• A case of Ollier's disease of the hand
• A mutant PTH/PTHrP type I receptor in enchondromatosis
• A new histologic approach to the differentiation of enchondroma and chondrosarcoma of the bones. A clinicopathologic analysis of 51 cases
• A rare case of enchondromatosis of the knees and hands with involvement of Hoffa's fat pad and peri-articular soft-tissues
• Absence of IHH and retention of PTHrP signalling in enchondromas and central chondrosarcomas
• Array-comparative genomic hybridization of central chondrosarcoma: identification of ribosomal protein S6 and cyclin-dependent kinase 4 as candidate target genes for genomic aberrations
• Benign and malignant cartilage tumors
• Benign and malignant cartilage tumors of bone and joint: their anatomic and theoretical basis with an emphasis on radiology, pathology and clinical biology. I. The intramedullary cartilage tumors
• Benign cartilage tumors
• Benign cartilage tumors. What should I do with incidental findings?
• Benign chondroid neoplasms of bone
• Benign phyllodes tumor associated with Maffucci's syndrome
• Bone scintigraphy in Maffucci syndrome
• Cartilaginous lesions of bone
• Characteristics of gliomas in patients with somatic IDH mosaicism
• Chest wall secondary chondrosarcoma arising from enchondroma in a young Asian female
• Chondroma, chondroblastoma and chondromyxoid fibroma
• Chondromas (enchondroma, periosteal chondroma, enchondromatosis)
• Chondrosarcoma of the short tubular bones of the hands and feet
• Coexistence of secondary chondrosarcoma and lung carcinoma metastasis in the humerus of a patient with Ollier's disease: A case report
• Composite hemangioendothelioma: report of 5 cases including one with associated Maffucci syndrome
• Concurrent enchondroma and periosteal chondroma of the humerus mimicking chondrosarcoma
• Concurrent periosteal chondroma and enchondroma of the fibula mimicking chondrosarcoma
• COX-2 expression in chondrosarcoma: a role for celecoxib treatment?
• Determination of malignancy of cartilaginous tumors (2). Determination of malignancy by nuclear DNA contents and their distribution patterns in cartilaginous tumors
• Do Glioblastomas with Syndromic Association Have Better Prognosis? A Case of Supratentorial Glioblastoma with Embryonal Tumor Differentiation in a Child with Multiple Enchondromatosis
• Enchondroma and chondrosarcoma
• Enchondroma of the Hand: Evaluation and Management
• Enchondroma of the hand. Clinical evaluation study of diagnosis, surgery and functional outcome
• Enchondroma of the nasal septum due to Ollier disease: a case report and review of the literature
• Enchondromatosis and Growth Plate Development
• ENCHONDROMATOSIS IN AN ADULT DOG
• Enchondromatosis: insights on the different subtypes
• Fibrous Dysplasia with Massive Cartilaginous Differentiation (Fibrocartilaginous Dysplasia) in the Proximal Femur: A Case Report and Review of the Literature
• Follow-up study of cartilaginous bone tumors
• From the benign to the ridiculous--a 15-year-old girl with a pathological fracture to left little finger--an interesting case of a pillow fight
• Functional results of open wedge osteotomies in lower limb angular deformities in teenagers
• Genochondromatosis II
• Genochondromatosis type II: report of a new patient and further delineation of the phenotype
• Genome-wide analysis of Ollier disease: Is it all in the genes?
• Giant Solitary Sinonasal Enchondroma: A Rare Case Report
• Hereditary bone tumors
• Hereditary bone tumors
• Hereditary multiple exostoses and enchondromatosis
• Hereditary multiple exostosis. Case report and differential diagnosis of enchondromatosis
• IDH2 and TP53 mutations are correlated with gliomagenesis in a patient with Maffucci syndrome
• Incidence, predictive factors, and prognosis of chondrosarcoma in patients with Ollier disease and Maffucci syndrome: an international multicenter study of 161 patients
• Insights into Enchondroma, Enchondromatosis and the risk of secondary Chondrosarcoma. Review of the literature with an emphasis on the clinical behaviour, radiology, malignant transformation and the follow up
• Large enchondroma of the thoracic spine: a rare case report and review of the literature
• Lipoid cell tumor of the ovary
• Maffucci Syndrome. An Interesting Case and a Review of the Literature
• Maffucci's syndrome in association with giant tubular adenoma of the breast: Case report and literature review
• Maffucci's syndrome with giant tumor of the thoracic wall
• Maffucci's syndrome--the result of neural abnormalities? Evidence of mitogenic neurotransmitters present in enchondromas and soft tissue hemangiomas
• Management of tumors and tumor-like lesions of the hand: a review of 191 patients
• Multiple enchondromatosis of the child apropos of 2 cases
• Multiple familial osteochondromatosis: presentation of a case
• Multiple hereditary exostoses and enchondromatosis
• Mutant IDH is sufficient to initiate enchondromatosis in mice
• Mutant IDH1 Dysregulates the Differentiation of Mesenchymal Stem Cells in Association with Gene-Specific Histone Modifications to Cartilage- and Bone-Related Genes
• Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature
• Ollier disease
• Ollier Disease: A Case Report and Review of Treatment Options
• Ollier Disease: A Case Series and Literature Review
• Ollier disease: benign tumours with risk of malignant transformation. A review of 17 cases
• Ollier's Disease - Rare Presentation of the Rare Disease
• Ovarian juvenile granulosa cell tumors in infants
• Plaster filling in surgical treatment of enchondroma--a justified therapeutic procedure?
• Proteoglycans and chondroitin sulfates from human multiple chondroma (enchondromatosis)
• Radiographic features of Ollier's disease - two case reports
• Sclerosing angiomatoid nodular transformation of the spleen in a patient with Maffucci syndrome: a case report and review of literature
• Secondary chondrosarcoma: radiopathological correlation
• Skull Base Enchondroma and Chondrosarcoma in Ollier Disease and Maffucci Syndrome
• Somatic <em>IDH1</em> variant (p.R132C) in an adult male with Maffucci syndrome
• Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome
• Spindle cell hemangioendothelioma: an immunohistochemical and flow cytometric study of six cases
• Spindle cell hemangioendothelioma. An analysis of 78 cases with reassessment of its pathogenesis and biologic behavior
• Spindle cell vulvar hemangiomatosis associated with enchondromatosis: a rare variant of Maffucci's syndrome
• The role of metabolic enzymes in mesenchymal tumors and tumor syndromes: genetics, pathology, and molecular mechanisms
• Unsatisfactory response to sirolimus in Maffucci syndrome-associated spindle cell hemangiomas
• Well-Differentiated Central Cartilage Tumors of Bone: An Overview