Vito Guarnieri
Foggia, 71013, Italy
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 71 publications
Functional and In Silico Characterization of ALPL Gene Variants Reveals Genotype-Phenotype Correlations in Italian Hypophosphatasia Patients.
Journal: Cells
Published: October 27, 2025
The clinical challenge of MEN1 phenocopies: insights from a multicentric national retrospective study.
Journal: Journal of endocrinological investigation
Published: July 25, 2025
Molecular spectrum of autosomal recessive osteogenesis imperfecta in 93 Italian children with bone fragility: a monocentric experience.
Journal: Journal of endocrinological investigation
Published: July 18, 2025
Phosphate metabolism in primary hyperparathyroidism: a real-life long-term study.
Journal: Endocrine
Published: December 03, 2024
Correction to: The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion.
Journal: Journal of endocrinological investigation
Published: June 09, 2024
Possible role of bone turnover markers in the diagnosis of adult hypophosphatasia.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: May 30, 2024
The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion.
Journal: Journal of endocrinological investigation
Published: July 28, 2023
Last Updated: 09/26/2026