Combined achondroplasia and short stature homeobox-containing (SHOX) gene deletion in [...]
#UNIAMOleforze Rare Disease Day Press Conference
#UNIAMOleforze Rare Disease Day Press Conference Following 2022 and 2023 [...]
Defining priorities in the transition from paediatric to adult healthcare for rare bone disease patients: a dialogic approach
Defining priorities in the transition from paediatric to adult healthcare [...]
European Reference Network ERN BOND and National Members. CHULN Multidisciplinary Team
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Osteogenesis imperfecta: a cross-sectional study of skeletal and extraskeletal features in a large cohort of Italian patients
Osteogenesis imperfecta: a cross-sectional study of skeletal and extraskeletal features [...]
ANDO Portugal Skeletal Dysplasia Seminar
The seminar took place in Azores on 20th January 2024 [...]
Rare skeletal disorders: a focus on ERN BOND’s experience
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Genetic and Genomics of Skeletal Disorders
Genetic and Genomics of Skeletal Disorders 'Genes' Journal Special Issues, [...]
Cost-effectiveness of bringing a nurse into an Italian genetic day clinic: a before and after study
Cost-effectiveness of bringing a nurse into an Italian genetic day [...]
Altered collagen I and premature pulmonary embryonic differentiation in patients with OI type II
Altered collagen I and premature pulmonary embryonic differentiation in patients [...]
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