Evidence map›Paper›PMID 39120005›Full record

ReviewTurkish journal of haematology : official journal of Turkish Society of Haematology2024

Deficiency of Adenosine Deaminase 2

Çağrı Coşkun, Şule Ünal

Abstract readReview
In one paragraph

Review in Turkish journal of haematology : official journal of Turkish Society of Haematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Extreme Phenotypic Variation in Siblings with Identical Homozygous Mutations Causing ADA2 Deficiency: A Case SeriesTurkish journal of haematology : official journal of Turkish Society of Haematology · 2025
    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

2 authors.

Çağrı CoşkunHacettepe University Faculty of Medicine, Department of Pediatric Hematology, Ankara, TürkiyeORCID 0000-0001-9725-8355
Şule ÜnalHacettepe University Faculty of Medicine, Department of Pediatric Hematology, Ankara, TürkiyeORCID 0000-0002-3842-8788

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adenosine deaminase 2 (

Indexed as

Adenosine DeaminaseAgammaglobulinemiaDisease ManagementGenetic TherapyHematopoietic Stem Cell TransplantationHereditary Autoinflammatory DiseasesHumansIntercellular Signaling Peptides and ProteinsMutationPhenotypeSevere Combined ImmunodeficiencyTumor Necrosis Factor-alphaADA2 protein, humanAdenosine DeaminaseIntercellular Signaling Peptides and ProteinsTumor Necrosis Factor-alphaADA2 geneAutoinflammatory diseaseDeficiency of adenosine deaminase 2ImmunodeficiencyPure red cell aplasia

Identifiers

PMID39120005
PMCPMC11589373

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.