Schwartz K - Search Results

1

A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy.

Friedrich FW, Bausero P, Sun Y, Treszl A, Krämer E, Juhr D, Richard P, Wegscheider K, Schwartz K, Brito D, Arbustini E, Waldenström A, Isnard R, Komajda M, Eschenhagen T, Carrier L; EUROGENE Heart Failure Project. Friedrich FW, et al. Among authors: schwartz k. Eur Heart J. 2009 Jul;30(13):1648-55. doi: 10.1093/eurheartj/ehp153. Epub 2009 May 8. Eur Heart J. 2009. PMID: 19429631

2

Diagnostic accuracy of a 2D left ventricle hypertrophy score for familial hypertrophic cardiomyopathy.

Forissier JF, Charron P, Tezenas du Montcel S, Hagège A, Isnard R, Carrier L, Richard P, Desnos M, Bouhour JB, Schwartz K, Komajda M, Dubourg O. Forissier JF, et al. Among authors: schwartz k. Eur Heart J. 2005 Sep;26(18):1882-6. doi: 10.1093/eurheartj/ehi276. Epub 2005 Apr 28. Eur Heart J. 2005. PMID: 15860513

3

Genotype-phenotype correlations in familial hypertrophic cardiomyopathy. A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes.

Charron P, Dubourg O, Desnos M, Isnard R, Hagege A, Bonne G, Carrier L, Tesson F, Bouhour JB, Buzzi JC, Feingold J, Schwartz K, Komajda M. Charron P, et al. Among authors: schwartz k. Eur Heart J. 1998 Jan;19(1):139-45. doi: 10.1053/euhj.1997.0575. Eur Heart J. 1998. PMID: 9503187

4

Familial hypertrophic cardiomyopathy. Cardiac ultrasonic abnormalities in genetically affected subjects without echocardiographic evidence of left ventricular hypertrophy.

Hagège AA, Dubourg O, Desnos M, Mirochnik R, Isnard G, Bonne G, Carrier L, Guicheney P, Bouhour JB, Schwartz K, Komajda M. Hagège AA, et al. Among authors: schwartz k. Eur Heart J. 1998 Mar;19(3):490-9. doi: 10.1053/euhj.1997.0735. Eur Heart J. 1998. PMID: 9568454

5

Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children.

Charron P, Dubourg O, Desnos M, Bouhour JB, Isnard R, Hagege A, Carrier L, Bonne G, Tesson F, Richard P, Hainque B, Schwartz K, Komajda M. Charron P, et al. Among authors: schwartz k. Eur Heart J. 1998 Sep;19(9):1377-82. doi: 10.1053/euhj.1998.1049. Eur Heart J. 1998. PMID: 9792264 Clinical Trial.

6

Nonsense-mediated mRNA decay and ubiquitin-proteasome system regulate cardiac myosin-binding protein C mutant levels in cardiomyopathic mice.

Vignier N, Schlossarek S, Fraysse B, Mearini G, Krämer E, Pointu H, Mougenot N, Guiard J, Reimer R, Hohenberg H, Schwartz K, Vernet M, Eschenhagen T, Carrier L. Vignier N, et al. Among authors: schwartz k. Circ Res. 2009 Jul 31;105(3):239-48. doi: 10.1161/CIRCRESAHA.109.201251. Epub 2009 Jul 9. Circ Res. 2009. PMID: 19590044

7

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.

Richard P, Charron P, Carrier L, Ledeuil C, Cheav T, Pichereau C, Benaiche A, Isnard R, Dubourg O, Burban M, Gueffet JP, Millaire A, Desnos M, Schwartz K, Hainque B, Komajda M; EUROGENE Heart Failure Project. Richard P, et al. Among authors: schwartz k. Circulation. 2003 May 6;107(17):2227-32. doi: 10.1161/01.CIR.0000066323.15244.54. Epub 2003 Apr 21. Circulation. 2003. PMID: 12707239

8

Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy.

Waldmüller S, Sakthivel S, Saadi AV, Selignow C, Rakesh PG, Golubenko M, Joseph PK, Padmakumar R, Richard P, Schwartz K, Tharakan JM, Rajamanickam C, Vosberg HP. Waldmüller S, et al. Among authors: schwartz k. J Mol Cell Cardiol. 2003 Jun;35(6):623-36. doi: 10.1016/s0022-2828(03)00050-6. J Mol Cell Cardiol. 2003. PMID: 12788380

9

Clinical and genetical heterogeneity of familial hypertrophic cardiomyopathy.

Hengstenberg C, Carrier L, Schwartz K, Maisch B. Hengstenberg C, et al. Among authors: schwartz k. Herz. 1994 Apr;19(2):84-90. Herz. 1994. PMID: 8194836 Review.

10

Familial hypertrophic cardiomyopathy: from mutations to functional defects.

Bonne G, Carrier L, Richard P, Hainque B, Schwartz K. Bonne G, et al. Among authors: schwartz k. Circ Res. 1998 Sep 21;83(6):580-93. doi: 10.1161/01.res.83.6.580. Circ Res. 1998. PMID: 9742053 Review.

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