Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Cancer Genetics|December 20, 2025
Multiple endocrine neoplasia type 1 syndrome due to novel Alu insertionAislinn Cragg, Hannah Boon, Treena Cranston, et al.
Human Mutation|January 7, 2010
Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumorsPaul J Newey, Michael R Bowl, Treena Cranston, et al.
Endocrine|June 17, 2016
Do patients with incidentally discovered bilateral adrenal nodules represent an early form of ARMC5-mediated bilateral macronodular hyperplasia?Holly Emms, Ioanna Tsirou, Treena Cranston, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|January 23, 2014
A patient with an apparently sporadic pheochromocytoma with a rearranged during transfection codon 635 variant: a mild form of multiple endocrine neoplasia type 2?Isabel Huguet, Treena Cranston, Lisa Walker, et al.
Journal of the Endocrine Society|December 22, 2017
Pachydermoperiostosis Masquerading as AcromegalyMunira M Karimova, Zamira Yu Halimova, Yulduz M Urmanova, et al.
The Journal of Clinical Endocrinology and Metabolism|September 3, 2009
A missense GATA3 mutation, Thr272Ile, causes the hypoparathyroidism, deafness, and renal dysplasia syndromeKatherine U Gaynor, Irina V Grigorieva, M Andrew Nesbit, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 24, 2017
Cinacalcet Rectifies Hypercalcemia in a Patient With Familial Hypocalciuric Hypercalcemia Type 2 (FHH2) Caused by a Germline Loss-of-Function Gα11 MutationCaroline M Gorvin, Fadil M Hannan, Treena Cranston, et al.
European Journal of Pediatrics|July 9, 2004
Neonatal severe hyperparathyroidism: genotype/phenotype correlation and the use of pamidronate as rescue therapySimon Waller, Tom Kurzawinski, Lewis Spitz, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 6, 2016
A G-protein Subunit-α11 Loss-of-Function Mutation, Thr54Met, Causes Familial Hypocalciuric Hypercalcemia Type 2 (FHH2)Caroline M Gorvin, Treena Cranston, Fadil M Hannan, et al.
The Journal of Clinical Endocrinology and Metabolism|May 15, 2014
CDC73 intragenic deletion in familial primary hyperparathyroidism associated with parathyroid carcinomaEeva Korpi-Hyövälti, Treena Cranston, Eeva Ryhänen, et al.
Pageof 4