Evidence map›Paper›PMID 38436911›Full record

ReviewCerebellum (London, England)2024

CHARON: An Imaging-Based Diagnostic Algorithm to Navigate Through the Sea of Hereditary Degenerative Ataxias.

Alessandra Scaravilli, Mario Tranfa, Giuseppe Pontillo, Bernard Brais, Giovanna De Michele, Roberta La Piana, Francesco Saccà, Filippo Maria Santorelli, Matthis Synofzik, Arturo Brunetti and 1 more

Open access · hybridAbstract readReview
In one paragraph

Review in Cerebellum (London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

11 authors at 4 institutions in 3 countries.

Alessandra ScaravilliDepartment of Advanced Biomedical Sciences, University of Naples "Federico II", Naples, Italy.
Mario TranfaDepartment of Advanced Biomedical Sciences, University of Naples "Federico II", Naples, Italy.
Giuseppe PontilloDepartment of Advanced Biomedical Sciences, University of Naples "Federico II", Naples, Italy.
Bernard BraisDepartment of Neurology and Neurosurgery, Montreal Neurological Hospital and Institute, Montreal, Canada.
Giovanna De MicheleDepartment of Neurosciences and Reproductive and Odontostomatological Sciences, University of Naples "Federico II", Naples, Italy.
Roberta La PianaDepartment of Neurology and Neurosurgery, Montreal Neurological Hospital and Institute, Montreal, Canada.
Francesco SaccàDepartment of Neurosciences and Reproductive and Odontostomatological Sciences, University of Naples "Federico II", Naples, Italy.
Filippo Maria SantorelliDepartment of Molecular Medicine, IRCCS Stella Maris Foundation, Pisa, Italy.
Matthis SynofzikGerman Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
Arturo BrunettiDepartment of Advanced Biomedical Sciences, University of Naples "Federico II", Naples, Italy.
Sirio CocozzaDepartment of Advanced Biomedical Sciences, University of Naples "Federico II", Naples, Italy. sirio.cocozza@unina.it.
University of Naples Federico II · ITMontreal Neurological Institute and Hospital · CAFondazione Stella Maris · ITUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The complexity in diagnosing hereditary degenerative ataxias lies not only in their rarity, but also in the variety of different genetic conditions that can determine sometimes similar and overlapping clinical findings. In this light, Magnetic Resonance Imaging (MRI) plays a key role in the evaluation of these conditions, being a fundamental diagnostic tool needed not only to exclude other causes determining the observed clinical phenotype, but also to proper guide to an adequate genetic testing. Here, we propose an MRI-based diagnostic algorithm named CHARON (Characterization of Hereditary Ataxias Relying On Neuroimaging), to help in disentangling among the numerous, and apparently very similar, hereditary degenerative ataxias. Being conceived from a neuroradiological standpoint, it is based primarily on an accurate evaluation of the observed MRI findings, with the first and most important being the pattern of cerebellar atrophy. Along with the evaluation of the presence, or absence, of additional signal changes and/or supratentorial involvement, CHARON allows for the identification of a small groups of ataxias sharing similar imaging features. The integration of additional MRI findings, demographic, clinical and laboratory data allow then for the identification of typical, and in some cases pathognomonic, phenotypes of hereditary ataxias.

Indexed as

AlgorithmsMagnetic Resonance ImagingHumansNeuroimagingAlgorithmAtaxiaMagnetic Resonance ImagingNeuroimaging

Identifiers

PMID38436911
PMCPMC11489197
OpenAlexW4392373246

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.