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Journal Abstract Search

75 related items for PubMed ID: 20804492

  • 1. Severe congenital lymphoedema not caused by mutations in known lymphoedema genes.
    Greenberger S, Reznik-Wolf H, Ghalamkarpour A, Marek-Yagel D, Vikkula M, Pras E.
    Br J Dermatol; 2010 Dec; 163(6):1358-60. PubMed ID: 20804492
    [No Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Early onset lymphoedema, recessive form--a new form of genetic lymphoedema syndrome.
    Mücke J, Hoepffner W, Scheerschmidt G, Gornig H, Beyreiss K.
    Eur J Pediatr; 1986 Aug; 145(3):195-8. PubMed ID: 3769974
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Possible new autosomal recessive syndrome of lymphedema, hydroceles, atrial septal defect, and characteristic facial changes.
    Irons MB, Bianchi DW, Geggel RL, Marx GR, Bhan I.
    Am J Med Genet; 1996 Dec 02; 66(1):69-71. PubMed ID: 8957515
    [Abstract] [Full Text] [Related]

  • 6. Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema.
    Evans AL, Bell R, Brice G, Comeglio P, Lipede C, Jeffery S, Mortimer P, Sarfarazi M, Child AH.
    J Med Genet; 2003 Sep 02; 40(9):697-703. PubMed ID: 12960217
    [No Abstract] [Full Text] [Related]

  • 7. Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema.
    Karkkainen MJ, Ferrell RE, Lawrence EC, Kimak MA, Levinson KL, McTigue MA, Alitalo K, Finegold DN.
    Nat Genet; 2000 Jun 02; 25(2):153-9. PubMed ID: 10835628
    [Abstract] [Full Text] [Related]

  • 8. 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 02; 46(8):3162-3171. PubMed ID: 29896974
    [Abstract] [Full Text] [Related]

  • 9. [Milroy's disease and primary lymphoedema. Exploration methods, therapeutic aspects (author's transl)].
    Stalder JF, Berger M.
    Ann Dermatol Venereol; 1980 Jul 02; 107(7):665-7. PubMed ID: 7436261
    [Abstract] [Full Text] [Related]

  • 10. Primary non-syndromic lymphoedema (Meige disease) is not caused by mutations in FOXC2.
    Rezaie T, Ghoroghchian R, Bell R, Brice G, Hasan A, Burnand K, Vernon S, Mansour S, Mortimer P, Jeffery S, Child A, Sarfarazi M.
    Eur J Hum Genet; 2008 Mar 02; 16(3):300-4. PubMed ID: 18197197
    [Abstract] [Full Text] [Related]

  • 11. Hereditary palmoplantar keratoderma associated with primary (congenital) lymphedema.
    Ogunbiyi SO, Deguara J, Moss C, Burnand KG.
    Lymphology; 2009 Jun 02; 42(2):85-7. PubMed ID: 19725273
    [Abstract] [Full Text] [Related]

  • 12. Possible new autosomal recessive syndrome of congenital lymphoedema, nail dystrophy and esotropia in a Saudi family.
    Fatinni Y, Asindi A, Al Falki Y, Al Harthi A, Al Fifi S, Al-Daama S.
    Acta Paediatr; 2001 Feb 02; 90(2):151-3. PubMed ID: 11236043
    [Abstract] [Full Text] [Related]

  • 13. A possible genetic factor in non-filarial elephantiasis of the lower legs.
    Price EW.
    Ethiop Med J; 1972 Jul 02; 10(3):87-93. PubMed ID: 4670473
    [No Abstract] [Full Text] [Related]

  • 14. 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 02; 45(2):59-61. PubMed ID: 15904433
    [Abstract] [Full Text] [Related]

  • 15. Massively parallel sequencing and identification of genes for primary lymphoedema: a perfect fit.
    Ostergaard P, Simpson MA, Jeffery S.
    Clin Genet; 2011 Aug 02; 80(2):110-6. PubMed ID: 21595654
    [Abstract] [Full Text] [Related]

  • 16. [A case of congenital hereditary lymphedema (Milroy-Nonne's disease].
    Beluschi C, Coraiola M, Pedrotti D.
    Pediatr Med Chir; 1982 Aug 02; 4(1-2):155-7. PubMed ID: 7111035
    [No Abstract] [Full Text] [Related]

  • 17. Expansion of the phenotype in Hennekam syndrome: a case with new manifestations.
    Angle B, Hersh JH.
    Am J Med Genet; 1997 Aug 08; 71(2):211-4. PubMed ID: 9217224
    [Abstract] [Full Text] [Related]

  • 18. Age of onset in hereditary lymphedema.
    Levinson KL, Feingold E, Ferrell RE, Glover TW, Traboulsi EI, Finegold DN.
    J Pediatr; 2003 Jun 08; 142(6):704-8. PubMed ID: 12838201
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 14(18):2619-27. PubMed ID: 16081467
    [Abstract] [Full Text] [Related]

  • 20. Primary congenital lymphedema. A case report.
    Gragnani SG, Michelotti F, Rocca R, Sardi R, Bardini N.
    Minerva Pediatr; 1999 Jun 15; 51(6):217-9. PubMed ID: 10544636
    [Abstract] [Full Text] [Related]

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