Publications in collaboration with researchers from Hospital Universitario La Paz (9)

2006

  1. Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population

    Archives of Neurology, Vol. 63, Núm. 1, pp. 107-111

2005

  1. Mitochondrial respiratory chain diseases. Evaluation and variability in 52 patients

    Revista de Neurologia, Vol. 41, Núm. 8, pp. 449-454

2003

  1. Prevalence and progression of mitochondrial diseases: A study of 50 patients

    Muscle and Nerve, Vol. 28, Núm. 6, pp. 690-695

1998

  1. Prospective study of serum and urinary nitrate levels in patients with systemic lupus erythematosus

    British Journal of Rheumatology, Vol. 37, Núm. 9, pp. 972-977

1997

  1. Gene dosage effect in one family with myoclonic epilepsy and ragged-red fibers (MERRF)

    Acta Neurologica Scandinavica, Vol. 96, Núm. 2, pp. 65-71

1994

  1. ABORDAJES CLINICO Y PARACLINICO DE LAS ENFERMEDADES MITOCONDRIALES. ESTUDIO DE 15 CASOS

    Neurologia, Vol. 9, Núm. 8, pp. 324-336

  2. Benign mitochondrial myopathy with decreased succinate cytochrome C reductase activity

    Acta Neurologica Scandinavica, Vol. 90, Núm. 4, pp. 281-284

  3. DEFICIENCIA DE LOS COMPLEJOS I Y IV DE LA CADENA RESPIRATORIA MITOCONDRIAL EN DOS HERMANOS CON ACIDURIA GLUTARICA TIPO I

    Neurologia, Vol. 9, Núm. 7, pp. 303-306

  4. POLIODISTROFIA CEREBRAL PROGRESIVA INFANTIL (SINDROME DE ALPERS)

    Anales Espanoles de Pediatria, Vol. 40, Núm. 3, pp. 232-234