Vosberg HP - Search Results

1

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.

Thierfelder L, Watkins H, MacRae C, Lamas R, McKenna W, Vosberg HP, Seidman JG, Seidman CE. Thierfelder L, et al. Among authors: vosberg hp. Cell. 1994 Jun 3;77(5):701-12. doi: 10.1016/0092-8674(94)90054-x. Cell. 1994. PMID: 8205619

2

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.

Geisterfer-Lowrance AA, Kass S, Tanigawa G, Vosberg HP, McKenna W, Seidman CE, Seidman JG. Geisterfer-Lowrance AA, et al. Among authors: vosberg hp. Cell. 1990 Sep 7;62(5):999-1006. doi: 10.1016/0092-8674(90)90274-i. Cell. 1990. PMID: 1975517

3

A molecular basis for familial hypertrophic cardiomyopathy: an alpha/beta cardiac myosin heavy chain hybrid gene.

Tanigawa G, Jarcho JA, Kass S, Solomon SD, Vosberg HP, Seidman JG, Seidman CE. Tanigawa G, et al. Among authors: vosberg hp. Cell. 1990 Sep 7;62(5):991-8. doi: 10.1016/0092-8674(90)90273-h. Cell. 1990. PMID: 2144212

4

Clinical features of hypertrophic cardiomyopathy caused by mutation of a "hot spot" in the alpha-tropomyosin gene.

Coviello DA, Maron BJ, Spirito P, Watkins H, Vosberg HP, Thierfelder L, Schoen FJ, Seidman JG, Seidman CE. Coviello DA, et al. Among authors: vosberg hp. J Am Coll Cardiol. 1997 Mar 1;29(3):635-40. doi: 10.1016/s0735-1097(96)00538-4. J Am Coll Cardiol. 1997. PMID: 9060904 Free article.

5

A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12.

Solomon SD, Geisterfer-Lowrance AA, Vosberg HP, Hiller G, Jarcho JA, Morton CC, McBride WO, Mitchell AL, Bale AE, McKenna WJ, et al. Solomon SD, et al. Among authors: vosberg hp. Am J Hum Genet. 1990 Sep;47(3):389-94. Am J Hum Genet. 1990. PMID: 1975475 Free PMC article.

6

A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance.

Moolman JA, Reith S, Uhl K, Bailey S, Gautel M, Jeschke B, Fischer C, Ochs J, McKenna WJ, Klues H, Vosberg HP. Moolman JA, et al. Among authors: vosberg hp. Circulation. 2000 Mar 28;101(12):1396-402. doi: 10.1161/01.cir.101.12.1396. Circulation. 2000. PMID: 10736283

7

Genetic polymorphisms in the renin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: a study of five polymorphic genes in a family with a disease causing mutation in the myosin binding protein C gene.

Ortlepp JR, Vosberg HP, Reith S, Ohme F, Mahon NG, Schröder D, Klues HG, Hanrath P, McKenna WJ. Ortlepp JR, et al. Among authors: vosberg hp. Heart. 2002 Mar;87(3):270-5. doi: 10.1136/heart.87.3.270. Heart. 2002. PMID: 11847170 Free PMC article.

8

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy.

Bonne G, Carrier L, Bercovici J, Cruaud C, Richard P, Hainque B, Gautel M, Labeit S, James M, Beckmann J, Weissenbach J, Vosberg HP, Fiszman M, Komajda M, Schwartz K. Bonne G, et al. Among authors: vosberg hp. Nat Genet. 1995 Dec;11(4):438-40. doi: 10.1038/ng1295-438. Nat Genet. 1995. PMID: 7493026

9

[Genetic causes of hypertrophic cardiomyopathy].

Vosberg HP. Vosberg HP. Med Klin (Munich). 1998 Apr 15;93(4):252-9. doi: 10.1007/BF03044801. Med Klin (Munich). 1998. PMID: 9594535 Review. German.

10

Myosin mutations in hypertrophic cardiomyopathy and functional implications.

Vosberg HP. Vosberg HP. Herz. 1994 Apr;19(2):75-83. Herz. 1994. PMID: 8194835 Review.

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