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Items: 1 to 20 of 34

1.

Lymphedema-distichiasis syndrome: a distinct type of primary lymphedema caused by mutations in the FOXC2 gene.

Vreeburg M, Heitink MV, Damstra RJ, Moog U, van Geel M, van Steensel MA.

Int J Dermatol. 2008 Nov;47 Suppl 1:52-5. doi: 10.1111/j.1365-4632.2008.03962.x.

PMID:
18986489
2.

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
3.

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
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.

Meige disease (familial lymphedema praecox) and cleft palate: report of a family and review of the literature.

Figueroa AA, Pruzansky S, Rollnick BR.

Cleft Palate J. 1983 Apr;20(2):151-7. Review.

PMID:
6342849
6.

Lymphedema-distichiasis syndrome: report of a case and review.

Johnson SM, Kincannon JM, Horn TD.

Arch Dermatol. 1999 Mar;135(3):347-8. Review. No abstract available.

PMID:
10086462
7.

Lymphedema-Distichiasis Syndrome.

Mansour S, Brice GW, Jeffery S, Mortimer P.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2005 Mar 29 [updated 2012 May 24].

8.

[Distichiasis-lymphedema syndrome].

Morooka K.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):284-5. Review. Japanese. No abstract available.

PMID:
11057230
9.

[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
10.

Literature watch. FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.

Pepper MS.

Lymphat Res Biol. 2003;1(3):245-9. Review. No abstract available.

PMID:
15624441
11.

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
12.

Research perspectives in inherited lymphatic disease: an update.

Ferrell RE, Finegold DN.

Ann N Y Acad Sci. 2008;1131:134-9. doi: 10.1196/annals.1413.012. Review.

PMID:
18519966
13.

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.

14.

Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunction.

De Baere E, Copelli S, Caburet S, Laissue P, Beysen D, Christin-Maitre S, Bouchard P, Veitia R, Fellous M.

Pediatr Endocrinol Rev. 2005 Jun;2(4):653-60. Review.

PMID:
16208278
15.

[Enigmatic lymphatic diseases involving the lung].

Khen-Dunlop N, Amiel J, Delacourt C, Révillon Y.

Rev Pneumol Clin. 2013 Oct;69(5):260-4. doi: 10.1016/j.pneumo.2013.02.001. Epub 2013 Apr 3. Review. French.

PMID:
23561737
16.

Yellow nail syndrome: not a genetic disorder? Eleven new cases and a review of the literature.

Hoque SR, Mansour S, Mortimer PS.

Br J Dermatol. 2007 Jun;156(6):1230-4. Epub 2007 Apr 25. Review.

PMID:
17459037
17.

Developmental disorders of the lymphatic system.

Greenlee R, Hoyme H, Witte M, Crowe P, Witte C.

Lymphology. 1993 Dec;26(4):156-68. Review.

PMID:
8121193
18.

The mutations and potential targets of the forkhead transcription factor FOXL2.

Moumné L, Batista F, Benayoun BA, Nallathambi J, Fellous M, Sundaresan P, Veitia RA.

Mol Cell Endocrinol. 2008 Jan 30;282(1-2):2-11. Epub 2007 Nov 19. Review.

PMID:
18155828
19.

Lymphedema praecox seen as isolated unilateral arm involvement: case report and review of the literature.

Harel L, Amir J, Nussinovitch M, Straussberg R, Varsano I.

J Pediatr. 1997 Mar;130(3):492-4. Review.

PMID:
9063433
20.

Syndromic classification of hereditary lymphedema.

Northup KA, Witte MH, Witte CL.

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

PMID:
14992570
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