Evidence map›Paper›PMID 29739732›Full record

ArticleJournal of clinical research in pediatric endocrinology2019

Inherited Deletion of 1q, Hyperparathyroidism and Signs of Y-chromosomal Influence in a Patient with Turner Syndrome

Alejandro F. Siller, Alex Shimony, Marwan Shinawi, Ina Amarillo, Louis P. Dehner, Katherine Semenkovich, Ana María Arbeláez

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

Article in Journal of clinical research in pediatric endocrinology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Primary Hyperparathyroidism in a 21 Year Old Patient of Turner Syndrome : A Rare Case Report.Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India · 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

7 authors.

Alejandro F. SillerWashington University Faculty of Medicine, Department of Pediatrics, Washington, USAORCID 0000-0003-1020-4552
Alex ShimonyWashington University Faculty of Medicine, Department of Pediatrics, Washington, USAORCID 0000-0002-8220-5020
Marwan ShinawiWashington University Faculty of Medicine, Department of Pediatrics, Washington, USAORCID 0000-0003-1329-4100
Ina AmarilloWashington University Faculty of Medicine, Department of Pathology and Immunology, Washington, USAORCID 0000-0001-8479-4298
Louis P. DehnerWashington University Faculty of Medicine, Department of Pathology and Immunology, Washington, USAORCID 0000-0002-2007-5638
Katherine SemenkovichWashington University Faculty of Medicine, Department of Pediatrics, Washington, USAORCID 0000-0003-1347-1525
Ana María ArbeláezWashington University Faculty of Medicine, Department of Pediatrics, Washington, USAORCID 0000-0001-6977-9786

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a detailed phenotypic, cytogenetic and molecular characterization of a patient prenatally diagnosed with Turner syndrome (TS). In addition to having typical TS clinical characteristics including webbed neck, high arched palate and coarctation of the aorta, the patient had features less frequently seen in TS. These included recurrent parathyroid adenomas, growth along the 75

Indexed as

HyperparathyroidismTurner SyndromeAdultChromosomes, Human, Pair 1Chromosomes, Human, XChromosomes, Human, YFemaleHumansMonosomySequence DeletionYoung Adultgenetic testinghyperparathyroidisminherited 1q deletionsigns of Y-chromosomal influenceTurner syndrome

Identifiers

PMID29739732
PMCPMC6398186
OpenAlexW2802961326

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.