ReviewJournal of pediatric genetics2016
Multiple Endocrine Neoplasia: A Genetically Diverse Group of Familial Tumor Syndromes.
Review in Journal of pediatric genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
What it found
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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.
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.
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Who cites it
10 citing papers in PubMed, 18 citations in OpenAlex.
- Case of Recurrent Primary Hyperparathyroidism, Congenital Granular Cell Tumor, and Aggressive Colorectal Cancer.Journal of the Endocrine Society · 2022Article
- Patients' perception on the quality of care for multiple endocrine neoplasia disorders in Europe: an online survey from a patient support group.Endocrine · 2021Article
- Clinical and genetic features of pediatric PCCs/PGLs patients: a single-center experience in China.Translational andrology and urology · 2020Article
- Parathyroid Pathology.Surgical pathology clinics · 2019Review
- Cryo-EM structure of the activated RET signaling complex reveals the importance of its cysteine-rich domain.Science advances · 2019Article
- Article
- Multiple endocrine neoplasia-like syndrome in 24 baboons (Papio spp.).Journal of medical primatology · 2018Article
- Inherited lung cancer syndromes targeting never smokers.Translational lung cancer research · 2018Review
- Identification of diverse target RNAs that are functionally regulated by human Pumilio proteins.Nucleic acids research · 2018Article
- Multiple Oral Mucosal Hamartomas in a 34-Year Old Female.Head and neck pathology · 2017Article
Corrections and comments
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Authors and funding
1 author at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Multiple endocrine neoplasia (MEN) syndrome is a familial cancer syndrome characterized by neuroendocrine tumors. The syndrome encompasses four major subtypes: MEN1, MEN2A, MEN2B, and MEN4. MEN1 is caused by mutations in the MEN1 gene, MEN2A and MEN2B are caused by mutations in RET, and MEN4 is caused by mutations in CDKNB1. All are inherited in an autosomal dominant pattern, but de novo cases do arise. While all subtypes are associated with neuroendocrine tumors, each has characteristic organ involvement. Identifying patients with the syndrome can aid in proper screening and treatment.
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What OpenQuestion holds
Registered trials
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.