Evidence map›Paper›PMID 37908481›Full record

ArticleJCEM case reports2023

Bartter Syndrome Type 1 Due to Novel

Zentaro Kiuchi, Kandai Nozu, Kunimasa Yan, Harald Jüppner

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

Article in JCEM case reports, 2023. 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
0.2field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

4 authors at 3 institutions in 2 countries.

Zentaro KiuchiDepartment of Pediatrics, Kyorin University School of Medicine, Mitaka, Tokyo, Japan.ORCID https://orcid.org/0000-0003-1302-7512
Kandai NozuDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.ORCID https://orcid.org/0000-0002-0290-3137
Kunimasa YanDepartment of Pediatrics, Kyorin University School of Medicine, Mitaka, Tokyo, Japan.
Harald JüppnerEndocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Kyorin University · JPHarvard University · USKobe University · JP

Funding

PTH/PTHRP RECEPTOR DEFECTS IN PSEUDOHYPOPARATHYROIDISMR01DK046718 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI JUEPPNER, HARALD W. · 1993 to 2024
$6.0M
NIDDK NIH HHS R01 DK046718
6 · The paper itself

Abstract

Bartter syndrome type 1 is caused by mutations in the solute carrier family 12 member 1 (

Indexed as

Bartter syndromeEllsworth Howard testhyperparathyroidismNSAIDpseudohypoparathyroidism type IISLC12A1

Identifiers

PMID37908481
PMCPMC10580512
OpenAlexW4321781315

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.