Disease: Hyperparathyroidism- familial- primary
- <em>CDC73</em>-Related Disorders
- <em>GCM2</em> p.Tyr394Ser variant in Ashkenazi Israeli patients with suspected familial isolated hyperparathyroidism
- 30 years of prophylactic thyroidectomy for hereditary medullary thyroid cancer : A milestone in translational medicine
- A Case of Delayed Diagnosis of Idiopathic Infantile Hypercalcemia Due to CYP24A1 Mutation: A 10-Year Journey
- A case report of primary hyperparathyroidism in an adolescent during Ramadan fast
- A family case report of parathyroid carcinoma associated with <em>CDC73</em> mutation in hyperparathyroidism-jaw tumor syndrome
- A family case report of parathyroid carcinoma associated with CDC73 mutation in hyperparathyroidism-jaw tumor syndrome
- A Germline ZFX Missense Variant in a Patient With Primary Hyperparathyroidism
- A Japanese Family Meeting the Clinical Diagnostic Criteria for MEN1 with a MEN1 Variant of Uncertain Significance
- A Knock-In Mouse Model of the <em>Gcm2</em> Variant p.Y392S Develops Normal Parathyroid Glands
- A novel likely pathogenetic variant p.(Cys235Arg) of the MEN1 gene in multiple endocrine neoplasia type 1 with multifocal glucagonomas
- A Novel Pathogenic <em>MEN1</em> Gene Variant Identified in a Family With Multiple Pancreatic Neuroendocrine Tumors
- Approach to Hypercalcemia
- Association of Hyperparathyroidism with Depression and Anxiety Among Chronic Hemodialysis Patients in the Al Baha Region, Kingdom of Saudi Arabia
- Brown tumor due to primary hyperparathyroidism in a familial case: a case report
- Brown tumors: Retrospective analysis of 26 cases
- Brown Tumors: The Hidden Face of Primary and Renal Hyperparathyroidism Amid Real-Life Settings
- Calcium Blood Level Elevation After Atorvastatin Initiation in a Patient With Hyperparathyroidism
- Case Presentation: Functional Assessment of a <em>CASR</em> Variant Identified in a Patient with Hypercalcaemia Confirms Familial Hypocalciuric Hypercalcaemia in the Patient and a Sister Previously Misdiagnosed with Primary Hyperparathyroidism
- Case Presentation: Functional Assessment of a CASR Variant Identified in a Patient with Hypercalcaemia Confirms Familial Hypocalciuric Hypercalcaemia in the Patient and a Sister Previously Misdiagnosed with Primary Hyperparathyroidism
- Case report: Comprehensive follow-up of a Colombian family carrying a novel MEN1 variant linked to a rare ACTH-producing pancreatic neuroendocrine carcinoma
- Case report: familial hypocalciuric hypercalcemia
- Challenges in the management of hypercalcemia in pregnancy - Case report of two cases
- Cinacalcet therapy in a child with novel homozygous CASR p.Glu353Lys mutation causing familial hypocalciuric hypercalcemia type 1: case report and review of the literature
- Clinical and outcome comparison of genetically positive vs. negative patients in a large cohort of suspected familial hypocalciuric hypercalcemia
- Clinical characteristics of a large familial cohort with Medullary thyroid cancer and germline Cys618Arg <em>RET</em> mutation in an Israeli multicenter study
- Clinical characteristics of a large familial cohort with Medullary thyroid cancer and germline Cys618Arg RET mutation in an Israeli multicenter study
- Clinical utility of untimed spot urine sampling in measuring calcium creatinine clearance in the diagnostic work-up of PTH-dependent hypercalcaemia
- Clinicopathological Study of Chronic Kidney Disease of Unknown Etiology in Odisha
- Coexistence of a Calcium-Sensing Receptor Mutation and Primary Hyperparathyroidism
- Complex Primary Hyperparathyroidism: Hereditary and Recurrent Disease
- Cutaneous lesions and other non-endocrine manifestations of Multiple Endocrine Neoplasia type 1 syndrome
- Delayed Diagnosis of Primary Hyperparathyroidism: A Case Report
- Differences in clinical characteristics, treatment, and outcomes of sporadic and MEN-1-related insulinomas
- Differences in the Presentation and Outcome between Premenopausal and Postmenopausal Primary Hyperparathyroidism Indian Women: A Single-Center Experience
- Electrolytes
- Expressions of Cushing's syndrome in multiple endocrine neoplasia type 1
- Familial Hypocalciuric Hypercalcemia
- Familial states of primary hyperparathyroidism: an update
- GCM2 p.Tyr394Ser variant in Ashkenazi Israeli patients with suspected familial isolated hyperparathyroidism
- Genetic and clinical screening for hereditary primary hyperparathyroidism in a large Chinese cohort: a single-center study
- Genetic profile of a large Spanish cohort with hypercalcemia
- Genetic testing for familial hyperparathyroidism: clinical-genetic profile in a Mediterranean cohort
- Genetics of hereditary forms of primary hyperparathyroidism
- Germline founder variant c.1998delinsTTCT in the RET oncogene: a cohort study in 15 Belgian families
- Hyperparathyroidism Jaw Tumor Syndrome, an Unforeseen Diagnosis
- Insights into Hyperparathyroidism-Jaw Tumour Syndrome: From Endocrine Acumen to the Spectrum of CDC73 Gene and Parafibromin-Deficient Tumours
- Management and surgical treatment of parathyroid carcinoma: a 6-year experience of a single centre of endocrine surgery unit
- Metabolic Bone Disease
- Multiple and hereditary renal tumors: a review for radiologists
- Multiple Endocrine Neoplasia Type 1, Type 2A, and Type 2B
- Multiple Endocrine Neoplasia Type 2
- Multiple Endocrine Neoplasia Type 4
- Multiple Endocrine Neoplasias Type 2
- Neonatal hypocalcaemic seizures unmasking asymptomatic maternal primary hyperparathyroidism
- Parathyroid carcinoma: molecular therapeutic targets
- Parathyroid tumors in the 5th edition of the WHO Classification of Tumors of the Endocrine Organs
- Pediatric Neuroendocrine Neoplasia of the Parathyroid Glands: Delving into Primary Hyperparathyroidism
- Phenotype and genotype of patients with multiple endocrine neoplasia type 1 studied in Argentina
- Predicting the presence of <em>MEN1</em> gene mutation based on the clinical phenotype of patients with primary hyperparathyroidism
- Predicting the presence of MEN1 gene mutation based on the clinical phenotype of patients with primary hyperparathyroidism
- Prevalence of Endocrine Manifestations and GIST in 108 Systematically Screened Patients With Neurofibromatosis Type 1
- Primary hyperparathyroidism associated with colorectal cancer: case report
- Primary Hyperparathyroidism in Older Adults: A Narrative Review of the Most Recent Literature on Epidemiology, Diagnosis and Management
- Primary Hyperparathyroidism overlapping with Multiple Sclerosis: a catastrophic marriage
- Primary hyperparathyroidism: predictors of sporadic multi-gland disease
- Primary hyperparathyroidism: predictors of sporadic multiglandular disease
- Recurrent multinodular goitre and primary hyperparathyroidism due to adenoma arising in a parathyroid autotransplant more than 20 years after near-total thyroidectomy
- Recurrent Primary Hyperparathyroidism in Hyperparathyroid Jaw Tumor Syndrome: A Case Report
- Special features of the diagnostics and treatment of hereditary primary hyperparathyroidism
- Sporadic parathyroid adenoma: an updated review of molecular genetics
- Surgical management of primary hyperparathyroidism
- The Role of Demographic and Clinical Factors in Germline Mutation Testing for Patients with Primary Hyperparathyroidism
- TRPC3 Is Downregulated in Primary Hyperparathyroidism
- Two Cases of Symptomatic Familial Hypocalciuric Hypercalcemia: Treatment Response to Calcimimetic Therapy
- Ultrasound-guided microwave ablation in the treatment of recurrent primary hyperparathyroidism in a patient with MEN1: a case report
- Uncovering genetic causes of hypophosphatemia
- Variant Tyr 394Ser in the <em>GCM2</em> Gene Is Rare in a Cohort of Ashkenazi Jews With Primary Hyperparathyroidism