María Barreda‐Sánchez

EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population

María Carmen Martínez-Romero, María Juliana Ballesta‐Martínez, Vanesa López‐González et al. · Orphanet Journal of Rare Diseases · 2019 · 43 citations · Full text

Health impact of acute intermittent porphyria in latent and non-recurrent attacks patients

Juan Buendía-Martínez, María Barreda‐Sánchez, Lidya Rodríguez-Peña et al. · Orphanet Journal of Rare Diseases · 2021 · 36 citations · Full text

Measurement of serum PON-3 concentration: method evaluation, reference values, and influence of genotypes in a population-based study

Gerard Aragonès, Marta Guardiola, María Barreda‐Sánchez et al. · Journal of Lipid Research · 2011 · 29 citations · Full text

High penetrance of acute intermittent porphyria in a Spanish founder mutation population and CYP2D6 genotype as a susceptibility factor

María Barreda‐Sánchez, Juan Buendía-Martínez, Guillermo Glover-López et al. · Orphanet Journal of Rare Diseases · 2019 · 27 citations · Full text

Presence of rare potential pathogenic variants in subjects under 65 years old with very severe or fatal COVID-19

Rosario López‐Rodríguez, Marta Del Pozo‐Valero, Marta Cortón et al. · Scientific Reports · 2022 · 10 citations · Full text