Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21.

Por van der Kooi, A J, van Meegen, M, Ledderhof, T M, McNally, E M, de Visser, M, Bolhuis, P A
Publicado em 1997

The heart in limb girdle muscular dystrophy

Por van der Kooi, A J, de Voogt, W G, Barth, P, Busch, H, Jennekens, F, Jongen, P, de Visser, M
Publicado em 1998

Extension of the clinical range of facioscapulohumeral dystrophy: report of six cases

Por van der Kooi, A J, Visser, M, Rosenberg, N, van den Berg-Vos, R, Wokke, J, Bakker, E, de Visser, M
Publicado em 2000

Recurrent and founder mutations in the Netherlands: the cardiac phenotype of DES founder mutations p.S13F and p.N342D

Por van Spaendonck-Zwarts, K. Y., van der Kooi, A. J., van den Berg, M. P., Ippel, E. F., Boven, L. G., Yee, W.-C., van den Wijngaard, A., Brusse, E., Hoogendijk, J. E., Doevendans, P. A., de Visser, M., Jongbloed, J. D. H., van Tintelen, J. P.
Publicado em 2012

Calpainopathy-a survey of mutations and polymorphisms.

Por Richard, I, Roudaut, C, Saenz, A, Pogue, R, Grimbergen, J E, Anderson, L V, Beley, C, Cobo, A M, de Diego, C, Eymard, B, Gallano, P, Ginjaar, H B, Lasa, A, Pollitt, C, Topaloglu, H, Urtizberea, J A, de Visser, M, van der Kooi, A, Bushby, K, Bakker, E, Lopez de Munain, A, Fardeau, M, Beckmann, J S
Publicado em 1999