Evidence map›Paper›PMID 31447678›Full record

ArticleFrontiers in pharmacology2019

Ambroxol Hydrochloride Improves Motor Functions and Extends Survival in a Mouse Model of Familial Amyotrophic Lateral Sclerosis.

Alexandra Bouscary, Cyril Quessada, Althéa Mosbach, Noëlle Callizot, Michael Spedding, Jean-Philippe Loeffler, Alexandre Henriques

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 44 citations in OpenAlex.

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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 at 3 institutions in 1 country.

Alexandra BouscaryUniversité de Strasbourg, UMR_S 1118, Fédération de Médecine Translationnelle, Strasbourg, France.
Cyril QuessadaUniversité de Strasbourg, UMR_S 1118, Fédération de Médecine Translationnelle, Strasbourg, France.
Althéa MosbachUniversité de Strasbourg, UMR_S 1118, Fédération de Médecine Translationnelle, Strasbourg, France.
Noëlle CallizotNeuro-sys SAS, Gardanne, France.
Michael SpeddingSpedding Research Solutions SAS, Le Vesinet, France.
Jean-Philippe LoefflerUniversité de Strasbourg, UMR_S 1118, Fédération de Médecine Translationnelle, Strasbourg, France.
Alexandre HenriquesUniversité de Strasbourg, UMR_S 1118, Fédération de Médecine Translationnelle, Strasbourg, France.
Inserm · FRMécanismes Centraux et Périphériques de la Neurodégénérescence · FRUniversité de Strasbourg · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is a multifactorial and fatal neurodegenerative disease. Growing evidence connects sphingolipid metabolism to the pathophysiology of ALS. In particular, levels of ceramides, glucosylceramides, and gangliosides are dysregulated in the central nervous system and at the neuromuscular junctions of both animal models and patients. Glucosylceramide is the main precursor of complex glycosphingolipids that is degraded by lysosomal (GBA1) or non-lysosomal (GBA2) glucocerebrosidase. Here, we report that GBA2, but not GBA1, activity is markedly increased in the spinal cord, of SOD1

Indexed as

ALSambroxolGBA2glucocerebrosidaseglucosylceramideneuromuscular junction

Identifiers

PMID31447678
PMCPMC6692493
OpenAlexW2959056005

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.