HuGE Literature Finder
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| FLT4 Mutations Are Associated with Segmental Lymphatic Dysfunction and Initial Lymphatic Aplasia in Patients with Milroy Disease. Genes 2021 10 12 (10): . Liu Ningfei, Gao Minz |
| Improvement of quality of life by intake of hydroxytyrosol in patients with lymphedema and association of lymphedema genes with obesity. European review for medical and pharmacological sciences 2021 12 25 (1 Suppl): 33-42. Dhuli K, Ceccarini M R, Precone V, Maltese P E, Bonetti G, Paolacci S, Dautaj A, Guerri G, Marceddu G, Beccari T, Michelini S, Bertelli |
| FOXC2 and FLT4 Gene Variants in Lymphatic Filariasis. Lymphatic research and biology 2015 Jun 13 (2): 112-9. Sheik Yasmeen, Qureshi Sameera Fatima, Mohhammed Basheeruddin, Nallari Pratib |
| Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema. Molecular syndromology 2013 Sep 4 (6): 257-66. Mendola A, Schlögel M J, Ghalamkarpour A, Irrthum A, Nguyen H L, Fastré E, Bygum A, van der Vleuten C, Fagerberg C, Baselga E, Quere I, Mulliken J B, Boon L M, Brouillard P, Vikkula M, |
| Connexin 47 mutations increase risk for secondary lymphedema following breast cancer treatment. Clinical cancer research : an official journal of the American Association for Cancer Research 2012 Apr 18 (8): 2382-90. Finegold David N, Baty Catherine J, Knickelbein Kelly Z, Perschke Shelley, Noon Sarah E, Campbell Diana, Karlsson Jenny M, Huang Diana, Kimak Mark A, Lawrence Elizabeth C, Feingold Eleanor, Meriney Stephen D, Brufsky Adam M, Ferrell Robert |
| HGF and MET mutations in primary and secondary lymphedema. Lymphatic research and biology 2008 6 (2): 65-8. Finegold David N, Schacht Vivien, Kimak Mark A, Lawrence Elizabeth C, Foeldi Etelka, Karlsson Jenny M, Baty Catherine J, Ferrell Robert |
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