Natalia Pérez Garrido

6PUBLICATIONS
38CO-AUTHORS
Paediatrics not elsewhere classifiedPharmacogenomicsGene and molecular therapyInfant and child healthHaematological tumours
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Publications (6)

|Jan 06, 2026
Primary hyperparathyroidism in a child with tuberous sclerosis.

Ana Feller, Mariana Aziz, Silvia Gil

|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

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

Natalia Gazek, Ana L Feller, Elisa Vaiani

|Feb 28, 2022
Growth in height and body proportion from birth to adulthood in hereditary hypophosphatemic rickets: a retrospective cohort study.

M Del Pino, G L Viterbo, M A Arenas

|Jun 05, 2020
Testis formation in XX individuals resulting from novel pathogenic variants in Wilms' tumor 1 (WT1) gene.

Caroline Eozenou, Nitzan Gonen, Maria Sol Touzon

|Sep 26, 2018
Androgen Insensitivity Syndrome: Clinical Phenotype and Molecular Analysis in a Single Tertiary Center Cohort

Maria Sol Touzon, Natalia Perez Garrido, Roxana Marino

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Frequent Collaborators

5 joint publications

Roxana Marino

3 joint publications

Pablo Ramirez

2 joint publications

Gisela Viterbo

2 joint publications

Alicia Belgorosky