Contribution of molecular analyses to the estimation of the risk of congenital myotonic dystrophy.

Por Cobo, A M, Poza, J J, Martorell, L, López de Munain, A, Emparanza, J I, Baiget, M
Publicado em 1995

Impaired calcium calmodulin kinase signaling and muscle adaptation response in the absence of calpain 3

Por Kramerova, I., Kudryashova, E., Ermolova, N., Saenz, A., Jaka, O., López de Munain, A., Spencer, M.J.
Publicado em 2012

Expansion of the myotonic dystrophy gene in Italian and Spanish patients.

Por Melchionda, S, Cobo, A, Gennarelli, M, Martorell, L, Fattorini, C, Baiget, M, Lopez de Munain, A, Johnson, K, Shelbourne, P, Novelli, G
Publicado em 1992

Influence of the sex of the transmitting grandparent in congenital myotonic dystrophy.

Por López de Munain, A, Cobo, A M, Poza, J J, Navarrete, D, Martorell, L, Palau, F, Emparanza, J I, Baiget, M
Publicado em 1995

Frequency of myotonic dystrophy gene carriers in cataract patients.

Por Cobo, A M, Poza, J J, Blanco, A, López de Munain, A, Saénz, A, Azpitarte, M, Marchessi, J, Martí Massó, J F
Publicado em 1996

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