Francesca M. Elli
Milan, Italy
Last Updated: 09/26/2026
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Found 62 publications
Targeted silencing of GNAS in a human model of osteoprogenitor cells results in the deregulation of the osteogenic differentiation program.
Journal: Frontiers in endocrinology
Published: September 21, 2023
Prevalence and clinical features of armadillo repeat-containing 5 mutations carriers in a single center cohort of patients with bilateral adrenal incidentalomas.
Journal: European journal of endocrinology
Published: February 23, 2023
Growth patterns and outcomes of growth hormone therapy in patients with acrodysostosis.
Journal: Journal of endocrinological investigation
Published: September 08, 2022
Fibroblast growth factor 23 level modulates the hepatocyte's alpha-2-HS-glycoprotein transcription through the inflammatory pathway TNFα/NFκB.
Journal: Frontiers in medicine
Published: September 07, 2022
Short stature in PRMT7 Mutations: first evidence of response to growth hormone treatment.
Journal: European journal of human genetics : EJHG
Published: April 28, 2022
Correction to: A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS gene.
Journal: Orphanet journal of rare diseases
Published: April 20, 2022
Is Encapsulated Medullary Thyroid Carcinoma Associated With a Better Prognosis? A Case Series and a Review of the Literature.
Journal: Frontiers in endocrinology
Published: January 31, 2022
Case Report: A Novel ARMC5 Germline Mutation in a Patient with Primary Bilateral Macronodular Adrenal Hyperplasia and Hypogammaglobulinemia.
Journal: Frontiers in genetics
Published: January 05, 2022
Corrigendum to "A comprehensive study on the effect of bentonite fining on wine charged model molecules" [Food Chem. 338 (2020) 127840].
Journal: Food chemistry
Published: July 22, 2021
Novel Pathogenetic Variants in PTHLH and TRPS1 Genes Causing Syndromic Brachydactyly.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: May 17, 2021
A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS gene.
Journal: Orphanet journal of rare diseases
Published: May 14, 2021
Last Updated: 09/26/2026