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	1.	New CTSA mutation in early infantile galactosialidosis. [electronic resource] by Aldámiz-Echevarría, Luis Couce, M Luz Villate, Olatz Fernández-Marmiesse, Ana Piñán, M Ángeles Producer: 20181024 In: Pediatrics international : official journal of the Japan Pediatric Society vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Development of electrospray ionization tandem mass spectrometry methods for the study of a high number of urine markers of inborn errors of metabolism. [electronic resource] by Rebollido-Fernandez, M Maira Castiñeiras, Daisy E Bóveda, M Dolores Couce, M Luz Cocho, José A Fraga, Jose M Producer: 20121023 In: Rapid communications in mass spectrometry : RCM vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Congenital hypothyroidism with neurological and respiratory alterations: a case detected using a variable diagnostic threshold for TSH. [electronic resource] by Barreiro, Jesús Alonso-Fernández, Jóse Ramón Castro-Feijoo, Lidia Colón, Cristóbal Cabanas, Paloma Heredia, Claudia Castaño, Luis Antonio Gómez-Lado, Carmen Couce, M Luz Pombo, Manuel Producer: 20120411 In: Journal of clinical research in pediatric endocrinology vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	[Epidemiological study of the metabolic diseases with homocystinuria in Spain]. [electronic resource] by García-Jiménez, M C Baldellou, A García-Silva, M T Dalmau-Serra, J García-Cazorla, A Gómez-López, L Giner, C Pedrón Luengo, O Alonso Peña Quintana, L Couce, M Luz Martínez-Pardo, M Lambruschini, N Producer: 20120723 In: Anales de pediatria (Barcelona, Spain : 2003) vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	[Transition process from paediatric to adult care in patients with inborn errors of metabolism. Consensus statement]. [electronic resource] by Pérez-López, Jordi Ceberio-Hualde, Leticia García Morillo, José Salvador Grau-Junyent, Josep M Hermida Ameijeiras, Álvaro López-Rodríguez, Mónica Morales-Conejo, Montserrat Nava Mateos, Juan José Aldámiz Echevarri Azuara, Luis José Campistol, Jaume Couce, M Luz García-Silva, María Teresa González Gutiérrez-Solana, Luis Del Toro, Mireia Producer: 20171122 In: Medicina clinica vol. 147 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Clinical and molecular diagnosis of non-phosphomannomutase 2 N-linked congenital disorders of glycosylation in Spain. [electronic resource] by Medrano, Celia Vega, Ana Navarrete, Rosa Ecay, M Jesús Calvo, Rocío Pascual, Samuel Ignacio Ruiz-Pons, Mónica Toledo, Laura García-Jiménez, Inmaculada Arroyo, Ignacio Campo, Andrea Couce, M Luz Domingo-Jiménez, M Rosario García-Silva, M Teresa González-Gutiérrez-Solana, Luis Hierro, Loreto Martín-Hernández, Elena Martínez-Pardo, Mercedes Roldán, Susana Tomás, Miguel Cabrera, Jose C Mártinez-Bugallo, Francisco Martín-Viota, Lucía Vitoria-Miñana, Isidro Lefeber, Dirk J Girós, M Luisa Serrano Gimare, Mercedes Ugarte, Magdalena Pérez, Belén Pérez-Cerdá, Celia Producer: 20200706 In: Clinical genetics vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)