Viviana Dalamón

9PUBLICATIONS
33CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Phonetics and speech scienceGene mappingOrganometallic chemistryCellular nervous system
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Publications (9)

|Dec 12, 2024
In silico and in vivo analyses of a novel variant in MYO6 identified in a family with postlingual non-syndromic hearing loss from Argentina.

Paula I Buonfiglio, Carlos D Bruque, Lucía Salatino

|Nov 27, 2024
Comment on De Rosa et al. Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin America. Genes 2024, 15, 178.

Ana Belén Elgoyhen, Paula Inés Buonfiglio, Viviana Dalamón

|Sep 28, 2024
Comprehensive Approach for the Genetic Diagnosis of Patients with Waardenburg Syndrome.

Paula Inés Buonfiglio, Agustín Izquierdo, Mariela Vanina Pace

|Aug 26, 2024
Co-release of GABA and ACh from medial olivocochlear neurons fine tunes cochlear efferent inhibition.

Tais Castagnola, Valeria C Castagna, Siân R Kitcher

|Aug 09, 2024
Key role of the TM2-TM3 loop in calcium potentiation of the α9α10 nicotinic acetylcholine receptor.

Sofia L Gallino, Lucía Agüero, Juan C Boffi

|Nov 25, 2023
Novel Pathogenic Variants in the Gene Encoding Stereocilin (STRC) Causing Non-Syndromic Moderate Hearing Loss in Spanish and Argentinean Subjects.

María Domínguez-Ruiz, Laura Ruiz-Palmero, Paula I Buonfiglio

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Frequent Collaborators

8 joint publications

Paula Inés Buonfiglio

8 joint publications

Ana Belén Elgoyhen

4 joint publications

Carlos David Bruque

2 joint publications

Vanesa Lotersztein