Evidence map›Paper›PMID 36544606›Full record

ArticleNagoya journal of medical science2022

Daisuke Watanabe, Yohei Hasebe, Shin Kasai, Tamao Shinohara, Yuki Maebayashi, Nobuyuki Katsumata, Atsushi Nemoto, Atsushi Naitoh

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Nagoya journal of medical science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Eighteen-years follow-up of congenital hypothyroidism byNagoya journal of medical science · 2023
    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

8 authors.

Daisuke WatanabeDepartment of Neonatology, Perinatal Center, Yamanashi Prefectural Central Hospital, Kofu, Japan.
Yohei HasebeDepartment of Neonatology, Perinatal Center, Yamanashi Prefectural Central Hospital, Kofu, Japan.
Shin KasaiDepartment of Neonatology, Perinatal Center, Yamanashi Prefectural Central Hospital, Kofu, Japan.
Tamao ShinoharaDepartment of Neonatology, Perinatal Center, Yamanashi Prefectural Central Hospital, Kofu, Japan.
Yuki MaebayashiDepartment of Neonatology, Perinatal Center, Yamanashi Prefectural Central Hospital, Kofu, Japan.
Nobuyuki KatsumataDepartment of Neonatology, Perinatal Center, Yamanashi Prefectural Central Hospital, Kofu, Japan.
Atsushi NemotoDepartment of Neonatology, Perinatal Center, Yamanashi Prefectural Central Hospital, Kofu, Japan.
Atsushi NaitohDepartment of Neonatology, Perinatal Center, Yamanashi Prefectural Central Hospital, Kofu, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent advances in molecular and genetic approaches have identified a number of genes responsible for Noonan syndrome (NS). However, there has been limited analysis of the genotype-phenotype correlation of NS patients. Here, we report the case of a Japanese patient with NS possessing a c.853T>C (p.Phe285Leu) mutation in the gene encoding protein-tyrosine phosphatase, nonreceptor-type 11 (

Indexed as

ChylothoraxNoonan SyndromeHumansMutationPhenotypeProtein Tyrosine Phosphatase, Non-Receptor Type 11Protein Tyrosine Phosphatase, Non-Receptor Type 11PTPN11 protein, humanc.853T>C (p.Phe285Leu)chylothoraxgenotype-phenotypeNoonan syndromePTPN11

Identifiers

PMID36544606
PMCPMC9748315

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.