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Frontiers in Endocrinology|March 14, 2022
Congenital Adrenal Hyperplasia and Ehlers-Danlos SyndromeRoxana Marino, Angélica Moresco, Natalia Perez Garrido, et al.
Medicina|May 23, 2020
Molecular analysis of the CYP21A2 gene in dried blood spot samplesSilvia Marino, Natalia Perez Garrido, Pablo Ramírez, et al.
Medicina|August 28, 2021
Growth hormone receptor gene polymorphism. Spontaneous catch up growth in small for gestational age patientsNatalia Perez Garrido, Matías Pujana, Malena Berger, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 19, 2021
Hereditary hypophosphatemic rickets and craniosynostosisMaría Alejandra Arenas, Sebastián Jaimovich, Natalia Perez Garrido, et al.
Molecular and Cellular Endocrinology|September 28, 2016
DNA methylation is not involved in specific down-regulation of HSD3B2, NR4A1 and RARB genes in androgen-secreting cells of human adrenal cortexMaría Sonia Baquedano, Natalia Perez Garrido, Javier Goñi, et al.
Journal of Clinical Research in Pediatric Endocrinology|September 26, 2018
Androgen Insensitivity Syndrome: Clinical Phenotype and Molecular Analysis in a Single Tertiary Center CohortMaria Sol Touzon, Natalia Perez Garrido, Roxana Marino, et al.
The Journal of Clinical Endocrinology and Metabolism|October 17, 2014
A novel missense mutation in the HSD3B2 gene, underlying nonsalt-wasting congenital adrenal hyperplasia. new insight into the structure-function relationships of 3β-hydroxysteroid dehidrogenase type IIMaría Sonia Baquedano, Marta Ciaccio, Roxana Marino, et al.
Hormone Research in Paediatrics|November 7, 2025
Clinical Impact of Genetic Alterations in Pediatric Papillary Thyroid Carcinoma: A Next-Generation Sequencing Study from ArgentinaNoelia Dujovne, Natalia Gazek, Elisa Vaiani, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 2021
Ehlers-Danlos Syndrome: Molecular and Clinical Characterization of TNXA/TNXB Chimeras in Congenital Adrenal HyperplasiaRoxana Marino, Natalia Perez Garrido, Pablo Ramirez, et al.
Hormone Research in Paediatrics|August 18, 2015
An Intron 9 CYP19 Gene Variant (IVS9+5G>A), Present in an Aromatase-Deficient Girl, Affects Normal Splicing and Is Also Present in Normal Human Steroidogenic TissuesNora Saraco, Suzana Nesi-Franca, Romina Sainz, et al.
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