• 'A child with Malpuech-Michels-Mingarelli-Carnevale syndrome and ADHD and major depressive disorder'
• A De Novo 8q22.2q22.3 Interstitial Microdeletion in a Girl with Developmental Delay and Congenital Defects
• A genotype and phenotype analysis of SMAD6 mutant patients with radioulnar synostosis
• A new technique for separating radioulnar synostosis with vascularized flap: a case report
• A newborn with a limited elbow function
• A novel MECOM variant associated with congenital amegakaryocytic thrombocytopenia and radioulnar synostosis
• A novel missense mutation in the MECOM gene in a Chinese boy with radioulnar synostosis with amegakaryocytic thrombocytopenia
• A novel mutation in MECOM affects MPL regulation in vitro and results in thrombocytopenia and bone marrow failure
• A Three-Step Method for the Treatment of Radioulnar Synostosis with Posterior Radial Head Dislocation
• Acquired Radial Club Hand: An Algorithm to Manage Radial Deficiency
• An anatomical classification of congenital proximal radioulnar synostosis based on retrospective MRI measurement combined with radiography
• Application of 3-Dimensional Printing Technology in Rotational Osteotomy of Congenital Radioulnar Synostosis
• Association of Polymorphisms of <em>MASP1/3</em>, <em>COLEC10</em>, and <em>COLEC11</em> Genes with 3MC Syndrome
• Bilateral congenital radioulnar synostosis in an Early Horizon subadult burial from the site of Atalla, Peru
• Cenani-Lenz syndactyly in siblings with a novel homozygous LRP4 mutation and recurrent hypoglycaemia
• Congenital middle radioulnar synostosis: Report of a probable subtype
• Congenital Proximal Radioulnar Synostosis in an Elite Athlete-Case Report
• Congenital proximal radioulnar synostosis-a case report
• Congenital Radioulnar Synostosis
• Congenital radioulnar synostosis presenting in adulthood - a case report
• Congenital Radioulnar Synostosis: A Case Report and Review of Various Osteotomies
• Congenital radioulnar synostosis: is prenatal diagnosis possible? - A case report
• Congenital unilateral proximal radioulnar synostosis: A surgical case report
• Correction: SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis
• Corrective derotation osteotomies to treat congenital radioulnar synostosis in children: results of a systematic review and meta-analysis
• Derotational Osteotomy and Plate Fixation of the Radius and Ulna for the Treatment of Congenital Proximal Radioulnar Synostosis
• Distal biceps tendon repair: outcome and complications with single incision anchor fixation
• Double-level Intraperiosteal Derotational Osteotomy for Congenital Radioulnar Synostosis
• Dynamic sonographic diagnosis of snapping elbow associated with congenital radioulnar synostosis
• Effects of simulated radioulnar synostosis on supination and pronation in cats. A cadaveric study
• Expanded phenotypic and hematologic abnormalities beyond bone marrow failure in MECOM-associated syndromes
• Expanding the phenotypic and genotypic characteristics of trichohepatoenteric syndrome: a report of eight patients from five unrelated families
• Expanding the phenotypic spectrum of COLEC10-Related 3MC syndrome: A glimpse into COLEC10-Related 3MC syndrome in the Ashkenazi Jewish population
• Fetal hydrops caused by a novel pathogenic MECOM variant
• Fibula flap in upper extremity segmental/critical size bone defects fixed with locking plates. Single-institution observational cohort
• Fracture of the two forearm bones and congenital radioulnar synostosis: A case report and review of literature
• Fractures of the proximal radius in children: management and results of 100 consecutive cases
• Functional outcome of campanacci grade 3 giant cell tumours of distal radius after resection and reconstruction with ulnar translocation technique: a case series
• Hand and Upper Limb Malformations in Italy: A Multicentric Study
• Heterotopic ossification formation after fractures about the elbow
• Homozygous <em>SMAD6</em> variants in two unrelated patients with craniosynostosis and radioulnar synostosis
• Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis
• Idiopathic Proximal Radioulnar Synostosis - A Rare Case Report and Review of Literature
• Improving the Accuracy of Corrective Osteotomy for Congenital Radio Ulnar Synostosis using the Axis of Rotation of the Forearm as a Guide
• Is short-term hand therapy effective in a child with congenital radioulnar synostosis? A case report
• Letter regarding 'Results after treatment of congenital radioulnar synostosis: a systematic review and pooled data analysis'
• Management of Monteggia Injuries in the Adult
• Measurement of compensatory wrist joint rotation using three-dimensional motion analysis in patients with unilateral proximal congenital radioulnar synostosis
• MECOM Deficiency: from Bone Marrow Failure to Impaired B-Cell Development
• Mecom mutation related to radioulnar synostosis with amegakaryocytic thrombocytopenia reduces HSPCs in mice
• MECOM-related disorder: Radioulnar synostosis without hematological aberration due to unique variants
• Melanotic Neuroectodermal Tumor of Infancy in the Ulna of an Infant: A Very Rare Tumor: A Case Report
• Musculoskeletal abnormalities in a large international cohort of boys with 49,XXXXY
• Nonlethal presentations of CYP26B1-related skeletal anomalies and multiple synostoses syndrome
• Not Kidding! Sequalae of elbow trauma in children
• OPerative versus non-opERAtive management of isolated ULNAr diaphyseal fractures (OPERA-Ulna): protocol for a randomized controlled trial
• Osteogenesis imperfecta type 1 with an incidental finding of bilateral radioulnar synostosis
• Outcomes of two-stage double-level rotational osteotomy in treating patients with congenital proximal radioulnar synostosis
• Patient and Caregiver Impressions of the Impact of Madelung Deformity: A CoULD Registry Analysis
• Perinatal-lethal nonimmune fetal hydrops attributed to <em>MECOM</em>-associated bone marrow failure
• Poland's syndrome concomitant with congenital proximal and distal radioulnar synostosis: A rare case report
• Post-traumatic proximal radioulnar synostosis: current concepts on the clinical presentations, classifications and open surgical approaches
• Post-traumatic proximal radioulnar synostosis: results of surgical treatment and review of the literature
• Post-Traumatic Radio-ulnar Synostosis Managed by the Excision of the Bone Bridge and Palmaris Longus Encircling Loop over the Ulna: A Case Report
• Post-traumatic Radioulnar Synostosis in Distal Forearm Fractures in Children: A Report of 2 Cases
• Post-traumatic radioulnar synostosis: a retrospective case series of 10 patients in Kuwait
• Posttraumatic proximal radioulnar synostosis: Current concepts on the clinical presentations, classifications, and open surgical approaches
• Preoperative radius head dislocation affects forearm rotation after mobilization of congenital radioulnar synostosis
• Proximal radioulnar synostosis following Monteggia fracture-dislocation: a case report
• Quantitative Analysis of Deformity in Digital Model of Congenital Radioulnar Synostosis
• Radial Head Prosthetic Replacement in Adolescents: A Report of 5 Cases
• Radial Pronation Angle: A Novel Radiological Evaluation Index of Congenital Proximal Radioulnar Synostosis
• Radioulnar Synostosis
• Radioulnar Synostosis
• Rare case of fracture of the two bones of the forearm in a patient with humerus bifurcation and an ulnar deficiency: humero-radioulnar synostosis
• Rare Complication of Distal Radius and Ulnar Styloid Fractures with Percutaneous Fixation: A Case Report on Distal Radioulnar Synostosis
• Rare complication of open reduction and internal fixation of fracture distal radius: A case report of distal radioulnar synostosis
• Rare complication of open reduction and internal fixation of fracture distal radius: A case report of distal radioulnar synostosis- letter to editor
• Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome
• Release of Extensive Post Traumatic Radio-Ulnar Synostosis with Vascularized Free Flap Interposition
• Results after treatment of congenital radioulnar synostosis: a systematic review and pooled data analysis
• Rotational osteotomy with single incision and elastic fixation for congenital radioulnar synostosis in children: a retrospective cohort study
• Severe coarctation of the aorta, developmental delay, and multiple dysmorphic features in a child with SMAD6 and SMARCA4 variants
• SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis
• SMAD6-deficiency in human genetic disorders
• Synostosis after fracture of both forearm bones treated by intramedullary nailing
• The Boyd approach: a valuable alternative to treating simple to complex elbow fractures and dislocations
• The One-Bone Forearm: A Review
• The relation between radiographic manifestation and clinical characteristics of congenital radioulnar synostosis in children: A retrospective study from multiple centers
• The Terrible Triad of the Elbow Accompanied by Capitellum and Humerus Shaft Fracture: A Rare Case Report
• Traumatic elbow dislocation in a patient with congenital radioulnar synostosis
• Treatment of Congenital Radioulnar Synostosis Using a Free Vascularized Fascia Lata Graft
• Treatment of congenital radioulnar synostosis with radial derotational osteotomy and local subcutaneous pedicled fat flap filling in fusion area
• Treatment of Recalcitrant Nonunion of the Radius With Posterior Interosseous Bone Flap in Children
• Unilateral congenital proximal radioulnar synostosis in a 4-year-old boy: A case report
• Unusual presentation of congenital radioulnar synostosis with osteoporosis, fragility fracture and nonunion: A case report and review of literature
• Use of Acellular Dermal Matrix to Prevent Recurrence of Radioulnar Heterotopic Ossification
• Vascularized ulnar periosteal pedicled flap for forearm nonunion in children
• Whole-exome sequencing identified first homozygous frameshift variant in the COLEC10 gene in an Iranian patient causing 3MC syndrome type 3
• ZMAT2, a newly-identified potential disease-causing gene in congenital radioulnar synostosis, modulates BMP signaling