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Search results (83)

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Refractory Hypocalcemia from Combined Autosomal Dominant Hypocalcemia Type 2 and Postsurgical Hypoparathyroidism.

Sonmez Ince M. et al, (2026), J Bone Miner Res

Long-acting parathyroid hormone receptor agonist rectifies hypocalcemia in autosomal dominant hypocalcemia type 1 mice.

Hannan FM. et al, (2026), J Clin Invest

MON-623 Insulin Influences Human Lactation and Promotes Mammary Mitochondrial Biogenesis

Hannan F. et al, (2025), Journal of the Endocrine Society, 9

Cohort Profile for the Heat in Pregnancy- India (HiP-India) Study

Thiruvengadam R. et al, (2025), Wellcome Open Research, 10, 472 - 472

Genetic variants predisposing to an increased risk of kidney stone disease.

Lovegrove CE. et al, (2025), J Clin Invest, 135

Characterization of quinazolinone calcilytic therapy for autosomal dominant hypocalcemia type 1 (ADH1).

Hannan FM. et al, (2025), J Biol Chem, 301

Cohort Profile for the Heat in Pregnancy- India (HiP-India) Study.

Thiruvengadam R. et al, (2025), Wellcome Open Res, 10

Endocrine effects of heat exposure and relevance to climate change.

Hannan FM. et al, (2024), Nat Rev Endocrinol, 20, 673 - 684

GNAQ/GNA11 Mosaicism Causes Aberrant Calcium Signaling Susceptible to Targeted Therapeutics.

Zecchin D. et al, (2024), J Invest Dermatol, 144, 811 - 819.e4

GNAQ/GNA11 Mosaicism Is Associated with Abnormal Serum Calcium Indices and Microvascular Neurocalcification.

Knöpfel N. et al, (2024), J Invest Dermatol, 144, 820 - 832.e9

Central Adiposity Increases Risk of Kidney Stone Disease through Effects on Serum Calcium Concentrations.

Lovegrove CE. et al, (2023), J Am Soc Nephrol, 34, 1991 - 2011

Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall-Smith Syndrome.

Kooblall KG. et al, (2023), JBMR Plus, 7

Hormonal regulation of mammary gland development and lactation.

Hannan FM. et al, (2023), Nat Rev Endocrinol, 19, 46 - 61

Epidemiology, Pathophysiology, and Genetics of Primary Hyperparathyroidism.

Minisola S. et al, (2022), J Bone Miner Res, 37, 2315 - 2329

Genetics of monogenic disorders of calcium and bone metabolism.

Newey PJ. et al, (2022), Clin Endocrinol (Oxf), 97, 483 - 501

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