Evidence map›Paper›PMID 35002956›Full record

ArticleFrontiers in endocrinology2021

Growth in Children With Noonan Syndrome and Effects of Growth Hormone Treatment on Adult Height.

Annachiara Libraro, Vito D'Ascanio, Marco Cappa, Mariangela Chiarito, Maria Cristina Digilio, Silvia Einaudi, Anna Grandone, Mohamad Maghnie, Laura Mazzanti, Alessandro Mussa and 7 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Frontiers in endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 30% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Domain-specific phenotypic profiles in RAF1-related Noonan syndrome.European journal of human genetics : EJHG · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. [Growth and development patterns of Noonan syndrome and advances in the treatment of short stature].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2025
    Review
  10. Article
  11. Review
  12. Growth Hormone Treatment for Non-GHD Disorders: Excitement Tempered by Biology.The Journal of clinical endocrinology and metabolism · 2024
    Review
  13. Article
  14. Noonan syndrome: rhGH treatment and PTPN11 mutation.Molecular genetics & genomic medicine · 2023
    Article
  15. Review
  16. Review
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

17 authors at 10 institutions in 1 country.

Annachiara LibraroDepartment of Biomedical Sciences and Human Oncology, Pediatric Unit, University of Bari "A. Moro", Bari, Italy.
Vito D'AscanioNational Research Council-Institute of Sciences of Food Production (CNR-ISPA), Bari, Italy.
Marco CappaUnit of Endocrinology, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome, Italy.
Mariangela ChiaritoDepartment of Biomedical Sciences and Human Oncology, Pediatric Unit, University of Bari "A. Moro", Bari, Italy.
Maria Cristina DigilioGenetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome, Italy.
Silvia EinaudiDepartment of Pediatric Endocrinology and Diabetology, Regina Margherita Children Hospital, University of Turin, Turin, Italy.
Anna GrandoneDepartment of Woman, Child and General and Specialized Surgery, University of Campania Luigi Vanvitelli, Naples, Italy.
Mohamad MaghnieDepartment of Pediatrics, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Istituto Giannina Gaslini, Genova, Italy.
Laura MazzantiPediatric Rare Diseases Unit, Department of Pediatrics, St. Orsola University Hospital, University of Bologna, Bologna, Italy.
Alessandro MussaDepartment of Public Health and Pediatrics, University of Torino, Torino, Italy.
Giuseppa PattiDepartment of Pediatrics, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Istituto Giannina Gaslini, Genova, Italy.
Emanuela ScaranoPediatric Rare Diseases Unit, Department of Pediatrics, St. Orsola University Hospital, University of Bologna, Bologna, Italy.
Antonietta SpinuzzaDepartment of Human Pathology of Adulthood and Childhood Gaetano Barresi, Gaetano Martino University Hospital, University of Messina, Messina, Italy.
Silvia VannelliDepartment of Pediatric Endocrinology and Diabetology, Regina Margherita Children Hospital, University of Turin, Turin, Italy.
Malgorzata Gabriela WasniewskaDepartment of Human Pathology of Adulthood and Childhood Gaetano Barresi, Gaetano Martino University Hospital, University of Messina, Messina, Italy.
Giovanni Battista FerreroDepartment of Clinical and Biological Sciences, University of Torino, Torino, Italy.
Maria Felicia FaienzaDepartment of Biomedical Sciences and Human Oncology, Pediatric Unit, University of Bari "A. Moro", Bari, Italy.
University of Bari Aldo Moro · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITIstituto Ortopedico Gaetano Pini · ITUniversity of Bologna · ITUniversity of Turin · ITBambino Gesù Children's Hospital · ITIstituto Giannina Gaslini · ITNational Research Council · ITOspedale Regina Margherita · ITUniversity of Campania "Luigi Vanvitelli" · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Growth impairment is a common manifestation in Noonan syndrome (NS). Recombinant human GH (rhGH) treatment has been shown to increase growth and adult height (AH) in a few studies. We aimed to evaluate the growth trajectory towards the AH, and the effects of rhGH treatment in a large cohort of NS children. Methods: Retrospective, multicenter, cohort study including subjects with genetic diagnosis of NS. A total of 228 NS patients, 154 with Results: ANOVA analysis showed a significant difference between birth length and height standard deviation scores (HSDS) at the different key ages ( Conclusions: rhGH treatment at the standard dose used for children with GH idiopathic deficiency is effective in improving growth and AH in NS with GHD. Further studies are needed to assess genotype-specific response to rhGH treatment in the different pathogenic variants of

Indexed as

AdolescentBody HeightChildChild, PreschoolFemaleHuman Growth HormoneHumansInfantMaleNoonan SyndromeRetrospective StudiesHuman Growth Hormoneadult heightchildrengrowthgrowth hormone treatmentNoonan Syndrome

Identifiers

PMID35002956
PMCPMC8730290
OpenAlexW4200018069

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.