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    Results: 19

    1.

    Thrombocytopenia resulting from mutations in filamin A can be expressed as an isolated syndrome.

    Nurden P, Debili N, Coupry I, Bryckaert M, Youlyouz-Marfak I, Solé G, Pons AC, Berrou E, Adam F, Kauskot A, Lamazière JM, Rameau P, Fergelot P, Rooryck C, Cailley D, Arveiler B, Lacombe D, Vainchenker W, Nurden A, Goizet C.

    Blood. 2011 Nov 24;118(22):5928-37. doi: 10.1182/blood-2011-07-365601. Epub 2011 Sep 29.

    PMID:
    21960593
    [PubMed - indexed for MEDLINE]
    Free Article
    2.

    Structure of filamin A immunoglobulin-like repeat 10 from Homo sapiens.

    Page RC, Clark JG, Misra S.

    Acta Crystallogr Sect F Struct Biol Cryst Commun. 2011 Aug 1;67(Pt 8):871-6. doi: 10.1107/S1744309111024249. Epub 2011 Jul 26.

    PMID:
    21821884
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    3.

    In-frame deletion in FLNA causing familial periventricular heterotopia with skeletal dysplasia in males.

    Parrini E, Rivas IL, Toral JF, Pucatti D, Giglio S, Mei D, Guerrini R.

    Am J Med Genet A. 2011 May;155A(5):1140-6. doi: 10.1002/ajmg.a.33880. Epub 2011 Apr 11.

    PMID:
    21484998
    [PubMed - indexed for MEDLINE]
    4.

    Bifid tongue, corneal clouding, and Dandy-Walker malformation in a male infant with otopalatodigital syndrome type 2.

    Murphy-Ryan M, Babovic-Vuksanovic D, Lindor N.

    Am J Med Genet A. 2011 Apr;155A(4):855-9. doi: 10.1002/ajmg.a.33901. Epub 2011 Mar 15.

    PMID:
    21412975
    [PubMed - indexed for MEDLINE]
    5.

    Lung disease associated with periventricular nodular heterotopia and an FLNA mutation.

    Masurel-Paulet A, Haan E, Thompson EM, Goizet C, Thauvin-Robinet C, Tai A, Kennedy D, Smith G, Khong TY, Solé G, Guerineau E, Coupry I, Huet F, Robertson S, Faivre L.

    Eur J Med Genet. 2011 Jan-Feb;54(1):25-8. doi: 10.1016/j.ejmg.2010.09.010. Epub 2010 Oct 1.

    PMID:
    20888935
    [PubMed - indexed for MEDLINE]
    6.

    Anesthesia in a child with otopalatodigital syndrome.

    Zachariah SK, Rai E, Ninan S.

    Paediatr Anaesth. 2010 Apr;20(4):367-8. doi: 10.1111/j.1460-9592.2010.03266.x. No abstract available.

    PMID:
    20470342
    [PubMed - indexed for MEDLINE]
    7.

    Mutational analysis of two boys with the severe perinatally lethal Melnick-Needles syndrome.

    Santos HH, Garcia PP, Pereira L, Leão LL, Aguiar RA, Lana AM, Carvalho MR, Aguiar MJ.

    Am J Med Genet A. 2010 Mar;152A(3):726-31. doi: 10.1002/ajmg.a.33260.

    PMID:
    20186808
    [PubMed - indexed for MEDLINE]
    8.

    Structure of the human filamin A actin-binding domain.

    Ruskamo S, Ylänne J.

    Acta Crystallogr D Biol Crystallogr. 2009 Nov;65(Pt 11):1217-21. doi: 10.1107/S0907444909037330. Epub 2009 Oct 22.

    PMID:
    19923718
    [PubMed - indexed for MEDLINE]
    9.

    Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders.

    Clark AR, Sawyer GM, Robertson SP, Sutherland-Smith AJ.

    Hum Mol Genet. 2009 Dec 15;18(24):4791-800. doi: 10.1093/hmg/ddp442. Epub 2009 Sep 22.

    PMID:
    19773341
    [PubMed - indexed for MEDLINE]
    Free Article
    10.

    The Erlenmeyer flask bone deformity in the skeletal dysplasias.

    Faden MA, Krakow D, Ezgu F, Rimoin DL, Lachman RS.

    Am J Med Genet A. 2009 Jun;149A(6):1334-45. doi: 10.1002/ajmg.a.32253. Review.

    PMID:
    19444897
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    11.

    Tracheomalacia in siblings with otopalatodigital syndrome.

    Johnson JN, Hartman TK, Krych EH, Seferian EG, Ouellette Y.

    Am J Med Genet A. 2008 May 15;146A(10):1347-9. doi: 10.1002/ajmg.a.32263. No abstract available.

    PMID:
    18412116
    [PubMed - indexed for MEDLINE]
    12.

    Syndromes and disorders associated with omphalocele (III): single gene disorders, neural tube defects, diaphragmatic defects and others.

    Chen CP.

    Taiwan J Obstet Gynecol. 2007 Jun;46(2):111-20. Review.

    PMID:
    17638618
    [PubMed - indexed for MEDLINE]
    13.

    Otopalatodigital syndrome type 2 in two siblings with a novel filamin A 629G>T mutation: clinical, pathological, and molecular findings.

    Mariño-Enríquez A, Lapunzina P, Robertson SP, Rodríguez JI.

    Am J Med Genet A. 2007 May 15;143A(10):1120-5.

    PMID:
    17431908
    [PubMed - indexed for MEDLINE]
    14.

    A new osteochondrodysplasia with severe osteopenia, preaxial polydactyly, clefting and dysmorphic features resembling filamin-related disorders.

    Colombani M, Laurent N, Le Merrer M, Delezoide AL, Thauvin-Robinet C, Huet F, Sagot P, Couvreur S, Rousseau T, Robertson SP, Faivre L.

    Prenat Diagn. 2006 Dec;26(12):1151-5.

    PMID:
    17009344
    [PubMed - indexed for MEDLINE]
    15.
    16.

    Distraction in a case of otopalatodigital syndrome type II.

    Batra P, Ryan FS, Witherow H, Calvert ML.

    Int J Paediatr Dent. 2006 Jul;16(4):286-91.

    PMID:
    16759327
    [PubMed - indexed for MEDLINE]
    17.

    Postzygotic mutation and germline mosaicism in the otopalatodigital syndrome spectrum disorders.

    Robertson SP, Thompson S, Morgan T, Holder-Espinasse M, Martinot-Duquenoy V, Wilkie AO, Manouvrier-Hanu S.

    Eur J Hum Genet. 2006 May;14(5):549-54.

    PMID:
    16538226
    [PubMed - indexed for MEDLINE]
    Free Article
    18.

    A novel filamin A D203Y mutation in a female patient with otopalatodigital type 1 syndrome and extremely skewed X chromosome inactivation.

    Hidalgo-Bravo A, Pompa-Mera EN, Kofman-Alfaro S, Gonzalez-Bonilla CR, Zenteno JC.

    Am J Med Genet A. 2005 Jul 15;136(2):190-3.

    PMID:
    15940695
    [PubMed - indexed for MEDLINE]
    19.

    Mutations in PITX2 may contribute to cases of omphalocele and VATER-like syndromes.

    Katz LA, Schultz RE, Semina EV, Torfs CP, Krahn KN, Murray JC.

    Am J Med Genet A. 2004 Oct 15;130A(3):277-83.

    PMID:
    15378534
    [PubMed - indexed for MEDLINE]

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