Evidence map›Paper›PMID 10906029›Full record

ArticleArchives of disease in childhood2000

An unusual concurrence of graft versus host disease caused by engraftment of maternal lymphocytes with DiGeorge anomaly.

J G Ocejo-Vinyals, M J Lozano, P Sánchez-Velasco, J Escribano de Diego, J E Paz-Miguel, F Leyva-Cobián

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Archives of disease in childhood, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Immunological aspects of 22q11.2 deletion syndrome.Cellular and molecular life sciences : CMLS · 2012
    Review
  5. Article
  6. Article
  7. 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

6 authors at 1 institution in 1 country.

J G Ocejo-VinyalsServicio de Inmunología, Hospital Universitario "Marqués de Valdecilla", Instituto Nacional de la Salud, 39008 Santander, Spain.
M J Lozano
P Sánchez-Velasco
J Escribano de Diego
J E Paz-Miguel
F Leyva-Cobián
Instituto Nacional de la Salud · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe a girl with DiGeorge anomaly and normal cytogenetic and molecular studies, whose clinical course was complicated by graft versus host disease caused by intrauterine materno-fetal transfusion, and several immunohematological alterations including a monoclonal gammapathy of undetermined significance (first IgG, which subsequently changed to IgM). The main clinical features and pathological findings are discussed.

Indexed as

Child, PreschoolChimeraChromosomes, Human, Pair 22DiGeorge SyndromeFatal OutcomeFemaleFetomaternal TransfusionGraft vs Host DiseaseHumansImmunoglobulin GImmunoglobulin MPedigreePregnancyT-LymphocytesImmunoglobulin GImmunoglobulin M

Identifiers

PMID10906029
PMCPMC1718418
OpenAlexW2168670634

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.