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Journal Abstract Search
89 related items for PubMed ID: 642583
1. The pathogenesis of congenital hereditary lymphedema in the pig. van der Putte SC. Lymphology; 1978 Mar; 11(1):10-21. PubMed ID: 642583 [Abstract] [Full Text] [Related]
2. Congenital hereditary lymphedema in the pig. van der Putte SC. Lymphology; 1978 Mar; 11(1):1-9. PubMed ID: 642582 [Abstract] [Full Text] [Related]
3. A syndrome of congenital lymphedema of the upper extremity and associated systemic lymphatic malformations. Fonkalsrud EW. Surg Gynecol Obstet; 1977 Aug; 145(2):228-34. PubMed ID: 877843 [No Abstract] [Full Text] [Related]
4. Developmental disorders of the lymphatic system. Greenlee R, Hoyme H, Witte M, Crowe P, Witte C. Lymphology; 1993 Dec; 26(4):156-68. PubMed ID: 8121193 [Abstract] [Full Text] [Related]
5. The early development of the lymphatic system in mouse embryos. van der Putte SC. Acta Morphol Neerl Scand; 1975 Dec; 13(4):245-86. PubMed ID: 1217547 [Abstract] [Full Text] [Related]
6. Aplasia of superficial lymphatic capillaries in hereditary and connatal lymphedema (Milroy's disease). Bollinger A, Isenring G, Franzeck UK, Brunner U. Lymphology; 1983 Mar; 16(1):27-30. PubMed ID: 6843174 [Abstract] [Full Text] [Related]
11. Negative pressure in pharyngo-oral cavity can treat lymphedema and related disorders. Fang Y, He Y, Liu Z. Med Hypotheses; 2008 Nov; 70(4):886-7. PubMed ID: 17964739 [Abstract] [Full Text] [Related]
12. Congenital lymphatic dysplasias: genetics review and resources for the lymphologist. Bellini C, Witte MH, Campisi C, Bonioli E, Boccardo F. Lymphology; 2009 Mar; 42(1):36-41. PubMed ID: 19499766 [Abstract] [Full Text] [Related]
13. Diameters of lymphatic capillaries in patients with different forms of primary lymphedema. Pfister G, Saesseli B, Hoffmann U, Geiger M, Bollinger A. Lymphology; 1990 Sep; 23(3):140-4. PubMed ID: 2250483 [Abstract] [Full Text] [Related]
19. 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; 45(2):59-61. PubMed ID: 15904433 [Abstract] [Full Text] [Related]
20. 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] Page: [Next] [New Search]