Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The genetic background and vitamin D supplementation can affect irisin levels in Prader-Willi syndrome.

Journal of endocrinological investigation - 1 Oct 2021

Faienza M F, Brunetti G, Grugni G, Fintini D, Convertino A, Pignataro P, Crinò A, Colucci S, Grano M

Abstract excerpt

BACKGROUND: Prader-Willi syndrome (PWS) is associated to distinctive clinical symptoms, including obesity, cognitive and behavioral disorders, and bone impairment. Irisin is a myokine that acts on several target organs including brain adipose tissue and bone. The present study was finalized to explore circulating levels of irisin in children and adult PWS patients. METHODS: Seventy-eight subjects with PWS, 26...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Biomarkers
Share to Dietary Supplements

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fibronectins

Share to Follow-Up Studies

Share to Prader-Willi Syndrome

Share to Prognosis

Share to Vitamin D

Share to Vitamins

Source

Open in PubMed Open full text

Identifiers

PMID: 33656700
DOI: 10.1007/s40618-021-01533-4
PMCID: PMC8421289

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The genetic background and vitamin D supplementation can affect irisin levels in Prader-Willi syndrome.PMID 33656700Read ↗

Irisin and the Metabolic Phenotype of Adults with Prader-Willi Syndrome.Semantic proximity Read ↗

Advances in genetic mechanisms of hypothalamic dysfunction in Prader-Willi syndrome.Semantic proximity Read ↗

Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation.Semantic proximity Read ↗

Prader-Willi Syndrome: Clinical AspectsSemantic proximity Read ↗

The Italian registry for patients with Prader-Willi syndromeSemantic proximity Read ↗

The Italian registry for patients with Prader–Willi syndromeSemantic proximity Read ↗

Case Series of Nizon-Isidor Syndrome by Heterozygous Variants in MED12L With Further Evidence of Mitotic Instability in One Case With Diploid-Triploid Mosaicism.Semantic proximity Read ↗

Role and Functions of Irisin: A Perspective on Recent Developments and Neurodegenerative DiseasesSemantic proximity Read ↗

Association of plasma Irisin levels with executive function in children: the role of weight statusSemantic proximity Read ↗

[Analysis of differences in clinical and biochemical characteristics and treatment effects in patients with different genotypes of Prader-Willi syndrome].Semantic proximity Read ↗

Circulating Inhibitory Factor 1 levels in adult patients with Prader-Willi syndrome.Semantic proximity Read ↗

Influence of molecular classes and growth hormone treatment on growth and dysmorphology in Prader-Willi syndrome: A multicenter study.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.