Evidence map›Paper›PMID 32849305›Full record

ReviewFrontiers in endocrinology2020

Auxological and Endocrinological Features in Children With McCune Albright Syndrome: A Review.

Maria Tufano, Daniele Ciofi, Antonella Amendolea, Stefano Stagi

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Burosumab treatment for FGF23-related hypophosphatemia in a two-year-old girl with McCune-Albright syndrome.Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. McCune-Albright Syndrome: A Case Report and Review of Literature.International journal of molecular sciences · 2023
    Review
  8. Review
  9. Review
  10. Review
  11. Thyroid Scan Conundrum in a Rare Case of McCune-Albright Syndrome.Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India
    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

4 authors at 2 institutions in 1 country.

Maria TufanoPediatric Unit, Mugello Hospital, Borgo San Lorenzo, Florence, Italy.
Daniele CiofiHealth Sciences Department, University of Florence, Anna Meyer Children's University Hospital, Florence, Italy.
Antonella AmendoleaPediatric Unit, Cecina Hospital, Livorno, Italy.
Stefano StagiHealth Sciences Department, University of Florence, Anna Meyer Children's University Hospital, Florence, Italy.
Meyer Children's Hospital · ITUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

McCune-Albright syndrome is a rare and challenging congenital sporadic disease involving the skin and skeletal and endocrine systems with a prevalence ranges from one in 100,000 to 1,000,000. In addition to the classical triad of fibrous dysplasia of bone,

Indexed as

ChildEndocrine System DiseasesFibrous Dysplasia, PolyostoticGrowth DisordersHumanscafé au lait skin pigmentationendocrinopathiesfibrous dysplasia of boneMcCune–Albright syndromeprecocious puberty

Identifiers

PMID32849305
PMCPMC7417367
OpenAlexW3047022630

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.