Evidence map›Paper›PMID 34573985›Full record

ArticleDiagnostics (Basel, Switzerland)2021

Coexistence of Primary Myelofibrosis and Paroxysmal Nocturnal Hemoglobinuria Clone with

Sholhui Park, Min-Kyung So, Min-Sun Cho, Dae-Young Kim, Jungwon Huh

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. The impact of SETBP1 mutations in neurological diseases and cancer.Genes to cells : devoted to molecular & cellular mechanisms · 2023
    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

5 authors at 1 institution in 1 country.

Sholhui ParkDepartment of Laboratory Medicine, College of Medicine, Ewha Womans University, Seoul 07804, Korea.ORCID 0000-0002-6467-427X
Min-Kyung SoDepartment of Laboratory Medicine, College of Medicine, Ewha Womans University, Seoul 07804, Korea.ORCID 0000-0001-9728-3008
Min-Sun ChoDepartment of Pathology, College of Medicine, Ewha Womans University, Seoul 07804, Korea.
Dae-Young KimDepartment of Internal Medicine, College of Medicine, Ewha Womans University, Seoul 07804, Korea.
Jungwon HuhDepartment of Laboratory Medicine, College of Medicine, Ewha Womans University, Seoul 07804, Korea.
Ewha Womans University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary myelofibrosis (PMF) and paroxysmal nocturnal hemoglobinuria (PNH) are very rare diseases, respectively, and it is uncommon to have both diseases together. Mutational profiling using next-generation sequencing in PMF and PNH detected additional mutations associated with myeloid neoplasms, suggesting a step-wise clonal evolution. We present here a very rare case with PMF and PNH with

Indexed as

case reportJAK2 V617Fparoxysmal nocturnal hemoglobinuriaprimary myelofibrosisSETBPT1 mutationU2AF1 mutation

Identifiers

PMID34573985
PMCPMC8466901
OpenAlexW3198815923

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.