Raffaele Buganza

Turin, Italy

Last Updated: 09/26/2026

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Found 23 publications

Correction: Understanding the burden of endocrine and metabolic disorders in Prader-Willi syndrome: data from the Italian registry.

Correction: Understanding the burden of endocrine and metabolic disorders in Prader-Willi syndrome: data from the Italian registry.

Journal: Journal of endocrinological investigation

Published: April 28, 2026

Diagnosis of Familial Hypercholesterolemia in Children: From Clinical Features Through Gene Variants to Polygenic Score.

Diagnosis of Familial Hypercholesterolemia in Children: From Clinical Features Through Gene Variants to Polygenic Score.

Journal: Genes

Published: January 14, 2026

Understanding the burden of endocrine and metabolic disorders in Prader-Willi syndrome: data from the Italian registry.

Understanding the burden of endocrine and metabolic disorders in Prader-Willi syndrome: data from the Italian registry.

Journal: Journal of endocrinological investigation

Published: November 23, 2025

Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea.

Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea.

Journal: JPGN reports

Published: June 27, 2025

Early Roots of Childhood Obesity: Risk Factors, Mechanisms, and Prevention Strategies.

Early Roots of Childhood Obesity: Risk Factors, Mechanisms, and Prevention Strategies.

Journal: International journal of molecular sciences

Published: May 26, 2025

The lysosomal acid lipase deficiency spectrum from infancy to adulthood: a multidisciplinary experience.

The lysosomal acid lipase deficiency spectrum from infancy to adulthood: a multidisciplinary experience.

Journal: Nutrition, metabolism, and cardiovascular diseases : NMCD

Published: May 16, 2025

Impact of Mediterranean Diet Adherence on Lipid Profiles in Pediatric Primary Dyslipidemia: Insights from the Updated KIDMED Score.

Impact of Mediterranean Diet Adherence on Lipid Profiles in Pediatric Primary Dyslipidemia: Insights from the Updated KIDMED Score.

Journal: Nutrients

Published: December 13, 2024

Lack of correlation between asprosin serum levels and hyperphagic behavior in subjects with prader-Willi Syndrome.

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

Impact of 12-SNP and 6-SNP Polygenic Scores on Predisposition to High LDL-Cholesterol Levels in Patients with Familial Hypercholesterolemia.

Impact of 12-SNP and 6-SNP Polygenic Scores on Predisposition to High LDL-Cholesterol Levels in Patients with Familial Hypercholesterolemia.

Journal: Genes

Published: March 08, 2024

Simplified Criteria for Identification of Familial Hypercholesterolemia in Children: Application in Real Life.

Simplified Criteria for Identification of Familial Hypercholesterolemia in Children: Application in Real Life.

Journal: Journal of cardiovascular development and disease

Published: March 05, 2024

Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation.

Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation.

Journal: Frontiers in endocrinology

Published: February 05, 2024

The treatment of obesity in children and adolescents: consensus position statement of the Italian society of pediatric endocrinology and diabetology, Italian Society of Pediatrics and Italian Society of Pediatric Surgery.

The treatment of obesity in children and adolescents: consensus position statement of the Italian society of pediatric endocrinology and diabetology, Italian Society of Pediatrics and Italian Society of Pediatric Surgery.

Journal: Italian journal of pediatrics

Published: February 21, 2023

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Last Updated: 09/26/2026