Evidence map›Paper›PMID 30411352›Full record

ArticleJournal of anatomy2019

Pre- and postnatal development of the otic ganglion in humans.

Dave Bandke, Konstantin Ebauer, Alexander Ebauer, Serge Weis

Open access · bronzeAbstract read
In one paragraph

Article in Journal of anatomy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 85% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

4 authors at 3 institutions in 2 countries.

Dave BandkeDivision of Neuropathology, Kepler University Hospital, Johannes Kepler University, Linz, Austria.ORCID 0000-0001-6668-1062
Konstantin EbauerInstitute of Neuropathology, Ludwig-Maximilians University, Munich, Germany.
Alexander EbauerInstitute of Anatomy, University of Tübingen, Tübingen, Germany.
Serge WeisDivision of Neuropathology, Kepler University Hospital, Johannes Kepler University, Linz, Austria.
Johannes Kepler University of Linz · ATLudwig-Maximilians-Universität München · DEUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Only a few papers exist dealing with the development and aging of the autonomic nervous system - and even rarer are studies that investigated the otic ganglion. Using a special trepan, we removed and investigated 172 samples from 86 corpses, ranging from 20 weeks of gestational age (GA) to 95 years of age. The aim of the study was to measure different morphometric parameters of the ganglionic neurons in order to study age-related changes from early development until old age. Fetuses show the highest numerical density of neurons. Then, in the first years of life, a rapid growth of the cytoplasm takes place, which is the main reason for the neuronal growth and the increase of the general size of the otic ganglion at this age. Also, the number of satellite cells increases till puberty. In adults, the parameters are relatively stable over decades and decrease slowly, in contrast to the steep increase in the first years of life. Moreover, neuronal degeneration, storage of pigments, neuro-axonal dystrophy, and lymphocytic infiltrates increase with age.

Indexed as

AdolescentAdultAgedAged, 80 and overChildChild, PreschoolEmbryonic DevelopmentFemaleGanglia, ParasympatheticHumansInfantInfant, NewbornMaleMiddle AgedYoung Adultagingautonomous nervous systemmorphologyotic ganglionparasympathetic nervous system

Identifiers

PMID30411352
PMCPMC6284433
OpenAlexW2899855174

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.