Romina I Armando

4PUBLICATIONS
58CO-AUTHORS
Neurology and neuromuscular diseasesGene and molecular therapyInfant and child healthGene expression (incl. microarray and other genome-wide approaches)
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Publications (4)

|Jul 21, 2026
[Neurofibromatosis Type 1 in Pediatrics: Recommendations for Diagnosis and Management].

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

Andrea A Arcari, María Eugenia Rodríguez, Romina Armando

|Nov 14, 2022
[Late diagnosis of spinal muscular atrophy in a patient with Down syndrome].

Magalí Squitín Tasende, Micaela Pauni, Romina Armando

|Sep 13, 2020
Implementation of chromosomal microarrays in a cohort of patients with intellectual disability at the Argentinean public health system.

Lucía Daniela Espeche, Andrea Paula Solari, María Ángeles Mori

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Frequent Collaborators

2 joint publications

María F Maccario

1 joint publications

Lucía Daniela Espeche

1 joint publications

Rubén Martín Arenas

1 joint publications

María Palomares