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Biomedica : Revista Del Instituto Nacional De Salud|April 17, 2003
[Evaluation as a function of granulocytes in hyperimmunoglobulinemia E syndrome with recurrent infections]Carlos Julio Montoya, Juan Alvaro López, Paula Andrea Velilla, et al.
Nucleic Acids Research|August 22, 2003
Import of mitochondrial transcription factor A (TFAM) into rat liver mitochondria stimulates transcription of mitochondrial DNAHeike L Garstka, Wolfgang E Schmitt, Jeanette Schultz, et al.
Investigacion Clinica|February 10, 2011
Autism associated to a deficiency of complexes III and IV of the mitochondrial respiratory chainJosé Guevara-Campos, Lucía González-Guevara, Paz Briones, et al.
Metabolic Brain Disease|April 25, 2013
Stressed cybrids model demyelinated axons in multiple sclerosisLaura Llobet, Aurora Gómez-Durán, Ruth Iceta, et al.
The European Journal of General Practice|April 3, 2019
At what stage in the undergraduate curriculum is it best to train in family medicine? A study from two medical schools in SpainMónica López-García, María Candelaria Ayuso-Raya, Jesús López-Torres-Hidalgo, et al.
Human Immunology|June 2, 2009
Frequency and function of circulating invariant NKT cells in autoimmune diabetes mellitus and thyroid diseases in Colombian patientsAlejandro Roman-Gonzalez, Maria Eugenia Moreno, Juan Manuel Alfaro, et al.
Journal of Pediatric Genetics|November 6, 2019
Mitochondrial m.13513G>A Point Mutation in ND5 in a 16-Year-Old Man with Leber Hereditary Optic Neuropathy Detected by Next-Generation SequencingDaniel Vázquez-Justes, Lidia Carreño-Gago, Elena García-Arumi, et al.
Drug Discovery Today|July 18, 2015
Can folic acid have a role in mitochondrial disorders?Aida Ormazabal, Mercedes Casado, Marta Molero-Luis, et al.
Journal of Assisted Reproduction and Genetics|January 26, 2023
m.4216 T > C polymorphism in JT cluster determines a lower pregnancy rate in response to controlled ovarian stimulation treatmentBelén Monge-Ochoa, Luis Montoro, Julio Montoya, et al.
Mutation Research. Reviews in Mutation Research|December 19, 2020
Genetic aspects of the oxidative phosphorylation dysfunction in dilated cardiomyopathyM Pilar Bayona-Bafaluy, Eldris Iglesias, Ester López-Gallardo, et al.
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