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    Results: 18

    1.

    Ectodermal, skeletal, and genitourinary abnormalities with neonatal hyperekplexia.

    McAbee GN, Santilli AM, Stone J, Schnur RE.

    Pediatr Neurol. 2011 May;44(5):381-4. doi: 10.1016/j.pediatrneurol.2010.12.006.

    PMID:
    21481749
    [PubMed - indexed for MEDLINE]
    2.

    Different lymphscintigraphic patterns in patients with lymphedema distichiasis.

    Sutkowska E, Bator A, Trompeta K, Szuba A.

    Lymphology. 2010 Jun;43(2):73-7.

    PMID:
    20848994
    [PubMed - indexed for MEDLINE]
    3.

    A novel missense mutation and two microrearrangements in the FOXC2 gene of three families with lymphedema-distichiasis syndrome.

    Fauret AL, Tuleja E, Jeunemaitre X, Vignes S.

    Lymphology. 2010 Mar;43(1):14-8.

    PMID:
    20552815
    [PubMed - indexed for MEDLINE]
    4.

    Spinal extradural arachnoid cysts in lymphedema-distichiasis syndrome.

    Sánchez-Carpintero R, Dominguez P, Núñez MT, Patiño-García A.

    Genet Med. 2010 Aug;12(8):532-5. doi: 10.1097/GIM.0b013e3181e5c7ea.

    PMID:
    20535019
    [PubMed - indexed for MEDLINE]
    5.

    A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation.

    Fabretto A, Shardlow A, Faletra F, Lepore L, Hladnik U, Gasparini P.

    Ophthalmic Genet. 2010 Jun;31(2):98-100. doi: 10.3109/13816811003620517.

    PMID:
    20450314
    [PubMed - indexed for MEDLINE]
    6.

    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]
    7.

    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]
    8.

    Rare association of immunoglobulin A nephropathy and lymphedema-distichiasis syndrome.

    Haran M, Lodha A, Rose M, Greenberg S.

    Am J Med Sci. 2010 Mar;339(3):288-9. doi: 10.1097/MAJ.0b013e3181c643c8.

    PMID:
    20124880
    [PubMed - indexed for MEDLINE]
    9.

    Novel missense mutations in the FOXC2 gene alter transcriptional activity.

    van Steensel MA, Damstra RJ, Heitink MV, Bladergroen RS, Veraart J, Steijlen PM, van Geel M.

    Hum Mutat. 2009 Dec;30(12):E1002-9. doi: 10.1002/humu.21127.

    PMID:
    19760751
    [PubMed - indexed for MEDLINE]
    10.

    Conjunctival edema and distichiasis in association with congenital lymphedema of the lower legs.

    Ramasubramanian A, Shields CL, Palamar M, Rousta ST, Shields JA.

    Ophthal Plast Reconstr Surg. 2009 Mar-Apr;25(2):148-50. doi: 10.1097/IOP.0b013e31819a44a1.

    PMID:
    19300167
    [PubMed - indexed for MEDLINE]
    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
    [PubMed - indexed for MEDLINE]
    12.

    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]
    13.

    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]
    14.

    Perinatal diagnosis of a lymphedema-distichiasis syndrome (LD).

    Büchner M, Dostert S, Falkert A, Huber G, Seelbach-Göbel B.

    Prenat Diagn. 2007 Nov;27(11):1069-71. No abstract available.

    PMID:
    17721865
    [PubMed - indexed for MEDLINE]
    15.

    Spinal extradural arachnoid cysts associated with distichiasis and lymphedema.

    Yabuki S, Kikuchi S, Ikegawa S.

    Am J Med Genet A. 2007 Apr 15;143A(8):884-7.

    PMID:
    17366583
    [PubMed - indexed for MEDLINE]
    16.

    Familial congenital non-immune hydrops, chylothorax, and pulmonary lymphangiectasia.

    Stevenson DA, Pysher TJ, Ward RM, Carey JC.

    Am J Med Genet A. 2006 Feb 15;140(4):368-72.

    PMID:
    16419129
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    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.

    Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndrome.

    Dagenais SL, Hartsough RL, Erickson RP, Witte MH, Butler MG, Glover TW.

    Gene Expr Patterns. 2004 Oct;4(6):611-9.

    PMID:
    15465483
    [PubMed - indexed for MEDLINE]

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