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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
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.
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
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
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome).
Ostergaard P, Simpson MA, Connell FC, Steward CG, Brice G, Woollard WJ, Dafou D, Kilo T, Smithson S, Lunt P, Murday VA, Hodgson S, Keenan R, Pilz DT, Martinez-Corral I, Makinen T, Mortimer PS, Jeffery S, Trembath RC, Mansour S. Ostergaard P, et al. Nat Genet. 2011 Sep 4;43(10):929-31. doi: 10.1038/ng.923. Nat Genet. 2011. PMID: 21892158
224 results