Albright's Hereditary Osteodystrophy Latest Advances
Find the Latest Research About Albright's Hereditary Osteodystrophy
Last Updated: 02/24/2026
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Found 1981 publications
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
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
Giant ischial osteochondroma causing ischiofemoral impingement and sciatic nerve compression in a pediatric patient with Albright's hereditary osteodystrophy.
Journal: Radiology case reports
Published: July 13, 2025
Three-generation familial transmission of a GNAS variant: from gestational phenotype in the mother to evolving prenatal/neonatal phenotype in the offspring.
Journal: Hormones (Athens, Greece)
Published: June 19, 2025
Natural History of Hyperphagia in Patients with Pseudohypoparathyroidism.
Journal: Journal of clinical medicine
Published: June 11, 2025
Imprinting and skeletal disorders: lessons from pseudohypoparathyroidism and related disorders.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: June 09, 2025
Pseudohypoparathyroidism type 1B mimicking gitelman syndrome: diagnostic pitfalls and molecular insights.
Journal: Frontiers in genetics
Published: May 30, 2025
Last Updated: 02/24/2026