Reference health

Primary Hyperparathyroidism: An Overview

https://doi.org/10.1155/2011/251410
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1 of 81 checkable references need attention · checked 2026-07-22

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.

11 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

References needing attention

does not resolve to a known work10.1210/jc.86.2.485
The 80 checked references that resolve
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Incidence of Primary Hyperparathyroidism in Rochester, Minnesota, 1993–2001: An Update on the Changing Epidemiology of the Disease
resolves10.1111/j.1365-2265.2007.02970.x
Asymptomatic hyperparathyroidism – need for multicentre studies
resolves10.1007/s00431-004-1591-x
Mucolipidosis II presenting as severe neonatal hyperparathyroidism
resolves10.1007/s12098-009-0289-5
Primary hyperparathyroidism in children and adolescents
resolves10.1016/j.jpedsurg.2010.02.074
What is the optimal treatment for children with primary hyperparathyroidism?
resolves10.1007/BF00878365
Transient neonatal distal renal tubular acidosis with secondary hyperparathyroidism
resolves10.1136/adc.56.7.565
Transient neonatal hyperparathyroidism secondary to maternal pseudohypoparathyroidism.
resolves10.1530/eje.0.1330151
Transient pseudohypoparathyroidism of the neonate
resolves10.1172/JCI119137
In 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-2007-999521
Spectrum and Natural History of Congenital Hyperparathyroidism Secondary to Maternal Hypocalcemia
resolves10.1007/BF00441557
Study of the bone pathology in early mucolipidosis II (I-cell disease)
resolves10.1016/S0140-6736(09)60507-9
Hyperparathyroidism
resolves10.1038/ncpendmet0388
Clinical lessons from the calcium-sensing receptor
resolves10.1152/ajpendo.00315.2009
The calcium-sensing receptor (CaSR) defends against hypercalcemia independently of its regulation of parathyroid hormone secretion
resolves10.1093/clinchem/37.2.162
Immunochemiluminometric and immunoradiometric determinations of intact and total immunoreactive parathyrin: performance in the differential diagnosis of hypercalcemia and hypoparathyroidism
resolves10.1093/clinchem/33.8.1364
Highly sensitive two-site immunoradiometric assay of parathyrin, and its clinical utility in evaluating patients with hypercalcemia.
resolves10.1359/jbmr.2001.16.4.605
Development 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.2002-021266
Clinical Utility of an Immunoradiometric Assay for Parathyroid Hormone (1–84) in Primary Hyperparathyroidism
resolves10.1093/ndt/gfm849
Third-generation parathyroid hormone assays and all-cause mortality in incident dialysis patients: the CHOICE study
resolves10.1373/clinchem.2005.065821
Comparison of 3 Third-Generation Assays for Bio-intact Parathyroid Hormone
resolves10.1159/000081788
Direct Comparison between Two 1-84PTH Assays in Dialysis Patients
resolves10.1016/0092-8674(93)90617-Y
Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
resolves10.1210/jc.2008-1758
Diagnosis of Asymptomatic Primary Hyperparathyroidism: Proceedings of the Third International Workshop
resolves10.1016/j.otc.2010.01.009
Primary Hyperparathyroidism
resolves10.1056/NEJM200012213432508
Hyperparathyroid and Hypoparathyroid Disorders
resolves10.1016/j.surg.2004.06.042
The coming of age of radiation-induced hyperparathyroidism: Evolving patterns of thyroid and parathyroid disease after head and neck irradiation
resolves10.1210/jc.83.8.2621
Mutation Analysis of the MEN1 Gene in Multiple Endocrine Neoplasia Type 1, Familial Acromegaly and Familial Isolated Hyperparathyroidism
resolves10.1038/ng1048
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome
resolves10.1210/jc.83.3.960
Absence of Germ-Line Mutations of the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene in Familial Pituitary Adenoma in Contrast to MEN1 in Japanese
resolves10.1210/jc.83.8.2617
Multiple Endocrine Neoplasia--Syndromes of the Twentieth Century
resolves10.1056/NEJMoa031237
Somatic 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.2003-030675
Familial Isolated Hyperparathyroidism Is Rarely Caused by Germline Mutation in<i>HRPT2</i>, the Gene for the Hyperparathyroidism-Jaw Tumor Syndrome
resolves10.1007/s100380050048
Mutational 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.32.12.934
Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.
resolves10.1073/pnas.0603877103
Germ-line mutations in p27 <i> <sup>Kip1</sup> </i> cause a multiple endocrine neoplasia syndrome in rats and humans
resolves10.1136/jmg.26.5.289
A new syndrome of autosomal recessive nephropathy, deafness, and hyperparathyroidism.
resolves10.1073/pnas.0712361105
A translocation causing increased α-Klotho level results in hypophosphatemic rickets and hyperparathyroidism
resolves10.1126/science.7701349
A Constitutively Active Mutant PTH-PTHrP Receptor in Jansen-Type Metaphyseal Chondrodysplasia
resolves10.1172/JCI2918
Absence of functional receptors for parathyroid hormone and parathyroid hormone-related peptide in Blomstrand chondrodysplasia.
resolves10.1007/BF00572767
A new familial skeletal dysplasia with severely retarded ossification and abnormal modeling of bones especially of the epiphyses, the hands, and feet
resolves10.1016/j.ajhg.2008.11.006
PTHR1 Loss-of-Function Mutations in Familial, Nonsyndromic Primary Failure of Tooth Eruption
resolves10.1002/ana.410150509
Severe neurological disease associated with hyperparathyroidism
resolves10.1210/jc.2008-1757
The Diagnosis and Management of Asymptomatic Primary Hyperparathyroidism Revisited
resolves10.1297/cpe.17.81
I-Cell Disease (Mucolipidosis II) Presenting as Neonatal Fractures: A Case for Continued Monitoring of Serum Parathyroid Hormone Levels
resolves10.1359/jbmr.1999.14.10.1700
Primary Hyperparathyroidism and the Risk of Fracture: A Population-Based Study
resolves10.1007/s00198-010-1226-1
Changes in trabecular and cortical bone microarchitecture at peripheral sites associated with 18 months of teriparatide therapy in postmenopausal women with osteoporosis
resolves10.1136/pgmj.2008.077842
Multimodality imaging in hyperparathyroidism
resolves10.2214/AJR.06.0938
Parathyroid Imaging: Technique and Role in the Preoperative Evaluation of Primary Hyperparathyroidism
resolves10.1210/jc.2008-1763
Guidelines for the Management of Asymptomatic Primary Hyperparathyroidism: Summary Statement from the Third International Workshop
resolves10.1093/ajcp/64.4.488
Primary Neonatal Hyperparathyroidism: Report of a Case and Review of the Literature
resolves10.1007/s00268-010-0569-2
Hyperparathyroidism in Pregnancy: Options for Localization and Surgical Therapy
resolves10.1007/BF01655086
Surgical treatment of ten cases of parathyroid carcinoma: Importance of an initial en bloc tumor resection
resolves10.1016/S0039-6060(98)70040-6
Primary and reoperative parathyroid operations in hyperparathyroidism of multiple endocrine neoplasia type 1
resolves10.1007/978-3-642-84749-3_9
Surgical Management of MEN 2
resolves10.1210/jc.85.1.165
Familial Isolated Hyperparathyroidism as a Variant of Multiple Endocrine Neoplasia Type 1 in a Large Danish Pedigree
resolves10.1016/j.jamcollsurg.2006.02.003
Consequences of Targeted Parathyroidectomy Guided by Localization Studies Without Intraoperative Parathyroid Hormone Monitoring
resolves10.1046/j.1445-2197.2002.02558.x
Minimal access thyroid surgery: Is it feasible, is it appropriate?
resolves10.1016/j.amjsurg.2005.01.029
Selective unilateral parathyroid exploration: an effective treatment for primary hyperparathyroidism
resolves10.1177/000313480707300404
Complications of Thyroidectomy and Parathyroidectomy in the Rural Community Hospital Setting
resolves10.1016/j.jamcollsurg.2009.01.048
Outpatient Minimally Invasive Parathyroidectomy Is Safe for Elderly Patients
resolves10.1111/j.1365-2265.2009.03540.x
Parathyroidectomy is safe and improves symptoms in elderly patients with primary hyperparathyroidism (PHPT)
resolves10.4158/EP08178.ORR
Alendronate Therapy in Men With Primary Hyperparathyroidism
resolves10.1016/S8756-3282(00)00291-X
Effects of two intermittent alendronate regimens in the prevention or treatment of postmenopausal osteoporosis
resolves10.1210/jc.2001-010385
Alendronate in the Treatment of Primary Hyperparathyroid-Related Osteoporosis: A 2-Year Study
resolves10.1016/j.jcms.2010.05.009
Osteoporosis and bisphosphonates-related osteonecrosis of the jaw: Not just a sporadic coincidence – a multi-centre study
resolves10.7326/0003-4819-125-5-199609010-00002
Effect of Hormone Replacement Therapy on Bone Mineral Density in Postmenopausal Women with Mild Primary Hyperparathyroidism
resolves10.1124/jpet.103.057273
Pharmacodynamics of the Type II Calcimimetic Compound Cinacalcet HCl
resolves10.1038/nrm1154
Extracellular calcium sensing and signalling
resolves10.1210/jc.2004-0842
Cinacalcet Hydrochloride Maintains Long-Term Normocalcemia in Patients with Primary Hyperparathyroidism
resolves10.1210/jc.2002-021597
The Calcimimetic Cinacalcet Normalizes Serum Calcium in Subjects with Primary Hyperparathyroidism
resolves10.1056/NEJM198907273210402
Clonality of Parathyroid Tumors in Familial Multiple Endocrine Neoplasia Type 1
resolves10.1067/msy.2002.128695
Limited versus radical parathyroidectomy in familial isolated primary hyperparathyroidism
resolves10.1097/RLU.0b013e3181b7dacf
Hybrid SPECT/CT Imaging for Primary Hyperparathyroidism
resolves10.1007/BF01665301
Surgical treatment of primary hyperparathyroidism: An institutional perspective
resolves10.1007/BF02067367
Findings and long‐term results of parathyroid surgery in multiple endocrine neoplasia type 1
resolves10.1016/S0889-8529(18)30122-1
Management of Individual Tumor Syndromes: Medullary Thyroid Carcinoma and Hyperparathyroidism
resolves10.1586/ERA.10.11
Fusion imaging for parathyroid localization in primary hyperparathyroidism
resolves10.1016/j.amjsurg.2010.02.001
Determinants of Tc-99m sestamibi SPECT scan sensitivity in primary hyperparathyroidism
The 11 references without a DOI — listed, not checked
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no DOI — not checkedRevision parathyroid surgery
no DOI — not checked93
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