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Clinical Biochemistry
|
January 17, 2009
Screening for congenital disorders of glycosylation (CDG): transferrin HPLC versus isoelectric focusing (IEF)
Ester Quintana, Aleix Navarro-Sastre, José María Hernández-Pérez, et al.
Scientific Reports
|
July 6, 2023
Amelogenin peptide analyses reveal female leadership in Copper Age Iberia (c. 2900-2650 BC)
Marta Cintas-Peña, Miriam Luciañez-Triviño, Raquel Montero Artús, et al.
Antioxidants (Basel, Switzerland)
|
March 25, 2022
Technical Aspects of Coenzyme Q<sub>10</sub> Analysis: Validation of a New HPLC-ED Method
Abraham J Paredes-Fuentes, Clara Oliva, Raquel Montero, et al.
Mitochondrion
|
April 16, 2013
Coenzyme Q₁₀ deficiency in mitochondrial DNA depletion syndromes
Raquel Montero, Manuela Grazina, Ester López-Gallardo, et al.
Cerebellum (London, England)
|
September 25, 2010
Combined therapy with idebenone and deferiprone in patients with Friedreich's ataxia
Daniel Velasco-Sánchez, Asuncion Aracil, Raquel Montero, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 15, 2010
Coenzyme Q(10)-responsive ataxia: 2-year-treatment follow-up
Merce Pineda, Raquel Montero, Asuncion Aracil, et al.
Antioxidants (Basel, Switzerland)
|
October 17, 2020
Coenzyme Q<sub>10</sub> Treatment Monitoring in Different Human Biological Samples
Abraham J Paredes-Fuentes, Raquel Montero, Anna Codina, et al.
Journal of Inherited Metabolic Disease
|
June 19, 2013
Characterization of CoQ₁₀ biosynthesis in fibroblasts of patients with primary and secondary CoQ₁₀ deficiency
Nuria Buján, Angela Arias, Raquel Montero, et al.
Clinical Biochemistry
|
April 5, 2008
Analysis of coenzyme Q10 in muscle and fibroblasts for the diagnosis of CoQ10 deficiency syndromes
Raquel Montero, José Antonio Sánchez-Alcázar, Paz Briones, et al.
Journal of Inherited Metabolic Disease
|
March 26, 2017
Longitudinal volumetric and 2D assessment of cerebellar atrophy in a large cohort of children with phosphomannomutase deficiency (PMM2-CDG)
Víctor de Diego, Antonio F Martínez-Monseny, Jordi Muchart, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 55) with videos related to
Sort By:
Page
of 6
Clinical Biochemistry
|
January 17, 2009
Screening for congenital disorders of glycosylation (CDG): transferrin HPLC versus isoelectric focusing (IEF)
Ester Quintana, Aleix Navarro-Sastre, José María Hernández-Pérez, et al.
Scientific Reports
|
July 6, 2023
Amelogenin peptide analyses reveal female leadership in Copper Age Iberia (c. 2900-2650 BC)
Marta Cintas-Peña, Miriam Luciañez-Triviño, Raquel Montero Artús, et al.
Antioxidants (Basel, Switzerland)
|
March 25, 2022
Technical Aspects of Coenzyme Q<sub>10</sub> Analysis: Validation of a New HPLC-ED Method
Abraham J Paredes-Fuentes, Clara Oliva, Raquel Montero, et al.
Mitochondrion
|
April 16, 2013
Coenzyme Q₁₀ deficiency in mitochondrial DNA depletion syndromes
Raquel Montero, Manuela Grazina, Ester López-Gallardo, et al.
Cerebellum (London, England)
|
September 25, 2010
Combined therapy with idebenone and deferiprone in patients with Friedreich's ataxia
Daniel Velasco-Sánchez, Asuncion Aracil, Raquel Montero, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 15, 2010
Coenzyme Q(10)-responsive ataxia: 2-year-treatment follow-up
Merce Pineda, Raquel Montero, Asuncion Aracil, et al.
Antioxidants (Basel, Switzerland)
|
October 17, 2020
Coenzyme Q<sub>10</sub> Treatment Monitoring in Different Human Biological Samples
Abraham J Paredes-Fuentes, Raquel Montero, Anna Codina, et al.
Journal of Inherited Metabolic Disease
|
June 19, 2013
Characterization of CoQ₁₀ biosynthesis in fibroblasts of patients with primary and secondary CoQ₁₀ deficiency
Nuria Buján, Angela Arias, Raquel Montero, et al.
Clinical Biochemistry
|
April 5, 2008
Analysis of coenzyme Q10 in muscle and fibroblasts for the diagnosis of CoQ10 deficiency syndromes
Raquel Montero, José Antonio Sánchez-Alcázar, Paz Briones, et al.
Journal of Inherited Metabolic Disease
|
March 26, 2017
Longitudinal volumetric and 2D assessment of cerebellar atrophy in a large cohort of children with phosphomannomutase deficiency (PMM2-CDG)
Víctor de Diego, Antonio F Martínez-Monseny, Jordi Muchart, et al.
Page
of 6