ReviewCancer genetics and cytogenetics2010
Solid tumors associated with multiple endocrine neoplasias.
Review in Cancer genetics and cytogenetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
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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.
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Who cites it
16 citing papers in PubMed, 63 citations in OpenAlex.
- Carney complex with PRKAR1A variant and breast/fibrolamellar carcinomas.Human genome variation · 2026Article
- Hereditary Gynecologic Cancer Syndromes - A Narrative Review.OncoTargets and therapy · 2022Review
- What Have We Learned from Molecular Biology of Paragangliomas and Pheochromocytomas?Endocrine pathology · 2021Review
- Multiple endocrine neoplasia type 1 (MEN1) presenting with renal stones: Case report and review.Radiology case reports · 2020Article
- Outcome and long-term follow-up of adrenal lesions in multiple endocrine neoplasia type 1.Archives of endocrinology and metabolism · 2019Article
- Multiple Endocrine Neoplasia Type 1: A Case Report With Review of Imaging Findings.Ochsner journal · 2018Article
- Hereditary syndromes predisposing to endocrine tumors and their skin manifestations.Reviews in endocrine & metabolic disorders · 2016Review
- Association Between Kidney Stones and Risk of Stroke: A Nationwide Population-Based Cohort Study.Medicine · 2016Article
- A Calcitonin-Negative Neuroendocrine Tumor Derived from Follicular Lesions of the Thyroid.Endocrinology and metabolism (Seoul, Korea) · 2015Article
- Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort.The Journal of clinical endocrinology and metabolism · 2015Article
- Association of carcinoid tumor and low grade glioma.World journal of surgical oncology · 2012Article
- Article
- Pituitary tumors in patients with MEN1 syndrome.Clinics (Sao Paulo, Brazil) · 2012Review
- Pancreatic endocrine tumors.North American journal of medical sciences · 2011Article
- Multiple Uterine Leiomyomas in Multiple Endocrine Neoplasia Type 1 with a Novel MEN1 Gene Mutation.Journal of human reproductive sciencesArticle
- Does Octreoscan add value in the differential diagnosis of parapharyngeal space lesions?Radiologia brasileiraArticle
Corrections and comments
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
Abstract
We present an update on molecular and clinical genetics of solid tumors associated with the various multiple endocrine neoplasias (MEN) syndromes. MEN type 1 (MEN1) describes the association of pituitary, parathyroid, and pancreatic islet cell tumors with a variety of many other lesions. MEN type 2 (MEN2) conditions represent at least four different syndromes that associate pheochromocytoma with medullary thyroid carcinoma, hyperparathyroidism, and a number of other manifestations. Other pheochromocytoma-associated syndromes include von Hippel-Lindau disease; neurofibromatosis 1; the recently defined paraganglioma syndromes type 1, 3, and 4; Carney-Stratakis syndrome; and the Carney triad. Carney-Stratakis syndrome is characterized by the association of paragangliomas and familial gastrointestinal stromal tumors. In the Carney triad, patients can manifest gastrointestinal stromal tumors, lung chondroma, paraganglioma, adrenal adenoma and pheochromocytoma, esophageal leiomyoma, and other conditions. The Carney complex is yet another form of MEN that is characterized by skin tumors and pigmented lesions, myxomas, schwannomas, and various endocrine neoplasias.
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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.