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Metyrapone as treatment in the neonatal McCune-Albright syndrome.
de Mingo C, Brugada M, León S, Moreno F, Vila N, Palanques-Pastor T, Poveda JL, Orti C, García-Robles A. de Mingo C, et al. J Pediatr Endocrinol Metab. 2020 Jul 22:/j/jpem.ahead-of-print/jpem-2020-0036/jpem-2020-0036.xml. doi: 10.1515/jpem-2020-0036. Online ahead of print. J Pediatr Endocrinol Metab. 2020. PMID: 32697759
Familial hyperaldosteronism type III a novel case and review of literature.
Pons Fernández N, Moreno F, Morata J, Moriano A, León S, De Mingo C, Zuñiga Á, Calvo F. Pons Fernández N, et al. Among authors: de mingo c. Rev Endocr Metab Disord. 2019 Mar;20(1):27-36. doi: 10.1007/s11154-018-9481-0. Rev Endocr Metab Disord. 2019. PMID: 30569443 Review.
GATA4 Variants in Individuals With a 46,XY Disorder of Sex Development (DSD) May or May Not Be Associated With Cardiac Defects Depending on Second Hits in Other DSD Genes.
Martinez de LaPiscina I, de Mingo C, Riedl S, Rodriguez A, Pandey AV, Fernández-Cancio M, Camats N, Sinclair A, Castaño L, Audi L, Flück CE. Martinez de LaPiscina I, et al. Among authors: de mingo c. Front Endocrinol (Lausanne). 2018 Apr 4;9:142. doi: 10.3389/fendo.2018.00142. eCollection 2018. Front Endocrinol (Lausanne). 2018. PMID: 29670578 Free PMC article.