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	1.	A new case of creatine transporter deficiency associated with mild clinical phenotype and a novel mutation in the SLC6A8 gene. [electronic resource] by Alcaide, Patricia Rodriguez-Pombo, Pilar Ruiz-Sala, Pedro Ferrer, Isaac Castro, Pedro Ruiz Martin, Yolanda Merinero, Begoña Ugarte, Magdalena Producer: 20100507 In: Developmental medicine and child neurology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Periventricular nodular heterotopia and dystonia due to an ARFGEF2 mutation. [electronic resource] by Bardón-Cancho, Eduardo Jesús Muñoz-Jiménez, Lucía Vázquez-López, María Ruíz-Martín, Yolanda García-Morín, Marina Barredo-Valderrama, Estíbaliz Producer: 20160331 In: Pediatric neurology vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Acute hemicerebellitis in children: case report and review of literature. [electronic resource] by Rodríguez-Cruz, Pedro M Janet-Signoret, Sophie Miranda-Herrero, María C Barredo-Valderrama, Estíbaliz Vázquez-López, María Ruiz-Martín, Yolanda Castro-De Castro, Pedro Producer: 20140403 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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