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	1.	Early mitochondrial dysfunction in an infant with Alexander disease. [electronic resource] by Cáceres-Marzal, Cristina Vaquerizo, Julián Galán, Enrique Fernández, Santiago Producer: 20061204 In: Pediatric neurology vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Decreased corneal opacity and improved vision in a patient with mucopolysaccharidosis I (Hurler-Scheie) treated with enzyme replacement therapy (laronidase, Aldurazyme). [electronic resource] by Cáceres-Marzal, Cristina García-Reymundo, Mercedes Solana, Jorge de Arévalo, Bernardo Vaquerizo, Julián Galán, Enrique Producer: 20080820 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A fatal mitochondrial disease is associated with defective NFU1 function in the maturation of a subset of mitochondrial Fe-S proteins. [electronic resource] by Navarro-Sastre, Aleix Tort, Frederic Stehling, Oliver Uzarska, Marta A Arranz, José Antonio Del Toro, Mireia Labayru, M Teresa Landa, Joseba Font, Aida Garcia-Villoria, Judit Merinero, Begoña Ugarte, Magdalena Gutierrez-Solana, Luis Gonzalez Campistol, Jaume Garcia-Cazorla, Angels Vaquerizo, Julian Riudor, Encarnació Briones, Paz Elpeleg, Orly Ribes, Antonia Lill, Roland Producer: 20120221 In: American journal of human genetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)