Autosomal Dominant Hypocalcemia Latest Advances
Find the Latest Research About Autosomal Dominant Hypocalcemia
Last Updated: 09/26/2026
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Found 198 publications
Autosomal Dominant Hypocalcemia With Hypercalciuria Due to a Calcium-Sensing Receptor Gain-of-Function Mutation: A Pediatric Case Report.
Journal: Cureus
Published: June 20, 2026
Regarding Non-Classical Presentations of Rare Hereditary Hypoparathyroidism: A Case Series of CASR, GNA11, and GATA3 Mutations in Parathyroidology.
Journal: Clinical endocrinology
Published: April 19, 2026
Case Report: Palopegteriparatide as a novel therapeutic option in pediatric autosomal dominant hypocalcemia type 1.
Journal: Frontiers in endocrinology
Published: March 24, 2026
Long-acting parathyroid hormone receptor agonist rectifies hypocalcemia in autosomal dominant hypocalcemia type 1 mice.
Journal: The Journal of clinical investigation
Published: February 19, 2026
A novel gain-of-function mutation (W818R) of calcium-sensing receptor in a family with autosomal dominant hypocalcemia type 1.
Journal: Frontiers in endocrinology
Published: February 08, 2026
Functional assessment of a constitutively activating CASR variant causing autosomal dominant hypocalcemia.
Journal: Journal of the Endocrine Society
Published: February 05, 2026
Teriparatide for the treatment of primary hypoparathyroidism in children.
Journal: American journal of translational research
Published: January 11, 2026
Continuous subcutaneous recombinant PTH(1-34) infusion improves serum calcium and phosphate homeostasis in children with autosomal dominant hypocalcemia type 1 refractory to standard-of-care treatment.
Journal: European journal of endocrinology
Published: January 09, 2026
Complications of Pseudohypoparathyroidism and Congenital Forms of Hypoparathyroidism in Children
Journal: Problemy endokrinologii
Published: December 26, 2025
Clinical and genetic insights into Autosomal Dominant Hypocalcemia type 1: a single-center case series including genotype-phenotype correlations, pregnancy outcomes, and novel CASR variants.
Journal: Journal of endocrinological investigation
Published: December 19, 2025
Observation of an index case of an autosomal dominant familial hypoparathyroidism revealed by recurrent hypocalcemia: a case report
Journal: The Pan African medical journal
Published: December 01, 2025
Non-Classical Presentations of Rare Hereditary Hypoparathyroidism: A Case Series of CASR, GNA11 and GATA3 Mutations.
Journal: Clinical endocrinology
Published: November 26, 2025
Last Updated: 09/26/2026