Evidence map›Paper›PMID 41975704›Full record

ArticleDiagnostics (Basel, Switzerland)2026

Challenges in Diagnosis and Management of Coffin-Lowry Syndrome-Single-Center Experience.

Ana Maria Chirilas, Alexandru Cărămizaru, Anca-Lelia Riza, Andreea Mitut-Veliscu, Andrei Costache, Rebecca-Cristiana Șerban, Aritina Morosanu, Carmen Niculescu, Alexandru-Cătălin Pâslaru, Florin Burada and 1 more

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2026. 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

11 authors.

Ana Maria ChirilasRegional Centre of Medical Genetics Dolj, Emergency County Hospital Craiova, 200642 Craiova, Romania.ORCID 0009-0000-5326-6361
Alexandru CărămizaruLaboratory of Human Genomics, University of Medicine and Pharmacy of Craiova, 200638 Craiova, Romania.ORCID 0009-0006-1422-0057
Anca-Lelia RizaRegional Centre of Medical Genetics Dolj, Emergency County Hospital Craiova, 200642 Craiova, Romania.
Andreea Mitut-VeliscuRegional Centre of Medical Genetics Dolj, Emergency County Hospital Craiova, 200642 Craiova, Romania.
Andrei CostacheDepartment of Biophysics, University of Medicine and Pharmacy of Craiova, 200638 Craiova, Romania.
Rebecca-Cristiana ȘerbanRegional Centre of Medical Genetics Dolj, Emergency County Hospital Craiova, 200642 Craiova, Romania.
Aritina MorosanuDepartment of Pediatrics, University of Medicine and Pharmacy of Craiova, 200638 Craiova, Romania.
Carmen NiculescuDepartment of Pediatrics, University of Medicine and Pharmacy of Craiova, 200638 Craiova, Romania.
Alexandru-Cătălin PâslaruFaculty of Medicine, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania.ORCID 0000-0002-9054-3257
Florin BuradaRegional Centre of Medical Genetics Dolj, Emergency County Hospital Craiova, 200642 Craiova, Romania.
Ioana StreataRegional Centre of Medical Genetics Dolj, Emergency County Hospital Craiova, 200642 Craiova, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Coffin–Lowry syndromeRPS6KA3 genesyndromic intellectual disability

Identifiers

PMID41975704
PMCPMC13073513

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.