Publicacións nas que colabora con Yolanda Campos Martín (10)

2003

  1. Lipomatosis simétrica múltiple asociada a polineuropatía, atrofia de cerebelo y citopatía mitocondrial

    Revista de Neurologia, Vol. 36, Núm. 11, pp. 1026-1029

2001

  1. Congenital hydranencephalic-hydrocephalic syndrome with proliferative vasculopathy: A possible relation with mitochondrial dysfunction

    Journal of Child Neurology, Vol. 16, Núm. 11, pp. 858-862

  2. Mitochondrial myopathy, cardiomyopathy and psychiatric illness in a Spanish family harbouring the mtDNA 3303C>T mutation

    Journal of Inherited Metabolic Disease, Vol. 24, Núm. 6, pp. 685-687

2000

  1. Benign congenital myopathy associated with a partial deficiency of complexes I and III of the mitochondrial respiratory chain

    Revista de neurologia, Vol. 31, Núm. 9, pp. 838-841

  2. Mitochondrial encephalomyopathies

    Revista de Neurologia

1999

  1. Congenital hydranencephalic-hydrocephalic syndrome associated with mitochondrial dysfunction

    Journal of Child Neurology, Vol. 14, Núm. 2, pp. 131-135

1998

  1. Clinical heterogeneity associated with mitochondrial DNA depletion in muscle

    Neuromuscular Disorders, Vol. 8, Núm. 8, pp. 568-573

  2. Congenital ocular motor apraxia associated with myopathy, external hydrocephalus and NADH dehydrogenase deficiency

    Brain and Development, Vol. 20, Núm. 3, pp. 175-178

  3. Erratum: Congenital ocular motor apraxia associated with myopathy, external hydrocephalus and NADH dehydrogenase deficiency (Brain and Development 20 (1998) (175-178) PII: S0387760498000096)

    Brain and Development

1996

  1. Leber's congenital amaurosis associated with mitochondrial dysfunction

    Journal of Child Neurology, Vol. 11, Núm. 2, pp. 108-111