Disease: Hyperparathyroidism- neonatal severe primary
- A Case of a Heterozygous Inactivating CASR Variant with Adult-Onset Symptomatic Hypercalcemia Requiring Extensive Surgery
- A Case of Neonatal Severe Hyperparathyroidism: Challenges in Management
- A novel CASR mutation associated with neonatal severe hyperparathyroidism transmitted as an autosomal recessive disorder
- A novel mutation in the calcium sensing receptor gene in a neonate with severe hyperparathyroidism
- A novel SLC12A1 gene mutation associated with hyperparathyroidism, hypercalcemia, nephrogenic diabetes insipidus, and nephrocalcinosis in four patients
- A rare case of hypercalcemia-induced pancreatitis in a first trimester pregnant woman
- A rare cause of neonatal hypercalcemia: Neonatal severe primary hyperparathyroidism: A case report and review of the literature
- A very rare type of primary hyperparathyroidism with severe hypercalcemia in an infant
- Aetiology, Diagnosis and Surgical Treatment of Primary Hyperparathyroidism in Children: New Trends
- Approach to the Patient: Management of Parathyroid Diseases Across Pregnancy
- Benign familial hypocalciuric hypercalcemia
- Bone and Nutrition. A prospect of calcium sensing receptor
- Calcium signaling regulates trafficking of familial hypocalciuric hypercalcemia (FHH) mutants of the calcium sensing receptor
- Calcium-sensing receptor (CaSR) mutations and disorders of calcium, electrolyte and water metabolism
- Calcium-sensing receptor: Role in health and disease
- Case report: acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation
- Case Report: Severe Neonatal Course in Paternally Derived Familial Hypocalciuric Hypercalcemia
- Case Report: Unusual Presentations of Loss-of-Function Mutations of the Calcium-Sensing Receptor
- Cell Surface Calcium-Sensing Receptor Heterodimers: Mutant Gene Dosage Affects Ca<sup>2+</sup> Sensing but Not G Protein Interaction
- Challenges in diagnosis and management of neonatal hyperparathyroidism in a resource-limited country: a case series from a Sudanese family
- Childhood Sustained Hypercalcemia: A Diagnostic Challenge
- Cinacalcet as a First-Line Treatment in Neonatal Severe Hyperparathyroidism Secondary to Calcium Sensing Receptor (CaSR) Mutation
- 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 molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes
- Clinical characteristics and genetic analysis of two children with neonatal severe hyperparathyroidism
- Clinical Presentation, Management, and Outcomes of Primary Hyperparathyroidism during Pregnancy
- Clinicopathological correlates of hyperparathyroidism
- Coexistent parathyroid adenoma and thyroid papillary carcinoma in pregnancy
- Different treatment strategies in primary hyperparathyroidism during pregnancy
- Diseases associated with calcium-sensing receptor
- Disorders of calcium metabolism and parathyroid disease
- Disorders of the Calcium Sensing Signaling Pathway: From Familial Hypocalciuric Hypercalcemia (FHH) to Life Threatening Conditions in Infancy
- Eclampsia as the First Manifestation of Primary Hyperparathyroidism: a Case Report
- Epidemiology, Pathophysiology, and Genetics of Primary Hyperparathyroidism
- Evolution of Our Understanding of the Hyperparathyroid Syndromes: A Historical Perspective
- Familial and Hereditary Forms of Primary Hyperparathyroidism
- Familial Hyperparathyroidism - Disorders of Growth and Secretion in Hormone-Secretory Tissue
- Familial Hypocalciuric Hypercalcemia and Neonatal Severe Hyperparathyroidism
- Familial states of primary hyperparathyroidism: an update
- Generation of an induced pluripotent stem cell line HPCASRi002-A from a patient with neonatal severe primary hyperparathyroidism caused by a compound heterozygous mutation in the CASR gene
- Genetic causes of neonatal and infantile hypercalcaemia
- Genetic defects associated with familial and sporadic hyperparathyroidism
- Genetics of hereditary forms of primary hyperparathyroidism
- Hereditary hyperparathyroidism--a consensus report of the European Society of Endocrine Surgeons (ESES)
- Hereditary syndromal and nonsyndromal forms of primary hyperparathyroidism
- Heritable forms of primary hyperparathyroidism: a current perspective
- Hypercalcaemia due to parathyroid carcinoma presenting in the third trimester of pregnancy
- Hypercalcemic Disorders in Children
- Hyperparathyroid crisis presenting with hyperemesis gravidarum
- Hyperparathyroidism in pregnancy and (99m)Tc-MIBI scintigraphy
- Hyperparathyroidism in pregnancy and <sup>99m</sup>Tc-MIBI scintigraphy
- Hyperplasia in glands with hormone excess
- Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites
- Idiopathic infantile hypercalcaemia in 5-month old girl
- Intraoperative parathyroid hormone monitoring in neonatal severe primary hyperparathyroidism
- Is calcium signaling relevant for long bone growth?
- Is minimally invasive parathyroid surgery an option for patients with gestational primary hyperparathyroidism?
- Late Presentation of Primary Oxalosis, Microcrystalline Arthropathy, and Tumoral Calcinosis: A Case Report and a Literature Review
- Management of familial hyperparathyroidism syndromes: MEN1, MEN2, MEN4, HPT-Jaw tumour, Familial isolated hyperparathyroidism, FHH, and neonatal severe hyperparathyroidism
- Management of primary hyperparathyroidism in pregnancy: a case series
- Management of severe and symptomatic primary hyperparathyroidism in the first trimester of unplanned pregnancy
- Molecular pathogenesis of primary hyperparathyroidism
- Needle in a haystack-parathyroid gland in a 10-day old infant: a case report and literature review
- Neonatal hypercalcemia due to a homozygous mutation in the calcium-sensing receptor: failure of cinacalcet
- Neonatal severe hyperparathyroidism due to a homozygous mutation of calcium-sensing receptor; a challenging case
- Neonatal severe hyperparathyroidism: A case report
- Neonatal severe hyperparathyroidism: further clinical and molecular delineation
- Neonatal Severe Hyperparathyroidism: Novel Insights From Calcium, PTH, and the CASR Gene
- Neonatal Severe Primary Hyperparathyroidism: A Series of Four Cases and their Long-term Management in India
- New diagnostic modalities and emerging treatments for neonatal bone disease
- Novel homozygous inactivating mutation of the calcium-sensing receptor gene in neonatal severe hyperparathyroidism responding to cinacalcet therapy: A case report and literature review
- Parathyroid Disease in Pregnancy and Lactation: A Narrative Review of the Literature
- Pediatric hyperparathyroidism: review and imaging update
- Personalised medicines for familial hypercalcemia and hyperparathyroidism
- Pheochromocytoma associated with primary hyperparathyroidism and type 1 neurofibromatosis
- Polyclonality of Parathyroid Tumors in Neonatal Severe Hyperparathyroidism
- Preeclampsia as an Inaugural Manifestation of Primary Hyperparathyroidism: A Case Report
- Preterm Parturient with Polyhydramnios and Pancreatitis: Primary Presentation of Hyperparathyroidism
- Primary Hyperparathyroidism
- Primary hyperparathyroidism can be mistaken as pregnancy inconvenience
- PRIMARY HYPERPARATHYROIDISM DURING PREGNANCY: A CASE SERIES OF 8 PATIENTS
- Primary hyperparathyroidism in children and adolescents
- Primary hyperparathyroidism in pregnancy
- Primary hyperparathyroidism in pregnancy: a case report highlighting uncommon complication
- Primary hyperparathyroidism in pregnancy: observations from the Indian PHPT registry
- Primary Hyperparathyroidism in Young and Adolescents: Alike or Unlike Adult Hyperparathyroidism? - A Series from South India
- Primary hyperparathyroidism presenting as a brown tumor with hypercalcemia crisis in a second-trimester pregnant woman: A case report
- Reduced affinity of calcium sensing-receptor heterodimers and reduced mutant homodimer trafficking combine to impair function in a model of familial hypocalciuric hypercalcemia type 1
- Reference values of parathyroid hormone in very low birth weight infants
- Sporadic and hereditary primary hyperparathyroidism
- Subtotal Parathyroidectomy Successfully Controls Calcium Levels of Patients with Neonatal Severe Hyperparathyroidism Carrying a Novel CASR Mutation
- Successful parathyroidectomy with intra-operative parathyroid hormone monitoring in a neonate with severe primary hyperparathyroidism caused by homozygous mutation in CASR gene
- Successful use of bisphosphonate and calcimimetic in neonatal severe primary hyperparathyroidism
- Surgical management of neonatal severe hyperparathyroidism
- Surgical treatment of children with hyperparathyroidism: single centre experience
- Ten-year follow-up report and neurologic sequelae in a case of neonatal severe primary hyperparathyroidism
- The Biochemical Profile of Familial Hypocalciuric Hypercalcemia and Primary Hyperparathyroidism during Pregnancy and Lactation: Two Case Reports and Review of the Literature
- The calcium sensing receptor: from calcium sensing to signaling
- The efficiency of cinacalcet treatment in delaying parathyroidectomy in a case with neonatal severe hyperparathyroidism caused by homozygous mutation in the CASR gene
- The role of the calcium-sensing receptor in human disease