Evidence map›Paper›PMID 29868001›Full record

ArticleFrontiers in immunology2018

Combined Immunodeficiency in Patients With Trichohepatoenteric Syndrome.

Frédéric Vély, Vincent Barlogis, Evelyne Marinier, Marie-Edith Coste, Béatrice Dubern, Emmanuelle Dugelay, Julie Lemale, Christine Martinez-Vinson, Noël Peretti, Ariane Perry and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  10. NovelTranslational pediatrics · 2022
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  11. Sensing of RNA stress by mTORC1 drives autoinflammation.The Journal of clinical investigation · 2022
    Article
  12. Article
  13. Review
  14. Article
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  16. A New Variant Mutation inPediatric reports · 2020
    Article
  17. Review
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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

16 authors at 7 institutions in 1 country.

Frédéric VélyAix Marseille Univ, CNRS, INSERM, CIML, Marseille, France.
Vincent BarlogisAPHM, Hôpital de la Timone, Service d'Hématologie et Oncologie Pédiatrique, Marseille, France.
Evelyne MarinierAPHP Robert Debré, Department of Pediatric Gastroenterology, Hepatology and Nutrition, Paris, France.
Marie-Edith CosteAPHM, Hôpital de la Timone Enfant, Service de Pédiatrie Multidisciplinaire, Marseille, France.
Béatrice DubernNutrition et Gastroentérologie Pédiatriques, Hôpital Armand-Trousseau, UMR-S U1166 Nutriomics, UPMC, Sorbonne University, Paris, France.
Emmanuelle DugelayAPHP Robert Debré, Department of Pediatric Gastroenterology, Hepatology and Nutrition, Paris, France.
Julie LemaleNutrition et Gastroentérologie Pédiatriques, Hôpital Armand-Trousseau, UMR-S U1166 Nutriomics, UPMC, Sorbonne University, Paris, France.
Christine Martinez-VinsonAPHP Robert Debré, Department of Pediatric Gastroenterology, Hepatology and Nutrition, Paris, France.
Noël PerettiDepartment of Pediatric Nutrition, University Pediatric Hospital of Lyon, Hospices Civils de Lyon HCL, INSERM U1060, CarMeN Laboratory, University Claude Bernard Univ Lyon-1, Lyon, France.
Ariane PerryAPHP, Hôpitaux Universitaires Paris Sud, Hôpital Antoine Béclère, Centre de référence des maladies héréditaires du métabolisme hépatique, Clamart, France.
Patrice BourgeoisAPHM, Hôpital de la Timone Enfant, Service de biologie moléculaire, Marseille, France.
Catherine BadensAPHM, Hôpital de la Timone Enfant, Service de biologie moléculaire, Marseille, France.
Olivier GouletAPHP, Necker-Enfants Malades Hospital, Department of Pediatric Gastroenterology, Hepatology and Nutrition, Paris-Descartes University, Intestinal Failure Rehabilitation Center, National Reference Centre for Rare Digestive Diseases, Paris, France.
Jean-Pierre HugotAPHP, Hôpital Robert Debré, Paris, France.
Catherine FarnarierAPHM, Hôpital de la Timone, Service d'Immunologie, Marseille-Immunopôle, Marseille, France.
Alexandre FabreAPHM, Hôpital de la Timone Enfant, Service de Pédiatrie Multidisciplinaire, Marseille, France.
Assistance Publique – Hôpitaux de Paris · FRInserm · FRHôpital de la Timone · FRSorbonne Université · FRCentre National de la Recherche Scientifique · FRHôpital Necker-Enfants Malades · FRUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The syndromic diarrhea/trichohepatoenteric syndrome (SD/THE) is a rare and multi-system genetic disorder caused by mutation in

Indexed as

B-LymphocytesCarrier ProteinsCohort StudiesDiarrhea, InfantileDNA HelicasesFaciesFetal Growth RetardationHair DiseasesHumansImmunologic Deficiency SyndromesImmunologic MemoryInfantInfant, NewbornInterferon-gammaKiller Cells, NaturalLymphocyte CountCarrier ProteinsDNA HelicasesInterferon-gammaSKIV2L protein, humanTTC37 protein, humanimmunodeficiencymemory B cellsNK cellsSKIV2Lsyndromic diarrhea/trichohepatoenteric syndromeT cellsTTC37

Identifiers

PMID29868001
PMCPMC5958188
OpenAlexW2801448773

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.