
Daniel
Fernández Moreira
Publications (16) Daniel Fernández Moreira publications
2022
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Biofilms en instalaciones alimentarias militares: comparación de técnicas rápidas de vigilancia y verificación
Sanidad militar: revista de sanidad de las Fuerzas Armadas de España, Vol. 78, Núm. 2, pp. 89-94
2019
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Control microbiológico de las comidas servidas en centros de educación infantil del Ministerio de Defensa durante el año 2017
Sanidad militar: revista de sanidad de las Fuerzas Armadas de España, Vol. 75, Núm. 1, pp. 7-13
2018
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Omentectomy Prevents Metabolic Syndrome by Reducing Appetite and Body Weight in A Diet-Induced Obesity Rat Model
Scientific Reports, Vol. 8, Núm. 1
2017
2016
2015
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In vitro treatment of HepG2 cells with saturated fatty acids reproduces mitochondrial dysfunction found in nonalcoholic steatohepatitis
DMM Disease Models and Mechanisms, Vol. 8, Núm. 2, pp. 183-191
2014
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High-fat diet decreases activity of the oxidative phosphorylation complexes and causes nonalcoholic steatohepatitis in mice
DMM Disease Models and Mechanisms, Vol. 7, Núm. 11, pp. 1287-1296
2013
2011
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Melatonin improves mitochondrial respiratory chain activity and liver morphology in ob/ob mice
Journal of Pineal Research, Vol. 51, Núm. 1, pp. 113-123
2010
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Mitochondrial complex i subunits are decreased in murine nonalcoholic fatty liver disease: Implication of peroxynitrite
Journal of Proteome Research, Vol. 9, Núm. 5, pp. 2450-2459
2008
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Recovery of Francisella tularensis from soil samples by filtration and detection by real-time PCR and cELISA
J Environ Monit.
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Recovery of Francisella tularensis from soil samples by filtration and detection by real-time PCR and cELISA
Journal of Environmental Monitoring, Vol. 10, Núm. 3, pp. 362-369
2007
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X-linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy
Annals of Neurology, Vol. 61, Núm. 1, pp. 73-83
2006
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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
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Does the C34T mutation in AMPD1 alter exercise capacity in the elderly?
International Journal of Sports Medicine, Vol. 27, Núm. 6, pp. 425-435
2005
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Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 gene
Archives of Neurology, Vol. 62, Núm. 4, pp. 659-661