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Raffaele Buganza

Observed names: BUGANZA, RAFFAELE, R. Buganza
ORCID: 0000-0003-1850-2300
Observed ORCID: 0000-0003-1850-2300
OpenAlex ID: A5084890123
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
2023 · Claudio Maffeis, Francesca Olivieri, et al. · The Italian Journal of Pediatrics/Italian journal of pediatrics · 79
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Early Roots of Childhood Obesity: Risk Factors, Mechanisms, and Prevention Strategies
2025 · Giuseppina Rosaria Umano, Simonetta Bellone, et al. · International Journal of Molecular Sciences · 45
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Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation
2024 · Simona F. Madeo, Luca Zagaroli, et al. · Frontiers in Endocrinology · 31
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Teriparatide (rhPTH 1–34) treatment in the pediatric age: long-term efficacy and safety data in a cohort with genetic hypoparathyroidism
2019 · Gerdi Tuli, Raffaele Buganza, et al. · Endocrine · 28
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Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy in Two Siblings: Same Mutations but Very Different Phenotypes
2021 · Andrea Carpino, Raffaele Buganza, et al. · Genes · 24
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Cardiovascular risk factors in children and adolescents with type 1 diabetes in Italy: a multicentric observational study
2020 · Elena Fornari, Claudia Piona, et al. · Pediatric Diabetes · 23
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Mediterranean Dietary Treatment in Hyperlipidemic Children: Should It Be an Option?
2022 · Giulia Massini, Nicolò Capra, et al. · Nutrients · 15
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“Primary Hyperparathyroidism (PHPT) in Children: Two Case Reports and Review of the Literature”
2021 · Gerdi Tuli, Jessica Munarin, et al. · Case Reports in Endocrinology · 15
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SHOX deficiency in children with growth impairment: evaluation of known and new auxological and radiological indicators
2020 · Silvia Vannelli, Maria Baffico, et al. · The Italian Journal of Pediatrics/Italian journal of pediatrics · 15
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Jaffe-Campanacci syndrome or neurofibromatosis type 1: a case report of phenotypic overlap with detection of NF1 gene mutation in non-ossifying fibroma
2020 · Silvia Vannelli, Raffaele Buganza, et al. · The Italian Journal of Pediatrics/Italian journal of pediatrics · 13
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Oestrogenic Activity in Girls with Signs of Precocious Puberty as Exposure Biomarker to Endocrine Disrupting Chemicals: A Pilot Study
2022 · Marta Gea, Anna Toso, et al. · International Journal of Environmental Research and Public Health · 12
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Multidisciplinary Approach for Hypothalamic Obesity in Children and Adolescents: A Preliminary Study
2021 · Daniele Tessaris, Patrizia Matarazzo, et al. · Children · 12
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Simplified Criteria for Identification of Familial Hypercholesterolemia in Children: Application in Real Life
2024 · Raffaele Buganza, Giulia Massini, et al. · Journal of Cardiovascular Development and Disease · 9
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Impact of 12-SNP and 6-SNP Polygenic Scores on Predisposition to High LDL-Cholesterol Levels in Patients with Familial Hypercholesterolemia
2024 · Giovanna Cardiero, Martina Ferrandino, et al. · Genes · 7
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Menorrhagia as main presentation sign of severe hypothyroidism in a pediatric patient: a case report
2022 · Arianna Barbero, Manuela Pagano, et al. · The Italian Journal of Pediatrics/Italian journal of pediatrics · 7
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Impact of Mediterranean Diet Adherence on Lipid Profiles in Pediatric Primary Dyslipidemia: Insights from the Updated KIDMED Score
2025 · Giulia Massini, Nicolò Capra, et al. · Nutrients · 6
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Diagnosis of Familial Hypercholesterolemia in Children: From Clinical Features Through Gene Variants to Polygenic Score
2026 · Raffaele Buganza, Cecilia Nobili, et al. · Genes · 3
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Lack of correlation between asprosin serum levels and hyperphagic behavior in subjects with prader-Willi Syndrome
2024 · Maria Felicia Faienza, Mariangela Chiarito, et al. · Journal of Endocrinological Investigation · 2
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Pediatric Myxedema Due to Autoimmune Hypothyroidism: A Rare Complication of a Common Disorder
2023 · Elisa Bonino, Patrizia Matarazzo, et al. · Children · 2
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Understanding the burden of endocrine and metabolic disorders in Prader-Willi syndrome: data from the Italian registry
2026 · Graziano Grugni, Adele Rocchetti, et al. · Journal of Endocrinological Investigation · 1
Evaluation of Classical and New Clinical Criteria for Diagnosing Familial Hypercholesterolemia in Childhood
2026 · Raffaele Buganza, Giulia Massini, et al. · Cardiogenetics
Correction: Understanding the burden of endocrine and metabolic disorders in Prader-Willi syndrome: data from the Italian registry
2026 · Graziano Grugni, Adele Rocchetti, et al. · Journal of Endocrinological Investigation
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Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea
2025 · Eleonora Saraceno, Angelo Corso Faini, et al. · JPGN Reports
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The lysosomal acid lipase deficiency spectrum from infancy to adulthood: a multidisciplinary experience
2025 · Raffaele Buganza, Riccardo Faletti, et al. · Nutrition Metabolism and Cardiovascular Diseases
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Impact of mediterranean diet adherence on lipid profiles in pediatric dyslipidemia: Insights from the updated KIDMED score
2025 · Giulia Massini, Raffaele Buganza, et al. · Atherosclerosis
Works count: 38
Citation count: 348
H-index: 12
I10-index: 12
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