Evidence map›Paper›PMID 31221777›Full record

ArticleHaematologica2019

Erdheim-Chester disease associated with chronic myelomonocytic leukemia harboring the same clonal mutation.

Pauline Bonnet, François Chasset, Philippe Moguelet, Noémie Abisror, Raphaël Itzykson, Jean-David Bouaziz, Pierre Hirsch, Annick Barbaud, Julien Haroche, Arsène Mekinian and 7 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Haematologica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

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  6. [Mutation pedigree and treatment selection of Erdheim-Chester disease].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2023
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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

17 authors at 7 institutions in 1 country.

Pauline BonnetFaculté de Médecine Sorbonne Université, AP-HP, Service de Dermatologie et Allergologie, Hôpital Tenon, Paris.
François ChassetFaculté de Médecine Sorbonne Université, AP-HP, Service de Dermatologie et Allergologie, Hôpital Tenon, Paris francois.chasset@aphp.fr.
Philippe MogueletFaculté de Médecine Sorbonne Université, AP-HP, Service de Pathologie, Hôpital Tenon, Paris.
Noémie AbisrorFaculté de Médecine Sorbonne Université, AP-HP, Service de Médecine Interne, Hôpital Saint-Antoine, Paris.
Raphaël ItzyksonFaculté de Médecine Paris Diderot, AP-HP, Service d'Hématologie, Hôpital Saint-Louis, Paris.
Jean-David BouazizFaculté de Médecine Paris Diderot, AP-HP, Service de Dermatologie, Hôpital Saint-Louis, Paris.
Pierre HirschFaculté de Médecine Sorbonne Université, AP-HP, Service de Biologie Cellulaire, Hôpital Saint-Antoine, Paris.
Annick BarbaudFaculté de Médecine Sorbonne Université, AP-HP, Service de Dermatologie et Allergologie, Hôpital Tenon, Paris.
Julien HarocheFaculté de Médecine Sorbonne Université, AP-HP, Service de Médecine Interne 2, Hôpital Pitié-Salpêtrière, Paris.
Arsène MekinianFaculté de Médecine Sorbonne Université, AP-HP, Service de Médecine Interne, Hôpital Saint-Antoine, Paris.
Zofia Hélias-RodzewiczFaculté de Médecine Université de Versailles, AP-HP, Service de Pathologie et laboratoire EA4340, Hôpital Ambroise Paré, Boulogne.
Emmanuelle ClappierFaculté de Médecine Paris Diderot, AP-HP, laboratoire Génome et Cancer, INSERM UMR944 et CNRS UMR7212, Hôpital Saint-Louis, Paris.
Pierre FenauxFaculté de Médecine Paris Diderot, AP-HP, Service d'Hématologie, Hôpital Saint-Louis, Paris.
Olivier FainFaculté de Médecine Sorbonne Université, AP-HP, Service de Médecine Interne, Hôpital Saint-Antoine, Paris.
Abdellatif TaziFaculté de Médecine Paris Diderot, AP-HP, Service de Pneumologie, Hôpital Saint-Louis, Paris, France.
Jean-François EmileFaculté de Médecine Université de Versailles, AP-HP, Service de Pathologie et laboratoire EA4340, Hôpital Ambroise Paré, Boulogne.
MINHEMON and EMSED
Assistance Publique – Hôpitaux de Paris · FRSorbonne Université · FRHôpital Ambroise-Paré · FRHôpital Saint-Antoine · FRHôpital Saint-Louis · FRHôpital Tenon · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic Predisposition to DiseaseMutationBiomarkersBiopsyBone MarrowClonal EvolutionErdheim-Chester DiseaseFemaleGenetic Association StudiesHumansImmunohistochemistryLeukemia, Myelomonocytic, ChronicMiddle AgedSkinBiomarkers

Identifiers

PMID31221777
PMCPMC6821636
OpenAlexW2950264247

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.