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    Results: 1 to 20 of 176

    1.

    Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience.

    Charron P, Héron D, Gargiulo M, Richard P, Dubourg O, Desnos M, Bouhour JB, Feingold J, Carrier L, Hainque B, Schwartz K, Komajda M.

    J Med Genet. 2002 Oct;39(10):741-6.PMID: 12362031 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Prenatal molecular diagnosis in hypertrophic cardiomyopathy: report of the first case.

    Charron P, Héron D, Gargiulo M, Feingold J, Oury JF, Richard P, Komajda M.

    Prenat Diagn. 2004 Sep;24(9):701-3.PMID: 15386449 [PubMed - indexed for MEDLINE]Related articles

    3.

    Diagnostic, prognostic, and therapeutic implications of genetic testing for hypertrophic cardiomyopathy.

    Bos JM, Towbin JA, Ackerman MJ.

    J Am Coll Cardiol. 2009 Jul 14;54(3):201-11. Review.PMID: 19589432 [PubMed - indexed for MEDLINE]Related articles

    4.

    Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling.

    Ingles J, Doolan A, Chiu C, Seidman J, Seidman C, Semsarian C.

    J Med Genet. 2005 Oct;42(10):e59.PMID: 16199542 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    [The contribution of molecular genetics to clinical cardiology: the example of hypertrophic cardiomyopathy]

    Fokstuen S, Blouin JL, Lyle R, Lerch R, Beghetti M, Mach F, Sztajzel J, Antonarakis SE, Sigwart U.

    Rev Med Suisse. 2005 May 25;1(21):1448, 1450, 1452-3. Review. French. PMID: 15997984 [PubMed - indexed for MEDLINE]Related articles

    6.

    Uptake of genetic counselling and predictive DNA testing in hypertrophic cardiomyopathy.

    Christiaans I, Birnie E, Bonsel GJ, Wilde AA, van Langen IM.

    Eur J Hum Genet. 2008 Oct;16(10):1201-7. Epub 2008 May 14.PMID: 18478037 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    [Genetic counseling in presymptomatic testing for Huntington disease]

    Helle JR, Braathen GJ, Pedersen JC, Skodje T, Stokke B, Berg K.

    Tidsskr Nor Laegeforen. 2000 Aug 30;120(20):2412-6. Norwegian. PMID: 11475227 [PubMed - indexed for MEDLINE]Related articles

    8.

    Genetic counseling and cardiac care in predictively tested hypertrophic cardiomyopathy mutation carriers: the patients' perspective.

    Christiaans I, van Langen IM, Birnie E, Bonsel GJ, Wilde AA, Smets EM.

    Am J Med Genet A. 2009 Jul;149A(7):1444-51.PMID: 19533783 [PubMed - indexed for MEDLINE]Related articles

    9.

    Family and population strategies for screening and counselling of inherited cardiac arrhythmias.

    van Langen IM, Hofman N, Tan HL, Wilde AA.

    Ann Med. 2004;36 Suppl 1:116-24.PMID: 15176433 [PubMed - indexed for MEDLINE]Related articles

    10.

    Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy.

    Olivotto I, Girolami F, Ackerman MJ, Nistri S, Bos JM, Zachara E, Ommen SR, Theis JL, Vaubel RA, Re F, Armentano C, Poggesi C, Torricelli F, Cecchi F.

    Mayo Clin Proc. 2008 Jun;83(6):630-8.PMID: 18533079 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy.

    Van Driest SL, Jaeger MA, Ommen SR, Will ML, Gersh BJ, Tajik AJ, Ackerman MJ.

    J Am Coll Cardiol. 2004 Aug 4;44(3):602-10.PMID: 15358028 [PubMed - indexed for MEDLINE]Related articles

    12.

    Genetic diagnosis and testing in clinical practice.

    McPherson E.

    Clin Med Res. 2006 Jun;4(2):123-9. Review.PMID: 16809405 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    [Genetic testing and bioethics]

    Fukushima Y.

    Rinsho Shinkeigaku. 2001 Dec;41(12):1187-9. Review. Japanese. PMID: 12235834 [PubMed - indexed for MEDLINE]Related articles

    14.

    Molecular genetic testing in pediatric practice: A subject review. Committee on Genetics.

    [No authors listed]

    Pediatrics. 2000 Dec;106(6):1494-7. Review.PMID: 11099612 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey.

    van Langen IM, Birnie E, Schuurman E, Tan HL, Hofman N, Bonsel GJ, Wilde AA.

    Clin Genet. 2005 Oct;68(4):360-8.PMID: 16143023 [PubMed - indexed for MEDLINE]Related articles

    16.

    Genetic testing for paediatric neurological disorders.

    Valente EM, Ferraris A, Dallapiccola B.

    Lancet Neurol. 2008 Dec;7(12):1113-26. Review.PMID: 19007736 [PubMed - indexed for MEDLINE]Related articles

    17.

    [Huntington disease: presymptomatic testing, prenatal diagnosis, preimplantation genetic diagnosis experience]

    Durr A, Viville S.

    Gynecol Obstet Fertil. 2007 Oct;35(10):1051-4. Epub 2007 Sep 25. French. PMID: 17897866 [PubMed - indexed for MEDLINE]Related articles

    18.

    Psychosocial impact of specialized cardiac genetic clinics for hypertrophic cardiomyopathy.

    Ingles J, Lind JM, Phongsavan P, Semsarian C.

    Genet Med. 2008 Feb;10(2):117-20.PMID: 18281919 [PubMed - indexed for MEDLINE]Related articles

    19.

    Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences.

    Doolan A, Tebo M, Ingles J, Nguyen L, Tsoutsman T, Lam L, Chiu C, Chung J, Weintraub RG, Semsarian C.

    J Mol Cell Cardiol. 2005 Feb;38(2):387-93. Epub 2005 Jan 27.PMID: 15698845 [PubMed - indexed for MEDLINE]Related articles

    20.

    Guidelines for the diagnosis and management of hypertrophic cardiomyopathy.

    Semsarian C; CSANZ Cardiovascular Genetics Working Group.

    Heart Lung Circ. 2007 Feb;16(1):16-8. Epub 2006 Dec 26. No abstract available. PMID: 17188934 [PubMed - indexed for MEDLINE]Related articles

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