moroni, I, Gonzalez, M, Hanna, MG, Bettencourt, C, Chabrol, E, Franke, A, von Au, K, Schilhabel, M, Kabzińska, D, Hausmanowa-Petrusewicz, I, Brandner, S, Lim, SC, Song, H, Choi, BO, Horvath, R, Chung, KW, Zuchner, S, Pareyson, D, Harms, M, Reilly, MM, Houlden, H

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Compensatory dynamics are rare in natural ecological communities von Houlahan, J.E, Currie, D.J, Cottenie, K, Cumming, G.S, Ernest, S.K.M, Findlay, C.S, Fuhlendorf, S.D, Gaedke, U, Legendre, P, Magnuson, J.J, McArdle, B.H, Muldavin, E.H, Noble, D, Russell, R, Stevens, R.D, Willis, T.J, Woiwod, I.P, Wondzell, S.M

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Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia von Oates, Emily C., Rossor, Alexander M., Hafezparast, Majid, Gonzalez, Michael, Speziani, Fiorella, MacArthur, Daniel G., Lek, Monkol, Cottenie, Ellen, Scoto, Mariacristina, Foley, A. Reghan, Hurles, Matthew, Houlden, Henry, Greensmith, Linda, Auer-Grumbach, Michaela, Pieber, Thomas R., Strom, Tim M., Schule, Rebecca, Herrmann, David N., Sowden, Janet E., Acsadi, Gyula, Menezes, Manoj P., Clarke, Nigel F., Züchner, Stephan, Muntoni, Francesco, North, Kathryn N., Reilly, Mary M.

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Negative relationships between species richness and temporal variability are common but weak in natural systems von Houlahan, J. E., Currie, D. J., Cottenie, K., Cumming, G. S., Findlay, C. S., Fuhlendorf, S. D., Legendre, P., Muldavin, E. H., Noble, D., Russell, R., Stevens, R. D., Willis, T. J., Wondzell, S. M.

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Zooplankton Metacommunity Structure: Regional vs. Local Processes in Highly Interconnected Ponds von Cottenie, Karl, Michels, Erik, Nuytten, Nele, de Meester, Luc

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Variation in space and time: a long-term examination of density-dependent dispersal in a woodland rodent von Denomme-Brown, Simon T., Cottenie, Karl, Falls, J. Bruce, Falls, E. Ann, Brooks, Ronald J., McAdam, Andrew G.

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Insight in the activity and diastereoselectivity of various Lewis acid catalysts for the citronellal cyclization von Vandichel, Matthias, Vermoortele, Frederik, Cottenie, Stijn, De Vos, Dirk E., Waroquier, Michel, Van Speybroeck, Veronique

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Reconciling seascape genetics and fisheries science in three codistributed flatfishes von Vandamme, Sara, Raeymaekers, Joost A. M., Maes, Gregory E., Cottenie, Karl, Calboli, Federico C. F., Diopere, Eveline, Volckaert, Filip A. M.

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Cryptic Amyloidogenic Elements in the 3′ UTRs of Neurofilament Genes Trigger Axonal Neuropathy von Rebelo, Adriana P., Abrams, Alexander J., Cottenie, Ellen, Horga, Alejandro, Gonzalez, Michael, Bis, Dana M., Sanchez-Mejias, Avencia, Pinto, Milena, Buglo, Elena, Markel, Kasey, Prince, Jeffrey, Laura, Matilde, Houlden, Henry, Blake, Julian, Woodward, Cathy, Sweeney, Mary G., Holton, Janice L., Hanna, Michael, Dallman, Julia E., Auer-Grumbach, Michaela, Reilly, Mary M., Zuchner, Stephan

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A Metacognitive Instructional Guide to Support Effective Studying Strategies von Bailey E. Bingham, Claire Coulter, Karl Cottenie, Shoshanah R. Jacobs

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Regional environmental pressure influences population differentiation in turbot (Scophthalmus maximus) von Vandamme, S. G, Maes, G. E, Raeymaekers, J. A. M, Cottenie, K, Imsland, A. K, Hellemans, B, Lacroix, G, Mac Aoidh, E, Martinsohn, J. T, Martínez, P, Robbens, J, Vilas, R, Volckaert, F. A. M

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Inscripciones sobre el cuerpo d'halmariano. Tatuajes, reflejos y fugas en Nirvana y La sombra del humo en el espejo von Cottenie, Sebastian

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