Bauce B - Search Results

1

The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathy.

De Bortoli M, Beffagna G, Bauce B, Lorenzon A, Smaniotto G, Rigato I, Calore M, Li Mura IE, Basso C, Thiene G, Lanfranchi G, Danieli GA, Nava A, Rampazzo A. De Bortoli M, et al. Among authors: bauce b. Eur J Hum Genet. 2010 Jul;18(7):776-82. doi: 10.1038/ejhg.2010.19. Epub 2010 Mar 3. Eur J Hum Genet. 2010. PMID: 20197793 Free PMC article.

2

Silent Threats of the Heart: A Case Series and Narrative Review on Suicide Left Ventricle Post-Aortic Valve Replacement in Patients with Dynamic LVOT Obstruction and Aortic Stenosis.

Romano S, D'Andrea E, Cozac DA, Savo MT, Cecchetto A, Baritussio A, Martini M, Napodano M, Bauce B, Pergola V. Romano S, et al. Among authors: bauce b. J Clin Med. 2024 Sep 19;13(18):5555. doi: 10.3390/jcm13185555. J Clin Med. 2024. PMID: 39337045 Free PMC article. Review.

3

Signal-averaged electrocardiogram in patients with arrhythmogenic right ventricular cardiomyopathy and ventricular arrhythmias.

Nava A, Folino AF, Bauce B, Turrini P, Buja GF, Daliento L, Thiene G. Nava A, et al. Among authors: bauce b. Eur Heart J. 2000 Jan;21(1):58-65. doi: 10.1053/euhj.1999.1733. Eur Heart J. 2000. PMID: 10610745

4

Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy map to chromosome 1q42-43.

Bauce B, Nava A, Rampazzo A, Daliento L, Muriago M, Basso C, Thiene G, Danieli GA. Bauce B, et al. Am J Cardiol. 2000 Mar 1;85(5):573-9. doi: 10.1016/s0002-9149(99)00814-0. Am J Cardiol. 2000. PMID: 11078270

5

Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy.

Nava A, Bauce B, Basso C, Muriago M, Rampazzo A, Villanova C, Daliento L, Buja G, Corrado D, Danieli GA, Thiene G. Nava A, et al. Among authors: bauce b. J Am Coll Cardiol. 2000 Dec;36(7):2226-33. doi: 10.1016/s0735-1097(00)00997-9. J Am Coll Cardiol. 2000. PMID: 11127465 Free article.

6

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2).

Tiso N, Stephan DA, Nava A, Bagattin A, Devaney JM, Stanchi F, Larderet G, Brahmbhatt B, Brown K, Bauce B, Muriago M, Basso C, Thiene G, Danieli GA, Rampazzo A. Tiso N, et al. Among authors: bauce b. Hum Mol Genet. 2001 Feb 1;10(3):189-94. doi: 10.1093/hmg/10.3.189. Hum Mol Genet. 2001. PMID: 11159936

7

Dispersion of ventricular depolarization-repolarization: a noninvasive marker for risk stratification in arrhythmogenic right ventricular cardiomyopathy.

Turrini P, Corrado D, Basso C, Nava A, Bauce B, Thiene G. Turrini P, et al. Among authors: bauce b. Circulation. 2001 Jun 26;103(25):3075-80. doi: 10.1161/01.cir.103.25.3075. Circulation. 2001. PMID: 11425771

8

Signal-averaged electrocardiographic parameter progression as a marker of increased electrical instability in two cases with an overt form of arrhythmogenic right ventricular cardiomyopathy.

Bauce B, Basso C, Nava A. Bauce B, et al. Pacing Clin Electrophysiol. 2002 Mar;25(3):362-4. doi: 10.1046/j.1460-9592.2002.00362.x. Pacing Clin Electrophysiol. 2002. PMID: 11990667

9

Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers.

Bauce B, Rampazzo A, Basso C, Bagattin A, Daliento L, Tiso N, Turrini P, Thiene G, Danieli GA, Nava A. Bauce B, et al. J Am Coll Cardiol. 2002 Jul 17;40(2):341-9. doi: 10.1016/s0735-1097(02)01946-0. J Am Coll Cardiol. 2002. PMID: 12106942 Free article.

10

Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy.

Rampazzo A, Nava A, Malacrida S, Beffagna G, Bauce B, Rossi V, Zimbello R, Simionati B, Basso C, Thiene G, Towbin JA, Danieli GA. Rampazzo A, et al. Among authors: bauce b. Am J Hum Genet. 2002 Nov;71(5):1200-6. doi: 10.1086/344208. Epub 2002 Oct 8. Am J Hum Genet. 2002. PMID: 12373648 Free PMC article.

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