Evidence map›Paper›PMID 33506078›Full record

ArticleBone reports2021

Multicentric carpotarsal osteolysis syndrome (MCTO) with generalized high bone turnover and high serum RANKL: Response to denosumab.

Ravit Regev, Etienne B Sochett, Yesmino Elia, Ronald M Laxer, Damien Noone, Kristi Whitney-Mahoney, Kornelia Filipowski, Amer Shamas, Reza Vali

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Bone reports, 2021. 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
1.3field-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

13 citing papers in PubMed, 18 citations in OpenAlex.

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  11. Monogenic disorders as mimics of juvenile idiopathic arthritis.Pediatric rheumatology online journal · 2022
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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

9 authors at 2 institutions in 1 country.

Ravit RegevDivision of Endocrinology, The Hospital for Sick Children, Toronto, ON, Canada.
Etienne B SochettDivision of Endocrinology, The Hospital for Sick Children, Toronto, ON, Canada.
Yesmino EliaDivision of Endocrinology, The Hospital for Sick Children, Toronto, ON, Canada.
Ronald M LaxerDivision of Rheumatology, The Hospital for Sick Children, Toronto, ON, Canada.
Damien NooneDivision of Nephrology, The Hospital for Sick Children, Toronto, ON, Canada.
Kristi Whitney-MahoneyDivision of Rheumatology, The Hospital for Sick Children, Toronto, ON, Canada.
Kornelia FilipowskiDivision of Endocrinology, The Hospital for Sick Children, Toronto, ON, Canada.
Amer ShamasDepartment of Paediatrics, The Hospital for Sick Children, Toronto, ON, Canada.
Reza ValiDepartment of Paediatrics, The Hospital for Sick Children, Toronto, ON, Canada.
Hospital for Sick Children · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MCTO is a rare disorder, caused by mutations in the

Indexed as

ACR, albumin to creatinine ratioBone turnoverCTX, C-telopeptideDenosumabESKD, end stage kidney diseaseHRpQCTHRpQCT, high resolution peripheral quantitative computed tomographyMafB, gene v-maf musculoaponeurotic fibrosarcoma oncogene ortholog BMCTOMCTO, Multicentric Carpotarsal Osteolysis SyndromeOPGOPG, osteoprotegerinOsteoporosisRANKLRANKL, receptor activator of nuclear factor-кB ligand

Identifiers

PMID33506078
PMCPMC7815641
OpenAlexW3119476937

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.