Concetta Schiavariello
Bologna, Italy
Last Updated: 09/26/2026
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Found 10 publications
Neuroimaging Abnormalities and Genotype-Phenotype Correlations in Noonan Syndrome: A Multicenter Cohort Study.
Journal: The Journal of clinical endocrinology and metabolism
Published: April 27, 2026
Impact of pubertal timing on growth progression and final height in subjects affected by RASopathies.
Journal: Frontiers in endocrinology
Published: November 20, 2024
Integrating vosoritide therapy with limb surgery in paediatric patients with achondroplasia: real-life experiences.
Journal: Orphanet journal of rare diseases
Published: June 28, 2024
Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation.
Journal: Frontiers in endocrinology
Published: February 05, 2024
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis.
Journal: European journal of human genetics : EJHG
Published: January 26, 2024
Lipid profile in Noonan syndrome and related disorders: trend by age, sex and genotype.
Journal: Frontiers in endocrinology
Published: April 20, 2023
The Italian registry for patients with Prader-Willi syndrome.
Journal: Orphanet journal of rare diseases
Published: September 09, 2022
Endocrinological manifestations in RASopathies.
Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: August 02, 2022
Viral bronchiolitis in children: a common condition with few therapeutic options.
Journal: Early human development
Published: August 27, 2013
Bordetella pertussis in infants hospitalized for acute respiratory symptoms remains a concern.
Journal: BMC infectious diseases
Published: July 08, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026