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Items: 1 to 20 of 109

1.

[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 Mar-Apr;34(2):100-3. Italian.

PMID:
22730636
2.

[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 Jan-Apr;27(1-2):106-8. Italian.

PMID:
16922055
3.

[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. French.

PMID:
2256646
4.

[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 Jan-Mar;94(1):189-92. Romanian.

PMID:
2075326
5.

[A case of congenital hereditary lymphedema (Milroy-Nonne's disease].

Beluschi C, Coraiola M, Pedrotti D.

Pediatr Med Chir. 1982 Jan-Apr;4(1-2):155-7. Italian. No abstract available.

PMID:
7111035
6.

[Hereditary congenital lymphedema with pseudosexual ambiguity].

Sarda P, Jalaguier J, Montoya F, Bonnet H.

J Genet Hum. 1988 Aug;36(4):353-60. French.

PMID:
3221210
7.

[Nonne-Milroy-Meige disease in 2 members of a family].

Jeske J, Ostrowska-Stach H, Hübner H.

Pol Tyg Lek. 1969 Sep 9;24(36):1389-90. Polish. No abstract available.

PMID:
5351081
8.

Congenital hereditary lymphedema (Nonne/Milroy).

Farhud DD, Farhud I, Walizadeh GR, Djaber-Ansari M.

Padiatr Padol. 1989;24(4):305-7.

PMID:
2616174
9.

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.

PMID:
16965327
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.

PMID:
15904433
11.

[Late isolated form of chronic trophic edema of the skin or Nonne-Milroy-Meige disease].

Brzecki A, Misztal S.

Neurol Neurochir Pol. 1972;6(3):487-90. Polish. No abstract available.

PMID:
5032301
12.

Prenatal ultrasonographic diagnosis of atypical Nonne-Milroy lymphedema.

Lev-Sagie A, Hamani Y, Raas-Rothschild A, Yagel S, Anteby EY.

Ultrasound Obstet Gynecol. 2003 Jan;21(1):72-4.

13.

[Etiopathogenetic unity of the Nonne-Milroy-Meige disease and various forms of exudative enteropathies].

Swicowa K, Foltyn H, Korzon M.

Pediatr Pol. 1971 Sep;46(9):1127-31. Polish. No abstract available.

PMID:
5114244
14.

Segregation analyses and a genome-wide linkage search confirm genetic heterogeneity and suggest oligogenic inheritance in some Milroy congenital primary lymphedema families.

Holberg CJ, Erickson RP, Bernas MJ, Witte MH, Fultz KE, Andrade M, Witte CL.

Am J Med Genet. 2001 Feb 1;98(4):303-12.

PMID:
11170072
15.

[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. French.

PMID:
7436261
16.

Milroy's primary congenital lymphedema in a male infant and review of the literature.

Kitsiou-Tzeli S, Vrettou C, Leze E, Makrythanasis P, Kanavakis E, Willems P.

In Vivo. 2010 May-Jun;24(3):309-14. Review.

PMID:
20555004
17.

Wide clinical spectrum in a family with hereditary lymphedema type I due to a novel missense mutation in VEGFR3.

Spiegel R, Ghalamkarpour A, Daniel-Spiegel E, Vikkula M, Shalev SA.

J Hum Genet. 2006;51(10):846-50. Epub 2006 Aug 19.

PMID:
16924388
18.

Kaposiform hemangioendothelioma associated with Milroy's disease (primary hereditary lymphedema).

Méndez R, Capdevila A, Tellado MG, Somoza I, Liras J, Pais E, Vela D.

J Pediatr Surg. 2003 Jul;38(7):E9-12.

PMID:
12861592
19.

A novel VEGFR3 mutation causes Milroy disease.

Butler MG, Dagenais SL, Rockson SG, Glover TW.

Am J Med Genet A. 2007 Jun 1;143A(11):1212-7.

20.

Mapping of primary congenital lymphedema to the 5q35.3 region.

Evans AL, Brice G, Sotirova V, Mortimer P, Beninson J, Burnand K, Rosbotham J, Child A, Sarfarazi M.

Am J Hum Genet. 1999 Feb;64(2):547-55.

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