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Journal Abstract Search

164 related items for PubMed ID: 24619057

  • 21. Cutaneous manifestations and massive genital involvement in Hennekam syndrome.
    Musumeci ML, Nasca MR, De Pasquale R, Schwartz RA, Micali G.
    Pediatr Dermatol; 2006; 23(3):239-42. PubMed ID: 16780470
    [Abstract] [Full Text] [Related]

  • 22. Primary lymphoedema associated with xanthomatosis, vaginal lymphorrhoea and intestinal lymphangiectasia.
    Karg E, Bereczki C, Kovacs J, Korom I, Varkonyi A, Megyeri P, Turi S.
    Br J Dermatol; 2002 Jan; 146(1):134-7. PubMed ID: 11841381
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  • 24. A child with diarrhea and recurrent otitis.
    Mönkemüller K, Fry LC, Heiduk M.
    Gastroenterology; 2012 Mar; 142(3):432, 677. PubMed ID: 22281272
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  • 27. Simultaneous multi-site lymphaticovenular anastomoses for primary lower extremity and genital lymphoedema complicated with severe lymphorrhea.
    Yamamoto T, Koshima I, Yoshimatsu H, Narushima M, Miahara M, Iida T.
    J Plast Reconstr Aesthet Surg; 2011 Jun; 64(6):812-5. PubMed ID: 21093398
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  • 29. Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome.
    Boone PM, Paterson S, Mohajeri K, Zhu W, Genetti CA, Tai DJC, Nori N, Agrawal PB, Bacino CA, Bi W, Talkowski ME, Hogan BM, Rodan LH.
    Am J Med Genet A; 2020 Jan; 182(1):189-194. PubMed ID: 31633297
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  • 30. Use of compression therapy in patients with lymphoedema.
    Hobday A.
    Nurs Stand; 2016 Mar 02; 30(27):50-8; quiz 60. PubMed ID: 26932650
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  • 32. A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family.
    Brice G, Ostergaard P, Jeffery S, Gordon K, Mortimer PS, Mansour S.
    Clin Genet; 2013 Oct 02; 84(4):378-81. PubMed ID: 23550541
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  • 34. Intestinal lymphangiectasia-A novel finding in Van Maldergem syndrome challenging the role of lymphedema for the distinction from Hennekam syndrome.
    de Meij TGJ, Zwijnenburg PJG, Broers CJM, Bökenkamp A.
    Am J Med Genet A; 2019 Jul 02; 179(7):1398-1399. PubMed ID: 31063239
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  • 35. A new classification system for primary lymphatic dysplasias based on phenotype.
    Connell F, Brice G, Jeffery S, Keeley V, Mortimer P, Mansour S.
    Clin Genet; 2010 May 02; 77(5):438-52. PubMed ID: 20447153
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  • 36. Primary upper-limb lymphoedema.
    Vignes S, Arrault M, Yannoutsos A, Blanchard M.
    Br J Dermatol; 2013 Feb 02; 168(2):272-6. PubMed ID: 22928742
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  • 37. Further delineation of Hennekam syndrome.
    Al-Gazali LI, Hertecant J, Ahmed R, Khan NA, Padmanabhan R.
    Clin Dysmorphol; 2003 Oct 02; 12(4):227-32. PubMed ID: 14564208
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  • 38. The VASCERN PPL working group patient pathway for primary and paediatric lymphoedema.
    Devoogdt N, Thomis S, Belva F, Dickinson-Blok J, Fourgeaud C, Giacalone G, Karlsmark T, Kavola H, Keeley V, Marques ML, Mansour S, Nissen CV, Nørregaard S, Oberlin M, Ručigaj TP, Somalo-Barranco G, Suominen S, Van Duinen K, Vignes S, Damstra R.
    Eur J Med Genet; 2024 Feb 02; 67():104905. PubMed ID: 38143023
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  • 39. Lymphoscintigraphic manifestations of Hennekam syndrome--a case report.
    Rockson SG, de los Santos M, Szuba A.
    Angiology; 1999 Dec 02; 50(12):1017-20. PubMed ID: 10609768
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  • 40. Exploration of Potential Immunodeficiency Unveils Hennekam Lymphangiectasia-Lymphedema Syndrome.
    Kaut S, Bucciol G, Moens L, Meyts I.
    J Clin Immunol; 2021 Oct 02; 41(7):1674-1676. PubMed ID: 34176065
    [No Abstract] [Full Text] [Related]

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