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1945 3
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1954 15
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1968 4
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1979 6
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1985 15
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1991 30
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1993 32
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1998 36
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1,543 results

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Page 1
Ollier disease.
Silve C, Jüppner H. Silve C, et al. Orphanet J Rare Dis. 2006 Sep 22;1:37. doi: 10.1186/1750-1172-1-37. Orphanet J Rare Dis. 2006. PMID: 16995932 Free PMC article. Review.
When multiple enchondromas are present, the condition is called enchondromatosis also known as Ollier disease (WHO terminology). The estimated prevalence of Ollier disease is 1/100,000. ...Enchondromas in Ollier disease present a r …
When multiple enchondromas are present, the condition is called enchondromatosis also known as Ollier disease (WHO term …
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. ...
Ollier disease (OD) and Maffucci syndrome (MS) are characterized by multiple enchondromas. ...
Ollier Disease: Pathogenesis, Diagnosis, and Management.
Kumar A, Jain VK, Bharadwaj M, Arya RK. Kumar A, et al. Orthopedics. 2015 Jun;38(6):e497-506. doi: 10.3928/01477447-20150603-58. Orthopedics. 2015. PMID: 26091223 Review.
Ollier disease (Spranger type I) is a rare bone disease that is characterized by multiple enchondromatosis with a typical asymmetrical distribution and confined to the appendicular skeleton. ...Clinically, Ollier disease has a wide variet
Ollier disease (Spranger type I) is a rare bone disease that is characterized by multiple enchondromatosis with
[Ollier disease].
Bellamlih H, El Bouazzi O, Belabbes S, El Haddad A, Zinoun B, Africha T. Bellamlih H, et al. Rev Prat. 2023 Jun;73(6):657. Rev Prat. 2023. PMID: 37458557 French. No abstract available.
Ollier disease.
D'Angelo L, Massimi L, Narducci A, Di Rocco C. D'Angelo L, et al. Childs Nerv Syst. 2009 Jun;25(6):647-53. doi: 10.1007/s00381-009-0873-z. Epub 2009 Mar 27. Childs Nerv Syst. 2009. PMID: 19326125
BACKGROUND: Ollier disease is a rare, nonfamilial disorder characterized by multiple enchondromatosis with an asymmetric distribution and areas of dysplastic cartilage. ...METHOD: We report on a 12-year-old boy affected with Ollier disease and o …
BACKGROUND: Ollier disease is a rare, nonfamilial disorder characterized by multiple enchondromatosis with an asymmetri …
[Ollier's disease].
Rexach Fumanya M, Castro Guardiola A, García-Bragado Dalmau F. Rexach Fumanya M, et al. Med Clin (Barc). 2012 Jun 30;139(3):e5. doi: 10.1016/j.medcli.2011.10.016. Epub 2011 Dec 23. Med Clin (Barc). 2012. PMID: 22197370 Spanish. No abstract available.
Ollier's disease.
BEGG J. BEGG J. Med J Aust. 1946 Jul 6;2:31. Med J Aust. 1946. PMID: 20991514 No abstract available.
Ollier's disease.
MARGOLIS J. MARGOLIS J. AMA Arch Intern Med. 1959 Feb;103(2):279-84. doi: 10.1001/archinte.1959.00270020107012. AMA Arch Intern Med. 1959. PMID: 13616764 No abstract available.
A case of Ollier's disease of the hand.
Miyawaki T, Kinoshita Y, Iizuka T. Miyawaki T, et al. Ann Plast Surg. 1997 Jan;38(1):77-80. doi: 10.1097/00000637-199701000-00015. Ann Plast Surg. 1997. PMID: 9015545 Review.
Enchondroma is a benign growth of cartilage arising in the bone metaphysis as a solitary or multiple primary lesions. The form of multiple enchondromatosis with unilateral predominance is termed Ollier's disease. We have recently treated a case of Ollier
Enchondroma is a benign growth of cartilage arising in the bone metaphysis as a solitary or multiple primary lesions. The form of multiple …
Skull Base Chondrosarcoma Caused by Ollier Disease: A Case Report and Literature Review.
Ding C, Chen W, Liu F, Xiong M, Chen J. Ding C, et al. World Neurosurg. 2019 Jul;127:103-108. doi: 10.1016/j.wneu.2019.03.037. Epub 2019 Mar 12. World Neurosurg. 2019. PMID: 30872199 Review.
BACKGROUND: Ollier disease (OD) is a rare, nonhereditary bone disease that is characterized by the presence of multiple enchondromatosis (3 or more) with a typical asymmetric distribution which is mainly confined to the appendicular skeleton. ...
BACKGROUND: Ollier disease (OD) is a rare, nonhereditary bone disease that is characterized by the presence of multiple …
1,543 results