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	1.	Acute striatal necrosis in hemiplegic migraine with de novo CACNA1A mutation. [electronic resource] by Carreño, Oriel García-Silva, María Teresa García-Campos, Óscar Martínez-de Aragón, Ana Cormand, Bru Macaya, Alfons Producer: 20120914 In: Headache vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Uniparental disomy as a cause of spinal muscular atrophy and progressive myoclonic epilepsy: phenotypic homogeneity due to the homozygous c.125C>T mutation in ASAH1. [electronic resource] by Giráldez, Beatriz G Guerrero-López, Rosa Ortega-Moreno, Laura Verdú, Alfonso Carrascosa-Romero, M Carmen García-Campos, Óscar García-Muñozguren, Susana Pardal-Fernández, José Manuel Serratosa, José M Producer: 20151123 In: Neuromuscular disorders : NMD vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening program. [electronic resource] by Navarrete, Rosa Leal, Fátima Vega, Ana I Morais-López, Ana Garcia-Silva, María Teresa Martín-Hernández, Elena Quijada-Fraile, Pilar Bergua, Ana Vives, Inmaculada García-Jiménez, Inmaculada Yahyaoui, Raquel Pedrón-Giner, Consuelo Belanger-Quintana, Amaya Stanescu, Sinziana Cañedo, Elvira García-Campos, Oscar Bueno-Delgado, María Delgado-Pecellín, Carmen Vitoria, Isidro Rausell, María Dolores Balmaseda, Elena Couce, Mari Luz Desviat, Lourdes R Merinero, Begoña Rodríguez-Pombo, Pilar Ugarte, Magdalena Pérez-Cerdá, Celia Pérez, Belén Producer: 20200615 In: European journal of human genetics : EJHG vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)