Fernando Santos
Oviedo, AS, Spain
Last Updated: 09/26/2026
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Found 66 publications
Erratum to "An update on clinical presentation and responses to therapy of patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH)." Kidney International 2023;105:1058-1076.
Journal: Kidney international
Published: June 21, 2024
Switching from immediate- to extended-release cysteamine in patients with nephropathic cystinosis: from clinical trials to clinical practice.
Journal: Clinical kidney journal
Published: December 01, 2023
An update on clinical presentation and responses to therapy of patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH).
Journal: Kidney international
Published: September 05, 2023
Is collagen X marker (CXM) a useful index of growth velocity in children with chronic kidney disease?
Journal: Pediatric nephrology (Berlin, Germany)
Published: July 14, 2023
Blocking FGF23 signaling improves the growth plate of mice with X-linked hypophosphatemia.
Journal: The Journal of endocrinology
Published: January 24, 2023
Evaluation of urinary acidification in children: Clinical utility.
Journal: Frontiers in pediatrics
Published: September 22, 2022
Burosumab for X-linked hypophosphatemia in children and adolescents: Opinion based on early experience in seven European countries.
Journal: Frontiers in endocrinology
Published: September 01, 2022
Cellular and Molecular Alterations Underlying Abnormal Bone Growth in X-Linked Hypophosphatemia.
Journal: International journal of molecular sciences
Published: December 09, 2021
Long-term complications of primary distal renal tubular acidosis.
Journal: Pediatric nephrology (Berlin, Germany)
Published: November 17, 2021
Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study.
Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Published: October 03, 2021
Correction to: Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population.
Journal: Orphanet journal of rare diseases
Published: April 02, 2021
Last Updated: 09/26/2026