Evidence map›Paper›PMID 17684762›Full record

ReviewVirchows Archiv : an international journal of pathology2007

Hereditary neuroendocrine tumors of the gastroenteropancreatic system.

Martin Anlauf, Nele Garbrecht, Juliane Bauersfeld, Anja Schmitt, Tobias Henopp, Paul Komminoth, Philipp U Heitz, Aurel Perren, Günter Klöppel

Abstract readReview
PubMed Publisher
In one paragraph

Review in Virchows Archiv : an international journal of pathology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Familial Hyperparathyroidism.Frontiers in endocrinology · 2021
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Nutrition and neuroendocrine tumors: An update of the literature.Reviews in endocrine & metabolic disorders · 2018
    Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Article
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

9 authors.

Martin AnlaufDepartment of Pathology, University of Kiel, Michaelisstr. 11, 24105, Kiel, Germany. manlauf@path.uni-kiel.de
Nele Garbrecht
Juliane Bauersfeld
Anja Schmitt
Tobias Henopp
Paul Komminoth
Philipp U Heitz
Aurel Perren
Günter Klöppel

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Approximately 5-10% of neuroendocrine tumors (NETs) of the gastroenteropancreatic system (GEP) have a hereditary background. The known inherited syndromes include multiple endocrine neoplasia type 1, neurofibromatosis type 1, von Hippel-Lindau disease, and the tuberous sclerosis complex. This review discusses for each of these syndromes the: (1) involved genes and specific types of mutations, (2) disease prevalence and penetrance, (3) affected neuroendocrine tissues and related clinical syndromes, (4) special morphological features of NETs and their putative precursor lesions. In addition, GEP-NETs clustering in individual families or associated with other malignancies without known genetic background are discussed.

Indexed as

Genetic Predisposition to DiseaseDigestive System NeoplasmsHumansNeuroendocrine Tumors

Identifiers

PMID17684762

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.