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Page 1
Multiple osteochondromas.
Bovée JV. Bovée JV. Orphanet J Rare Dis. 2008 Feb 13;3:3. doi: 10.1186/1750-1172-3-3. Orphanet J Rare Dis. 2008. PMID: 18271966 Free PMC article. Review.
Multiple osteochondromas (MO) is characterised by development of two or more cartilage capped bony outgrowths (osteochondromas) of the long bones. ...Osteochondromas are benign lesions and do not affect life expectancy. Management includes remov
Multiple osteochondromas (MO) is characterised by development of two or more cartilage capped bony outgrowths (osteo
Multiple osteochondromas (MO) in the forearm: a 12-year single-centre experience.
Ham J, Flipsen M, Koolen M, van der Zwan A, Mader K. Ham J, et al. Strategies Trauma Limb Reconstr. 2016 Nov;11(3):169-175. doi: 10.1007/s11751-016-0267-1. Epub 2016 Oct 13. Strategies Trauma Limb Reconstr. 2016. PMID: 27738974 Free PMC article.
Multiple osteochondromas (MO) are a rare autosomal dominant disorder characterized by the presence of osteochondromas located on the long bones and axial skeleton. ...Several surgical procedures are offered from excision of symptomatic osteochondrom
Multiple osteochondromas (MO) are a rare autosomal dominant disorder characterized by the presence of osteochondroma
Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb).
Jennes I, Pedrini E, Zuntini M, Mordenti M, Balkassmi S, Asteggiano CG, Casey B, Bakker B, Sangiorgi L, Wuyts W. Jennes I, et al. Hum Mutat. 2009 Dec;30(12):1620-7. doi: 10.1002/humu.21123. Hum Mutat. 2009. PMID: 19810120 Review.
Multiple osteochondromas (MO) is an autosomal dominant skeletal disease characterized by the formation of multiple cartilage-capped bone tumors growing outward from the metaphyses of long tubular bones. ...In this article, the clinical aspects and mole
Multiple osteochondromas (MO) is an autosomal dominant skeletal disease characterized by the formation of multiple
Multiple Osteochondromas Comorbid With Enlarged Parietal Foramina, Elongated Styloid Processes, and Tibiofibular Synostosis.
Baugher EC, Batarseh TR, Becker AK, Cantu AJ, Carr EW, Sakthi Velavan S. Baugher EC, et al. Am J Clin Pathol. 2021 Sep 8;156(4):513-520. doi: 10.1093/ajcp/aqaa282. Am J Clin Pathol. 2021. PMID: 33769443 Review.
OBJECTIVES: This study investigates a unique case of multiple osteochondromas (MO) comorbid with enlarged parietal foramina and correlates the findings with the existing literature. ...CONCLUSIONS: In combination with the histopathologic examination, the case …
OBJECTIVES: This study investigates a unique case of multiple osteochondromas (MO) comorbid with enlarged parietal fora …
[Osteochondroma and multiple osteochondromas: recommendations on the diagnostics and follow-up with special consideration to the occurrence of secondary chondrosarcoma].
Herget GW, Kontny U, Saueressig U, Baumhoer D, Hauschild O, Elger T, Südkamp NP, Uhl M. Herget GW, et al. Radiologe. 2013 Dec;53(12):1125-36. doi: 10.1007/s00117-013-2571-9. Radiologe. 2013. PMID: 24129968 Review. German.
Clinical manifestations include deformity of bone, compression of surrounding tissue and vascular or neurological compromise. Osteochondromas may be solitary (solitary osteochondroma, SO) or multiple (multiple osteochondromas MO). ...According t …
Clinical manifestations include deformity of bone, compression of surrounding tissue and vascular or neurological compromise. Osteochondr
The Impact of Isolated Versus Multiple Osteochondromas: Analysis of the CoULD Registry.
Wessel LE, Goldfarb CA, Vuillermin C, Hutchinson DT, Bohn D, Steinman S, Wall LB; CoULD Study Group. Wessel LE, et al. J Pediatr Orthop. 2022 Aug 1;42(7):387-392. doi: 10.1097/BPO.0000000000002167. Epub 2022 Jun 24. J Pediatr Orthop. 2022. PMID: 35749762
PURPOSE: The burden of upper extremity (UE) osteochondromas on function and self-perception among pediatric patients is unclear. The purpose of our study was to study the impact of osteochondromas in comparison to population norms and to evaluate solitary versus …
PURPOSE: The burden of upper extremity (UE) osteochondromas on function and self-perception among pediatric patients is unclear. The …
Signaling systems affecting the severity of multiple osteochondromas.
Piombo V, Jochmann K, Hoffmann D, Wuelling M, Vortkamp A. Piombo V, et al. Bone. 2018 Jun;111:71-81. doi: 10.1016/j.bone.2018.03.010. Epub 2018 Mar 13. Bone. 2018. PMID: 29545125 Free article.
Multiple osteochondromas (MO) syndrome is a dominant autosomal bone disorder characterized by the formation of cartilage-capped bony outgrowths that develop at the juxtaposition of the growth plate of endochondral bones. ...Reduced Ihh signaling does not chan
Multiple osteochondromas (MO) syndrome is a dominant autosomal bone disorder characterized by the formation of cartilag
Clinical and Genetic Analysis of Multiple Osteochondromas in A Cohort of Argentine Patients.
Caino S, Cubilla MA, Alba R, Obregón MG, Fano V, Gómez A, Zecchini L, Lapunzina P, Aza-Carmona M, Heath KE, Asteggiano CG. Caino S, et al. Genes (Basel). 2022 Nov 7;13(11):2063. doi: 10.3390/genes13112063. Genes (Basel). 2022. PMID: 36360300 Free PMC article.
Multiple Osteochondromatosis (MO, MIM 133700 & 133701), an autosomal dominant O-glycosylation disorder (EXT1/EXT2-CDG), can be associated with a reduction in skeletal growth, bony deformity, restricted joint motion, shortened stature and pathogenic varian
Multiple Osteochondromatosis (MO, MIM 133700 & 133701), an autosomal dominant O-glycosylation disorder (EXT1/EXT2-C
Pain and fatigue in adult patients with multiple osteochondromas: The Netherlands.
Amajjar I, Vergauwen K, Willigenburg NW, Ham SJ, Smeets RJEM. Amajjar I, et al. PLoS One. 2024 Jul 17;19(7):e0305640. doi: 10.1371/journal.pone.0305640. eCollection 2024. PLoS One. 2024. PMID: 39018287 Free PMC article.
BACKGROUND: Multiple Osteochondromas (MO) is a rare genetic disorder characterised by the presence of numerous benign bone tumours, known as osteochondromas. ...This study aims to (1) assess the level of pain and fatigue in adult patients with MO
BACKGROUND: Multiple Osteochondromas (MO) is a rare genetic disorder characterised by the presence of numerous benign b …
The Rizzoli Multiple Osteochondromas Classification revised: describing the phenotype to improve clinical practice.
Mordenti M, Gnoli M, Boarini M, Trisolino G, Evangelista A, Pedrini E, Corsini S, Tremosini M, Staals EL, Antonioli D, Stilli S, Donati DM, Sangiorgi L. Mordenti M, et al. Am J Med Genet A. 2021 Nov;185(11):3466-3475. doi: 10.1002/ajmg.a.62470. Epub 2021 Sep 3. Am J Med Genet A. 2021. PMID: 34477285 Free PMC article.
Multiple osteochondromas (MO) is a rare disorder, characterized by benign osteocartilaginous tumors (osteochondromas), arising from the perichondrium of bones. The osteochondromas increase during growth, frequently causing deformities and limita
Multiple osteochondromas (MO) is a rare disorder, characterized by benign osteocartilaginous tumors (osteochondromas
117 results