• 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 frameshift variant in the EXT1 gene in a feline leukemia virus-negative cat with osteochondromatosis
• A Genotype-Phenotype Study of Multiple Hereditary Exostoses in Forty-Three Patients
• A Missed Case of Synovial Osteochondromatosis
• A New Classification System for Forearm Deformities Caused by Hereditary Multiple Osteochondromas
• A patient with pseudohypoparathyroidism type 1A previously misdiagnosed as hereditary multiple exostosis: A case report
• 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
• Advanced colon cancer coexisting with multiple Osteochondromatosis in a child; coincidence or causality? - A case report
• An Easy-to-Use Approach to Detect CNV From Targeted NGS Data: Identification of a Novel Pathogenic Variant in MO Disease
• An unusual cause of inguinal swelling: Primary synovial osteochondromatosis
• Ankle synovial chondromatosis: Clinical, radiological, and surgical findings: A case report
• Anterior Ankle Synovial Osteochondromatosis: a Rare Case in an Adolescent
• Arthroscopic Synovectomy and Removal of Loose Bodies in Synovial Osteochondromatosis of the Knee
• 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?
• Clinical and Genetic Analysis of Multiple Osteochondromas in A Cohort of Argentine Patients
• Combined arthroscopic and open removal of loose bodies in synovial chondromatosis: a case report with technical note
• 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
• Concurrent intraosseous cartilaginous lesions in patients with multiple osteochondromas identified on total-body MR imaging
• Conventional Chondrosarcoma with Clear Cell Features in the Rib: Report of Two Cases and Review of the Literature
• Correction of tibial multiplanar deformities using single Taylor external fixator combined with biplanar osteotomy
• Defining priorities in the transition from paediatric to adult healthcare for rare bone disease patients: a dialogic approach
• 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
• Enlarged Reactional Periostitis of the Peroneal Tubercle Mimicking Osteochondromatosis of the Calcaneus: A Case Report
• Extra-articular synovial osteochondromatosis of the knee in a recreational runner
• Extraarticular Synovial Osteochondromatosis in Baker's Cysts Bilaterally: a Rare Presentation
• Feline osteochondromatosis in a 12-year-old feline leukaemia virus-negative cat
• Forearm deformity in multiple hereditary exostosis. Radiologic predictors of radial head dislocation
• Functional Impairment of Hip Joint and Activities of Daily Living Failure in Patients with Multiple Hereditary Exostoses
• Giant pleomorphic lipoma in patient with multiple osteochondromatosis
• Guided Growth Improves Coxa Valga and Hip Subluxation in Children With Hereditary Multiple Exostoses
• 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
• Incidental Finding of Synovial Osteochondromatosis: A Case Report
• 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
• Management of Primary Synovial Osteochondromatosis in the Ankle Joint With a Combined Posterior-Anterior Arthroscopic Procedure: A Case Report
• Medullary Compression by a Cervical Osteochondroma in a Patient with Multiple Hereditary Exostoses: A Case Report
• Metachondromatosis: A Confusing Disease
• Millennium-old pathogenic Mendelian mutation discovery for multiple osteochondromas from a Gaelic Medieval graveyard
• Modified Technique of Single-Bone Forearm in the Treatment of Deformities
• 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
• Multiple Hereditary Exostoses-Family "Bone History" Revealed
• Mutations in LIFR rewire the JAK/STAT signaling pathway: A study unveiling mechanistic details of Stüve-Wiedemann syndrome
• Neurologic recovery following laminectomy and tumor resection of a pediatric cervical synovial osteochondromatosis causing paralysis
• 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
• Osteochondroma
• Osteochondroma
• Pain and fatigue in adult patients with multiple osteochondromas: The Netherlands
• Pain, popping, and episodic locking of the knee: osteochondromatosis
• Pediatric diaphragmatic hernia induced by a rib osteochondroma
• Pediatric Synovial Osteochondromatosis of the Knee with Leg Length Discrepancy: A Case Report
• 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
• Potocki-Shaffer syndrome revealed in a WAGR syndrome case with multiple exostoses
• Primary Synovial Chondromatosis of the Ankle in a Child: A Rare Case Presentation and Review of Literature
• Primary synovial chondromatosis of the hip joint (PrSC of the hip): A retrospective cohort analysis and review of the literature
• Primary synovial osteochondromatosis of the ankle: A case report and review of the literature
• Primary Synovial Osteochondromatosis of the Shoulder in Pediatric Patient: Case Report and Review of the Literature
• 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
• Reliability of the Masada Classification for Forearm Involvement in Patients With Hereditary Multiple Osteochondromas (HMO)
• 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
• Sacroiliac joint involvement in osteochondromatosis: identifying its prevalence and characteristics from cross-sectional imaging
• 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 Dislocation of the Hip through Lateral Approach for the Treatment of Synovial Chondromatosis
• Surgical Proposition of a Slow-Growing Calvarial Exostosis in a Female Patient With a Congenital Iris Cyst of the Anterior Chamber and Mandibular Tori
• Synovial Chondromatosis
• Synovial Chondromatosis
• Synovial Chondromatosis in a Rural Healthcare Setting
• Synovial Chondromatosis in a Young Athlete: A Report of a Rare Case
• Synovial Osteochondromatosis: Clinical Characteristics Unique to the Shoulder
• The identification of a novel frameshift insertion mutation in the <em>EXT1</em> gene in a Chinese family with hereditary multiple exostoses
• The identification of a novel frameshift insertion mutation in the EXT1 gene in a Chinese family with hereditary multiple exostoses
• The Impact of Isolated Versus Multiple Osteochondromas: Analysis of the CoULD Registry
• The Perils of Sleeper Plates in Multiple Hereditary Exostosis: Tibial Deformity Overcorrection Due to Tether at Empty Metaphyseal Hole
• Total Knee Arthroplasty With Patient-Specific Instrumentation to Correct Severe Valgus Deformity in a Patient With Hereditary Multiple Exostoses
• UHMWPE suture induced pseudotumor following arthroscopic rotator cuff repair: A case report
• 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