At the dated check, the references listed below either did not resolve in
Crossref or DataCite, or carried a retraction notice. Each one is shown with the
registry record that put it there.
The 80 checked references that resolve
resolves10.1359/JBMR.050910Incidence of Primary Hyperparathyroidism in Rochester, Minnesota, 1993–2001: An Update on the Changing Epidemiology of the Disease
resolves10.1007/BF00878365Transient neonatal distal renal tubular acidosis with secondary hyperparathyroidism
resolves10.1136/adc.56.7.565Transient neonatal hyperparathyroidism secondary to maternal pseudohypoparathyroidism.
resolves10.1172/JCI119137In vivo and in vitro characterization of neonatal hyperparathyroidism resulting from a de novo, heterozygous mutation in the Ca2+-sensing receptor gene: normal maternal calcium homeostasis as a cause of secondary hyperparathyroidism in familial benign hypocalciuric hypercalcemia.
resolves10.1055/s-2007-999521Spectrum and Natural History of Congenital Hyperparathyroidism Secondary to Maternal Hypocalcemia
resolves10.1007/BF00441557Study of the bone pathology in early mucolipidosis II (I-cell disease)
resolves10.1152/ajpendo.00315.2009The calcium-sensing receptor (CaSR) defends against hypercalcemia independently of its regulation of parathyroid hormone secretion
resolves10.1093/clinchem/37.2.162Immunochemiluminometric and immunoradiometric determinations of intact and total immunoreactive parathyrin: performance in the differential diagnosis of hypercalcemia and hypoparathyroidism
resolves10.1093/clinchem/33.8.1364Highly sensitive two-site immunoradiometric assay of parathyrin, and its clinical utility in evaluating patients with hypercalcemia.
resolves10.1359/jbmr.2001.16.4.605Development of a Novel Immunoradiometric Assay Exclusively for Biologically Active Whole Parathyroid Hormone 1–84: Implications for Improvement of Accurate Assessment of Parathyroid Function
resolves10.1210/jc.2002-021266Clinical Utility of an Immunoradiometric Assay for Parathyroid Hormone (1–84) in Primary Hyperparathyroidism
resolves10.1093/ndt/gfm849Third-generation parathyroid hormone assays and all-cause mortality in incident dialysis patients: the CHOICE study
resolves10.1159/000081788Direct Comparison between Two 1-84PTH Assays in Dialysis Patients
resolves10.1016/0092-8674(93)90617-YMutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
resolves10.1210/jc.2008-1758Diagnosis of Asymptomatic Primary Hyperparathyroidism: Proceedings of the Third International Workshop
resolves10.1016/j.surg.2004.06.042The coming of age of radiation-induced hyperparathyroidism: Evolving patterns of thyroid and parathyroid disease after head and neck irradiation
resolves10.1210/jc.83.8.2621Mutation Analysis of the MEN1 Gene in Multiple Endocrine Neoplasia Type 1, Familial Acromegaly and Familial Isolated Hyperparathyroidism
resolves10.1038/ng1048HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome
resolves10.1210/jc.83.3.960Absence of Germ-Line Mutations of the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene in Familial Pituitary Adenoma in Contrast to MEN1 in Japanese
resolves10.1056/NEJMoa031237Somatic and Germ-Line Mutations of the<i>HRPT2</i>Gene in Sporadic Parathyroid Carcinoma
resolves10.1136/jmg.40.9.657<i>HRPT2</i> mutations are associated with malignancy in sporadic parathyroid tumours
resolves10.1210/jc.2003-030675Familial Isolated Hyperparathyroidism Is Rarely Caused by Germline Mutation in<i>HRPT2</i>, the Gene for the Hyperparathyroidism-Jaw Tumor Syndrome
resolves10.1007/s100380050048Mutational analysis of the RET proto-oncogene in 71 Japanese patients with medullary thyroid carcinoma
resolves10.1210/jc.2007-1005<i>RET</i>
Genetic Screening in Patients with Medullary Thyroid Cancer and Their Relatives: Experience with 807 Individuals at One Center
resolves10.1136/jmg.32.12.934Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.
resolves10.1073/pnas.0603877103Germ-line mutations in p27
<i>
<sup>Kip1</sup>
</i>
cause a multiple endocrine neoplasia syndrome in rats and humans
resolves10.1136/jmg.26.5.289A new syndrome of autosomal recessive nephropathy, deafness, and hyperparathyroidism.
resolves10.1073/pnas.0712361105A translocation causing increased α-Klotho level results in hypophosphatemic rickets and hyperparathyroidism
resolves10.1126/science.7701349A Constitutively Active Mutant PTH-PTHrP Receptor in Jansen-Type Metaphyseal Chondrodysplasia
resolves10.1172/JCI2918Absence of functional receptors for parathyroid hormone and parathyroid hormone-related peptide in Blomstrand chondrodysplasia.
resolves10.1007/BF00572767A new familial skeletal dysplasia with severely retarded ossification and abnormal modeling of bones especially of the epiphyses, the hands, and feet
resolves10.1210/jc.2008-1757The Diagnosis and Management of Asymptomatic Primary Hyperparathyroidism Revisited
resolves10.1297/cpe.17.81I-Cell Disease (Mucolipidosis II) Presenting as Neonatal Fractures: A Case for Continued Monitoring of Serum Parathyroid Hormone Levels
resolves10.1007/s00198-010-1226-1Changes in trabecular and cortical bone microarchitecture at peripheral sites associated with 18 months of teriparatide therapy in postmenopausal women with osteoporosis
resolves10.2214/AJR.06.0938Parathyroid Imaging: Technique and Role in the Preoperative Evaluation of Primary Hyperparathyroidism
resolves10.1210/jc.2008-1763Guidelines for the Management of Asymptomatic Primary Hyperparathyroidism: Summary Statement from the Third International Workshop
resolves10.1093/ajcp/64.4.488Primary Neonatal Hyperparathyroidism: Report of a Case and Review of the Literature
resolves10.1007/BF01655086Surgical treatment of ten cases of parathyroid carcinoma: Importance of an initial en bloc tumor resection
resolves10.1016/S0039-6060(98)70040-6Primary and reoperative parathyroid operations in hyperparathyroidism of multiple endocrine neoplasia type 1
resolves10.1210/jc.85.1.165Familial Isolated Hyperparathyroidism as a Variant of Multiple Endocrine Neoplasia Type 1 in a Large Danish Pedigree
resolves10.1016/j.jamcollsurg.2006.02.003Consequences of Targeted Parathyroidectomy Guided by Localization Studies Without Intraoperative Parathyroid Hormone Monitoring
resolves10.1016/S8756-3282(00)00291-XEffects of two intermittent alendronate regimens in the prevention or treatment of postmenopausal osteoporosis
resolves10.1210/jc.2001-010385Alendronate in the Treatment of Primary Hyperparathyroid-Related Osteoporosis: A 2-Year Study
resolves10.1016/j.jcms.2010.05.009Osteoporosis and bisphosphonates-related osteonecrosis of the jaw: Not just a sporadic coincidence – a multi-centre study
resolves10.1210/jc.2004-0842Cinacalcet Hydrochloride Maintains Long-Term Normocalcemia in Patients with Primary Hyperparathyroidism
resolves10.1210/jc.2002-021597The Calcimimetic Cinacalcet Normalizes Serum Calcium in Subjects with Primary Hyperparathyroidism
resolves10.1067/msy.2002.128695Limited versus radical parathyroidectomy in familial isolated primary hyperparathyroidism
resolves10.1007/BF01665301Surgical treatment of primary hyperparathyroidism: An institutional perspective
resolves10.1007/BF02067367Findings and long‐term results of parathyroid surgery in multiple endocrine neoplasia type 1
resolves10.1586/ERA.10.11Fusion imaging for parathyroid localization in primary hyperparathyroidism
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