• <em>PHF21A</em> Related Disorder: Description of a New Case
• 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 potentially fatal cranial pathology in a specimen of Tarchia
• 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
• Anesthetic management using costoclavicular brachial plexus block with patient-controlled analgesia in Pediatrics: A case report
• Association between statins and progression of osteoarthritis features on magnetic resonance imaging in a predominantly pre-radiographic cohort: the Vancouver Longitudinal Study of Early Knee Osteoarthritis (VALSEKO): a cohort study
• Benign Brain and Spinal Tumors Originating from Bone or Cartilage
• Biomechanical properties of splint materials while curing
• Case report: Initial atypical skeletal symptoms and dental anomalies as first signs of Gardner syndrome: the importance of genetic analysis in the early diagnosis
• CC-Chemokine Receptor-2 Expression in Osteoblasts Contributes to Cartilage and Bone Damage during Post-Traumatic Osteoarthritis
• Cervical Osteoma in Hereditary Multiple Exostoses
• 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
• Clinical Features and Surgical Outcomes of Osteochondroma of the Spine
• 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
• Conservative and Surgical Treatment of Osteochondromas in Children, Particularly with or without Surgical Lengthening of the Ulna
• Deep dental phenotyping and a novel FAM20A variant in patients with amelogenesis imperfecta type IG
• Defining priorities in the transition from paediatric to adult healthcare for rare bone disease patients: a dialogic approach
• Disease-Modifying Effects of Lenvatinib, a Multiple Receptor Tyrosine Kinase Inhibitor, on Posttraumatic Osteoarthritis of the Knee
• 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
• Early ablation of Ccr2 in aggrecan-expressing cells following knee injury ameliorates joint damage and pain during post-traumatic osteoarthritis
• Evaluation of clinical signs and magnetic resonance imaging findings in patients with temporomandibular disorders
• Expanding the clinical and molecular features of trichorhino- phalangeal syndrome with a novel variant
• Factors influencing postoperative bleeding after dental extraction in older adult patients receiving anticoagulation therapy
• Feline osteochondromatosis in a 12-year-old feline leukaemia virus-negative cat
• Fibrodysplasia Ossificans Progressiva: A rare disease due to unawareness, case report and literature review
• 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
• Genetics implicates overactive osteogenesis in the development of diffuse idiopathic skeletal hyperostosis
• 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
• Hemothorax caused by costal exostosis injuring diaphragm: a case report and literature review
• 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
• Heterozygous Variants in <em>FREM2</em> Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas
• Heterozygous Variants in FREM2 Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas
• 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
• Interplay between fat, muscle, bone mass, and oteophytes and risk for tophaceous gout
• 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
• Millennium-old pathogenic Mendelian mutation discovery for multiple osteochondromas from a Gaelic Medieval graveyard
• 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
• Neuroparalytic keratopathy in Stüve-Wiedemann syndrome treated with tarsoconjunctival flap
• NFATC1 and NFATC2 expression patterns in human osteochondromas
• Not All Osteophytes Are Located on the Right Side of the Vertebrae in Diffuse Idiopathic Skeletal Hyperostosis: A Quantitative Analysis in Relation to the Position of Aorta
• One-Bone Forearm Procedure for Severe Recalcitrant Forearm Deformities in Masada IIb Hereditary Multiple Exostoses
• Osteochondroma
• Osteochondroma of the atlas vertebra causing high grade spinal canal stenosis: a rare case report
• Osteochondroma of the Rib: A Potentially Life-Threatening Benign Tumor
• Outcomes and Vertebral Osteophytes and Bulging Intervertebral Discs Occupancy as a Decision-Making Tool for Surgical Success in Patients Undergoing Microendoscopic Foraminotomy for Lumbar Foraminal Stenosis
• Pain and fatigue in adult patients with multiple osteochondromas: The Netherlands
• Pathological progress and remission strategies of osteoarthritic lesions caused by long-term joint immobilization
• Pediatric diaphragmatic hernia induced by a rib osteochondroma
• Peroneal Nerve Decompression in Patients with Multiple Hereditary Exostoses: Indications, Complications, and Recurrence
• Piezo1 expression in chondrocytes controls endochondral ossification and osteoarthritis development
• Popliteal artery pseudoaneurysm and secondary ipsilateral deep vein thrombosis caused by an exostosis in a mature adult
• Popliteal pseudoaneurysm in a young patient with multiple hereditary exostosis
• Potocki-Shaffer syndrome revealed in a WAGR syndrome case with multiple exostoses
• 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
• Rare retro-patellar multiple osteochondromas in patellar tendon: A case report
• Rare Variants in <em>LRP4</em> Are Associated with Mesiodens, Root Maldevelopment, and Oral Exostoses in Humans
• Rare Variants in LRP4 Are Associated with Mesiodens, Root Maldevelopment, and Oral Exostoses in Humans
• 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
• Secondary peripheral chondrosarcoma in multiple osteochondromas: a retrospective single-institution case series
• Skeletal fluorosis: an uncommon cause, yet a rescue treatment?
• Solitary Osteochondroma at Unusual Sites: A Case Report and Literature Review
• Spontaneous absorption of osteophytic calcification associated with chronic dural tear and ventral spinal CSF leak
• Successful treatment of forelimb osteochondroma in a ferret (Mustela putorius furo)
• Surgical Approach and Considerations for Compressive Thoracic Intraspinal Osteochondroma in Familial Hereditary Multiple Exostosis
• Surgical Proposition of a Slow-Growing Calvarial Exostosis in a Female Patient With a Congenital Iris Cyst of the Anterior Chamber and Mandibular Tori
• Surgical restabilization reduces the progression of post-traumatic osteoarthritis initiated by ACL rupture in mice
• 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 Perils of Sleeper Plates in Multiple Hereditary Exostosis: Tibial Deformity Overcorrection Due to Tether at Empty Metaphyseal Hole
• Tibia Valga Correction by Extraperiosteal Fibular Release in Multiple Exostosis Disease
• 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