Simona F. Madeo
Modena, Italy
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 25 publications
Screening practices for diabetic peripheral neuropathy in pediatric type 1 diabetes: a nationwide survey by the ISPED Diabetes Study Group.
Journal: Acta diabetologica
Published: October 17, 2025
Megalencephalic leukoencephalopathy with subcortical cysts: a multicenter Italian experience.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: August 27, 2025
Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross-Sectional Study and Systematic Literature Review.
Journal: American journal of medical genetics. Part A
Published: July 28, 2025
Mometasone Furoate-Induced Iatrogenic Cushing's Syndrome and Secondary Adrenal Insufficiency: A Case Report.
Journal: Case reports in pediatrics
Published: February 27, 2025
Lack of correlation between asprosin serum levels and hyperphagic behavior in subjects with prader-Willi Syndrome.
Journal: Journal of endocrinological investigation
Published: September 26, 2024
The Approach to a Child with Dysmorphic Features: What the Pediatrician Should Know.
Journal: Children (Basel, Switzerland)
Published: April 03, 2024
Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation.
Journal: Frontiers in endocrinology
Published: February 05, 2024
Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature.
Journal: Journal of medical genetics
Published: January 03, 2023
The impact of BMI on long-term anthropometric and metabolic outcomes in girls with idiopathic central precocious puberty treated with GnRHas.
Journal: Frontiers in endocrinology
Published: July 29, 2022
Growth hormone deficiency in a child with benign hereditary chorea caused by a de novo mutation of the TITF1/NKX2-1 gene.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: June 14, 2021
Last Updated: 09/26/2026