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Journal Abstract Search

123 related items for PubMed ID: 10544636

  • 21. [You make the diagnosis: congenital hereditary lymphedema].
    Schober PH, Kratky M, Müller WD.
    Padiatr Padol; 1984; 19(4):409-11. PubMed ID: 6504549
    [No Abstract] [Full Text] [Related]

  • 22. Disarticulation of the left upper extremity for treatment of giant primary lymphedema--case report.
    Fraga MF, Júnior AH, Guedes Neto HJ.
    Lymphology; 2004 Dec; 37(4):199-201. PubMed ID: 15693537
    [Abstract] [Full Text] [Related]

  • 23. [Congenital primary chylous lymphedema (author's transl)].
    Schönenberg H.
    Klin Padiatr; 1974 May; 186(3):222-7. PubMed ID: 4472786
    [No Abstract] [Full Text] [Related]

  • 24. 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
    [Abstract] [Full Text] [Related]

  • 25. 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]

  • 26. [Nonne-Milroy's syndrome (hereditary lymphedema type I). Report of a clinical case].
    La Placa G, Andreotti M, Pradella C, Russo F, Besana R.
    Pediatr Med Chir; 2005 Jun; 27(1-2):106-8. PubMed ID: 16922055
    [Abstract] [Full Text] [Related]

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

  • 28. Surgical correction of congenital lymphoedema of external female genitalia: case report and review of the literature.
    Papacharalabous EN, Myles RW, Antonarakis ES.
    J Obstet Gynaecol; 2004 Jun; 24(4):469-70. PubMed ID: 15203604
    [No Abstract] [Full Text] [Related]

  • 29. Physiotherapy results in a baby with congenital lymphedema: a follow-up study.
    Akbayrak T, Citak I, Demirtürk F, Kerem M, Akarcali I.
    Turk J Pediatr; 2002 Jun; 44(4):349-53. PubMed ID: 12458815
    [Abstract] [Full Text] [Related]

  • 30. Severe lymphedema, intestinal lymphangiectasia, seizures and mild mental retardation: further case of Hennekam syndrome with a severe phenotype.
    Forzano F, Faravelli F, Loy A, Di Rocco M.
    Am J Med Genet; 2002 Jul 22; 111(1):68-70. PubMed ID: 12124738
    [Abstract] [Full Text] [Related]

  • 31. [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]

  • 32. 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 09; 163(6):1358-60. PubMed ID: 20804492
    [No Abstract] [Full Text] [Related]

  • 33. Three children with Milroy disease and de novo mutations in VEGFR3.
    Carver C, Brice G, Mansour S, Ostergaard P, Mortimer P, Jeffery S, Lymphodema Consortium.
    Clin Genet; 2007 Feb 09; 71(2):187-9. PubMed ID: 17250670
    [No Abstract] [Full Text] [Related]

  • 34. Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome.
    Frühwirth M, Janecke AR, Müller T, Carlton VE, Kronenberg F, Offner F, Knisely AS, Geleff S, Song EJ, Simma B, Königsrainer A, Margreiter R, van der Hagen CB, Eiklid K, Aagenaes O, Bull L, Ellemunter H.
    J Pediatr; 2003 Apr 09; 142(4):441-7. PubMed ID: 12712065
    [Abstract] [Full Text] [Related]

  • 35. [Sporadic congenital lymphedema. (Description of a case)].
    Mensi E, Manca M.
    Minerva Nipiol; 1968 Apr 09; 18():Suppl 6:295-9. PubMed ID: 5745331
    [No Abstract] [Full Text] [Related]

  • 36. Functional magnetic resonance evidence of cortical alterations in a case of reversible congenital lymphedema of the lower limb: a pilot study.
    Pardini M, Bonzano L, Roccatagliata L, Boccardo F, Mancardi G, Campisi C.
    Lymphology; 2007 Mar 09; 40(1):19-25. PubMed ID: 17539461
    [Abstract] [Full Text] [Related]

  • 37. [Case of Milroy's disease].
    Sikorski S.
    Wiad Lek; 1971 Dec 01; 24(23):2229-30. PubMed ID: 5164929
    [No Abstract] [Full Text] [Related]

  • 38. Dominantly inherited syndrome of microcephaly and congenital lymphedema.
    Leung AK.
    Clin Genet; 1985 Jun 01; 27(6):611-2. PubMed ID: 4017282
    [Abstract] [Full Text] [Related]

  • 39. [Description of a case of sporadic congenital lymphedema associated with chronic steatorrhea].
    Masarone M.
    Minerva Pediatr; 1970 Feb 04; 22(5):254-7. PubMed ID: 5436274
    [No Abstract] [Full Text] [Related]

  • 40. [A case report of congenital lymphedema with chylothorax].
    Kitahara M.
    Nihon Kyobu Shikkan Gakkai Zasshi; 1985 Jan 04; 23(1):106-13. PubMed ID: 4010098
    [No Abstract] [Full Text] [Related]

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