These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
180 related articles for article (PubMed ID: 19002718)
1. 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; Hum Genet; 2009 Jan; 124(6):625-31. PubMed ID: 19002718 [TBL] [Abstract][Full Text] [Related]
2. Mutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedema. Gordon K; Schulte D; Brice G; Simpson MA; Roukens MG; van Impel A; Connell F; Kalidas K; Jeffery S; Mortimer PS; Mansour S; Schulte-Merker S; Ostergaard P Circ Res; 2013 Mar; 112(6):956-60. PubMed ID: 23410910 [TBL] [Abstract][Full Text] [Related]
4. A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease. Balboa-Beltran E; Fernández-Seara MJ; Pérez-Muñuzuri A; Lago R; García-Magán C; Couce ML; Sobrino B; Amigo J; Carracedo A; Barros F J Med Genet; 2014 Jul; 51(7):475-8. PubMed ID: 24744435 [TBL] [Abstract][Full Text] [Related]
5. Recessive primary congenital lymphoedema caused by a VEGFR3 mutation. Ghalamkarpour A; Holnthoner W; Saharinen P; Boon LM; Mulliken JB; Alitalo K; Vikkula M J Med Genet; 2009 Jun; 46(6):399-404. PubMed ID: 19289394 [TBL] [Abstract][Full Text] [Related]
6. A novel mutation in the conserved sequence of vascular endothelial growth factor receptor 3 leads to primary lymphoedema. Dai T; Li B; He B; Yan L; Gu L; Liu X; Qi J; Li P; Zhou X J Int Med Res; 2018 Aug; 46(8):3162-3171. PubMed ID: 29896974 [TBL] [Abstract][Full Text] [Related]
7. Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations. Ghalamkarpour A; Morlot S; Raas-Rothschild A; Utkus A; Mulliken JB; Boon LM; Vikkula M Clin Genet; 2006 Oct; 70(4):330-5. PubMed ID: 16965327 [TBL] [Abstract][Full Text] [Related]
8. Wide clinical spectrum in a family with hereditary lymphedema type I due to a novel missense mutation in VEGFR3. Spiegel R; Ghalamkarpour A; Daniel-Spiegel E; Vikkula M; A Shalev S J Hum Genet; 2006; 51(10):846-850. PubMed ID: 16924388 [TBL] [Abstract][Full Text] [Related]
9. A novel FLT4 mutation identified in a patient with Milroy disease. DiGiovanni RM; Erickson RP; Ohlson EC; Bernas M; Witte MH Lymphology; 2014 Mar; 47(1):44-7. PubMed ID: 25109169 [TBL] [Abstract][Full Text] [Related]
10. A Novel Splice-Site Mutation in Nadarajah N; Schulte D; McConnell V; Martin-Almedina S; Karapouliou C; Mortimer PS; Jeffery S; Schulte-Merker S; Gordon K; Mansour S; Ostergaard P Int J Mol Sci; 2018 Aug; 19(8):. PubMed ID: 30071673 [TBL] [Abstract][Full Text] [Related]
11. Splice-site mutations in VEGFC cause loss of function and Nonne-Milroy-like primary lymphedema. Fastré E; Lanteigne LE; Helaers R; Giacalone G; Revencu N; Dionyssiou D; Demiri E; Brouillard P; Vikkula M Clin Genet; 2018 Jul; 94(1):179-181. PubMed ID: 29542815 [No Abstract] [Full Text] [Related]
12. Milroy's primary congenital lymphedema in a male infant and review of the literature. Kitsiou-Tzeli S; Vrettou C; Leze E; Makrythanasis P; Kanavakis E; Willems P In Vivo; 2010; 24(3):309-14. PubMed ID: 20555004 [TBL] [Abstract][Full Text] [Related]
13. [Identification of VEGFR3 gene mutation in a Chinese family with autosomal dominant primary congenital lymphoedema]. Sheng JQ; Zeng F; Li C; Liu JY; Wang Q; Liu MG Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):371-5. PubMed ID: 20677139 [TBL] [Abstract][Full Text] [Related]
14. Three children with Milroy disease and de novo mutations in VEGFR3. Carver C; Brice G; Mansour S; Ostergaard P; Mortimer P; Jeffery S; Clin Genet; 2007 Feb; 71(2):187-9. PubMed ID: 17250670 [No Abstract] [Full Text] [Related]
15. A Milroy case with FLT4/VEGFR3 mutation and an unusual skin biopsy. Liu NF; Yu ZY; Lou Y; Sun D Br J Dermatol; 2019 Jan; 180(1):223-224. PubMed ID: 30169892 [No Abstract] [Full Text] [Related]
16. FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update. Gordon K; Spiden SL; Connell FC; Brice G; Cottrell S; Short J; Taylor R; Jeffery S; Mortimer PS; Mansour S; Ostergaard P Hum Mutat; 2013 Jan; 34(1):23-31. PubMed ID: 23074044 [TBL] [Abstract][Full Text] [Related]
17. Liu N; Gao M Genes (Basel); 2021 Oct; 12(10):. PubMed ID: 34681005 [TBL] [Abstract][Full Text] [Related]
18. A family with Milroy disease caused by the FLT4/VEGFR3 gene variant c.2774 T > A. Sui Y; Lu Y; Lin M; Ni X; Chen X; Li H; Jiang M BMC Med Genomics; 2021 Jun; 14(1):151. PubMed ID: 34103024 [TBL] [Abstract][Full Text] [Related]
19. A Novel Missense Mutation in FLT4 Causes Autosomal Recessive Hereditary Lymphedema. Melikhan-Revzin S; Kurolap A; Dagan E; Mory A; Gershoni-Baruch R Lymphat Res Biol; 2015 Jun; 13(2):107-11. PubMed ID: 26091405 [TBL] [Abstract][Full Text] [Related]
20. The physiological and pathological functions of VEGFR3 in cardiac and lymphatic development and related diseases. Monaghan RM; Page DJ; Ostergaard P; Keavney BD Cardiovasc Res; 2021 Jul; 117(8):1877-1890. PubMed ID: 33067626 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]