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Items: 19

1.

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
2.

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
3.

FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update.

Gordon K, Spiden SL, Connell FC, Brice G, Cottrell S, Short J, Taylor R, Jeffery S, Mortimer PS, Mansour S, Ostergaard P.

Hum Mutat. 2013 Jan;34(1):23-31. doi: 10.1002/humu.22223. Epub 2012 Oct 16. Review.

PMID:
23074044
4.

Research perspectives in inherited lymphatic disease.

Ferrell RE.

Ann N Y Acad Sci. 2002 Dec;979:39-51; discussion 76-9. Review.

PMID:
12543715
5.

Lymphangiosarcoma in late-onset hereditary lymphedema: case report and nosological implications.

Andersson HC, Parry DM, Mulvihill JJ.

Am J Med Genet. 1995 Mar 13;56(1):72-5. Review.

PMID:
7747790
6.

Milroy Disease.

Brice GW, Mansour S, Ostergaard P, Connell F, Jeffery S, Mortimer P.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2006 Apr 27 [updated 2014 Sep 25].

7.

Milroy disease and the VEGFR-3 mutation phenotype.

Brice G, Child AH, Evans A, Bell R, Mansour S, Burnand K, Sarfarazi M, Jeffery S, Mortimer P.

J Med Genet. 2005 Feb;42(2):98-102. Review.

8.

The genetics of vascular anomalies.

Frigerio A, Stevenson DA, Grimmer JF.

Curr Opin Otolaryngol Head Neck Surg. 2012 Dec;20(6):527-32. doi: 10.1097/MOO.0b013e3283587415. Review.

PMID:
22913934
9.

Phenotypic characterization of primary lymphedema.

Connell F, Brice G, Mortimer P.

Ann N Y Acad Sci. 2008;1131:140-6. doi: 10.1196/annals.1413.013. Review.

PMID:
18519967
10.

Syndromic classification of hereditary lymphedema.

Northup KA, Witte MH, Witte CL.

Lymphology. 2003 Dec;36(4):162-89. Review.

PMID:
14992570
11.

Novel FOXC2 missense mutation identified in patient with lymphedema-distichiasis syndrome and review.

Dellinger MT, Thome K, Bernas MJ, Erickson RP, Witte MH.

Lymphology. 2008 Sep;41(3):98-102. Review.

PMID:
19013876
12.

Lymphangiosarcoma of the pubic region: a rare complication arising in congenital non-hereditary lymphedema.

Cerri A, Gianni C, Corbellino M, Pizzuto M, Moneghini L, Crosti C.

Eur J Dermatol. 1998 Oct-Nov;8(7):511-4. Review.

PMID:
9854166
13.

Genetics of lymphatic anomalies.

Brouillard P, Boon L, Vikkula M.

J Clin Invest. 2014 Mar;124(3):898-904. doi: 10.1172/JCI71614. Epub 2014 Mar 3. Review.

14.

[Yellow nail syndrome].

Hausmann M, Keller R.

Pneumologie. 1994 Jan;48(1):30-3. Review. German.

PMID:
8153117
15.

[Primary lymphedema of limbs].

Vaillant L, Tauveron V.

Presse Med. 2010 Dec;39(12):1279-86. doi: 10.1016/j.lpm.2010.09.010. Epub 2010 Oct 28. Review. French.

PMID:
21035299
16.

[Primary lymphedema].

Gregl A, von Heyden D, Jentsch F, Yu D.

Z Lymphol. 1983 Jul;7(1):21-8. Review. German.

PMID:
6353789
17.

The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings.

Connell FC, Gordon K, Brice G, Keeley V, Jeffery S, Mortimer PS, Mansour S, Ostergaard P.

Clin Genet. 2013 Oct;84(4):303-14. doi: 10.1111/cge.12173. Epub 2013 Jun 27. Review.

PMID:
23621851
18.

[The trophedema (Nonne-Milroy-Meige). Carcinogenesis as a rare complication].

Köstler E.

Dermatol Monatsschr. 1976 Jun;162(6):465-77. Review. German.

PMID:
786757
19.

[Lymphedema].

Izumikawa Y.

Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):121. Review. Japanese. No abstract available.

PMID:
11528651

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