Kannu P - Search Results

1

Premature arthritis is a distinct type II collagen phenotype.

Kannu P, Bateman JF, Randle S, Cowie S, du Sart D, McGrath S, Edwards M, Savarirayan R. Kannu P, et al. Arthritis Rheum. 2010 May;62(5):1421-30. doi: 10.1002/art.27354. Arthritis Rheum. 2010. PMID: 20131279 Free article.

2

Employing molecular genetics of chondrodysplasias to inform the study of osteoarthritis.

Kannu P, Bateman JF, Belluoccio D, Fosang AJ, Savarirayan R. Kannu P, et al. Arthritis Rheum. 2009 Feb;60(2):325-34. doi: 10.1002/art.24251. Arthritis Rheum. 2009. PMID: 19180483 Free article. Review. No abstract available.

3

Clinical phenotypes associated with type II collagen mutations.

Kannu P, Bateman J, Savarirayan R. Kannu P, et al. J Paediatr Child Health. 2012 Feb;48(2):E38-43. doi: 10.1111/j.1440-1754.2010.01979.x. Epub 2011 Feb 18. J Paediatr Child Health. 2012. PMID: 21332586 Review.

4

Two novel COL2A1 mutations associated with a Legg-Calvé-Perthes disease-like presentation.

Kannu P, Irving M, Aftimos S, Savarirayan R. Kannu P, et al. Clin Orthop Relat Res. 2011 Jun;469(6):1785-90. doi: 10.1007/s11999-011-1850-x. Epub 2011 Mar 26. Clin Orthop Relat Res. 2011. PMID: 21442341 Free PMC article.

5

Metatropic dysplasia: clinical and radiographic findings in 11 patients demonstrating long-term natural history.

Kannu P, Aftimos S, Mayne V, Donnan L, Savarirayan R. Kannu P, et al. Am J Med Genet A. 2007 Nov 1;143A(21):2512-22. doi: 10.1002/ajmg.a.31941. Am J Med Genet A. 2007. PMID: 17879966

6

Andreucci E, Aftimos S, Alcausin M, Haan E, Hunter W, Kannu P, Kerr B, McGillivray G, McKinlay Gardner RJ, Patricelli MG, Sillence D, Thompson E, Zacharin M, Zankl A, Lamandé SR, Savarirayan R. Andreucci E, et al. Among authors: kannu p. Orphanet J Rare Dis. 2011 Jun 9;6:37. doi: 10.1186/1750-1172-6-37. Orphanet J Rare Dis. 2011. PMID: 21658220 Free PMC article.

7

Rapp-Hodgkin ectodermal dysplasia syndrome: the clinical and molecular overlap with Hay-Wells syndrome.

Kannu P, Savarirayan R, Ozoemena L, White SM, McGrath JA. Kannu P, et al. Am J Med Genet A. 2006 Apr 15;140(8):887-91. doi: 10.1002/ajmg.a.31187. Am J Med Genet A. 2006. PMID: 16532463

8

Primary skeletal dysplasia as a major manifesting feature in an infant with congenital disorder of glycosylation type Ia.

Coman D, Bostock D, Hunter M, Kannu P, Irving M, Mayne V, Fietz M, Jaeken J, Savarirayan R. Coman D, et al. Among authors: kannu p. Am J Med Genet A. 2008 Feb 1;146A(3):389-92. doi: 10.1002/ajmg.a.32119. Am J Med Genet A. 2008. PMID: 18203160 No abstract available.

9

An unclassifiable short rib-polydactyly syndrome with acromesomelic hypomineralization and campomelia in siblings.

Kannu P, McFarlane JH, Savarirayan R, Aftimos S. Kannu P, et al. Am J Med Genet A. 2007 Nov 1;143A(21):2607-11. doi: 10.1002/ajmg.a.31989. Am J Med Genet A. 2007. PMID: 17935248

10

Thiemann disease and familial digital arthropathy - brachydactyly: two sides of the same coin?

Damseh N, Stimec J, O'Brien A, Marshall C, Savarirayan R, Jawad A, Laxer R, Kannu P. Damseh N, et al. Among authors: kannu p. Orphanet J Rare Dis. 2019 Jun 27;14(1):156. doi: 10.1186/s13023-019-1138-x. Orphanet J Rare Dis. 2019. PMID: 31248428 Free PMC article. Review.

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