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	1.	Comparison of predose vs 2-h postdose blood metabolites/cyclosporine ratios in kidney and liver transplant patients. [electronic resource] by Fernández-Marmiesse, A Hermida, J Tutor, J C Producer: 20001130 In: Clinical biochemistry vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Paucisymptomatic hyperCKemia due to a mutation in the ANO5 gene. [electronic resource] by Alcahut-Rodríguez, C Díaz-Maroto, I Fernández-Marmiesse, A García-García, J Producer: 20210908 In: Neurologia vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	[De novo sporadic mutation in the KCND3 gene in a patient with early onset chronic ataxia]. [electronic resource] by Carrasco-Marina, M L Quijada-Fraile, P Fernandez-Marmiesse, A Gutierrez-Cruz, N Martin-Del Valle, F Producer: 20200820 In: Revista de neurologia vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Molecular epidemiology and BH4-responsiveness in patients with phenylalanine hydroxylase deficiency from Galicia region of Spain. [electronic resource] by Couce, M L Bóveda, M D Fernández-Marmiesse, A Mirás, A Pérez, B Desviat, L R Fraga, J M Producer: 20130708 In: Gene vol. 521 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Evolution of maple syrup urine disease in patients diagnosed by newborn screening versus late diagnosis. [electronic resource] by Couce, M L Ramos, F Bueno, M A Díaz, J Meavilla, S Bóveda, M D Fernández-Marmiesse, A García-Cazorla, A Producer: 20160523 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	[18F-fluoro-L-DOPA PET-CT imaging combined with genetic analysis for optimal classification and treatment in a child with severe congenital hyperinsulinism]. [electronic resource] by Arbizu Lostao, J Fernández-Marmiesse, A Garrastachu Zumarrán, P Martino Casado, E Azcona San Julián, C Carracedo, A Richter Echevarría, J A Producer: 20080909 In: Anales de pediatria (Barcelona, Spain : 2003) vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Septo-optic dysplasia caused by a novel FLNA splice site mutation: a case report. [electronic resource] by Fernández-Marmiesse, A Pérez-Poyato, M S Fontalba, A Marco de Lucas, E Martínez, M T Cabero Pérez, M J Couce, M L Producer: 20191202 In: BMC medical genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)