Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

An Analysis of Primary Hyperparathyroidism in Individuals Diagnosed with Multiple Endocrine Neoplasia Type 2

27 Mar 2025

Abstract excerpt

Background: Primary hyperparathyroidism (PHPT) represents a multi-faced disease with a wide spectrum of manifestations. Familial forms of PHPT (affecting up to 10% of the cases) involve a particular category that encompasses a large range of hereditary syndromes, including parathyroid hyper-function, frequently in the setting of a multi-glandular disease. Objective: The aim was to analyze the most recent findings...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Metabolism, Diabetes, and Cancer
Share to Neuroendocrine Tumor Research Advances
Share to Parathyroid Disorders and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 40277809
DOI: 10.3390/diseases13040098

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

An Analysis of Primary Hyperparathyroidism in Individuals Diagnosed with Multiple Endocrine Neoplasia Type 2PMID 40277809Read ↗

Primary Hyperparathyroidism in Multiple Endocrine Neoplasia Type 2A in Denmark 1930–2021: A Nationwide Population-Based Retrospective StudySemantic proximity Read ↗

Epidemiology, Pathophysiology, and Genetics of Primary HyperparathyroidismSemantic proximity Read ↗

Primary hyperparathyroidism as first manifestation in multiple endocrine neoplasia type 2A: an international multicenter studySemantic proximity Read ↗

Does Genotype-Specific Phenotype in Patients with Multiple Endocrine Neoplasia Type 2 Occur as Current Guidelines Predict?Semantic proximity Read ↗

Germline Mutations Related to Primary Hyperparathyroidism Identified by Next-Generation SequencingSemantic proximity Read ↗

Heritable forms of primary hyperparathyroidism: a current perspective.Semantic proximity Read ↗

Molecular genetics in familial primary hyperparathyroidism: A study from Northern IndiaSemantic proximity Read ↗

Primary hyperparathyroidism: Disease of diverse genetic, symptomatic, and biochemical phenotypes.Semantic proximity Read ↗

Molecular Pathophysiology of Parathyroid Tumorigenesis—The Lesson from a Rare Disease: The “MEN1 Model”Semantic proximity Read ↗

Evolution of Our Understanding of the Hyperparathyroid Syndromes: A Historical PerspectiveSemantic proximity Read ↗

Molecular genetics in primary hyperparathyroidism: the role of genetic tests in differential diagnosis, disease prevention strategy, and therapeutic planning. A 2017 updateSemantic proximity Read ↗

Molecular and Clinical Spectrum of Primary HyperparathyroidismSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.