C. Cáceres-Marzal

Early mitochondrial dysfunction in an infant with Alexander disease.

C. Cáceres-Marzal, J. Vaquerizo, E. Galán, 2006, Pediatric neurology.

Methotrexate‐induced subacute neurotoxicity in a child with acute lymphoblastic leukemia carrying genetic polymorphisms related to folate homeostasis

G. Gervasini, C. Cáceres-Marzal, J. Vagace, 2011, American journal of hematology.

Central nervous system chemotoxicity during treatment of pediatric acute lymphoblastic leukemia/lymphoma.

G. Gervasini, C. Cáceres-Marzal, J. Vagace, 2012, Critical reviews in oncology/hematology.

Early response to idursulfase treatment in a 3 year-old boy affected of Hunter syndrome.

E. Galán-Gómez, J. Cardesa-García, C. Cáceres-Marzal, 2008, European journal of medical genetics.

Decreased corneal opacity and improved vision in a patient with mucopolysaccharidosis I (Hurler–Scheie) treated with enzyme replacement therapy (laronidase, Aldurazyme®)

C. Cáceres-Marzal, J. Vaquerizo, E. Galán, 2008, American journal of medical genetics. Part A.

[Idiopathic focal epilepsies in childhood. Diagnostic difficulties].

C. Cáceres-Marzal, J. Vaquerizo-Madrid, A. Guerrero-Rico, 2011, Revista de neurología (Ed. impresa).