Laura Valinotto
6PUBLICATIONS
16CO-AUTHORS
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Publications (6)
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|Apr 13, 2026
Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot.Sheetal Kumar, Sohail Ahmed, Pietro Incardona
|Nov 17, 2025
Epidermolysis Bullosa Simplex with Mottled Pigmentation and Migratory Circinate Erythema: Distinct Subtypes or a Continuum?Laura E Valinotto, Mónica Natale, Silvina B Lusso
|Jun 28, 2023
The Lambda Variant in Argentina: Analyzing the Evolution and Spread of SARS-CoV-2 Lineage C.37.Mercedes Soledad Nabaes Jodar, Carolina Torres, Laura Mojsiejczuk
|Aug 18, 2022
Analysis of COL7A1 pathogenic variants in a large cohort of dystrophic epidermolysis bullosa patients from Argentina reveals a new genotype-phenotype correlation.Mónica Inés Natale, Graciela Beatriz Manzur, Silvina Beatriz Lusso
|Mar 20, 2021
Ichthyosis follicularis, atrichia and photophobia (IFAP) and hereditary mucoepithelial dysplasia: Two syndromes that share a common clinical spectrum.Inés Irurzun, Mónica I Natale, María L Agostinelli
|Jan 21, 2020
A novel pathogenic FERMT1 variant in four families with Kindler syndrome in Argentina.Laura Elena Valinotto, Mónica Inés Natale, Silvina Beatriz Lusso
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Frequent Collaborators
2 joint publications
Mónica Natale
2 joint publications
Graciela Manzur
1 joint publications
Maria Del Carmen Boente
1 joint publications
Mercedes Soledad Nabaes Jodar
1 joint publications
Carolina Torres
1 joint publications
Matias Irazoqui
1 joint publications
Paula Aulicino
1 joint publications
Elisa Bolatti
1 joint publications
Humberto Debat
1 joint publications
Maria Jose Dus Santos
