Núria Camats-Tarruella
8PUBLICATIONS
35CO-AUTHORS
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Publications (8)
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|Sep 28, 2024
NR5A1/SF-1 Collaborates with Inhibin α and the Androgen Receptor.Rawda Naamneh Elzenaty, Chrysanthi Kouri, Idoia Martinez de Lapiscina
|Sep 28, 2024
Genetic and Functional Studies of Patients with Thyroid Dyshormonogenesis and Defects in the TSH Receptor (TSHR).Diego Yeste, Noelia Baz-Redón, María Antolín
|Aug 10, 2024
Patients with Thyroid Dyshormonogenesis and DUOX2 Variants: Molecular and Clinical Description and Genotype-Phenotype Correlation.Noelia Baz-Redón, María Antolín, María Clemente
|Mar 27, 2024
Primary Ciliary Dyskinesia and Retinitis Pigmentosa: Novel RPGR Variant and Possible Modifier Gene.Noelia Baz-Redón, Laura Sánchez-Bellver, Mónica Fernández-Cancio
|May 22, 2023
Genetics and Natural History of Non-pancreatectomized Patients With Congenital Hyperinsulinism Due to Variants in ABCC8.María Clemente, Patricia Cobo, María Antolín
|Nov 13, 2020
Immunofluorescence Analysis as a Diagnostic Tool in a Spanish Cohort of Patients with Suspected Primary Ciliary Dyskinesia.Noelia Baz-Redón, Sandra Rovira-Amigo, Mónica Fernández-Cancio
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Frequent Collaborators
5 joint publications
Noelia Baz-Redón
3 joint publications
Diego Yeste
2 joint publications
Eduard Mogas
2 joint publications
Núria González-Llorens
2 joint publications
Mónica Fernández-Cancio
2 joint publications
Maria Cols
2 joint publications
Cristina Aguilar-Riera
2 joint publications
María Clemente
2 joint publications
Antonio Moreno-Galdó
1 joint publications
Sandra Rovira-Amigo
