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	21.	Myopathy with lobulated muscle fibers: evidence for heterogeneous etiology and clinical presentation. [electronic resource] by Figarella-Branger, D El-Dassouki, M Saenz, A Cobo, A M Malzac, P Tong, S Cassotte, E Azulay, J P Pouget, J Pellissier, J F Producer: 20020301 In: Neuromuscular disorders : NMD vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	[Alterations in functional proteins. Calpaine-3 deficiency]. [electronic resource] by López de Munain, A Urtasun, A Poza, J J Ruiz, J Sáenz, A Cobo, A M Lasa, A Gallano, P Baiget, M Martí-Massó, J F Producer: 19990608 In: Revista de neurologia vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	23.	Cognitive/personality pattern and triplet expansion size in adult myotonic dystrophy type 1 (DM1): CTG repeats, cognition and personality in DM1. [electronic resource] by Sistiaga, A Urreta, I Jodar, M Cobo, A M Emparanza, J Otaegui, D Poza, J J Merino, J J Imaz, H Martí-Massó, J F López de Munain, A Producer: 20100625 In: Psychological medicine vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Autosomal dominant nocturnal frontal lobe epilepsy in a Spanish family with a Ser252Phe mutation in the CHRNA4 gene. [electronic resource] by Sáenz, A Galán, J Caloustian, C Lorenzo, F Márquez, C Rodríguez, N Jiménez, M D Poza, J J Cobo, A M Grid, D Prud'homme, J F López de Munain, A Producer: 19990915 In: Archives of neurology vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q. [electronic resource] by Poza, J J Sáenz, A Martínez-Gil, A Cheron, N Cobo, A M Urtasun, M Martí-Massó, J F Grid, D Beckmann, J S Prud'homme, J F López de Munain, A Producer: 19990329 In: Annals of neurology vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain). [electronic resource] by Urtasun, M Sáenz, A Roudaut, C Poza, J J Urtizberea, J A Cobo, A M Richard, I García Bragado, F Leturcq, F Kaplan, J C Martí Massó, J F Beckmann, J S López de Munain, A Producer: 19981021 In: Brain : a journal of neurology vol. 121 ( Pt 9) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Aplasia cutis congenita with dystrophic epidermolysis bullosa: clinical and mutational study. [electronic resource] by Chiaverini, C Charlesworth, A Fernandez, A Barbarot, S Bessis, D Bodemer, C Bursztejn, A-C Cobo, A-M Del Rio, M D'Incan, M Labrèze, C Langlet, C Mazereeuw, J Miquel, J Vabres, P Meneguzzi, G Lacour, J-P Producer: 20150528 In: The British journal of dermatology vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome. [electronic resource] by Donaldson, M R Jensen, J L Tristani-Firouzi, M Tawil, R Bendahhou, S Suarez, W A Cobo, A M Poza, J J Behr, E Wagstaff, J Szepetowski, P Pereira, S Mozaffar, T Escolar, D M Fu, Y-H Ptácek, L J Producer: 20040224 In: Neurology vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene. [electronic resource] by Sáenz, A Leturcq, F Cobo, A M Poza, J J Ferrer, X Otaegui, D Camaño, P Urtasun, M Vílchez, J Gutiérrez-Rivas, E Emparanza, J Merlini, L Paisán, C Goicoechea, M Blázquez, L Eymard, B Lochmuller, H Walter, M Bonnemann, C Figarella-Branger, D Kaplan, J C Urtizberea, J A Martí-Massó, J F López de Munain, A Producer: 20050420 In: Brain : a journal of neurology vol. 128 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Calpainopathy-a survey of mutations and polymorphisms. [electronic resource] by 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 Producer: 19990624 In: American journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease. [electronic resource] by Gutiérrez Gutiérrez, G Díaz-Manera, J Almendrote, M Azriel, S Eulalio Bárcena, J Cabezudo García, P Camacho Salas, A Casanova Rodríguez, C Cobo, A M Díaz Guardiola, P Fernández-Torrón, R Gallano Petit, M P García Pavía, P Gómez Gallego, M Gutiérrez Martínez, A J Jericó, I Kapetanovic García, S López de Munaín Arregui, A Martorell, L Morís de la Tassa, G Moreno Zabaleta, R Muñoz-Blanco, J L Olivar Roldán, J Pascual Pascual, S I Peinado Peinado, R Pérez, H Poza Aldea, J J Rabasa, M Ramos, A Rosado Bartolomé, A Rubio Pérez, M Á Urtizberea, J A Zapata-Wainberg, G Gutiérrez-Rivas, E Producer: 20210208 In: Neurologia vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)