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Journal Abstract Search

82 related items for PubMed ID: 4010046

  • 1. Congenital lymphedema in two siblings.
    Kajii T, Tsukahara M.
    Jinrui Idengaku Zasshi; 1985 Mar; 30(1):31-4. PubMed ID: 4010046
    [No Abstract] [Full Text] [Related]

  • 2. A genetic association between microcephaly and lymphedema.
    Crowe CA, Dickerman LH.
    Am J Med Genet; 1986 May; 24(1):131-5. PubMed ID: 3706402
    [Abstract] [Full Text] [Related]

  • 3. Puffy feet in a female neonate.
    Espírito Santo R, Moldovan O, Costa P, Graça A, Abrantes M.
    BMJ Case Rep; 2016 Aug 10; 2016():. PubMed ID: 27511750
    [No Abstract] [Full Text] [Related]

  • 4. 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 10; 45(2):59-61. PubMed ID: 15904433
    [Abstract] [Full Text] [Related]

  • 5. Hydrops fetalis: an unusual prenatal presentation of hereditary congenital lymphedema.
    Daniel-Spiegel E, Ghalamkarpour A, Spiegel R, Weiner E, Vikkula M, Shalev E, Shalev SA.
    Prenat Diagn; 2005 Nov 10; 25(11):1015-8. PubMed ID: 16231305
    [Abstract] [Full Text] [Related]

  • 6. [Congenital elephantitis in children].
    Troshkov AA, Mateshuk RV, Liapis MA.
    Khirurgiia (Mosk); 1971 Apr 10; 47(4):100-4. PubMed ID: 5122398
    [No Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. 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]

  • 9. Primary congenital lymphedema. A case report.
    Gragnani SG, Michelotti F, Rocca R, Sardi R, Bardini N.
    Minerva Pediatr; 1999 Jun 02; 51(6):217-9. PubMed ID: 10544636
    [Abstract] [Full Text] [Related]

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

  • 11. [Congenital lymphedema].
    Yebra Sotillo I, Ortega Resinas M, Camacho Martínez F.
    Med Cutan Ibero Lat Am; 1986 Jun 02; 14(4):247-50. PubMed ID: 3537585
    [Abstract] [Full Text] [Related]

  • 12. Congenital hereditary lymphedema (Nonne/Milroy).
    Farhud DD, Farhud I, Walizadeh GR, Djaber-Ansari M.
    Padiatr Padol; 1989 Jun 02; 24(4):305-7. PubMed ID: 2616174
    [Abstract] [Full Text] [Related]

  • 13. [Hereditary congenital lymphedema with pseudosexual ambiguity].
    Sarda P, Jalaguier J, Montoya F, Bonnet H.
    J Genet Hum; 1988 Aug 02; 36(4):353-60. PubMed ID: 3221210
    [Abstract] [Full Text] [Related]

  • 14. Presentation one: a neonate with swollen feet.
    Paul SP, Patton MA.
    J Fam Health Care; 2012 Aug 02; 22(5):34-5. PubMed ID: 23311286
    [No Abstract] [Full Text] [Related]

  • 15. Distichiasis-lymphedema. A hereditary syndrome of multiple congenital defects.
    Robinow M, Johnson GF, Verhagen AD.
    Am J Dis Child; 1970 Apr 02; 119(4):343-7. PubMed ID: 5434594
    [No Abstract] [Full Text] [Related]

  • 16. [Congenital diseases of the lymphatic system].
    Godart S.
    Acta Paediatr Belg; 1966 Apr 02; 20(2):101-18. PubMed ID: 5947182
    [No Abstract] [Full Text] [Related]

  • 17. [Lymphedema. In Ullrich-Turner syndrome it is congenital].
    Butenandt O.
    MMW Fortschr Med; 2001 Apr 12; 143(15):10. PubMed ID: 11349310
    [No Abstract] [Full Text] [Related]

  • 18. [Nonne-Milroy-Meige disease in 2 members of a family].
    Jeske J, Ostrowska-Stach H, Hübner H.
    Pol Tyg Lek; 1969 Sep 09; 24(36):1389-90. PubMed ID: 5351081
    [No Abstract] [Full Text] [Related]

  • 19. Familial congenital pulmonary lymphangectasia, non-immune hydrops fetalis, facial and lower limb lymphedema: confirmation of Njolstad's report.
    Jacquemont S, Barbarot S, Bocéno M, Stalder JF, David A.
    Am J Med Genet; 2000 Aug 14; 93(4):264-8. PubMed ID: 10946350
    [Abstract] [Full Text] [Related]

  • 20. Distichiasis and lymphedema: a hereditary syndrome with possible multiple defects. A report of a family.
    Hoover RE, Kelley JS.
    Trans Am Ophthalmol Soc; 1971 Aug 14; 69():293-306. PubMed ID: 5154265
    [No Abstract] [Full Text] [Related]

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