Ostergaard P - Search Results

1

Update and audit of the St George's classification algorithm of primary lymphatic anomalies: a clinical and molecular approach to diagnosis.

Gordon K, Varney R, Keeley V, Riches K, Jeffery S, Van Zanten M, Mortimer P, Ostergaard P, Mansour S. Gordon K, et al. Among authors: ostergaard p. J Med Genet. 2020 Oct;57(10):653-659. doi: 10.1136/jmedgenet-2019-106084. Epub 2020 May 14. J Med Genet. 2020. PMID: 32409509 Free PMC article. Review.

2

Three children with Milroy disease and de novo mutations in VEGFR3.

Carver C, Brice G, Mansour S, Ostergaard P, Mortimer P, Jeffery S; Lymphodema Consortium. Carver C, et al. Among authors: ostergaard p. Clin Genet. 2007 Feb;71(2):187-9. doi: 10.1111/j.1399-0004.2007.00741.x. Clin Genet. 2007. PMID: 17250670 No abstract available.

3

A family with lymphoedema-distichiasis where identical twins have a discordant phenotype.

Kumar S, Carver C, McCall S, Brice G, Ostergaard P, Mortimer P, Jeffery S; Lymphoedema Consortium. Kumar S, et al. Among authors: ostergaard p. Clin Genet. 2007 Mar;71(3):285-7. doi: 10.1111/j.1399-0004.2007.00758.x. Clin Genet. 2007. PMID: 17309653 No abstract available.

4

Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas.

Connell FC, Ostergaard P, Carver C, Brice G, Williams N, Mansour S, Mortimer PS, Jeffery S; Lymphoedema Consortium. Connell FC, et al. Among authors: ostergaard p. Hum Genet. 2009 Jan;124(6):625-31. doi: 10.1007/s00439-008-0586-5. Epub 2008 Nov 12. Hum Genet. 2009. PMID: 19002718

5

Pit-1 mutation and lipoedema in a family.

Bano G, Mansour S, Brice G, Ostergaard P, Mortimer PS, Jeffery S, Nussey S. Bano G, et al. Among authors: ostergaard p. Exp Clin Endocrinol Diabetes. 2010 Jun;118(6):377-80. doi: 10.1055/s-0029-1224154. Epub 2009 Jul 16. Exp Clin Endocrinol Diabetes. 2010. PMID: 19609847

6

Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia.

Connell F, Kalidas K, Ostergaard P, Brice G, Homfray T, Roberts L, Bunyan DJ, Mitton S, Mansour S, Mortimer P, Jeffery S; Lymphoedema Consortium. Connell F, et al. Among authors: ostergaard p. Hum Genet. 2010 Feb;127(2):231-41. doi: 10.1007/s00439-009-0766-y. Epub 2009 Nov 13. Hum Genet. 2010. PMID: 19911200

7

Lipedema: an inherited condition.

Child AH, Gordon KD, Sharpe P, Brice G, Ostergaard P, Jeffery S, Mortimer PS. Child AH, et al. Among authors: ostergaard p. Am J Med Genet A. 2010 Apr;152A(4):970-6. doi: 10.1002/ajmg.a.33313. Am J Med Genet A. 2010. PMID: 20358611

8

Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new cases.

Mansour S, Connell F, Steward C, Ostergaard P, Brice G, Smithson S, Lunt P, Jeffery S, Dokal I, Vulliamy T, Gibson B, Hodgson S, Cottrell S, Kiely L, Tinworth L, Kalidas K, Mufti G, Cornish J, Keenan R, Mortimer P, Murday V; Lymphoedema Research Consortium. Mansour S, et al. Among authors: ostergaard p. Am J Med Genet A. 2010 Sep;152A(9):2287-96. doi: 10.1002/ajmg.a.33445. Am J Med Genet A. 2010. PMID: 20803646

9

Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype.

Ostergaard P, Simpson MA, Brice G, Mansour S, Connell FC, Onoufriadis A, Child AH, Hwang J, Kalidas K, Mortimer PS, Trembath R, Jeffery S. Ostergaard P, et al. J Med Genet. 2011 Apr;48(4):251-5. doi: 10.1136/jmg.2010.085563. Epub 2011 Jan 25. J Med Genet. 2011. PMID: 21266381

10

Massively parallel sequencing and identification of genes for primary lymphoedema: a perfect fit.

Ostergaard P, Simpson MA, Jeffery S. Ostergaard P, et al. Clin Genet. 2011 Aug;80(2):110-6. doi: 10.1111/j.1399-0004.2011.01706.x. Epub 2011 Jun 13. Clin Genet. 2011. PMID: 21595654

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