C. Busquets

Cohort Profile: Design and methods of the PREDIMED-Plus randomized trial

Miguel Ángel Martínez‐González, Pilar Buil‐Cosiales, Dolores Corella et al. · International Journal of Epidemiology · 2018 · 327 citations · Full text

Medicine, Health Promotion, Nutrition +17

Biochemical and molecular studies in 26 Spanish patients with congenital disorder of glycosylation type Ia

P. Briones, Marta Vilaseca, Els Schollen et al. · Journal of Inherited Metabolic Disease · 2003 · 51 citations

Life Sciences, Biochemistry, Molecular Biology +14

Mutational study in the<i>PDHA1</i>gene of 40 patients suspected of pyruvate dehydrogenase complex deficiency

Ester Quintana, Laura Gort, C. Busquets et al. · Clinical Genetics · 2009 · 41 citations

Life Sciences, Genetics, Molecular Genetics +16

Compound heterozygosity in the glutaryl‐CoA dehydrogenase gene with R227P mutation in one allele is associated with no or very low free glutarate excretion

E. Christensen, Antònia Ribes, C. Busquets et al. · Journal of Inherited Metabolic Disease · 1997 · 36 citations

Life Sciences, Genetics, Molecular Genetics +9

Glutaric aciduria type I with high residual glutaryl‐CoA dehydrogenase activity

Manuel Pineda, Antònia Ribes, C. Busquets et al. · Developmental Medicine & Child Neurology · 1998 · 25 citations · Full text

Life Sciences, Neurology, Neuroscience +9