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5. [Congenital Milroy Oedema: a case report of a family]. Raffa V; Campra D; Guarino R; Angellotti P; Ballardini G; Boscardini L; Guala A Pediatr Med Chir; 2012; 34(2):100-3. PubMed ID: 22730636 [TBL] [Abstract][Full Text] [Related]
6. [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; 27(1-2):106-8. PubMed ID: 16922055 [TBL] [Abstract][Full Text] [Related]
7. Puffy feet in an 11-month-old infant: a quiz. Milroy disease. Yilmaz AE; Sarifakioglu E; Gorpelioglu C; Karabel M; Dogan G Acta Derm Venereol; 2009 Nov; 89(6):668, 670. PubMed ID: 19997714 [No Abstract] [Full Text] [Related]
8. [Meige-Milroy-Nonne disease. Report of a case in a six-month-old infant]. Kubryk N; Roger M Ann Pediatr (Paris); 1990 Sep; 37(7):481-2. PubMed ID: 2256646 [TBL] [Abstract][Full Text] [Related]
9. [Primary congenital lymphedema: Milroy disease: the first case observed in the Department of Pediatrics at the University Hospital Yalgado Ouedraogo, Ouagadougou]. Ouattara CZ; Kalmogho A; Yonaba C; Bouda CG; Yaméogo G; Kam L Pan Afr Med J; 2017; 27():21. PubMed ID: 28748022 [TBL] [Abstract][Full Text] [Related]
10. 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 [TBL] [Abstract][Full Text] [Related]
16. [Nonne-Milroy-Meige disease in 2 members of a family]. Jeske J; Ostrowska-Stach H; Hübner H Pol Tyg Lek; 1969 Sep; 24(36):1389-90. PubMed ID: 5351081 [No Abstract] [Full Text] [Related]
17. 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 [TBL] [Abstract][Full Text] [Related]