Evidence map›Paper›PMID 42074341›Full record

ReviewInternational journal of molecular sciences2026

Pompe Disease: Pathogenesis, Molecular Mechanisms, Neurological Aspects, Diagnostics and Modern Therapeutic Approaches.

Alexandra Sharshakova, Alisa Fattakhova, Valeriya Solovyeva, Albert Sufianov, Galina Sufianova, Grigorii Kutovoi, Albert Rizvanov

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Alexandra SharshakovaInstitute for Fundamental Medicine and Biology, Kazan Federal University, 420008 Kazan, Russia.ORCID 0009-0002-2486-0518
Alisa FattakhovaInstitute for Fundamental Medicine and Biology, Kazan Federal University, 420008 Kazan, Russia.
Valeriya SolovyevaInstitute for Fundamental Medicine and Biology, Kazan Federal University, 420008 Kazan, Russia.ORCID 0000-0002-8776-3662
Albert SufianovDepartment of Neurosurgery, Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University), 119991 Moscow, Russia.
Galina SufianovaDepartment of Pharmacology, Tyumen State Medical University, 625023 Tyumen, Russia.
Grigorii KutovoiInstitute for Fundamental Medicine and Biology, Kazan Federal University, 420008 Kazan, Russia.
Albert RizvanovInstitute for Fundamental Medicine and Biology, Kazan Federal University, 420008 Kazan, Russia.ORCID 0000-0002-9427-5739

Funding

Ministry of Science and Higher Education of the Russian Federation This paper has been supported by the Kazan Federal University Strategic Academic Leadership Program (PRIORITY-2030)
6 · The paper itself

Abstract

Pompe disease (PD) is a neuromuscular autosomal recessive disorder caused by mutation in the

Indexed as

alpha-GlucosidasesGlycogen Storage Disease Type IIAnimalsAutophagyDisease Models, AnimalEnzyme Replacement TherapyHumansalpha-GlucosidasesGAA protein, humanautophagyCRIM statusenzyme replacement therapygene therapylysosomal storage diseaseneurodegenerationPompe disease

Identifiers

PMID42074341
PMCPMC13116368

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.