Dov Tiosano

Haifa, HA, Israel

Last Updated: 09/26/2026

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Found 49 publications

Characterizing the metabolome of children with growth hormone deficiency.

Characterizing the metabolome of children with growth hormone deficiency.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: February 23, 2025

Nephrocalcinosis tendency does not worsen under burosumab treatment for X-linked hypophosphatemic rickets: a multicenter pediatric study.

Nephrocalcinosis tendency does not worsen under burosumab treatment for X-linked hypophosphatemic rickets: a multicenter pediatric study.

Journal: Frontiers in pediatrics

Published: August 28, 2024

A family with an atypical presentation of TBX3-related disorder.

A family with an atypical presentation of TBX3-related disorder.

Journal: European journal of medical genetics

Published: February 20, 2024

Linear growth of children with X-linked hypophosphatemia treated with burosumab: a real-life observational study.

Linear growth of children with X-linked hypophosphatemia treated with burosumab: a real-life observational study.

Journal: European journal of pediatrics

Published: June 16, 2023

The effect of etanercept therapy on adrenal steroid metabolism in juvenile idiopathic arthritis: a steroid metabolomics approach.

The effect of etanercept therapy on adrenal steroid metabolism in juvenile idiopathic arthritis: a steroid metabolomics approach.

Journal: Pediatric rheumatology online journal

Published: November 25, 2022

PI(3,4)P2-mediated cytokinetic abscission prevents early senescence and cataract formation.

PI(3,4)P2-mediated cytokinetic abscission prevents early senescence and cataract formation.

Journal: Science (New York, N.Y.)

Published: December 09, 2021

An Expert Perspective on Phosphate Dysregulation With a Focus on Chronic Hypophosphatemia.

An Expert Perspective on Phosphate Dysregulation With a Focus on Chronic Hypophosphatemia.

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Published: July 21, 2021

Expanding the spectrum of endocrinopathies identified in Schaaf-Yang syndrome - A case report and review of the literature.

Expanding the spectrum of endocrinopathies identified in Schaaf-Yang syndrome - A case report and review of the literature.

Journal: European journal of medical genetics

Published: January 18, 2021

Pathogenic variants in SMARCA5, a chromatin remodeler, cause a range of syndromic neurodevelopmental features.

Pathogenic variants in SMARCA5, a chromatin remodeler, cause a range of syndromic neurodevelopmental features.

Journal: Science advances

Published: October 14, 2020

SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling.

SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling.

Journal: American journal of human genetics

Published: September 23, 2020

Lessons Learned from Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets Patients on Vitamin D Functions.

Lessons Learned from Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets Patients on Vitamin D Functions.

Journal: The Journal of nutrition

Published: August 19, 2020

In Silico Structural and Biochemical Functional Analysis of a Novel CYP21A2 Pathogenic Variant.

In Silico Structural and Biochemical Functional Analysis of a Novel CYP21A2 Pathogenic Variant.

Journal: International journal of molecular sciences

Published: June 22, 2020

Showing 1-12 of 49

Last Updated: 09/26/2026