Maffucci Syndrome-Reference-Cited by-同舟云学术

Maffucci Syndrome

Published:2015-12 Issue:12 Volume:42 Page:2434-2435
ISSN:0315-162X
Container-title:The Journal of Rheumatology
language:en
Short-container-title:J Rheumatol

Author:

TSAO YEN-PO,TSAI CHANG-YOUH,CHEN WEI-SHENG

Publisher

The Journal of Rheumatology

Subject

Immunology,Immunology and Allergy,Rheumatology

Reference5 articles.

1. Bovee JV Alman BA . Enchondromatosis: Ollier disease and Maffucci syndrome. In: Fletcher CD Hogendoorn P , editors. WHO classification of tumours of soft tissue and bone, 4th ed. Lyon: IARC Press; 2013:376–8.

2. Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome

3. Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2

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

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

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. An osteolytic lesion of the proximal ulna in a patient with Maffucci syndrome: a case report;Archives of Hand and Microsurgery;2024-09-01

2. Osteopathies from Anarchic Tissue Development;Prenatal Diagnosis of Fetal Osteopathologies;2024

3. A possible case of “kissing” osteochondroma and multiple enchondromas in a medieval skeleton from the church of Sant’ Agostino in Caravate (Northern Italy);Anthropologischer Anzeiger;2023-03-16

4. Multicentric infantile myofibromatosis with extensive involvement limited to bone;Skeletal Radiology;2021-12-04

5. IDH1 R132C and ERC2 L309I Mutations Contribute to the Development of Maffucci’s Syndrome;Frontiers in Endocrinology;2021-11-01