Fernando Revert
San Vicent Del Raspeig, VC 46001, Spain
Last Updated: 09/26/2026
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Found 9 publications
XLA-MTS: a distinct clinical genetic entity characterized by immunodeficiency and neurodevelopmental delay.
Journal: Orphanet journal of rare diseases
Published: January 28, 2026
A novel TIMM8A mutation in Mohr-Tranebjaerg syndrome without hearing loss and with basal ganglia iron deposition.
Journal: Orphanet journal of rare diseases
Published: May 12, 2025
Polyribonucleotide phosphorylase is overexpressed in hepatocellular cancer, promoting epithelial phenotype maintenance and tumor progression.
Journal: Pathology, research and practice
Published: October 02, 2024
The Versatility of Collagen in Pharmacology: Targeting Collagen, Targeting with Collagen.
Journal: International journal of molecular sciences
Published: May 08, 2024
More Than Three Years for Normalisation of Routine Laboratory Values after Gluten Withdrawal in Paediatric Coeliac Patients.
Journal: Children (Basel, Switzerland)
Published: September 03, 2023
SP1 and NFY Regulate the Expression of PNPT1, a Gene Encoding a Mitochondrial Protein Involved in Cancer.
Journal: International journal of molecular sciences
Published: July 29, 2022
Selective improvement by rifaximin of changes in the immunophenotype in patients who improve minimal hepatic encephalopathy.
Journal: Journal of translational medicine
Published: March 13, 2019
Unicellular ancestry and mechanisms of diversification of Goodpasture antigen-binding protein.
Journal: The Journal of biological chemistry
Published: October 12, 2018
Showing 1-9 of 9
Last Updated: 09/26/2026