Disease: Ollier disease
- A Longitudinal Clinical Trajectory Analysis Examining the Accumulation of Co-morbidity in People with Type 2 Diabetes (T2D) Compared with Non-T2D Individuals
- A Rare Co-Occurrence of Maffucci Syndrome and Astrocytoma with IDH1 R132H Mutation: A Case Report
- A study to investigate genetic factors associated with weight gain in people with diabetes: analysis of polymorphisms in four relevant genes
- Advanced colon cancer coexisting with multiple Osteochondromatosis in a child; coincidence or causality? - A case report
- Benign Brain and Spinal Tumors Originating from Bone or Cartilage
- Brain and/or Spinal Cord Tumors Accompanied with Other Diseases or Syndromes
- Can digital health researchers make a difference during the pandemic? Results of the single-arm, chatbot-led Elena+: Care for COVID-19 interventional study
- Comparison of clinical features between patients with anti-synthetase syndrome and dermatomyositis: Results from the MYONET registry
- 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
- IDH mutations in G2-3 conventional central bone chondrosarcoma: a mono institutional experience
- Intracranial Metastasis of Extracranial Chondrosarcoma: Systematic Review With Illustrative Case
- Investigating <em>in vivo Mycobacterium avium</em> subsp. <em>paratuberculosis</em> microevolution and mixed strain infections
- Juvenile granulosa cell tumor in a transgender male with Ollier disease: A case report
- Local design and manufacturing of patient-specific implant using Anatomage Medical Design Studio software: proof of concept - Botswana's 1st case report
- Lower limb lymphangioma circumscriptum: The guiding sign for the diagnosis of Maffucci syndrome
- Malignant Transformation in Ollier's Disease: A Novel Stem for a Tibial Megaprosthesis
- 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
- Proteomic biomarkers for survival in systemic sclerosis-associated pulmonary hypertension
- Sars-Cov-2 Infection in People with Type 1 Diabetes and Hospital Admission: An Analysis of Risk Factors for England
- Supratentorial multifocal gliomas associated with Ollier disease harboring IDH1 R132H mutation: A case report
- Targeting amyotrophic lateral sclerosis by neutralizing seeding-competent TDP-43 in CSF
- The change in glycaemic control immediately after the 3rd COVID-19 vaccination in people with type 1 diabetes
- The Utility of PET/CT for the Diagnosis of Periosteal Chondrosarcoma in a Patient With Maffucci's Syndrome
- Two Ways of Targeting a CD19 Positive Relapse of Acute Lymphoblastic Leukaemia after Anti-CD19 CAR-T Cells
- Unraveling the molecular diagnosis of metaphyseal enchondromatosis with D-2-hydroxyglutaric aciduria: A 22-year quest
- Vascular Malformation? It's Maffucci Syndrome