Ignacia Fuentes
8PUBLICATIONS
28CO-AUTHORS
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Publications (8)
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|May 14, 2025
A Novel Homozygous 9385 bp Deletion in the FERMT1 (KIND1) Gene in a Malaysian Family with Kindler Epidermolysis bullosa and a Review of Large Deletions.Alfred Klausegger, Fabian Leditzky, Susanne Krämer
|Jan 08, 2025
Prevalence of Crown Resorption in Amelogenesis Imperfecta due to Junctional Epidermolysis Bullosa.Colomba Besa-Witto, Ana Ortega-Pinto, Sebastián Véliz
|Dec 05, 2024
Novel variants impairing Sp1 transcription factor binding in the COL7A1 promoter cause mild cases of recessive dystrophic epidermolysis bullosa.Nathalie Pironon, Artyom Gasparyan, María Joao Yubero
|Mar 11, 2024
Antiviral drugs prolong survival in murine recessive dystrophic epidermolysis bullosa.Grace Tartaglia, Ignacia Fuentes, Neil Patel
|Feb 23, 2024
Patients suffering from dystrophic epidermolysis bullosa are prone to developing autoantibodies against skin proteins: A longitudinal confirmational study.J Bremer, H H Pas, G F H Diercks
|Mar 21, 2022
Characterisation of the pathophysiology of neuropathy and sensory dysfunction in a mouse model of recessive dystrophic epidermolysis bullosa.Daniela Schmidt, Paula Díaz, Daniela Muñoz
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Frequent Collaborators
3 joint publications
Susanne Krämer
2 joint publications
Francis Palisson
1 joint publications
J Bremer
1 joint publications
Daniela Schmidt
1 joint publications
Paula Díaz
1 joint publications
Daniela Muñoz
1 joint publications
Fernanda Espinoza
1 joint publications
Alexander Nystrom
1 joint publications
Johann Wolfgang Bauer
1 joint publications
Margarita Calvo