Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature

The association of enchondromatosis with malignant transformed chondrosarcoma and ovarian juvenile granulosa cell tumor (Ollier disease)

(2017) Andrea Burgetova et al.   Taiwanese Journal of Obstetrics & Gynecology

Ollier Disease: Pathogenesis, Diagnosis, and Management

(2015) Avinash Kumar et al.   ORTHOPEDICS

IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours

(2011) M Fernanda Amary et al.   JOURNAL OF PATHOLOGY

Incidence, Predictive Factors, and Prognosis of Chondrosarcoma in Patients with Ollier Disease and Maffucci Syndrome: An International Multicenter Study of 161 Patients

(2011) S. H. M. Verdegaal et al.   ONCOLOGIST

Genome-wide analysis of Ollier disease: Is it all in the genes?

(2011) Twinkal C Pansuriya et al.   Orphanet Journal of Rare Diseases

DO INTRACRANIAL NEOPLASMS DIFFER IN OLLIER DISEASE AND MAFFUCCI SYNDROME? AN IN-DEPTH ANALYSIS OF THE LITERATURE

(2009) Adrianna Ranger et al.   NEUROSURGERY

PTHR1 mutations associated with Ollier disease result in receptor loss of function

(2008) Alain Couvineau et al.   HUMAN MOLECULAR GENETICS