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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

211 related articles for article (PubMed ID: 22768468)

  • 1. Clinical and genetic study of 46 Italian patients with primary lymphedema.
    Michelini S; Degiorgio D; Cestari M; Corda D; Ricci M; Cardone M; Mander A; Famoso L; Contini E; Serrani R; Pinelli L; Cecchin S; Bertelli M
    Lymphology; 2012 Mar; 45(1):3-12. PubMed ID: 22768468
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Age of onset in hereditary lymphedema.
    Levinson KL; Feingold E; Ferrell RE; Glover TW; Traboulsi EI; Finegold DN
    J Pediatr; 2003 Jun; 142(6):704-8. PubMed ID: 12838201
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rare Variants in LAMA5 Gene associated with FLT4 and FOXC2 Mutations in Primary Lymphedema May Contribute to Severity.
    Liu NF; Yu ZY; Sun D; Lou Y
    Lymphology; 2016 Dec; 49(4):192-204. PubMed ID: 29908552
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Defective valves and abnormal mural cell recruitment underlie lymphatic vascular failure in lymphedema distichiasis.
    Petrova TV; Karpanen T; Norrmén C; Mellor R; Tamakoshi T; Finegold D; Ferrell R; Kerjaschki D; Mortimer P; Ylä-Herttuala S; Miura N; Alitalo K
    Nat Med; 2004 Sep; 10(9):974-81. PubMed ID: 15322537
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis.
    Berry FB; Tamimi Y; Carle MV; Lehmann OJ; Walter MA
    Hum Mol Genet; 2005 Sep; 14(18):2619-27. PubMed ID: 16081467
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel missense mutation and two microrearrangements in the FOXC2 gene of three families with lymphedema-distichiasis syndrome.
    Fauret AL; Tuleja E; Jeunemaitre X; Vignes S
    Lymphology; 2010 Mar; 43(1):14-8. PubMed ID: 20552815
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Lymphedema-distichiasis syndrome: a distinct type of primary lymphedema caused by mutations in the FOXC2 gene.
    Vreeburg M; Heitink MV; Damstra RJ; Moog U; van Geel M; van Steensel MA
    Int J Dermatol; 2008 Nov; 47 Suppl 1():52-5. PubMed ID: 18986489
    [TBL] [Abstract][Full Text] [Related]  

  • 9. FOXC2 and FLT4 Gene Variants in Lymphatic Filariasis.
    Sheik Y; Qureshi SF; Mohhammed B; Nallari P
    Lymphat Res Biol; 2015 Jun; 13(2):112-9. PubMed ID: 26091406
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic Screening in a Large Cohort of Italian Patients Affected by Primary Lymphedema Using a Next Generation Sequencing (NGS) Approach.
    Michelini S; Vettori A; Maltese PE; Cardone M; Bruson A; Fiorentino A; Cappellino F; Sainato V; Guerri G; Marceddu G; Tezzele S; Bertelli M
    Lymphology; 2016 Jun; 49(2):57-72. PubMed ID: 29906362
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lymphedema-distichiasis syndrome without FOXC2 mutation: evidence for chromosome 16 duplication upstream of FOXC2.
    Witte MH; Erickson RP; Khalil M; Dellinger M; Bernas M; Grogan T; Nitta H; Feng J; Duggan D; Witte CL
    Lymphology; 2009 Dec; 42(4):152-60. PubMed ID: 20218083
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutation.
    Mizuno S; Yamada Y; Yamada K; Nomura N; Wakamatsu N
    Congenit Anom (Kyoto); 2005 Jun; 45(2):59-61. PubMed ID: 15904433
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel FOXC2 missense mutation identified in patient with lymphedema-distichiasis syndrome and review.
    Dellinger MT; Thome K; Bernas MJ; Erickson RP; Witte MH
    Lymphology; 2008 Sep; 41(3):98-102. PubMed ID: 19013876
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation.
    Fabretto A; Shardlow A; Faletra F; Lepore L; Hladnik U; Gasparini P
    Ophthalmic Genet; 2010 Jun; 31(2):98-100. PubMed ID: 20450314
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Evaluation of FOXC2 as a candidate gene for chronic progressive lymphedema in draft horses.
    Young AE; Bower LP; Affolter VK; De Cock HE; Ferraro GL; Bannasch DL
    Vet J; 2007 Sep; 174(2):397-9. PubMed ID: 16884936
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.