Elisa Vaiani

4PUBLICATIONS
33CO-AUTHORS
Gene mappingPharmacogenomicsInfant and child healthGene and molecular therapy
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Publications (4)

|Jun 22, 2026
Compound Heterozygous Variants in the Phospholipase Gene PNPLA6 Cause Hypopituitarism and Vision Loss.

|Nov 19, 2025
A Novel POR G88S Mutation Causes Severe PORD and Establishes a Critical Pharmacogenomic Risk Profile.

Maria Natalia Rojas Velazquez, Jimena Lopez Dacal, Flemming S Jørgensen

|Aug 05, 2024
Characterization of a cohort of patients with hypercalcemia in a tertiary pediatric hospital.

Ana Feller, Mariana Aziz, Silvia Gil

|Mar 08, 2023
Treatment with TRIAC in pediatric patients with MCT8.

Natalia Gazek, Ana L Feller, Elisa Vaiani

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Frequent Collaborators

2 joint publications

Ana L Feller

2 joint publications

Natalia Pérez Garrido

2 joint publications

Marta Ciaccio

1 joint publications

Natalia Gazek