Vosberg HP - Search Results

1

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.

2

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

3

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

4

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

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

Identification of a mutation near a functional site of the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy.

Dufour C, Dausse E, Fetler L, Dubourg O, Bouhour JB, Vosberg HP, Guicheney P, Komajda M, Schwartz K. Dufour C, et al. Among authors: vosberg hp. J Mol Cell Cardiol. 1994 Sep;26(9):1241-7. doi: 10.1006/jmcc.1994.1142. J Mol Cell Cardiol. 1994. PMID: 7815466

7

[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.

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: vosberg hp. 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

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

10

Gene symbol: MYBPC3. Disease: Hypertrophic cardiomyopathy.

Golubenko MV, Puzyrev KV, Puzyrev VP, Pavlukova EN, Makeeva OA, Vosberg HP. Golubenko MV, et al. Among authors: vosberg hp. Hum Genet. 2004 Mar;114(4):406. Hum Genet. 2004. PMID: 15046084 No abstract available.

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