Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2014 2
2015 14
2016 7
2017 5
2018 3
2019 7
2020 2
2021 7
2022 7
2023 6
2024 3

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

51 results

Results by year

Filters applied: . Clear all
Page 1
Multiple hereditary exostoses and enchondromatosis.
Jurik AG. Jurik AG. Best Pract Res Clin Rheumatol. 2020 Jun;34(3):101505. doi: 10.1016/j.berh.2020.101505. Epub 2020 Apr 4. Best Pract Res Clin Rheumatol. 2020. PMID: 32253147 Review.
Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature.
El Abiad JM, Robbins SM, Cohen B, Levin AS, Valle DL, Morris CD, de Macena Sobreira NL. El Abiad JM, et al. Am J Med Genet A. 2020 May;182(5):1093-1103. doi: 10.1002/ajmg.a.61530. Epub 2020 Mar 7. Am J Med Genet A. 2020. PMID: 32144835 Free PMC article.
Ollier disease (OD) and Maffucci syndrome (MS) are characterized by multiple enchondromas. Patients with MS also have benign vascular overgrowths that become malignant in 8.5% of cases. ...
Ollier disease (OD) and Maffucci syndrome (MS) are characterized by multiple enchondromas. Patients with MS also have benign v …
Maffucci Syndrome.
Tsao YP, Tsai CY, Chen WS. Tsao YP, et al. J Rheumatol. 2015 Dec;42(12):2434-5. doi: 10.3899/jrheum.150216. J Rheumatol. 2015. PMID: 26628708 No abstract available.
Monomelic Maffucci syndrome.
Verma GG, Jain VK, Iyengar KP. Verma GG, et al. BMJ Case Rep. 2021 Mar 3;14(3):e239619. doi: 10.1136/bcr-2020-239619. BMJ Case Rep. 2021. PMID: 33658216 Free PMC article.
Maffucci syndrome is a rare congenital, non-hereditary condition characterised by presence of multiple enchondromas and haemangiomas. ...We describe a 12-year-old girl with monomelic Maffucci syndrome affecting her left lower limb. She presented with p …
Maffucci syndrome is a rare congenital, non-hereditary condition characterised by presence of multiple enchondromas and haeman …
Update on the imaging features of the enchondromatosis syndromes.
Sharif B, Lindsay D, Saifuddin A. Sharif B, et al. Skeletal Radiol. 2022 Apr;51(4):747-762. doi: 10.1007/s00256-021-03870-0. Epub 2021 Jul 24. Skeletal Radiol. 2022. PMID: 34302201 Review.
Ollier disease and Maffucci syndrome are the commonest enchondromatosis subtypes, arising from non-hereditary mutations in the IDH1 and IDH2 genes, presenting in childhood and being characterised by multiple enchondromas. ...In this review, we outline the molecular …
Ollier disease and Maffucci syndrome are the commonest enchondromatosis subtypes, arising from non-hereditary mutations in the …
Maffucci syndrome and neoplasms: a case report and review of the literature.
Prokopchuk O, Andres S, Becker K, Holzapfel K, Hartmann D, Friess H. Prokopchuk O, et al. BMC Res Notes. 2016 Feb 27;9:126. doi: 10.1186/s13104-016-1913-x. BMC Res Notes. 2016. PMID: 26920730 Free PMC article. Review.
Patients with Maffucci syndrome are at increased risk of developing different kinds of malignant tumors. ...IHCC) and also with Maffucci syndrome. For IHCC, mutations in IDH1/IDH2 are associated with higher survival rates. ...
Patients with Maffucci syndrome are at increased risk of developing different kinds of malignant tumors. ...IHCC) and also wit …
Maffucci Syndrome. An Interesting Case and a Review of the Literature.
Ngai C, Ding DY, Rapp TB. Ngai C, et al. Bull Hosp Jt Dis (2013). 2015 Dec;73(4):282-5. Bull Hosp Jt Dis (2013). 2015. PMID: 26630472 Free article. Review.
Maffucci syndrome, a rare sporadic form of enchondromatosis, is characterized by hemangiomas and multiple enchondromas, benign cartilaginous tumors that arise near growth plates. Previous studies demonstrate that individuals diagnosed with Maffucci syndrom …
Maffucci syndrome, a rare sporadic form of enchondromatosis, is characterized by hemangiomas and multiple enchondromas, benign …
Malignant Transformation of Maffucci Syndrome.
Triki W, Belem A, Labbene E, Riahi H, Chelli-Bouaziz M. Triki W, et al. J Clin Rheumatol. 2021 Oct 1;27(7):e266-e268. doi: 10.1097/RHU.0000000000001424. J Clin Rheumatol. 2021. PMID: 32530866 No abstract available.
Somatic mosaic mutations of IDH1 and NPM1 associated with cup-like acute myeloid leukemia in a patient with Maffucci syndrome.
Akiyama M, Yamaoka M, Mikami-Terao Y, Ohyama W, Yokoi K, Arakawa Y, Takita J, Suzuki H, Yamada H. Akiyama M, et al. Int J Hematol. 2015 Dec;102(6):723-8. doi: 10.1007/s12185-015-1892-z. Epub 2015 Oct 27. Int J Hematol. 2015. PMID: 26508204 Review.
Maffucci syndrome is a nonhereditary congenital disorder characterized by multiple enchondromas and with soft-tissue hemangiomas. ...However, hematopoietic malignancies arising in Maffucci syndrome are rare. We report a 7-year-old girl with Maffucci …
Maffucci syndrome is a nonhereditary congenital disorder characterized by multiple enchondromas and with soft-tissue hemangiom …
Synovial sarcoma complicating Maffucci syndrome.
Gammoudi R, Aounallah A, Belajouza C, Nouira R. Gammoudi R, et al. Indian J Dermatol Venereol Leprol. 2019 May-Jun;85(3):291-294. doi: 10.4103/ijdvl.IJDVL_547_17. Indian J Dermatol Venereol Leprol. 2019. PMID: 29667613 Free article.
Maffucci syndrome is a rare nonhereditary disorder comprising of lymphovascular malformations and multiple enchondromas, which may be associated with several internal malignancies. This report describes a new association of Maffucci syndrome with pedal …
Maffucci syndrome is a rare nonhereditary disorder comprising of lymphovascular malformations and multiple enchondromas, which …
51 results