Disease: Exostoses- multiple
- <em>PHF21A</em> Related Disorder: Description of a New Case
- A Case Report of Trevor's Disease in a Pediatric Patient with Hereditary Multiple Exostoses Disease
- 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 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
- An Easy-to-Use Approach to Detect CNV From Targeted NGS Data: Identification of a Novel Pathogenic Variant in MO Disease
- Anesthetic management using costoclavicular brachial plexus block with patient-controlled analgesia in Pediatrics: A case report
- Ankle Mortise Instability in Multiple Hereditary Exostoses
- Atypical medial femoral condylar fracture in Stuve-Wiedemann syndrome
- Autosomal recessive EXT2 syndrome - extending the phenotypic spectrum of an emerging condition, a further case?
- Biomechanical properties of splint materials while curing
- C1 C2 spinal cord compression in hereditary multiple exostoses: case report and review of the literature
- 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 overview and outcome of the Stuve-Wiedemann syndrome: a systematic review
- Clinical survey of a pedigree with hereditary multiple exostoses and identification of EXT-2 gene deletion mutation
- Clinical survey of a pedigree with hereditary multiple exostoses and identification of EXT‑2 gene deletion mutation
- 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
- Computer Navigation-Aided Excision of Proximal Femoral Osteochondroma: Surgical Technique
- 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
- 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
- Endoscopic endonasal extreme far-medial approach for a lower clivus osteochondroma in a patient with hereditary multiple exostoses: illustrative case
- 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
- 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
- Genetic and functional analyses detect an EXT1 splicing pathogenic variant in a Chinese hereditary multiple exostosis (HME) family
- 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 spinal canal involvement
- Hereditary Multiple Exostoses-A Review of the Molecular Background, Diagnostics, and Potential Therapeutic Strategies
- Hereditary multiple exostoses: A case report and literature review
- 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
- Hinge positioning method of Ilizarov apparatus in correcting radial head luxation caused by multiple hereditary exostoses
- 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 acetabular osteochondroma in patients with multiple hereditary exostoses
- 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
- Lower limb deformities and limb length discrepancies in hereditary multiple exostoses
- 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 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
- 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 Arising From the Inferior Articular Process of the Lumbar Spine in a Geriatric Patient: A Case Report and Literature Review
- Osteochondroma formation is independent of heparanase expression as revealed in a mouse model of hereditary multiple exostoses
- 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
- Pediatric diaphragmatic hernia induced by a rib osteochondroma
- Peroneal Nerve Decompression in Patients with Multiple Hereditary Exostoses: Indications, Complications, and Recurrence
- Perturbed body fluid distribution and osmoregulation in response to high salt intake in patients with hereditary multiple exostoses
- Popliteal artery pseudoaneurysm and secondary ipsilateral deep vein thrombosis caused by an exostosis in a mature adult
- Postzygotic mosaicism of a novel PTPN11 mutation in monozygotic twins discordant for metachondromatosis
- Potential influence of factors for genu valgus with hereditary multiple exostoses
- 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
- Rapidly acquired valgus deformity of the knee after osteochondroma resection in multiple hereditary exostoses pediatric patients: A report of two cases
- Rare coexistence of multiple osteochondromas and solitary osteoid osteoma: 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
- Rebound predictors of varus-valgus deformities around the knee corrected by guided growth
- 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
- Solitary Osteochondroma at Unusual Sites: A Case Report and Literature Review
- Spontaneous pneumothorax in a 17-year-old male patient with multiple exostoses: A case report and review of the literature
- Surgical outcomes of spinal osteochondroma in children: A multicentre observational study
- 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 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 Largest Germline Heterozygous Deletion Encompassing Potocki-Shaffer and WAGR Syndromes Loci to Date: A Case Report
- 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
- 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