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

Year Number of Results
1974 2
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1976 1
1977 1
1978 1
1983 1
1987 1
1989 1
1992 1
1993 1
2001 2
2004 1
2005 1
2006 1
2007 2
2009 2
2010 3
2011 2
2012 2
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2015 3
2016 3
2017 1
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2019 1
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40 results

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Page 1
Winchester syndrome.
Matthiesen G, Pedersen VF, Helin P, Jacobsen GK, Nielsen NS. Matthiesen G, et al. Int Orthop. 2001;25(5):331-3. doi: 10.1007/s002640100276. Int Orthop. 2001. PMID: 11794271 Free PMC article.
Winchester syndrome was first described in 1969 and since then nine patients have been reported in the literature. ...
Winchester syndrome was first described in 1969 and since then nine patients have been reported in the literature. ...
[Winchester syndrome].
Matsuo M. Matsuo M. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):817-8. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11529039 Review. Japanese. No abstract available.
Anaesthesia management for Winchester syndrome.
Sharma A, Sharma P, Sasidharan S. Sharma A, et al. Indian J Anaesth. 2021 Feb;65(2):165-167. doi: 10.4103/ija.IJA_984_20. Epub 2021 Feb 10. Indian J Anaesth. 2021. PMID: 33776097 Free PMC article. No abstract available.
A child with Winchester syndrome responding to oral betamethasone and methotrexate.
Dash G, Pradhan S, Sinha U, Sinha R. Dash G, et al. Pediatr Dermatol. 2024 Jul-Aug;41(4):688-691. doi: 10.1111/pde.15543. Epub 2024 Jan 30. Pediatr Dermatol. 2024. PMID: 38291559
Winchester syndrome (WS) is a rare genetic disorder with a handful of cases reported to date. ...
Winchester syndrome (WS) is a rare genetic disorder with a handful of cases reported to date. ...
Winchester syndrome caused by a homozygous mutation affecting the active site of matrix metalloproteinase 2.
Zankl A, Bonafé L, Calcaterra V, Di Rocco M, Superti-Furga A. Zankl A, et al. Clin Genet. 2005 Mar;67(3):261-6. doi: 10.1111/j.1399-0004.2004.00402.x. Clin Genet. 2005. PMID: 15691365
Three osteolysis syndromes show autosomal recessive inheritance and multicentric involvement: Torg syndrome (OMIM 259600), Winchester syndrome (OMIM 277950) and Nodulosis-Arthropathy-Osteolysis syndrome (NAO; OMIM 605156). ...We report a homozygous missense mutation …
Three osteolysis syndromes show autosomal recessive inheritance and multicentric involvement: Torg syndrome (OMIM 259600), Winchester …
Torg syndrome is caused by inactivating mutations in MMP2 and is allelic to NAO and Winchester syndrome.
Zankl A, Pachman L, Poznanski A, Bonafé L, Wang F, Shusterman Y, Fishman DA, Superti-Furga A. Zankl A, et al. J Bone Miner Res. 2007 Feb;22(2):329-33. doi: 10.1359/jbmr.061013. J Bone Miner Res. 2007. PMID: 17059372 Free article.
MMP2 mutations were previously identified in patients with NAO and Winchester syndrome. Our findings suggest that Torg, NAO, and Winchester syndrome are allelic disorders. ...Gelatin zymography indicated complete loss of MMP2 activity. CONCLUSIONS: Tor …
MMP2 mutations were previously identified in patients with NAO and Winchester syndrome. Our findings suggest that Torg, NAO, a …
Winchester syndrome: the progression of radiological findings over a 23-year period.
Vanatka R, Rouzier C, Lambert JC, Leroux C, Coussement A. Vanatka R, et al. Skeletal Radiol. 2011 Mar;40(3):347-51. doi: 10.1007/s00256-010-1033-y. Epub 2010 Sep 24. Skeletal Radiol. 2011. PMID: 20865259
Winchester syndrome (WS) is a rare autosomal recessive syndrome resulting in multicentric osteolysis. ...
Winchester syndrome (WS) is a rare autosomal recessive syndrome resulting in multicentric osteolysis. ...
Winchester syndrome: a case report.
Grover S, Grewal RS, Verma R, Mani NS, Mehta A, Sinha P. Grover S, et al. Int J Dermatol. 2009 Feb;48(2):175-7. doi: 10.1111/j.1365-4632.2009.03872.x. Int J Dermatol. 2009. PMID: 19200197 No abstract available.
Multicentric Osteolysis Nodulosis and Arthropathy.
Bhavani GS, Shah H, Shukla A, Girisha KM. Bhavani GS, et al. 2016 Jul 14 [updated 2023 Mar 30]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026. 2016 Jul 14 [updated 2023 Mar 30]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026. PMID: 27413800 Free Books & Documents. Review.
Taurodontism in dental genetics.
Chetty M, Roomaney IA, Beighton P. Chetty M, et al. BDJ Open. 2021 Jul 9;7(1):25. doi: 10.1038/s41405-021-00081-6. BDJ Open. 2021. PMID: 34244468 Free PMC article.
Sixty-four individuals with Osteogenesis imperfecta (OI), one individual with Pyle disease and one with Torg-Winchester syndrome respectively, were assessed clinically, radiographically and at a molecular level. Ten patients with OI XI and those with Pyle disease an …
Sixty-four individuals with Osteogenesis imperfecta (OI), one individual with Pyle disease and one with Torg-Winchester syndrome …
40 results