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1991 30
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1993 32
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1998 36
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2009 41
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1,525 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 …
[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: 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 …
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.
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.
BEGG J. BEGG J. Med J Aust. 1946 Jul 6;2:31. Med J Aust. 1946. PMID: 20991514 No abstract available.
Ollier's disease: dyschondroplasia.
NARDELL SG. NARDELL SG. Br Med J. 1950 Sep 2;2(4678):555-7. doi: 10.1136/bmj.2.4678.555. Br Med J. 1950. PMID: 15434456 Free PMC article. No abstract available.
Ollier's disease (dyschondroplasia).
POTTER CT. POTTER CT. Proc R Soc Med. 1949 Jul;42(7):559. Proc R Soc Med. 1949. PMID: 18228986 Free PMC article. No abstract available.
[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.
[Enchondromatosis (Ollier disease)].
Kosho T. Kosho T. Ryoikibetsu Shokogun Shirizu. 2001;(33):631-2. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462603 Review. Japanese. No abstract available.
1,525 results

Searches related to "ollier disease"