Evidence map›Paper›PMID 31485549›Full record

ArticleJBMR plus2019

Neonatal McCune-Albright Syndrome: A Unique Syndromic Profile With an Unfavorable Outcome.

Alessandro Corsi, Natasha Cherman, David L Donaldson, Pamela G Robey, Michael T Collins, Mara Riminucci

Open access · goldAbstract read
In one paragraph

Article in JBMR plus, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Bone pain in fibrous dysplasia does not rely on aberrant sensory nerve sprouting or neuroma formation.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2025
    Article
  3. Article
  4. Article
  5. Article
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  7. Article
  8. Article
  9. Article
  10. Article
  11. Delayed Diagnosis of McCune-Albright Syndrome.Case reports in genetics · 2021
    Article
  12. RANKL Inhibition in Fibrous Dysplasia of Bone: A Preclinical Study in a Mouse Model of the Human Disease.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019
    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 2 countries.

Alessandro CorsiDepartment of Molecular Medicine Sapienza University Rome Italy.
Natasha ChermanSkeletal Biology Section National Institute of Dental and Craniofacial Research National Institutes of Health Bethesda MD USA.
David L DonaldsonDepartment of Pediatrics University of Utah, School of Medicine Salt Lake City UT USA.
Pamela G RobeySkeletal Biology Section National Institute of Dental and Craniofacial Research National Institutes of Health Bethesda MD USA.
Michael T CollinsSkeletal Disorders and Mineral Homeostasis Section National Institute of Dental and Craniofacial Research National Institutes of Health Bethesda MD USA.
Mara RiminucciDepartment of Molecular Medicine Sapienza University Rome Italy.
National Institutes of Health · USSapienza University of Rome · ITUniversity of Utah · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Somatic gain-of-function mutations of

Indexed as

CHOLESTASISCUSHING SYNDROMEGNASMCCUNE‐ALBRIGHT SYNDROMENEONATAL

Identifiers

PMID31485549
PMCPMC6715781
OpenAlexW2904687104

What Socratic 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 Socratic graph.