Mitochondrial encephalomyopathy with coenzyme Q <sub>10</sub> deficiencyCláudia Ferreira da Rosa Sobreira, S. DiMauro, Michio Hirano et al.|Neurology|1997Cited by 196
Deficient Muscle Carnitine Transport in Primary Carnitine DeficiencyRoser Pons, Darryl C. De Vivo, Linda J. Addonizio et al.|Pediatric Research|1997Cited by 40
Dihydrorhodamine 123 identifies impaired mitochondrial respiratory chain function in cultured cells harboring mitochondrial DNA mutations.Cláudia Ferreira da Rosa Sobreira, Armand F. Miranda, Michael T. Davidson et al.|Journal of Histochemistry & Cytochemistry|1996Cited by 31
Long-Term Analysis of Differentiation in Human Myoblasts Repopulated with Mitochondria Harboring mtDNA MutationsCláudia Ferreira da Rosa Sobreira, Armand F. Miranda, Hye Jeong Park et al.|Biochemical and Biophysical Research Communications|1999Cited by 11