Evidence map›Paper›PMID 28091863›Full record

ArticleCerebellum (London, England)2017

Fast Progression of Cerebellar Atrophy in PLA2G6-Associated Infantile Neuronal Axonal Dystrophy.

Mario Mascalchi, Francesco Mari, Beatrice Berti, Emanuele Bartolini, Matteo Lenge, Andrea Bianchi, Laura Antonucci, Filippo M Santorelli, Barbara Garavaglia, Renzo Guerrini

Abstract read
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In one paragraph

Article in Cerebellum (London, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. [Progressive psychomotor regression for 2.5 years in a boy aged 5 years].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2022
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. [Clinical features of infantile neuroaxonal dystrophy and PLA2G6 gene testing].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2019
    Article
  8. Review
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

10 authors at 4 institutions in 1 country.

Mario MascalchiNeuroradiology, Meyer Children's Hospital, Florence, Italy. mario.mascalchi@unifi.it.
Francesco MariNeurology Unit and Laboratories, Meyer Children's Hospital, University of Florence, Florence, Italy.
Beatrice BertiNeurology Unit and Laboratories, Meyer Children's Hospital, University of Florence, Florence, Italy.
Emanuele BartoliniNeurology Unit and Laboratories, Meyer Children's Hospital, University of Florence, Florence, Italy.
Matteo LengeNeurology Unit and Laboratories, Meyer Children's Hospital, University of Florence, Florence, Italy.
Andrea BianchiNeuroradiology, Meyer Children's Hospital, Florence, Italy.
Laura AntonucciNeuroradiology, Meyer Children's Hospital, Florence, Italy.
Filippo M SantorelliIRCCS Stella Maris Foundation, Pisa, Italy.
Barbara GaravagliaMolecular Neurogenetics Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Renzo GuerriniNeurology Unit and Laboratories, Meyer Children's Hospital, University of Florence, Florence, Italy.
Meyer Children's Hospital · ITUniversity of Florence · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITFondazione Stella Maris · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infantile neuronal axonal dystrophy (INAD) is characterized by progressive cerebellar atrophy. MRI has been recommended as a marker of disease progression in cerebellar diseases. We performed a longitudinal brain volumetry study in a couple of bicorial twins with PLA2G6-positive INAD. Brain volumetry was calculated with FreeSurfer software on 3T T1-weighted images acquired at age 28 (t

Indexed as

AtrophyAxonsCerebellar DiseasesChild, PreschoolDisease ProgressionFemaleGroup VI Phospholipases A2HumansInfantMagnetic Resonance ImagingMaleNeuroaxonal DystrophiesGroup VI Phospholipases A2Brain mappingCerebellar degenerationMRIPediatric

Identifiers

PMID28091863
OpenAlexW2572993538

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.