Evidence map›Paper›PMID 39519139›Full record

ReviewInternational journal of molecular sciences2024

Molecular Pathophysiology of Parathyroid Tumorigenesis-The Lesson from a Rare Disease: The "MEN1 Model".

Alessandro Brunetti, Roberta Cosso, Fabio Vescini, Alberto Falchetti

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Observational
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Alessandro BrunettiSC Endocrinologia, Ospedale Santa Maria della Misericordia, 33100 Udine, Italy.ORCID 0000-0001-6651-4117
Roberta CossoMedical Center Amedic, 47521 Cesena, Italy.
Fabio VesciniSC Endocrinologia, Ospedale Santa Maria della Misericordia, 33100 Udine, Italy.ORCID 0000-0003-1892-9785
Alberto FalchettiSC Endocrinologia, ASST Grande Ospedale Metropolitano Niguarda, Piazza dell'Ospedale Maggiore, 3, 20162 Milano, Italy.ORCID 0000-0002-6739-4417

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary hyperparathyroidism represents the third most prevalent endocrine disease in the general population, consisting of an excessive secretion of parathyroid hormone from one or, more frequently, more of the parathyroid glands, leading to a dysregulation of calcium homeostasis. Schematically, its development occurs primarily by pathophysiological events with genetic mutation, at the germline and/or somatic level, that favor the neoplastic transformation of parathyroid cells and promote their aberrant proliferation, and mutations determining the shift in the PTH "set-point", thus interfering with the normal pathways of PTH secretion and leading to a "resetting" of Ca

Indexed as

Multiple Endocrine Neoplasia Type 1Parathyroid NeoplasmsAnimalsCarcinogenesisCell Transformation, NeoplasticHumansHyperparathyroidism, PrimaryMutationParathyroid GlandsParathyroid HormoneProto-Oncogene ProteinsRare DiseasesMEN1 protein, humanParathyroid HormoneProto-Oncogene ProteinsCDKN1B geneepigeneticsfamilial hyperparathyroidismgenetics of parathyroid tumorsMEN1 geneMEN1 syndromeMEN4 syndromemeninmiRNAsprimary hyperparathyroidism

Identifiers

PMID39519139
PMCPMC11545851

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.