Search Results - "Gallano Petit, M P"

Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease 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

“…Steinert's disease or myotonic dystrophy type 1 (MD1), (OMIM 160900), is the most prevalent myopathy in adults. It is a multisystemic disorder with dysfunction…”
Get full text

Clinical practice guidelines for the diagnosis and management of Charcot-Marie-Tooth disease by Sivera Mascaró, R, García Sobrino, T, Horga Hernández, A, Pelayo Negro, A L, Alonso Jiménez, A, Antelo Pose, A, Calabria Gallego, M D, Casasnovas, C, Cemillán Fernández, C A, Esteban Pérez, J, Fenollar Cortés, M, Frasquet Carrera, M, Gallano Petit, M P, Giménez Muñoz, A, Gutiérrez Gutiérrez, G, Gutiérrez Martínez, A, Juntas Morales, R, Ciano-Petersen, N L, Martínez Ulloa, P L, Mederer Hengstl, S, Millet Sancho, E, Navacerrada Barrero, F J, Navarrete Faubel, F E, Pardo Fernández, J, Pascual Pascual, S I, Pérez Lucas, J, Pino Mínguez, J, Rabasa Pérez, M, Sánchez González, M, Sotoca, J, Rodríguez Santiago, B, Rojas García, R, Turon-Sans, J, Vicent Carsí, V, Sevilla Mantecón, T

“…Charcot-Marie-Tooth disease (CMT) is classified according to neurophysiological and histological findings, the inheritance pattern, and the underlying genetic…”
Get full text