Maria C. Salerno
Naples, Italy
Last Updated: 09/26/2026
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Found 9 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
Unmet needs of Italian centers for pediatric diabetes care: analysis of a survey among pediatric diabetologists facing the national screening program for Type 1 Diabetes.
Journal: Italian journal of pediatrics
Published: July 17, 2024
Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene.
Journal: European journal of endocrinology
Published: April 19, 2019
Novel GLI2 mutations identified in patients with Combined Pituitary Hormone Deficiency (CPHD): Evidence for a pathogenic effect by functional characterization.
Journal: Clinical endocrinology
Published: August 28, 2018
Multiplex Ligation-Dependent Probe Amplification Accurately Detects Turner Syndrome in Girls with Short Stature.
Journal: Hormone research in paediatrics
Published: June 20, 2016
Stories of experiences of care for growth hormone deficiency: the CRESCERE project.
Journal: Future science OA
Published: August 06, 2015
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations.
Journal: European journal of endocrinology
Published: March 06, 2015
Complex chromosomal rearrangements causing Langer-Giedion syndrome atypical phenotype: genotype-phenotype correlation and literature review.
Journal: American journal of medical genetics. Part A
Published: February 15, 2013
Serum thyrotropin concentration in children with isolated thyroid nodules.
Journal: The Journal of pediatrics
Published: December 31, 2012
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Last Updated: 09/26/2026