M. Martí-Herrero

Natural History, Outcome, and Treatment Efficacy in Children and Adults with Glutaryl-CoA Dehydrogenase Deficiency

A. Ribes, M. Wajner, B. Merinero, 2006, Pediatric Research.

First experience of enzyme replacement therapy with idursulfase in Spanish patients with Hunter syndrome under 5 years of age: case observations from the Hunter Outcome Survey (HOS).

G. Pintos-Morell, R. Cancho-Candela, M. Martí-Herrero, 2010, European journal of medical genetics.

[Moebius syndrome. Three different forms of presentation].

M. Martí-Herrero, L. Toledo, D. Bonnet, 1998, Revista de neurologia.