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4. [Familial case of Milroy-Meige-Nonne disease]. Ouvry PA; Davy A; Sauzeau MF; Lesieur P Phlebologie; 1986; 39(3):497-508. PubMed ID: 3786423 [TBL] [Abstract][Full Text] [Related]
5. Lymphangiosarcoma in late-onset hereditary lymphedema: case report and nosological implications. Andersson HC; Parry DM; Mulvihill JJ Am J Med Genet; 1995 Mar; 56(1):72-5. PubMed ID: 7747790 [TBL] [Abstract][Full Text] [Related]
6. [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]
8. 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]
10. A genetic association between microcephaly and lymphedema. Crowe CA; Dickerman LH Am J Med Genet; 1986 May; 24(1):131-5. PubMed ID: 3706402 [TBL] [Abstract][Full Text] [Related]
11. [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]
12. [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]
13. [Hereditary lymphedema (Milroy's disease)]. Eliachar E; Servelle M; Tassy R; Gamerman H Ann Pediatr (Paris); 1970 Nov; 17(11):750-3. PubMed ID: 5484619 [No Abstract] [Full Text] [Related]
14. 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]
15. [Hereditary lymphedema (Nonne-Milroy-Meige syndrome) associated with chylothorax. Comments on 2 cases]. Zbranca V; Aramă A; Mihăescu T; Covic M Rev Med Chir Soc Med Nat Iasi; 1990; 94(1):189-92. PubMed ID: 2075326 [TBL] [Abstract][Full Text] [Related]
17. Dominantly inherited syndrome of microcephaly and congenital lymphedema. Leung AK Clin Genet; 1985 Jun; 27(6):611-2. PubMed ID: 4017282 [TBL] [Abstract][Full Text] [Related]
18. [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]
19. [Milroy's disease and primary lymphoedema. Exploration methods, therapeutic aspects (author's transl)]. Stalder JF; Berger M Ann Dermatol Venereol; 1980 Jul; 107(7):665-7. PubMed ID: 7436261 [TBL] [Abstract][Full Text] [Related]
20. 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; 142(4):441-7. PubMed ID: 12712065 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]