Evidence map›Paper›PMID 42295520›Full record

ArticleClinical autonomic research : official journal of the Clinical Autonomic Research Society2026

Co-occurrence of Chiari malformation type 1 and small fiber neuropathy in a family with a novel COL6A5 null variant.

Francesca Masciarelli, Domenico Dell'Aversana, Floriana Vitale, Giuseppina Ciccarelli, Lucia Micale, Silvia Morlino, Giuseppe Caporaso, Stefano Tozza, Vincenzo Provitera, Marco Castori and 1 more

Abstract readLetter
PubMed Publisher
In one paragraph

Article in Clinical autonomic research : official journal of the Clinical Autonomic Research Society, 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.

Francesca MasciarelliDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples Federico II, 80131, Naples, Italy.
Domenico Dell'AversanaDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples Federico II, 80131, Naples, Italy.
Floriana VitaleDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples Federico II, 80131, Naples, Italy.
Giuseppina CiccarelliDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples Federico II, 80131, Naples, Italy.
Lucia MicaleDivision of Medical Genetics and Inborn Errors of Morphogenesis Research Unit, Fondazione IRCCS-Casa Sollievo Della Sofferenza, Viale Cappuccini Snc, 71013, San Giovanni Rotondo (FG), Italy.
Silvia MorlinoDivision of Medical Genetics and Inborn Errors of Morphogenesis Research Unit, Fondazione IRCCS-Casa Sollievo Della Sofferenza, Viale Cappuccini Snc, 71013, San Giovanni Rotondo (FG), Italy.
Giuseppe CaporasoIstituti Clinici Scientifici Maugeri IRCCS, Skin Biopsy Lab, Neurological Rehabilitation Unit of Telese Terme Institute, 82037, Telese Terme, Benevento, Italy.
Stefano TozzaDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples Federico II, 80131, Naples, Italy.
Vincenzo ProviteraIstituti Clinici Scientifici Maugeri IRCCS, Skin Biopsy Lab, Neurological Rehabilitation Unit of Telese Terme Institute, 82037, Telese Terme, Benevento, Italy.
Marco CastoriDivision of Medical Genetics and Inborn Errors of Morphogenesis Research Unit, Fondazione IRCCS-Casa Sollievo Della Sofferenza, Viale Cappuccini Snc, 71013, San Giovanni Rotondo (FG), Italy.
Maria NolanoDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples Federico II, 80131, Naples, Italy. maria.nolano@unina.it.ORCID http://orcid.org/0000-0002-4849-1318

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Autonomic nervous systemChiari malformation type 1GeneticsSkin biopsySmall fiber neuropathy (SFN)

Identifiers

PMID42295520

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.