Evidence map›Paper›PMID 29147350›Full record

ArticleWorld journal of oncology2013

A Rare Disease in Adult: Langerhans Cell Histiocytosis.

Ilhami Berber, Mehmet Ali Erkurt, Irfan Kuku, Mustafa Koroglu, Emin Kaya, Serkan Unlu

Open access · greenAbstract readCase Reports
In one paragraph

Article in World journal of oncology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Iranian journal of pathology · 2017
    Article
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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

6 authors at 1 institution in 1 country.

Ilhami BerberDepartment of Hematology, Inonu University Faculty of Medicine, Malatya, Turkey.
Mehmet Ali ErkurtDepartment of Hematology, Inonu University Faculty of Medicine, Malatya, Turkey.
Irfan KukuDepartment of Hematology, Inonu University Faculty of Medicine, Malatya, Turkey.
Mustafa KorogluDepartment of Hematology, Inonu University Faculty of Medicine, Malatya, Turkey.
Emin KayaDepartment of Hematology, Inonu University Faculty of Medicine, Malatya, Turkey.
Serkan UnluDepartment of Radiology, Inonu University Faculty of Medicine, Malatya, Turkey.
Inonu University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Langerhans cell histiocytosis is a rare histiocytic disorder and has been diagnosed in all age groups, but is most common in children. This disease is very rare in adults. We presented a patient who was 62 years old man diagnosed langerhans cell histiocytosis.

Indexed as

AdultHistiocytosisLangerhans cell

Identifiers

PMID29147350
PMCPMC5649783
OpenAlexW2056758502

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.