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Author

L. de Sanctis

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Open access Sep 2026

Selective Whole-Blood Expression of Interferon-Stimulated Genes and TLR3/TLR7 in Type 1 Diabetes with Minimal Enterovirus-Targeted Amplification in Whole Blood

These findings indicate group-specific differences in whole-blood transcript expression of selected RNA-sensing and IFN-related genes in T1D under conditions in which enterovirus-targeted amplification was observed in only one sample, and do not establish the presence or absence of systemic enterovirus infection or fun...

I. Galliano, Francesca Nardò, D. Tinti et al. · 0 citations
Review Open access Sep 2026

Adrenal insufficiency in individuals with Duchenne muscular dystrophy treated with glucocorticoids: Insights from the past, current challenges, and future directions

Duchenne muscular dystrophy (DMD) is an X-linked recessive dystrophinopathy characterized by progressive loss of muscle strength, respiratory insufficiency, cardiac dysfunction, and premature death. Despite a rapidly evolving therapeutic landscape that now includes multiple disease modifying treatments including exon s...

D. Weber, Alexandra Ahmet, K. Kinnett et al. · 0 citations
Review Open access Sep 2026

Diagnosis and management of bone fragility fractures in children and adolescents: Good Clinical Practice Recommendations of the Italian Society of Pediatric Endocrinology and Diabetology (ISPED)

These recommendations, revised and approved by the Italian National Institute of Health, aim to provide clinicians with a structured and evidence-based approach to improve the early identification, diagnostic work-up, and management of pediatric patients with bone fragility, promoting standardized care and reducing var...

L. de Sanctis, G. Baroncelli, B. Pintaudi et al. · 0 citations

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