20122019
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International and National Collaboration Publications and projects within past five years.

Publications 2012 2019

Dominantly inherited distal nemaline/cap myopathy caused by a large deletion in the nebulin gene

Kiiski, K. J., Lehtokari, V-L., Vihola, A. K., Laitila, J. M., Huovinen, S., Sagath, L. J., Evilä, A. E., Paetau, A. E., Sewry, C. A., Hackman, P. B., Pelin, K. B., Wallgren-Pettersson, C. & Udd, B., Feb 2019, In : Neuromuscular Disorders. 29, 2, p. 97-107 11 p.

Research output: Contribution to journalArticleScientificpeer-review

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Interpreting Genetic Variants in Titin in Patients With Muscle Disorders

Savarese, M., Maggi, L., Vihola, A., Jonson, P. H., Tasca, G., Ruggiero, L., Bello, L., Magri, F., Giugliano, T., Torella, A., Evilä, A., Di Fruscio, G., Vanakker, O., Gibertini, S., Vercelli, L., Ruggieri, A., Antozzi, C., Luque, H., Janssens, S., Pasanisi, M. B. & 21 othersFiorillo, C., Raimondi, M., Ergoli, M., Politano, L., Bruno, C., Rubegni, A., Pane, M., Santorelli, F. M., Minetti, C., Angelini, C., De Bleecker, J., Moggio, M., Mongini, T., Comi, G. P., Santoro, L., Mercuri, E., Pegoraro, E., Mora, M., Hackman, P., Udd, B. & Nigro, V., May 2018, In : JAMA neurology. 75, 5, p. 557-565 9 p.

Research output: Contribution to journalArticleScientificpeer-review

Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families

Jonson, P. H., Palmio, J., Johari, M., Penttilä, S., Evila, A., Nelson, I., Bonne, G., Wiart, N., Meyer, V., Boland, A., Deleuze, J. -F., Masson, C., Stojkovic, T., Chapon, F., Romero, N. B., Sole, G., Ferrer, X., Ferreiro, A., Hackman, P., Richard, I. & 1 othersUdd, B., May 2018, In : European Journal of Neurology. 25, 5, p. 790-794 5 p.

Research output: Contribution to journalArticleScientificpeer-review

TIA1 variant drives myodegeneration in multisystem proteinopathy with SQSTM1 mutations

Lee, Y., Jonson, P. H., Sarparanta, J., Palmio, J., Sarkar, M., Vihola, A., Evilä, A., Suominen, T., Penttila, S., Savarese, M., Johari, M., Minot, M-C., Hilton-Jones, D., Maddison, P., Chinnery, P., Reimann, J., Kornblum, C., Kraya, T., Zierz, S., Sue, C. & 8 othersGoebel, H., Azfer, A., Ralston, S. H., Hackman, P., Bucelli, R. C., Taylor, J. P., Weihl, C. C. & Udd, B., 1 Mar 2018, In : Journal of Clinical Investigation. 128, 3, p. 1164-1177 14 p.

Research output: Contribution to journalArticleScientificpeer-review

A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy

Rossi, D., Palmio, J., Evila, A., Galli, L., Barone, V., Caldwell, T. A., Policke, R. A., Aldkheil, E., Berndsen, C. E., Wright, N. T., Malfatti, E., Brochier, G., Pierantozzi, E., Jordanova, A., Guergueltcheva, V., Romero, N. B., Hackman, P., Eymard, B., Udd, B. & Sorrentino, V., 26 Oct 2017, In : PLoS One. 12, 10, 21 p., 0186642.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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