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Clinical Biochemistry|March 15, 2011
Folate analysis for the differential diagnosis of profound cerebrospinal fluid folate deficiencyAida Ormazábal, Belén Perez-Dueñas, Cristina Sierra, et al.Mitochondrion|October 28, 2008
Human mitochondrial variants influence on oxygen consumptionAna Marcuello, Diana Martínez-Redondo, Yahya Dahmani, et al.Biochemical and Biophysical Research Communications|April 23, 2005
In vitro transcription termination activity of the Drosophila mitochondrial DNA-binding protein DmTTFMarina Roberti, Patricio Fernandez-Silva, Paola Loguercio Polosa, et al.Mitochondrion|April 16, 2013
Coenzyme Q₁₀ deficiency in mitochondrial DNA depletion syndromesRaquel Montero, Manuela Grazina, Ester López-Gallardo, et al.Pediatric Research|May 7, 2004
Peripheral neuropathy with ataxia in childhood as a result of the G8363A mutation in mitochondrial DNAMercedes Pineda, Abelardo Solano, Rafael Artuch, et al.Journal of Applied Measurement|December 14, 2012
Development and validation of a questionnaire to evaluate attitudes toward family medicineFrancisco Escobar Rabadán, Jesús López-Torres Hidalgo, Julio Montoya Fernández, et al.Nature Structural & Molecular Biology|November 1, 2011
Human mitochondrial transcription factor A induces a U-turn structure in the light strand promoterAnna Rubio-Cosials, Jasmin F Sidow, Nereida Jiménez-Menéndez, et al.Cells|November 14, 2019
Uridine Prevents Negative Effects of OXPHOS Xenobiotics on Dopaminergic Neuronal DifferentiationEldris Iglesias, M Pilar Bayona-Bafaluy, Alba Pesini, et al.Neurogenetics|October 28, 2019
Infectious stress triggers a POLG-related mitochondrial diseasePaula Gaudó, Sonia Emperador, Nuria Garrido-Pérez, et al.Acta Neuropathologica|December 10, 2002
The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunctionKurenai Tanji, Josep Gamez, Carles Cervera, et al.Pageof 16