Evidence map›Paper›PMID 36830903›Full record

ArticleBiomedicines2023

A Broad Characterization of Glycogen Storage Disease IV Patients: A Clinical, Genetic, and Histopathological Study.

Matheus Vernet Machado Bressan Wilke, Bibiana Mello de Oliveira, Rodrigo Tzovenos Starosta, Marwan Shinawi, Liang Lu, Mai He, Yamin Ma, Janis Stoll, Carolina Fischinger Moura de Souza, Ana Cecilia Menezes de Siqueira and 4 more

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

Article in Biomedicines, 2023. 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
1.7field-weighted citation impact, top 16% 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, 7 citations in OpenAlex.

  1. 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

14 authors at 4 institutions in 2 countries.

Matheus Vernet Machado Bressan WilkeMedical Genetics Service, Hospital de Clínicas de Porto Alegre, Ramiro Barcelos St., 2350, 3rd Floor, Porto Alegre 90035-903, Brazil.ORCID 0000-0002-8302-7705
Bibiana Mello de OliveiraMedical Genetics Service, Hospital de Clínicas de Porto Alegre, Ramiro Barcelos St., 2350, 3rd Floor, Porto Alegre 90035-903, Brazil.ORCID 0000-0002-2679-6858
Rodrigo Tzovenos StarostaDivision of Medical Genetics and Genomics, Washington University in Saint Louis, Saint Louis, MO 63130, USA.ORCID 0000-0002-2350-7192
Marwan ShinawiDivision of Medical Genetics and Genomics, Washington University in Saint Louis, Saint Louis, MO 63130, USA.
Liang LuDepartment of Pathology and Immunology, Washington University in Saint Louis, Saint Louis, MO 63130, USA.
Mai HeDepartment of Pathology and Immunology, Washington University in Saint Louis, Saint Louis, MO 63130, USA.
Yamin MaDepartment of Pathology and Immunology, Washington University in Saint Louis, Saint Louis, MO 63130, USA.
Janis StollDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Washington University in Saint Louis, Saint Louis, MO 63130, USA.
Carolina Fischinger Moura de SouzaMedical Genetics Service, Hospital de Clínicas de Porto Alegre, Ramiro Barcelos St., 2350, 3rd Floor, Porto Alegre 90035-903, Brazil.
Ana Cecilia Menezes de SiqueiraTreatment Center of Inborn Errors of Metabolism, Instituto de Medicina Integral Professor Fernando Figueira, Recife 50070-902, Brazil.
Sandra Maria Gonçalves VieiraPediatrics Gastroenterology Service, Hospital de Clínicas de Porto Alegre, Porto Alegre 90035-903, Brazil.
Carlos Thadeu CerskiPathology Service, Hospital de Clínicas de Porto Alegre, Porto Alegre 90035-903, Brazil.
Lilia Farret RefoscoMedical Genetics Service, Hospital de Clínicas de Porto Alegre, Ramiro Barcelos St., 2350, 3rd Floor, Porto Alegre 90035-903, Brazil.
Ida Vanessa Doederlein SchwartzMedical Genetics Service, Hospital de Clínicas de Porto Alegre, Ramiro Barcelos St., 2350, 3rd Floor, Porto Alegre 90035-903, Brazil.
Washington University in St. Louis · USUniversidade Federal do Rio Grande do Sul · BRHospital de Clínicas de Porto Alegre · BRInstituto de Medicina Integral Professor Fernando Figueira · BR

Funding

the Fundo de Incentivo à Pesquisa e Eventos (FIPE) of the HCPA
6 · The paper itself

Abstract

Glycogen storage disease type IV (GSD IV) is an ultra-rare autosomal recessive disease caused by variants in the

Indexed as

dietary treatmentglycogen storage disease IVliver transplantation

Identifiers

PMID36830903
PMCPMC9953126
OpenAlexW4318204436

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.