Evidence map›Paper›PMID 38847890›Full record

ArticleJournal of clinical immunology2024

Double Trouble: Novel Digenic CD19-RABEP2 Deletion in Predominantly Antibody Deficiency with Syndromic Features.

Neha Jodhawat, Umair Ahmed Bargir, Goutham Rawal, Priti Kamble, Shweta Shinde-Vhatkar, Aparna Dalvi, Suhas Kulkarni, Manisha Madkaikar

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In one paragraph

Article in Journal of clinical immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Neha JodhawatDepartment of Pediatric immunology and leukocyte biology,, ICMR-National institute of immunohaematology (NIIH), Parel, Mumbai, 400012, Maharashtra, India.
Umair Ahmed BargirDepartment of Pediatric immunology and leukocyte biology,, ICMR-National institute of immunohaematology (NIIH), Parel, Mumbai, 400012, Maharashtra, India.
Goutham RawalDepartment of Pediatric immunology and leukocyte biology,, ICMR-National institute of immunohaematology (NIIH), Parel, Mumbai, 400012, Maharashtra, India.
Priti KambleDepartment of Pediatrics, D Y Patil Hospital and Research Centre, Kolhapur, 416005, India.
Shweta Shinde-VhatkarDepartment of Pediatric immunology and leukocyte biology,, ICMR-National institute of immunohaematology (NIIH), Parel, Mumbai, 400012, Maharashtra, India.
Aparna DalviDepartment of Pediatric immunology and leukocyte biology,, ICMR-National institute of immunohaematology (NIIH), Parel, Mumbai, 400012, Maharashtra, India.
Suhas KulkarniDepartment of Pediatrics, D Y Patil Hospital and Research Centre, Kolhapur, 416005, India.
Manisha MadkaikarDepartment of Pediatric immunology and leukocyte biology,, ICMR-National institute of immunohaematology (NIIH), Parel, Mumbai, 400012, Maharashtra, India. madkaikarmanisha@gmail.com.

Funding

Indian Council of Medical Research 33/27/2019-TF/Rare/BMSIndian Council of Medical Research 45/05/2022/HAE/BMS
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Antigens, CD19FemaleGene DeletionHumansImmunologic Deficiency SyndromesMaleSequence DeletionAntigens, CD19CD19 molecule, human

Identifiers

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.