Albright's Hereditary Osteodystrophy Latest Advances
Find the Latest Research About Albright's Hereditary Osteodystrophy
Last Updated: 04/28/2026
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Found 1984 publications
Pseudohypoparathyroidism in a Chinese girl: A case report.
Journal: The Journal of international medical research
Published: April 12, 2026
Clinical and genetic characteristics of pseudohypoparathyroidism type 1
Journal: Zhonghua yi xue za zhi
Published: April 07, 2026
A maternal exon H splice-site variant leading to pseudohypoparathyroidism type 1B with broad methylation defects in GNAS-differentially methylated regions.
Journal: Clinical epigenetics
Published: January 20, 2026
From hypercalcemia to the diagnosis of pseudohypoparathyroidism type 1b: a case report.
Journal: Frontiers in endocrinology
Published: December 31, 2025
A Rare Familial Case of Pseudohypoparathyroidism Type 1b in Two Brothers Presenting With Recurrent Leg Cramps and Learning Difficulties.
Journal: Cureus
Published: December 18, 2025
Gsα, Albright's hereditary osteodystrophy, and craniosynostosis.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: December 15, 2025
The association of GNAS defects with pro-inflammatory adipokine levels in pseudohypoparathyroidism type 1.
Journal: Journal of endocrinological investigation
Published: October 19, 2025
Six cases of ectopic cutaneous ossification associated with GNAS gene variants.
Journal: European journal of dermatology : EJD
Published: September 18, 2025
Defective GNAS imprinting due to splice site variants in pseudohypoparathyroidism type 1B.
Journal: JCI insight
Published: September 02, 2025
Last Updated: 04/28/2026