• A Case Report on Surgical Excision of Intracapsular Osteochondroma of Femur Neck using Mini-Arthrotomy without Hip Dislocation in a Young Female with Hereditary Multiple Exostoses
• A New Classification System for Forearm Deformities Caused by Hereditary Multiple Osteochondromas
• A Rare Case of Hereditary Multiple Exostoses in a Woman
• A rare presentation of osteochondroma at the spinous process of the cervical spine: a case report
• A solitary osteochondroma of the sixth cervical spine: A case report
• Challenges in Diagnosing Fibrodysplasia Ossificans Progressiva: A Case Report
• Chest wall osteochondroma resection with biologic acellular bovine dermal mesh reconstruction in pediatric hereditary multiple exostoses: A case report and review of literature
• Chondrosarcoma secondary to hereditary multiple osteochondromas with spinal cord compression: A case report and systematic review
• Chondrosarcoma transformation in hereditary multiple exostosis: When to suspect?
• Comment on the article: Distraction osteogenesis at the proximal third of the ulna for the treatment of Masada type I/IIb deformities in children with hereditary multiple exostoses: a retrospective review of twenty cases
• Defining priorities in the transition from paediatric to adult healthcare for rare bone disease patients: a dialogic approach
• Haploinsufficiency of EXT1 and Heparan Sulphate Deficiency Associated with Hereditary Multiple Exostoses in a Pakistani Family
• Health-related quality of life and associated risk factors in patients with Multiple Osteochondromas: a cross-sectional study
• Hemiepiphysiodesis for Genu Valgum in Patients With Multiple Hereditary Exostoses
• Hereditary multiple exostoses caused by a chromosomal inversion removing part of EXT1 gene
• Hereditary multiple exostoses with a giant osteochondroma degenerated into chondrosarcoma
• Hereditary multiple exostoses with spinal canal involvement
• Imaging of solitary and multiple osteochondromas: From head to toe - A review
• Implications of neuropathy and management of the corneal surface in a patient with Stuve-Wiedemann syndrome
• Insights into pathogenesis, clinical complications and potential treatments of multiple osteochondromas in children: A case report
• Insights into pathogenesis, clinical complications, and potential treatments of multiple osteochondroma in children: A case report
• Intra-articular exostosis on the glenoid neck in a patient with hereditary multiple exostoses: a case report
• Is total-body MRI useful as a screening tool to rule out malignant progression in patients with multiple osteochondromas? Results in a single-center cohort of 319 adult patients
• Long-term outcome of total hip arthroplasty in patients with multiple hereditary exostosis
• Medullary Compression by a Cervical Osteochondroma in a Patient with Multiple Hereditary Exostoses: A Case Report
• Modified ulnar lengthening for correction of the Masada type 2 forearm deformity in hereditary multiple exostosis
• Multiple Distal Femoral Osteochondromas Encasing Popliteal Neurovascular Bundle
• Multiple Hereditary Exostoses instigating a popliteal pseudoaneurysm in a young Middle Eastern male: A case report and literature review
• Mutations in LIFR rewire the JAK/STAT signaling pathway: A study unveiling mechanistic details of Stüve-Wiedemann syndrome
• Neuroparalytic keratopathy in Stüve-Wiedemann syndrome treated with tarsoconjunctival flap
• NFATC1 and NFATC2 expression patterns in human osteochondromas
• One-Bone Forearm Procedure for Severe Recalcitrant Forearm Deformities in Masada IIb Hereditary Multiple Exostoses
• Pain and fatigue in adult patients with multiple osteochondromas: The Netherlands
• Pediatric diaphragmatic hernia induced by a rib osteochondroma
• Peroneal Nerve Decompression in Patients with Multiple Hereditary Exostoses: Indications, Complications, and Recurrence
• Popliteal artery pseudoaneurysm and secondary ipsilateral deep vein thrombosis caused by an exostosis in a mature adult
• Radiation exposure in multiple hereditary exostoses: A retrospective review
• Radiographic evaluation of ulnar deformity in patients with hereditary multiple osteochondroma and its relationship with radial head dislocation
• Rare coexistence of multiple osteochondromas and solitary osteoid osteoma: A case report
• Response to Jacques Caton, MD's comments on the article "Distraction osteogenesis at the proximal third of the ulna for the treatment of Masada type I/IIb deformities in children with hereditary multiple exostoses: a retrospective review of twen
• Secondary peripheral chondrosarcoma in multiple osteochondromas: a retrospective single-institution case series
• Solitary Osteochondroma at Unusual Sites: A Case Report and Literature Review
• Successful treatment of forelimb osteochondroma in a ferret (Mustela putorius furo)
• Surgical Proposition of a Slow-Growing Calvarial Exostosis in a Female Patient With a Congenital Iris Cyst of the Anterior Chamber and Mandibular Tori
• The Perils of Sleeper Plates in Multiple Hereditary Exostosis: Tibial Deformity Overcorrection Due to Tether at Empty Metaphyseal Hole
• Use of Pediatric Outcomes Data Collection Instrument to Evaluate Functional Outcomes in Multiple Hereditary Exostoses
• Venous malformation may be a feature of EXT1-related hereditary multiple exostoses: A report of two unrelated probands