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Results: 1 to 20 of 238

1.

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
[PubMed - indexed for MEDLINE]
2.

Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24.

Brice G, Mansour S, Bell R, Collin JR, Child AH, Brady AF, Sarfarazi M, Burnand KG, Jeffery S, Mortimer P, Murday VA.

J Med Genet. 2002 Jul;39(7):478-83.

PMID:
12114478
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

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

Kriederman BM, Myloyde TL, Witte MH, Dagenais SL, Witte CL, Rennels M, Bernas MJ, Lynch MT, Erickson RP, Caulder MS, Miura N, Jackson D, Brooks BP, Glover TW.

Hum Mol Genet. 2003 May 15;12(10):1179-85.

PMID:
12719382
[PubMed - indexed for MEDLINE]
Free Article
4.

FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate.

Bahuau M, Houdayer C, Tredano M, Soupre V, Couderc R, Vazquez MP.

Clin Genet. 2002 Dec;62(6):470-3.

PMID:
12485195
[PubMed - indexed for MEDLINE]
5.

Lymphedema-distichiasis syndrome and FOXC2 gene mutation.

Traboulsi EI, Al-Khayer K, Matsumoto M, Kimak MA, Crowe S, Wilson SE, Finegold DN, Ferrell RE, Meisler DM.

Am J Ophthalmol. 2002 Oct;134(4):592-6.

PMID:
12383817
[PubMed - indexed for MEDLINE]
6.

Research perspectives in inherited lymphatic disease.

Ferrell RE.

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

PMID:
12543715
[PubMed - indexed for MEDLINE]
7.

Hereditary lymphedema and distichiasis.

Kolin T, Johns KJ, Wadlington WB, Butler MG, Sunalp MA, Wright KW.

Arch Ophthalmol. 1991 Jul;109(7):980-1.

PMID:
2064580
[PubMed - indexed for MEDLINE]
8.

Truncating mutations in FOXC2 cause multiple lymphedema syndromes.

Finegold DN, Kimak MA, Lawrence EC, Levinson KL, Cherniske EM, Pober BR, Dunlap JW, Ferrell RE.

Hum Mol Genet. 2001 May 15;10(11):1185-9.

PMID:
11371511
[PubMed - indexed for MEDLINE]
Free Article
9.

Mutation of the FOXC2 gene in familial distichiasis.

Brooks BP, Dagenais SL, Nelson CC, Glynn MW, Caulder MS, Downs CA, Glover TW.

J AAPOS. 2003 Oct;7(5):354-7.

PMID:
14566319
[PubMed - indexed for MEDLINE]
10.

Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome.

Fang J, Dagenais SL, Erickson RP, Arlt MF, Glynn MW, Gorski JL, Seaver LH, Glover TW.

Am J Hum Genet. 2000 Dec;67(6):1382-8. Epub 2000 Nov 8.

PMID:
11078474
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

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
[PubMed - indexed for MEDLINE]
12.

Lymphedema-distichiasis syndrome without FOXC2 mutation: evidence for chromosome 16 duplication upstream of FOXC2.

Witte MH, Erickson RP, Khalil M, Dellinger M, Bernas M, Grogan T, Nitta H, Feng J, Duggan D, Witte CL.

Lymphology. 2009 Dec;42(4):152-60.

PMID:
20218083
[PubMed - indexed for MEDLINE]
13.

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
[PubMed - indexed for MEDLINE]
14.

Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia.

Irrthum A, Devriendt K, Chitayat D, Matthijs G, Glade C, Steijlen PM, Fryns JP, Van Steensel MA, Vikkula M.

Am J Hum Genet. 2003 Jun;72(6):1470-8. Epub 2003 May 8.

PMID:
12740761
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patient.

Tanpaiboon P, Kantaputra P, Wejathikul K, Piyamongkol W.

Am J Med Genet A. 2010 Mar;152A(3):737-40. doi: 10.1002/ajmg.a.33273.

PMID:
20186799
[PubMed - indexed for MEDLINE]
16.

Lymphedema-distichiasis and FOXC2 gene mutations.

Erickson RP.

Lymphology. 2001 Mar;34(1):1. No abstract available.

PMID:
11307659
[PubMed - indexed for MEDLINE]
17.

A novel frameshift mutation of FOXC2 gene in a family with hereditary lymphedema-distichiasis syndrome associated with renal disease and diabetes mellitus.

Yildirim-Toruner C, Subramanian K, El Manjra L, Chen E, Goldstein S, Vitale E.

Am J Med Genet A. 2004 Dec 15;131(3):281-6.

PMID:
15523639
[PubMed - indexed for MEDLINE]
18.

Age of onset in hereditary lymphedema.

Levinson KL, Feingold E, Ferrell RE, Glover TW, Traboulsi EI, Finegold DN.

J Pediatr. 2003 Jun;142(6):704-8.

PMID:
12838201
[PubMed - indexed for MEDLINE]
19.

Hereditary palmoplantar keratoderma associated with primary (congenital) lymphedema.

Ogunbiyi SO, Deguara J, Moss C, Burnand KG.

Lymphology. 2009 Jun;42(2):85-7.

PMID:
19725273
[PubMed - indexed for MEDLINE]
20.

Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations.

Erickson RP, Dagenais SL, Caulder MS, Downs CA, Herman G, Jones MC, Kerstjens-Frederikse WS, Lidral AC, McDonald M, Nelson CC, Witte M, Glover TW.

J Med Genet. 2001 Nov;38(11):761-6.

PMID:
11694548
[PubMed - indexed for MEDLINE]
Free PMC Article

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