María Eugenia Rodríguez

2PUBLICATIONS
11CO-AUTHORS
Gene and molecular therapyAdolescent health
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Publications (2)

|Dec 24, 2025
MCT8 Deficiency in Two Brothers With a Novel Deletion Mutation in SLC16A2.

Andrea A Arcari, María Eugenia Rodríguez, Romina Armando

|Oct 31, 2024
Peripheral precocious puberty secondary to severe hypothyroidism.

Melina Gil, Florencia Martino, Gonzalo Besseghine

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