Evidence map›Paper›PMID 31965886›Full record

ArticleThe Journal of international medical research2020

Hepatic fibrinogen storage disease and hypofibrinogenemia caused by fibrinogen Aguadilla mutation: a case report.

Leilei Gu, Bin Wang, Lu Liu, Qiaorong Gan, Xiaolong Liu, Lihong Chen, Li Chen

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

Article in The Journal of international medical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Hereditary Hypofibrinogenemia with Hepatic Storage.International journal of molecular sciences · 2020
    Review
  6. 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.

Leilei GuDepartment of Gastroenterology, Ruijin Hospital North, Shanghai JiaoTong University, School of Medicine, Shanghai, China.ORCID https://orcid.org/0000-0002-3878-7262
Bin WangDepartment of Pathology, School of Basic Medical Sciences of Fujian Medical University, Fuzhou, China.
Lu LiuDepartment of Hepatology, Mengchao Hepatobiliary Hospital, Fujian Medical University, Fuzhou, Fujian, China.
Qiaorong GanDepartment of Hepatology, Mengchao Hepatobiliary Hospital, Fujian Medical University, Fuzhou, Fujian, China.
Xiaolong LiuDepartment of Hepatology, Mengchao Hepatobiliary Hospital, Fujian Medical University, Fuzhou, Fujian, China.
Lihong ChenDepartment of Pathology, School of Basic Medical Sciences of Fujian Medical University, Fuzhou, China.
Li ChenDepartment of Gastroenterology, Ruijin Hospital North, Shanghai JiaoTong University, School of Medicine, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AfibrinogenemiaChild, PreschoolEndoplasmic ReticulumEosinophilsFibrinogenHumansInclusion BodiesLiverLiver DiseasesMaleMutation, MissensePolymorphism, Single NucleotideFibrinogenfibrinogen Aalphaafibrinogenemiadifferential diagnosisfibrinogengenetic diagnosisHepatic endoplasmic reticulum storage diseaseinclusion bodiespathologysingle nucleotide polymorphism

Identifiers

PMID31965886
PMCPMC7169362

What OpenQuestion holds

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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.