Towbin JA - Search Results

1

Novel mutations in domain I of SCN5A cause Brugada syndrome.

Vatta M, Dumaine R, Antzelevitch C, Brugada R, Li H, Bowles NE, Nademanee K, Brugada J, Brugada P, Towbin JA. Vatta M, et al. Among authors: towbin ja. Mol Genet Metab. 2002 Apr;75(4):317-24. doi: 10.1016/S1096-7192(02)00006-9. Mol Genet Metab. 2002. PMID: 12051963

2

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity.

Jiang C, Atkinson D, Towbin JA, Splawski I, Lehmann MH, Li H, Timothy K, Taggart RT, Schwartz PJ, Vincent GM, et al. Jiang C, et al. Among authors: towbin ja. Nat Genet. 1994 Oct;8(2):141-7. doi: 10.1038/ng1094-141. Nat Genet. 1994. PMID: 7842012

3

Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families.

Towbin JA, Li H, Taggart RT, Lehmann MH, Schwartz PJ, Satler CA, Ayyagari R, Robinson JL, Moss A, Hejtmancik JF. Towbin JA, et al. Circulation. 1994 Dec;90(6):2635-44. doi: 10.1161/01.cir.90.6.2635. Circulation. 1994. PMID: 7994803

4

Delineation of the Marfan phenotype associated with mutations in exons 23-32 of the FBN1 gene.

Putnam EA, Cho M, Zinn AB, Towbin JA, Byers PH, Milewicz DM. Putnam EA, et al. Among authors: towbin ja. Am J Med Genet. 1996 Mar 29;62(3):233-42. doi: 10.1002/(SICI)1096-8628(19960329)62:3<233::AID-AJMG7>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8882780

5

Viral infection of the myocardium in endocardial fibroelastosis. Molecular evidence for the role of mumps virus as an etiologic agent.

Ni J, Bowles NE, Kim YH, Demmler G, Kearney D, Bricker JT, Towbin JA. Ni J, et al. Among authors: towbin ja. Circulation. 1997 Jan 7;95(1):133-9. doi: 10.1161/01.cir.95.1.133. Circulation. 1997. PMID: 8994428

6

Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy.

Ortiz-Lopez R, Li H, Su J, Goytia V, Towbin JA. Ortiz-Lopez R, et al. Among authors: towbin ja. Circulation. 1997 May 20;95(10):2434-40. doi: 10.1161/01.cir.95.10.2434. Circulation. 1997. PMID: 9170407

7

Molecular genetics of long QT syndrome from genes to patients.

Wang Q, Chen Q, Li H, Towbin JA. Wang Q, et al. Among authors: towbin ja. Curr Opin Cardiol. 1997 May;12(3):310-20. doi: 10.1097/00001573-199705000-00013. Curr Opin Cardiol. 1997. PMID: 9243089 Review.

8

Association of parvovirus B19 genome in children with myocarditis and cardiac allograft rejection: diagnosis using the polymerase chain reaction.

Schowengerdt KO, Ni J, Denfield SW, Gajarski RJ, Bowles NE, Rosenthal G, Kearney DL, Price JK, Rogers BB, Schauer GM, Chinnock RE, Towbin JA. Schowengerdt KO, et al. Among authors: towbin ja. Circulation. 1997 Nov 18;96(10):3549-54. doi: 10.1161/01.cir.96.10.3549. Circulation. 1997. PMID: 9396454

9

Prospects for adenovirus-mediated gene therapy of inherited diseases of the myocardium.

Bowles NE, Wang Q, Towbin JA. Bowles NE, et al. Among authors: towbin ja. Cardiovasc Res. 1997 Sep;35(3):422-30. doi: 10.1016/s0008-6363(97)00162-4. Cardiovasc Res. 1997. PMID: 9415286 Review. No abstract available.

10

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation.

Chen Q, Kirsch GE, Zhang D, Brugada R, Brugada J, Brugada P, Potenza D, Moya A, Borggrefe M, Breithardt G, Ortiz-Lopez R, Wang Z, Antzelevitch C, O'Brien RE, Schulze-Bahr E, Keating MT, Towbin JA, Wang Q. Chen Q, et al. Among authors: towbin ja. Nature. 1998 Mar 19;392(6673):293-6. doi: 10.1038/32675. Nature. 1998. PMID: 9521325

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