Last Updated: 09/26/2026
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Found 21 publications
Secondary Deformity After Hemiepiphysiodesis in Hypophosphatemic Rickets: The Role of Metabolic Control.
Journal: Journal of pediatric orthopedics
Published: November 11, 2025
Bone Health in Youth with Congenital Adrenal Hyperplasia: Abdominal and Total Adiposity Is Associated with Bone Mineral Density.
Journal: Hormone research in paediatrics
Published: June 13, 2025
Bidirectional disruption of GNAS transcripts causes broad methylation defects in pseudohypoparathyroidism type 1B.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 18, 2025
Obesity Management in Youth with Duchenne Muscular Dystrophy: A Review of Metformin and Alternative Pharmacotherapies.
Journal: Childhood obesity (Print)
Published: October 11, 2024
Pediatric Endocrine Society Statement on Considerations for Use of Teplizumab (Tzield™) in Clinical Practice.
Journal: Hormone research in paediatrics
Published: February 06, 2024
A Novel De Novo Frameshift Pathogenic Variant in the FAM111B Resulting in Progressive Osseous Heteroplasia Phenotype.
Journal: Calcified tissue international
Published: October 21, 2022
A Unique Case of Aggressive Central Giant Cell Granuloma in a 10-Year-Old Boy With 16p13.11 Microdeletion Syndrome.
Journal: Journal of investigative medicine high impact case reports
Published: September 26, 2022
Quantifying RANKL and OPG levels in healthy children: A large cross-sectional analysis.
Journal: Bone
Published: May 03, 2019
Evaluating RANKL and OPG levels in patients with Duchenne muscular dystrophy.
Journal: Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA
Published: April 29, 2019
Meeting Report: 2018 Annual Meeting of the Pediatric Endocrine Society, Toronto, Canada, May 5-8, 2018, Selected Highlights.
Journal: Pediatric endocrinology reviews : PER
Published: December 18, 2018
A case of severe TBCE-negative hypoparathyroidism-retardation-dysmorphism syndrome: Case report and literature review.
Journal: American journal of medical genetics. Part A
Published: February 25, 2018
Last Updated: 09/26/2026