Evidence map›Paper›PMID 34440204›Full record

ReviewBiomedicines2021

NAD

Elena Obrador, Rosario Salvador-Palmer, Rafael López-Blanch, Ryan W Dellinger, José M Estrela

Abstract readReview
In one paragraph

Review in Biomedicines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Role of Senataxin in Amyotrophic Lateral Sclerosis.Journal of molecular neuroscience : MN · 2023
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. 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

5 authors.

Elena ObradorDepartment of Physiology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.ORCID 0000-0002-5934-5543
Rosario Salvador-PalmerDepartment of Physiology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.ORCID 0000-0002-0784-6776
Rafael López-BlanchDepartment of Physiology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.
Ryan W DellingerElysium Health Inc., New York, NY 10013, USA.
José M EstrelaDepartment of Physiology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.

Funding

University of Valencia and Elysium Health Inc. OTR2017-18255INVESUniversity of Valencia and Elysium Health Inc. OTR2018-19337INVES
6 · The paper itself

Abstract

Charcot first described amyotrophic lateral sclerosis (ALS) between 1865 and 1874 as a sporadic adult disease resulting from the idiopathic progressive degeneration of the motor neuronal system, resulting in rapid, progressive, and generalized muscle weakness and atrophy. There is no cure for ALS and no proven therapy to prevent it or reverse its course. There are two drugs specifically approved for the treatment of ALS, riluzol and edaravone, and many others have already been tested or are following clinical trials. However, at the present moment, we still cannot glimpse a true breakthrough in the treatment of this devastating disease. Nevertheless, our understanding of the pathophysiology of ALS is constantly growing. Based on this background, we know that oxidative stress, alterations in the NAD

Indexed as

amyotrophic lateral sclerosisantioxidantsmotor neuronsNAD+oxidative stress

Identifiers

PMID34440204
PMCPMC8394119

What OpenQuestion holds

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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.