• A Rare Co-Occurrence of Maffucci Syndrome and Astrocytoma with IDH1 R132H Mutation: A Case Report
• A rare presentation of Maffucci syndrome: A case report and literature review
• Advanced colon cancer coexisting with multiple Osteochondromatosis in a child; coincidence or causality? - A case report
• An intermediate phenotype in IDH related enchondromatosis spectrum
• Benign Brain and Spinal Tumors Originating from Bone or Cartilage
• Brain and/or Spinal Cord Tumors Accompanied with Other Diseases or Syndromes
• Clinical and radiological response of Maffucci related enchondromas to mutant IDH1 inhibitor Ivosidenib
• Defining priorities in the transition from paediatric to adult healthcare for rare bone disease patients: a dialogic approach
• Defining priorities in the transition from paediatric to adult healthcare for rare bone disease patients. A dialogic approach
• Disastrous evolution of ollier disease: a rare case report
• Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome
• Giant Solitary Sinonasal Enchondroma: A Rare Case Report
• Haploinsufficiency of EXT1 and Heparan Sulphate Deficiency Associated with Hereditary Multiple Exostoses in a Pakistani Family
• Intracranial Metastasis of Extracranial Chondrosarcoma: Systematic Review With Illustrative Case
• Lower limb lymphangioma circumscriptum: The guiding sign for the diagnosis of Maffucci syndrome
• Malignant transformation of Ollier disease-related multiple glioma with IDH1 p.R132C mutation
• Multiple enchondromas and hobnail hemangiomas revealing a rare type of Maffucci syndrome
• New bone formation accelerates during lower limb lengthening and deformity correction in children with Ollier's disease
• Ollier disease
• Ollier disease: A case report and literature review
• Ollier Disease: A Case Report and Review of Treatment Options
• Ovarian juvenile granulosa cell tumors with Ollier's disease in children with IDH1 gene somatic mutation
• Pelvic Vascular Malformations and Recurrent Rectal Prolapse in a Patient With Maffucci Syndrome: A Diagnostic and Therapeutic Challenge
• Rare radiological manifestation of enchondromatosis in children: Columnar pattern: A retrospective cohort study
• Robotic mitral valve repair and resection of a pericardial cyst in Maffucci syndrome with sternal manifestations: A case report
• Single-cell transcriptomic analyses of mouse idh1 mutant growth plate chondrocytes reveal distinct cell populations responsible for longitudinal growth and enchondroma formation
• Successful sirolimus treatment of spindle cell haemangiomas in a paediatric patient with Maffucci syndrome
• Successful sirolimus treatment of spindle cell hemangiomas in a pediatric patient of Maffucci syndrome
• Supratentorial multifocal gliomas associated with Ollier disease harboring IDH1 R132H mutation: A case report
• Surgical Resection Combined with Sclerotherapy Treating Maffucci Syndrome's Venous Malformation in Head and Neck Region
• The Utility of PET/CT for the Diagnosis of Periosteal Chondrosarcoma in a Patient With Maffucci's Syndrome
• Unraveling the molecular diagnosis of metaphyseal enchondromatosis with D-2-hydroxyglutaric aciduria: A 22-year quest
• Vascular Malformation? It's Maffucci Syndrome