1.
Gastroenteropancreatic neuroendocrine tumours
by Modlin, Irvin M, Prof
The lancet oncology, 2008, Vol.9 (1), p.61-72
2.
Epidemiology and Diagnosis of Hypoparathyroidism
by Clarke, Bart L
The journal of clinical endocrinology and metabolism, 2016, Vol.101 (6), p.2284-2299
3.
The Calcilytic Agent NPS 2143 Rectifies Hypocalcemia in a Mouse Model With an Activating Calcium-Sensing Receptor (CaSR) Mutation: Relevance to Autosomal Dominant Hypocalcemia Type...
by Hannan, Fadil M
Endocrinology (Philadelphia), 2015, Vol.156 (9), p.3114-3121
4.
Whole-Exome Sequencing Studies of Nonhereditary (Sporadic) Parathyroid Adenomas
by Newey, Paul J
The journal of clinical endocrinology and metabolism, 2012, Vol.97 (10), p.E1995-E2005
5.
Pasireotide Therapy of Multiple Endocrine Neoplasia Type 1–Associated Neuroendocrine Tumors in Female Mice Deleted for an Men1 Allele Improves Survival and Reduces Tumor Progressio...
by Walls, Gerard V
Endocrinology (Philadelphia), 2016, Vol.157 (5), p.1789-1798
6.
Genetic causes of hypercalciuric nephrolithiasis
by Stechman, Michael J
Pediatric nephrology (Berlin, West), 2008, Vol.24 (12), p.2321-2332
7.
CDC73 Intragenic Deletion in Familial Primary Hyperparathyroidism Associated With Parathyroid Carcinoma
by Korpi-Hyövälti, Eeva
The journal of clinical endocrinology and metabolism, 2014, Vol.99 (9), p.3044-3048
8.
Mutant Mice With Calcium-Sensing Receptor Activation Have Hyperglycemia That Is Rectified by Calcilytic Therapy
by Babinsky, Valerie N
Endocrinology (Philadelphia), 2017, Vol.158 (8), p.2486-2502
9.
Whole-Exome Sequencing Studies of Nonfunctioning Pituitary Adenomas
by Newey, Paul J
The journal of clinical endocrinology and metabolism, 2013, Vol.98 (4), p.E796-E800
10.
Clinical Practice Guidelines for Multiple Endocrine Neoplasia Type 1 (MEN1)
by Thakker, Rajesh V
The journal of clinical endocrinology and metabolism, 2012, Vol.97 (9), p.2990-3011
11.
An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess
by Bentley, Liz
Endocrinology (Philadelphia), 2014, Vol.155 (3), p.908-922
12.
Diagnosis of Asymptomatic Primary Hyperparathyroidism: Proceedings of the Fourth International Workshop
by Eastell, Richard
The journal of clinical endocrinology and metabolism, 2014, Vol.99 (10), p.3570-3579
13.
Management of Hypoparathyroidism: Summary Statement and Guidelines
by Brandi, Maria Luisa
The journal of clinical endocrinology and metabolism, 2016, Vol.101 (6), p.2273-2283
14.
Mutational Analysis of the Adaptor Protein 2 Sigma Subunit (AP2S1) Gene: Search for Autosomal Dominant Hypocalcemia Type 3 (ADH3)
by Rogers, Angela
The journal of clinical endocrinology and metabolism, 2014, Vol.99 (7), p.E1300-E1305
15.
Proliferation Rates of Multiple Endocrine Neoplasia Type 1 (MEN1)-Associated Tumors
by Walls, Gerard V
Endocrinology (Philadelphia), 2012, Vol.153 (11), p.5167-5179
16.
Presentation of Hypoparathyroidism: Etiologies and Clinical Features
by Shoback, Dolores M
The journal of clinical endocrinology and metabolism, 2016, Vol.101 (6), p.2300-2312
17.
Heterogeneous Genetic Background of the Association of Pheochromocytoma/Paraganglioma and Pituitary Adenoma: Results From a Large Patient Cohort
by Dénes, Judit
The journal of clinical endocrinology and metabolism, 2015, Vol.100 (3), p.E531-E541
18.
Whole-Exome Sequencing Studies of Parathyroid Carcinomas Reveal Novel PRUNE2 Mutations, Distinctive Mutational Spectra Related to APOBEC-Catalyzed DNA Mutagenesis and Mutational En...
by Yu, Willie
The journal of clinical endocrinology and metabolism, 2015, Vol.100 (2), p.E360-E364
19.
CONSENSUS: Guidelines for Diagnosis and Therapy of MEN Type 1 and Type 2
by Brandi, Maria Luisa
The journal of clinical endocrinology and metabolism, 2001, Vol.86 (12), p.5658-5671
20.
A Missense Glial Cells Missing Homolog B (GCMB) Mutation, Asn502His, Causes Autosomal Dominant Hypoparathyroidism
by Mirczuk, Samantha M
The journal of clinical endocrinology and metabolism, 2010, Vol.95 (7), p.3512-3516
