Evidence map›Paper›PMID 33790768›Full record

ArticleCase reports in neurology

A Patient with Noonan Syndrome with a

Yoshihito Ando, Mikio Sawada, Tadataka Kawakami, Mitsuya Morita, Yoko Aoki

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Case reports in neurology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. MRI and MR neurography features of a patient with Noonan syndrome associated with diffuse thickening of peripheral and cranial nerves.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2022
    Article
  3. Review
  4. A rigorousFrontiers in molecular neuroscience · 2022
    Article
  5. 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 at 3 institutions in 1 country.

Yoshihito AndoDepartment of Internal Medicine, Josai Hospital, Yuki, Japan.
Mikio SawadaDivision of Neurology, Department of Internal Medicine, Jichi Medical University Hospital, Shimotsuke, Japan.
Tadataka KawakamiDivision of Neurology, Department of Internal Medicine, Jichi Medical University Hospital, Shimotsuke, Japan.
Mitsuya MoritaDivision of Neurology, Department of Internal Medicine, Jichi Medical University Hospital, Shimotsuke, Japan.
Yoko AokiDepartment of Medical Genetics, Tohoku University School of Medicine, Sendai, Japan.
Jichi Medical University · JPJichi Medical University Hospital · JPTohoku University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a 45-year-old female with clinical features resembling Noonan syndrome (NS) who presented with significant nerve root hypertrophy. She was initially diagnosed with Charcot-Marie-Tooth disease because her gait disturbance gradually deteriorated and nerve conduction velocity was reduced. However, she did not carry a

Indexed as

KRAS gene mutationNerve root hypertrophyNoonan syndromeRas/MAPK pathwayRASopathy

Identifiers

PMID33790768
PMCPMC7989852
OpenAlexW3131242077

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.