Evidence map›Paper›PMID 25132997›Full record

ReviewInternational journal of hepatology2014

Genetic diseases that predispose to early liver cirrhosis.

Manuela Scorza, Ausilia Elce, Federica Zarrilli, Renato Liguori, Felice Amato, Giuseppe Castaldo

Open access · goldAbstract readReview
In one paragraph

Review in International journal of hepatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Cell therapy for liver disorders: past, present and future.Nature reviews. Gastroenterology & hepatology · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Lycopene: A Potent Antioxidant with Multiple Health Benefits.Journal of nutrition and metabolism · 2024
    Review
  9. Article
  10. Review
  11. Cellular Mechanisms of Liver Fibrosis.Frontiers in pharmacology · 2021
    Review
  12. Organoids: a novel modality in disease modeling.Bio-design and manufacturing · 2021
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

6 authors at 3 institutions in 1 country.

Manuela ScorzaCEINGE-Biotecnologie Avanzate Scarl, Via Gaetano Salvatore 486, 80145 Napoli, Italy ; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, Via Sergio Pansini 5, 80131 Napoli, Italy.ORCID 0000-0002-0671-3664
Ausilia ElceCEINGE-Biotecnologie Avanzate Scarl, Via Gaetano Salvatore 486, 80145 Napoli, Italy ; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, Via Sergio Pansini 5, 80131 Napoli, Italy ; Università Telematica Pegaso, Piazza Trieste e Trento 48, 80132 Napoli, Italy.ORCID 0000-0002-7421-6176
Federica ZarrilliCEINGE-Biotecnologie Avanzate Scarl, Via Gaetano Salvatore 486, 80145 Napoli, Italy ; Dipartimento di Bioscienze e Territorio, Università del Molise, Contrada Fonte Lappone, Pesche, 86090 Isernia, Italy.ORCID 0000-0003-1614-6816
Renato LiguoriCEINGE-Biotecnologie Avanzate Scarl, Via Gaetano Salvatore 486, 80145 Napoli, Italy ; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, Via Sergio Pansini 5, 80131 Napoli, Italy.
Felice AmatoCEINGE-Biotecnologie Avanzate Scarl, Via Gaetano Salvatore 486, 80145 Napoli, Italy ; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, Via Sergio Pansini 5, 80131 Napoli, Italy.ORCID 0000-0002-0596-2933
Giuseppe CastaldoCEINGE-Biotecnologie Avanzate Scarl, Via Gaetano Salvatore 486, 80145 Napoli, Italy ; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, Via Sergio Pansini 5, 80131 Napoli, Italy.ORCID 0000-0002-4036-0874
Ceinge Biotecnologie Avanzate (Italy) · ITPegaso University · ITUniversity of Molise · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited liver diseases are a group of metabolic and genetic defects that typically cause early chronic liver involvement. Most are due to a defect of an enzyme/transport protein that alters a metabolic pathway and exerts a pathogenic role mainly in the liver. The prevalence is variable, but most are rare pathologies. We review the pathophysiology of such diseases and the diagnostic contribution of laboratory tests, focusing on the role of molecular genetics. In fact, thanks to recent advances in genetics, molecular analysis permits early and specific diagnosis for most disorders and helps to reduce the invasive approach of liver biopsy.

Identifiers

PMID25132997
PMCPMC4123515
OpenAlexW2122701100

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.