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Journal Abstract Search

115 related items for PubMed ID: 3786423

  • 21. Scintilymphangiography with 99 mTc-antimony sulfide colloid in hereditary lymphedema (Nonne-Milroy diseases).
    Jackson FI, Bowen P, Lentle BC.
    Clin Nucl Med; 1978 Jul; 3(7):296-8. PubMed ID: 709985
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  • 22. [Meige-Milroy-Nonne disease or chronic hereditary trophedema].
    VERGER P, BLAQUIERE R.
    Pediatrie; 1957 Jul; 12(1):37-41. PubMed ID: 13431326
    [No Abstract] [Full Text] [Related]

  • 23. 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
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  • 24. [Clinical aspects of genuine hereditary elephantiasis (Nonne-Milroy-Meige)].
    ALSLEV J, FRANK H.
    Arztl Wochensch; 1957 Aug 30; 12(35-36):769-72. PubMed ID: 13508444
    [No Abstract] [Full Text] [Related]

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  • 26. Aplasia of superficial lymphatic capillaries in hereditary and connatal lymphedema (Milroy's disease).
    Bollinger A, Isenring G, Franzeck UK, Brunner U.
    Lymphology; 1983 Mar 30; 16(1):27-30. PubMed ID: 6843174
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  • 30. [Fabry's disease and familial lymphedema. Description of 2 cases].
    Savi M, Neri TM, Asinari G, Pietrini V, Tagliavini F, Migone L.
    Minerva Med; 1980 Oct 13; 71(39):2851-6. PubMed ID: 6776448
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  • 32. [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 Oct 13; 27(1-2):106-8. PubMed ID: 16922055
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  • 35. Investigation on the role of biallelic variants in VEGF-C found in a patient affected by Milroy-like lymphedema.
    Mukenge S, Jha SK, Catena M, Manara E, Leppänen VM, Lenti E, Negrini D, Bertelli M, Brendolan A, Jeltsch M, Aldrighetti L.
    Mol Genet Genomic Med; 2020 Sep 13; 8(9):e1389. PubMed ID: 32592340
    [Abstract] [Full Text] [Related]

  • 36. A family study of lymphedema of the leg in a lymphatic filariasis-endemic area.
    Cuenco KT, Halloran ME, Louis-Charles J, Lammie PJ.
    Am J Trop Med Hyg; 2004 Feb 13; 70(2):180-4. PubMed ID: 14993630
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  • 37. Syndromic classification of hereditary lymphedema.
    Northup KA, Witte MH, Witte CL.
    Lymphology; 2003 Dec 13; 36(4):162-89. PubMed ID: 14992570
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  • 38. [Recessively hereditary chronic lymphedema (Nonne-Milroy-Meige disease)].
    DORET M, KLEIN D.
    Bibl Ophthalmol; 1957 Dec 13; 12(47):576-83. PubMed ID: 13382786
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  • 39. [Elastolytic granulomas of the legs in familial visceral lymphangiodysplasia with chronic lymphedema].
    Baltaci M, Sepp N, Obermoser G, Kaiserling E, Zelger B, Fritsch P.
    J Dtsch Dermatol Ges; 2004 Sep 13; 2(9):766-9. PubMed ID: 16279221
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  • 40. [A case of the Meige-Milroy-Nonne disease].
    PERALTA SERRANO A.
    Acta Pediatr Esp; 1961 Jul 13; 19():405-9. PubMed ID: 14485194
    [No Abstract] [Full Text] [Related]

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