Evidence map›Paper›PMID 31652573›Full record

ReviewInternational journal of molecular sciences2019

Insights into the Pathophysiology of Infertility in Females with Classical Galactosaemia.

Zaza Abidin, Eileen P Treacy

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. A Rare Cause of Hypergonadotropic Hypogonadism: Transaldolase Deficiency in Two SiblingsJournal of clinical research in pediatric endocrinology · 2025
    Article
  2. Article
  3. Article
  4. Selected Genetic Factors Associated with Primary Ovarian Insufficiency.International journal of molecular sciences · 2023
    Review
  5. Review
  6. Current and Future Treatments for Classic Galactosemia.Journal of personalized medicine · 2021
    Review
  7. 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

2 authors at 2 institutions in 1 country.

Zaza AbidinNational Centre for Inherited Metabolic Disorders, Adult Services, Mater Misericordiae University Hospital, Dublin, Ireland. zazaabidin@mater.ie.
Eileen P TreacyNational Centre for Inherited Metabolic Disorders, Adult Services, Mater Misericordiae University Hospital, Dublin, Ireland. etreacy@mater.ie.ORCID 0000-0002-6226-1615
Mater Misericordiae University Hospital · IEUniversity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Classical galactosaemia (CG) (OMIM 230400) is a rare inborn error of galactose metabolism caused by the deficiency of the enzyme galactose-1-phosphate uridylyltransferase (GALT, EC 2.7.7.12). Primary ovarian insufficiency (POI) is the most common long-term complication experienced by females with CG, presenting with hypergonadotrophic hypoestrogenic infertility affecting at least 80% of females despite new-born screening and lifelong galactose dietary restriction. In this review, we describe the hypothesized pathophysiology of POI from CG, implications of timing of the ovarian dysfunction, and the new horizons and future prospects for treatments and fertility preservation.

Indexed as

FemaleFertility PreservationGalactoseGalactosemiasHumansGalactoseclassical galactosaemiafertility preservationpathophysiologyprimary ovarian insufficiency

Identifiers

PMID31652573
PMCPMC6834160
OpenAlexW2981479807

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.