Evidence map›Paper›PMID 39641820›Full record

ArticleCerebellum (London, England)2024

Hereditary Spastic Paraplegia Associated with Ultra-Rare Variant Enrichment Encompassing the SYNE1, CAPN1 and PGAP1 Genes.

E Fratto, Maurizio Morelli, J Buonocore, A Quattrone, R Procopio, M Gagliardi, E Tinelli, F Fortunato, A Gambardella

Abstract readLetter
PubMed Publisher
In one paragraph

Article 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Novel homozygousTherapeutic advances in neurological disorders · 2026
    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

9 authors.

E FrattoDepartment of Medical and Surgical Sciences, Institute of Neurology, "Magna Graecia" University, Catanzaro, Calabria, Italy.ORCID https://orcid.org/0000-0003-3422-972X
Maurizio MorelliDepartment of Medical and Surgical Sciences, Institute of Neurology, "Magna Graecia" University, Catanzaro, Calabria, Italy. m.morelli@unicz.it.ORCID https://orcid.org/0000-0002-7263-1229
J BuonocoreDepartment of Medical and Surgical Sciences, Institute of Neurology, "Magna Graecia" University, Catanzaro, Calabria, Italy.ORCID https://orcid.org/0000-0002-3813-283X
A QuattroneDepartment of Medical and Surgical Sciences, Institute of Neurology, "Magna Graecia" University, Catanzaro, Calabria, Italy.ORCID https://orcid.org/0000-0003-2071-2083
R ProcopioDepartment of Medical and Surgical Sciences, Neuroscience Research Center, "Magna Graecia" University, Catanzaro, Calabria, Italy.ORCID https://orcid.org/0000-0001-7141-2123
M GagliardiDepartment of Medical and Surgical Sciences, Neuroscience Research Center, "Magna Graecia" University, Catanzaro, Calabria, Italy.ORCID https://orcid.org/0000-0002-3386-9808
E TinelliDepartment of Medical and Surgical Sciences, Institute of Neuroradiology, "Magna Graecia" University, Catanzaro, Calabria, Italy.ORCID https://orcid.org/0000-0002-3007-4022
F FortunatoDepartment of Medical and Surgical Sciences, Institute of Neurology, "Magna Graecia" University, Catanzaro, Calabria, Italy.ORCID https://orcid.org/0000-0001-8395-7809
A GambardellaDepartment of Medical and Surgical Sciences, Institute of Neurology, "Magna Graecia" University, Catanzaro, Calabria, Italy.ORCID https://orcid.org/0000-0001-7384-3074

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Complex inheritanceHereditary ataxiaHereditary spastic paraplegiaNext-generation sequencingSYNE1

Identifiers

PMID39641820

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.