Evidence map›Paper›PMID 31406617›Full record

ArticleJournal of pediatric genetics2019

SHOX Deficiency in Argentinean Cohort: Long-Term Auxological Follow-Up and a Family's New Mutation.

Mariana Del Pino, Miriam Aza-Carmona, David Medino-Martín, Abel Gomez, Karen E Heath, Virginia Fano, María Gabriela Obregon

Open access · bronzeAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of pediatric genetics, 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 31% 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, 5 citations in OpenAlex.

  1. Skeletal dysplasias in Latin America.American journal of medical genetics. Part C, Seminars in medical genetics · 2020
    Review
  2. 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 at 2 institutions in 2 countries.

Mariana Del PinoDepartment of Growth and Development, Hospital Garrahan, Buenos Aires, Argentina.ORCID 0000-0001-6095-7080
Miriam Aza-CarmonaInstitute of Medical and Molecular Genetics (INGEMM), Hospital Universitario La Paz, UAM, IdiPAZ, Madrid, Spain.
David Medino-MartínInstitute of Medical and Molecular Genetics (INGEMM), Hospital Universitario La Paz, UAM, IdiPAZ, Madrid, Spain.
Abel GomezDepartment of Genetics, Hospital Garrahan, Buenos Aires, Argentina.
Karen E HeathInstitute of Medical and Molecular Genetics (INGEMM), Hospital Universitario La Paz, UAM, IdiPAZ, Madrid, Spain.
Virginia FanoDepartment of Growth and Development, Hospital Garrahan, Buenos Aires, Argentina.
María Gabriela ObregonDepartment of Genetics, Hospital Garrahan, Buenos Aires, Argentina.
Garrahan Hospital · ARHospital Universitario La Paz · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A cohort study on the growth of 19 Argentinean children, aged 0 to 18 years, and 11 of their first-degree relatives with alterations in the

Indexed as

body disproportionLeri–Weill dyschondrosteosisSHOX gene

Identifiers

PMID31406617
PMCPMC6688879
OpenAlexW2947994984

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.