D. Esteban-Oliva

Long-term follow-up of a patient with primary hypomagnesaemia and secondary hypocalcaemia due to a novel TRPM6 mutation

M. Konrad, G. Pintos-Morell, D. Esteban-Oliva, 2009, European Journal of Pediatrics.

Transient type I 2nd-degree congenital atrioventricular block: a case report

Marc Roguera-Sopena, D. Esteban-Oliva, W. Coroleu-Lletget, 2022, Archivos de Cardiología de México.

Síndrome de Sotos: nueva mutación «sin sentido» del gen NSD1 que presenta cutis laxa neonatal

G. Pintos-Morell, P. Martín-Jiménez, D. Esteban-Oliva, 2011 .