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Number of items: 4.

Maggi, L; Scoto, M; Cirak, S; Robb, S A; Klein, A; Lillis, S; Cullup, T; Feng, L; Manzur, A Y; Sewry, C A; Abbs, S; Jungbluth, H; Muntoni, F (2013). Congenital myopathies--clinical features and frequency of individual subtypes diagnosed over a 5-year period in the United Kingdom. Neuromuscular Disorders : NMD, 23(3):195-205.

Clement, E; Mercuri, E; Godfrey, C; Smith, J; Robb, S; Kinali, M; Straub, V; Bushby, K; Manzur, A; Talim, B; Cowan, F; Quinlivan, R; Klein, A; Longman, C; McWilliam, R; Topaloglu, H; Mein, R; Abbs, S; North, K; Barkovich, A J; Rutherford, M; Muntoni, F (2008). Brain involvement in muscular dystrophies with defective dystroglycan glycosylation. Annals of Neurology, 64(5):573-582.

Klein, A; Clement, E; Mercuri, E; Muntoni, F (2008). Differential diagnosis of congenital muscular dystrophies. European Journal of Paediatric Neurology, 12(5):371-377.

Budde, B S; Namavar, Y; Barth, P G; Poll-The, B T; Nürnberg, G; Becker, C; van Ruissen, F; Weterman, M A J; Fluiter, K; te Beek, E T; Aronica, E; van der Knaap, M S; Höhne, W; Toliat, M R; Crow, Y J; Steinling, M; Voit, T; Roelens, F; Brussel, W; Brockmann, K; Kyllerman, M; Boltshauser, E; Hammersen, G; Willemsen, M A; Basel-Vanagaite, L; Krägeloh-Mann, I; de Vries, L S; Sztriha, L; Muntoni, F; Ferrie, C D; Battini, R; Hennekam, R C M; Grillo, E; Beemer, F A; Stoets, L M E; Wollnik, B; Nürnberg, P; Baas, F (2008). tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia. Nature Genetics, 40(9):1113-1118.

This list was generated on Thu Apr 25 22:00:32 2019 CEST.