Yolanda Campos

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

Patrizia Amati‐Bonneau, Maria Lucia Valentino, Pascal Reynier et al. · Brain · 2007 · 510 citations · Full text

Opa1 Gene, Genome Instability, Mitochondrial Biogenesis +15

Complex I Defect in muscle from patients with Huntington's disease

Joaquı́n Arenas, Yolanda Campos, René Ribacoba et al. · Annals of Neurology · 1998 · 173 citations · Full text

Genetics, Muscle Morphology, Mitochondrial Myopathy +19

Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease

Yohei Kirino, Yu‐ichi Goto, Yolanda Campos et al. · Proceedings of the National Academy of Sciences · 2005 · 166 citations · Full text

Renal pathology in children with mitochondrial diseases

Elena Martín‐Hernández, M.T. García‐Silva, Julia Vara et al. · Pediatric Nephrology · 2005 · 108 citations

Glomerulonephritis, Urology, Mitochondrial Function +8

Plasma carnitine insufficiency and effectiveness of <scp>L</scp>‐carnitine therapy in patients with mitochondril myopathy

Yolanda Campos, Rosa Huertas, Gustavo Lorenzo et al. · Muscle & Nerve · 1993 · 97 citations