Profil bibliographique

Luca Sangiorgi

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173Publications signalées

6568Citations signalées

1Affiliations récentes

Institutions déclarées

Domaines associés

Bone Tumor Diagnosis and TreatmentsSarcoma Diagnosis and TreatmentConnective tissue disorders researchGenomics and Rare DiseasesBone health and treatments

Publications récentes

2026 articleOpenAlex

Biobanks and Patient Representatives Together in a Participatory Process: From the BBMRI.it Informed Consent Matrix to the Informed Consent Model of TNGB—Fondazione Telethon Network of Genetic Biobanks

Sara Casati, Chiara Baldo, Laura Casareto, Monica Locatelli et autres

0 citationsBiopreservation and Biobanking

Accès ouvert 2026 articleOpenAlex

Crisis readiness for rare disease populations: learnings and recommendations by the European Reference Networks

Hélène Dollfus, Alexis Arzimanoglou, Teresinha Evangelista, Holm Graessner et autres

0 citationsThe Lancet Regional Health - Europe

Accès ouvert 2026 articleOpenAlex

Opportunities and challenges in automated coding of electronic health records: a pilot study for rare disease registries

Damiano Paoli, Marcella Lanza, Federico Banchelli, Manila Boarini et autres

0 citationsFrontiers in Digital Health

Accès ouvert 2026 articleOpenAlex

Fibrous dysplasia: clinical and pathologic characteristics, surgical approaches, and outcomes in a large Italian cohort

Marina Mordenti, Giovanni Trisolino, Alice Moroni, Stefania Claudia Parisi et autres

0 citationsJournal of Orthopaedics and Traumatology

Accès ouvert 2026 articleOpenAlex

European Reference Networks as core health structures where referring genetic newborn screening positive infants: an innovative operational research framework

F. Fortunato, Rita Selvatici, J Kirschner, Stefaan Sansen et autres

0 citationsFrontiers in Public Health

Accès ouvert 2026 articleOpenAlex

Osteogenesis imperfecta: a registry-based study of the clinical symptoms of disease in a large cohort of Italian patients

Marina Mordenti, James Clancy, Matthew Dyer, Manila Boarini et autres

0 citationsFrontiers in Endocrinology

Accès ouvert 2026 articleOpenAlex

Blended adapted sailing therapy with telerehabilitation for rare skeletal disorders: protocol for a pilot randomised controlled feasibility trial in Italy (PaS2-EXTEND)

Manila Boarini, Federico Banchelli, Davide Scognamiglio, Giuseppina Mariagrazia Farella et autres

0 citationsBMJ Open

Accès ouvert 2026 articleOpenAlex

European Reference Networks – a flagship activity of the EU in the field of rare and complex diseases: from 2017 to 2025

Holm Graeßner, Sophie Ripp, Alberto M. Pereira, F Schaefer et autres

8 citationsOrphanet Journal of Rare Diseases

2026 articleOpenAlex

Methodological considerations and clinical implications of pain assessment in rare bone diseases

Mattia Morri, Elena Pedrini, Alice Moroni, Luca Sangiorgi

0 citationsBone

Accès ouvert 2026 preprintOpenAlex

The Italian Rare Diseases Network: Moving across the Regional, National and European Dimension

Monica Mazzucato, Laura Visonà Dalla Pozza, Luca Sangiorgi, See PDF

0 citationsSSRN Electronic Journal

Accès ouvert 2026 articleOpenAlex

Characteristics of Pain in Patients Diagnosed With Ehlers–Danlos Syndrome and Hypermobility Spectrum Disorders. An Observational Study

Mattia Morri, Morena Tremosini, Cristiana Forni, Alice Moroni et autres

0 citationsPain Research and Management

Accès ouvert 2025 articleOpenAlex

Matrix-directed therapy losartan to identify the effect on the bone resorption marker carboxy-terminal crosslink of type I collagen telopeptide (CTX) in older adolescents and adults with osteogenesis imperfecta recruited from secondary care sites: the ‘MOI-A’ study; a randomised, phase 2/pilot, dose-escalating trial

Mahboobeh Haji Sadeghi, Judith Cohen, Bronwen Williams, Sarah Sumpter et autres

0 citationsBMJ Open

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