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  1. Article

    Open Access

    Skeletal dysplasias: approach to the clinical diagnosis and implication of appropriate diagnosis for knowledge and research studies in these rare diseases. Hereditary multiple Osteochondromas as example/paradigm

    Maria Gnoli, Elena Pedrini, Marina Mordenti in Italian Journal of Pediatrics (2014)

  2. Article

    Open Access

    Hereditary multiple exostoses and solitary osteochondroma associated with growth hormone deficiency: to treat or not to treat?

    Osteochondroma generally occurs as a single lesion and it is not a heritable disease. When two or more osteochondroma are present, this condition represents a genetic disorder named hereditary multiple exostos...

    Mauro Bozzola, Chiara Gertosio, Maria Gnoli in Italian Journal of Pediatrics (2015)

  3. No Access

    Article

    Histological and molecular features of solitary fibrous tumor of the extremities: clinical correlation

    Solitary fibrous tumor is a rare mesenchymal neoplasm that exhibits a broad spectrum of biological behaviors. Few studies relative to clinical-pathologic features and predictive factors have been reported, all...

    Giuseppe Bianchi, Andrea Sambri, Elena Pedrini, Laura Pazzaglia in Virchows Archiv (2020)

  4. Article

    Open Access

    Secondary peripheral chondrosarcoma arising in solitary osteochondroma: variables influencing prognosis and survival

    Secondary peripheral chondrosarcomas arising in solitary osteochondromas is an unusual complication, reported in small series. In this study, we aimed to present our experience with this rare variant of chondr...

    Alberto Righi, Marina Pacheco, Stefania Cocchi in Orphanet Journal of Rare Diseases (2022)

  5. Article

    Open Access

    Cost-effectiveness of bringing a nurse into an Italian genetic day clinic: a before and after study

    Only a few studies explore the role of nurses in genetic counselling and genetic health care, and none of them is related to orphan diseases. In addition, few studies address the issue of finding variables tha...

    Marina Mordenti, Morena Tremosini, Manuela Locatelli in BMC Health Services Research (2023)

  6. Article

    Open Access

    Secondary peripheral chondrosarcoma in multiple osteochondromas: a retrospective single-institution case series

    Multiple osteochondromas is genetic disorder characterized by the formation of multiple benign cartilage-capped bone tumors, named osteochondromas, during skeletal development. The most feared complication is ...

    Maria Gnoli, Marco Gambarotti, Alberto Righi in Orphanet Journal of Rare Diseases (2024)

  7. Article

    Open Access

    Health-related quality of life and associated risk factors in patients with Multiple Osteochondromas: a cross-sectional study

    To evaluate the health-related quality of life and associated risk factors for Multiple Osteochondromas patients.

    Manila Boarini, Morena Tremosini, Alessia Di Cecco, Maria Gnoli in Quality of Life Research (2024)

  8. No Access

    Article

    Aneurysmal bone cyst-like changes developed in melorheostosis with epiphyseal osteopoikilosis

    Aneurysmal bone cyst (ABC) is a rare and usually painful condition, representing about 1% of all bone tumors. A geographical lytic, expansile, and septated radiological pattern, with fluid–fluid levels on MRI,...

    Paolo Spinnato, Marco Colangeli, Elena Pedrini, Anna Parmeggiani in Skeletal Radiology (2024)