Flavia Napoli

Genoa, 16147, Italy

Last Updated: 09/26/2026

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Found 56 publications

Arginine Vasopressin Deficiency in Children - A Practical Guide to Etiological Diagnosis and Long-Term Surveillance.

Arginine Vasopressin Deficiency in Children - A Practical Guide to Etiological Diagnosis and Long-Term Surveillance.

Journal: The Journal of clinical endocrinology and metabolism

Published: July 25, 2026

Neonatal hypocalcemia and hydrocephalus as early manifestations of intermediate osteopetrosis: successful hematopoietic stem cell transplantation despite negative genetic testing: a case report.

Neonatal hypocalcemia and hydrocephalus as early manifestations of intermediate osteopetrosis: successful hematopoietic stem cell transplantation despite negative genetic testing: a case report.

Journal: Frontiers in endocrinology

Published: June 15, 2026

Teaching Video NeuroImage: Eating-Related Cataplexy in Prader-Willi Syndrome.

Teaching Video NeuroImage: Eating-Related Cataplexy in Prader-Willi Syndrome.

Journal: Neurology

Published: May 05, 2026

Neuroimaging Abnormalities and Genotype-Phenotype Correlations in Noonan Syndrome: A Multicenter Cohort Study.

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

Distinguishing central precocious puberty from nonprogressive breast development: adiposity and DXA body composition.

Distinguishing central precocious puberty from nonprogressive breast development: adiposity and DXA body composition.

Journal: Journal of the Endocrine Society

Published: March 31, 2026

Bone and body composition by DXA in girls with precocious puberty, premature thelarche, and prepubertal controls.

Bone and body composition by DXA in girls with precocious puberty, premature thelarche, and prepubertal controls.

Journal: Journal of the Endocrine Society

Published: October 08, 2025

PEG10 loss of function causes Silver-Russell syndrome: a familial case with paternal deletion.

PEG10 loss of function causes Silver-Russell syndrome: a familial case with paternal deletion.

Journal: Scientific reports

Published: September 09, 2025

GH Response to Glucagon in Transition: Role of Body Mass Index and Etiology in Childhood-onset GH Deficiency.

GH Response to Glucagon in Transition: Role of Body Mass Index and Etiology in Childhood-onset GH Deficiency.

Journal: The Journal of clinical endocrinology and metabolism

Published: July 04, 2025

Foramen magnum stenosis, cervicomedullary decompression, and growth in children with achondroplasia: a retrospective cohort study.

Foramen magnum stenosis, cervicomedullary decompression, and growth in children with achondroplasia: a retrospective cohort study.

Journal: Orphanet journal of rare diseases

Published: February 22, 2025

Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver-Russell Syndrome and Focus on the IGF1R Gene.

Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver-Russell Syndrome and Focus on the IGF1R Gene.

Journal: The Journal of clinical endocrinology and metabolism

Published: June 26, 2024

SPISE INDEX (Single point insulin sensitivity estimator): indicator of insulin resistance in children and adolescents with overweight and obesity.

SPISE INDEX (Single point insulin sensitivity estimator): indicator of insulin resistance in children and adolescents with overweight and obesity.

Journal: Frontiers in endocrinology

Published: May 28, 2024

Accuracy of Glucagon Testing Across Transition in Young Adults With Childhood-Onset GH Deficiency.

Accuracy of Glucagon Testing Across Transition in Young Adults With Childhood-Onset GH Deficiency.

Journal: The Journal of clinical endocrinology and metabolism

Published: March 15, 2024

Showing 1-12 of 56

Last Updated: 09/26/2026