Matteo Vatta

Matteo Vatta

UNVERIFIED PROFILE

Are you Matteo Vatta?   Register this Author

Register author
Matteo Vatta

Matteo Vatta

Publications by authors named "Matteo Vatta"

Are you Matteo Vatta?   Register this Author

92Publications

1620Reads

45Profile Views

Angiotensin-related genetic determinants of cardiovascular disease in patients undergoing hemodialysis.

Nephrol Dial Transplant 2019 Nov;34(11):1924-1931

Division of Nephrology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/ndt/gfy191DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826165PMC
November 2019

Clinical characterisation of a novel variant associated with progressive malignant arrhythmia and dilated cardiomyopathy.

Cardiol Young 2019 Oct;29(10):1257-1263

Department of Pediatrics, Division of Pediatric Cardiology, Indiana University School of Medicine, Indianapolis, IN, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1017/S1047951119001860DOI Listing
October 2019

Fibroblast Growth Factor 23 Genotype and Cardiovascular Disease in Patients Undergoing Hemodialysis.

Am J Nephrol 2019 22;49(2):125-132. Epub 2019 Jan 22.

Division of Nephrology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA,

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000496060DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6473180PMC
January 2019

Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).

Genet Med 2018 09 14;20(9):899-909. Epub 2018 Jun 14.

Departments of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/s41436-018-0039-zDOI Listing
September 2018

Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline.

J Card Fail 2018 May 19;24(5):281-302. Epub 2018 Mar 19.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana; Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana.

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S10719164183010
Publisher Site
http://dx.doi.org/10.1016/j.cardfail.2018.03.004DOI Listing
May 2018

Editorial commentary: Targeting TYMP for cardiovascular disease: How far are we?

Authors:
Matteo Vatta

Trends Cardiovasc Med 2018 04 7;28(3):172-173. Epub 2017 Dec 7.

Invitae, San Francisco, CA; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN. Electronic address:

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S10501738173018
Publisher Site
http://dx.doi.org/10.1016/j.tcm.2017.12.002DOI Listing
April 2018

Genetic analyses in a bonobo (Pan paniscus) with arrhythmogenic right ventricular cardiomyopathy.

Sci Rep 2018 03 12;8(1):4350. Epub 2018 Mar 12.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/s41598-018-22334-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847517PMC
March 2018

Editorial: Current Challenges in Cardiovascular Molecular Diagnostics.

Front Cardiovasc Med 2017 1;4:54. Epub 2017 Sep 1.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, United States.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3389/fcvm.2017.00054DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5585151PMC
September 2017

A Novel SCN5A Mutation Associated with Drug Induced Brugada Type ECG.

PLoS One 2016 25;11(8):e0161872. Epub 2016 Aug 25.

Cardiovascular and Respiratory Medicine, Shiga Univ. School of Medicine, Otsu, Japan.

View Article

Download full-text PDF

Source
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0161872PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999187PMC
August 2017

Calcium-Sensing Receptor Genotype and Response to Cinacalcet in Patients Undergoing Hemodialysis.

Clin J Am Soc Nephrol 2017 Jul 19;12(7):1128-1138. Epub 2017 Jun 19.

Division of Nephrology, Department of Medicine, Stanford School of Medicine, Stanford, California.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.2215/CJN.11141016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498355PMC
July 2017

Validation and Utilization of a Clinical Next-Generation Sequencing Panel for Selected Cardiovascular Disorders.

Front Cardiovasc Med 2017 15;4:11. Epub 2017 Mar 15.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA; Division of Cardiology, Department of Medicine, Krannert Institute of Cardiology, Indiana University School of Medicine, Indianapolis, IN, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3389/fcvm.2017.00011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350117PMC
March 2017

Intragenic CFTR Duplication and 5T/12TG Variant in a Patient with Non-Classic Cystic Fibrosis.

Sci Rep 2016 12 20;6:38776. Epub 2016 Dec 20.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/srep38776DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5172161PMC
December 2016

Molecular Diagnosis of Myotonic Dystrophy.

Curr Protoc Hum Genet 2016 10 11;91:9.29.1-9.29.19. Epub 2016 Oct 11.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/cphg.22DOI Listing
October 2016

Arrhythmogenic calmodulin mutations impede activation of small-conductance calcium-activated potassium current.

Heart Rhythm 2016 08 7;13(8):1716-23. Epub 2016 May 7.

Krannert Institute of Cardiology and Division of Cardiology, Department of Medicine, Indiana University, Indianapolis, Indiana. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.hrthm.2016.05.009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4958519PMC
August 2016

Editorial Commentary: Reprogramming autologous mesenchymal stem cells to regenerate the lost myocardium in chronic heart failure: Reboot and restore?

Authors:
Matteo Vatta

Trends Cardiovasc Med 2016 07 4;26(5):405-6. Epub 2016 Mar 4.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN; Division of Cardiology, Department of Medicine, Krannert Institute of Cardiology, Indianapolis, IN. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.tcm.2016.02.001DOI Listing
July 2016

Mitochondria, contractile apparatus, and ion channels in the failing myocardium: Special relationships or dangerous liaisons?

Authors:
Matteo Vatta

Heart Rhythm 2016 05 25;13(5):1140-1141. Epub 2016 Jan 25.

Department of Medical and Molecular Genetics, and Krannert Institute of Cardiology and the Division of Cardiology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.hrthm.2016.01.023DOI Listing
May 2016

MY APPROACH to genetic testing in cardiology practice.

Authors:
Matteo Vatta

Trends Cardiovasc Med 2016 Jan 22;26(1):97-8. Epub 2015 Oct 22.

Department of Medical and Molecular Genetics, Indiana University School of Medicine; Department of Clinical Medicine, Indiana University School of Medicine. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.tcm.2015.05.018DOI Listing
January 2016

ZASP interacts with the mechanosensing protein Ankrd2 and p53 in the signalling network of striated muscle.

PLoS One 2014 19;9(3):e92259. Epub 2014 Mar 19.

International Centre for Genetic Engineering and Biotechnology, Trieste, Italy; Centro di Ricerca Interdipartimentale per le Biotecnologie Innovative, University of Padua, Padova, Italy.

View Article

Download full-text PDF

Source
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0092259PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3960238PMC
December 2015

Use of genetic testing to identify sudden cardiac death syndromes.

Trends Cardiovasc Med 2015 Nov 12;25(8):738-48. Epub 2015 Mar 12.

Department of Medicine, Krannert Institute of Cardiology, Indiana University School of Medicine, Indianapolis, IN.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.tcm.2015.03.007DOI Listing
November 2015

Genetic mutations in African patients with atrial fibrillation: Rationale and design of the Study of Genetics of Atrial Fibrillation in an African Population (SIGNAL).

Am Heart J 2015 Sep 14;170(3):455-64.e5. Epub 2015 Jun 14.

AMPATH Partnership, Eldoret, Kenya; Department of Medicine, Indiana University, Indianapolis, IN; Department of Medicine, School of Medicine, College of Health Sciences, Moi University, Eldoret, Kenya.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ahj.2015.06.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4575772PMC
September 2015

Coronary artery disease: the magnificent fifty?

Trends Cardiovasc Med 2015 Apr 6;25(3):179-80. Epub 2014 Nov 6.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN; Krannert Institute of Cardiology, Indianapolis, IN; Division of Cardiology, Department of Medicine, Indiana University School of Medicine, Indianapolis, IN. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.tcm.2014.10.027DOI Listing
April 2015

Dysfunction in the βII spectrin-dependent cytoskeleton underlies human arrhythmia.

Circulation 2015 Feb 28;131(8):695-708. Epub 2015 Jan 28.

From Dorothy M. Davis Heart and Lung Research Institute (S.A.S., A.C.S., J.C., C.F.K., S.C.L., I.M.B., V.P.L., M.M., I.P., L.D.H., T.R.W., P.W., R.W., P.F.B., P.M.J., A.K., R.S.H., M.S., J.M., C.A.C., T.J.H., P.J.M.), Department of Internal Medicine, Division of Cardiovascular Medicine (S.A.S., R.W., P.F.B., P.J.M.), Department of Internal Medicine, Division of Human Genetics (A.C.S., P.M.J.), Department of Physiology and Cell Biology (J.C., C.F.K., S.C.L., M.M., I.P., L.D.H., T.R.W., P.W., P.M.J., P.J.M.), and Department of Surgery (A.K., R.S.H., M.S., J.M.), The Ohio State University Wexner Medical Center; Columbus; College of Pharmacy (I.M.B., V.P.L., C.A.C.) and Department of Biomedical Engineering, College of Engineering (T.J.H.), The Ohio State University, Columbus; Division of Life Science and Institute for Advanced Study, Hong Kong University of Science and Technology, Clear Water Bay Kowloon, Hong Kong (Z.W., M.Z.); Department of Biology, South University of Science and Technology of China, Shenzhen, Guangdong, China (Z.W.); Institute of Pharmacology, Faculty of Medicine, University Duisburg-Essen, Essen, Germany (N.V., D.D.); Krannert Institute of Cardiology and Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis (D.B., K.G.S., M.V.); and Department of Neuroscience, Baylor College of Medicine; Houston, TX (C.Z., M.N.R.).

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1161/CIRCULATIONAHA.114.013708DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4342332PMC
February 2015

Taking a peek at the border of the sarcomere in heart failure and cardiac resynchronization therapy.

J Mol Cell Cardiol 2014 Sep 2;74:1-3. Epub 2014 May 2.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indianapolis, IN, USA; Krannert Institute of Cardiology and the Division of Cardiology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indianapolis, IN, USA. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.yjmcc.2014.04.015DOI Listing
September 2014

Evidence for replicative mechanism in a CHD7 rearrangement in a patient with CHARGE syndrome.

Am J Med Genet A 2013 Dec 16;161A(12):3182-6. Epub 2013 Aug 16.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas; Krannert Institute of Cardiology, Indiana University School of Medicine, Indianapolis, Indiana; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.36178DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3926511PMC
December 2013

Biological pacemakers: are we at the dawn of a new treatment era?

J Am Coll Cardiol 2013 Mar 6;61(11):1202-3. Epub 2013 Feb 6.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jacc.2012.11.063DOI Listing
March 2013

CaMKII and ryanodine receptor as new antiarrhythmic targets.

Heart Rhythm 2012 Dec 14;9(12):2042-3. Epub 2012 Sep 14.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.hrthm.2012.09.011DOI Listing
December 2012

Myocardial alternative RNA splicing and gene expression profiling in early stage hypoplastic left heart syndrome.

PLoS One 2012 27;7(1):e29784. Epub 2012 Jan 27.

Division of Cardiothoracic Surgery, University of Miami Miller School of Medicine and Holtz Children's Hospital/Jackson Memorial Hospital, Miami, Florida, United States of America.

View Article

Download full-text PDF

Source
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0029784PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3267718PMC
July 2012

A novel STXBP1 mutation causes focal seizures with neonatal onset.

J Child Neurol 2012 Jun;27(6):811-4

Department of Molecular and Human Genetics, Baylor College of Medicine, TX 77030, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/0883073811435246DOI Listing
June 2012

Coffin-Lowry syndrome and left ventricular noncompaction cardiomyopathy with a restrictive pattern.

Am J Med Genet A 2011 Dec 18;155A(12):3030-4. Epub 2011 Oct 18.

The Section of Pediatric Cardiology, Texas Children's Hospital, Houston, Texas, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.33856DOI Listing
December 2011

LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype.

Cardiogenetics 2011 Oct;1(1)

Division of Cardiovascular Medicine, Department of Medicine, University of Wisconsin, Madison, WI, USA ; Department of Forensic Pathology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong, China.

View Article

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852898PMC
http://dx.doi.org/10.4081/cardiogenetics.2011.e13DOI Listing
October 2011

Left ventricular non compaction in children.

Congenit Heart Dis 2010 Sep-Oct;5(5):384-97

Department of Cardiology, Second University of Naples, Monaldi Hospital, Naples, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1747-0803.2010.00446.xDOI Listing
March 2011

Genetics of heart failure and sudden death.

Heart Fail Clin 2010 Oct;6(4):507-14, ix

Department of Pediatrics Cardiology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX 77030, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.hfc.2010.05.008DOI Listing
October 2010

[Molecular basis of arrhythmias in patients with genetically-based cardiomyopathies: when the cytoskeleton meets the ion channels].

Authors:
Matteo Vatta

G Ital Cardiol (Rome) 2010 Oct;11(10):746-52

Department of Pediatrics (Cardiology) and Molecular Physiology and Biophysics, Baylor College of Medicine and Texas Children's Hospital, Houston, TX 77030, USA.

View Article

Download full-text PDF

Source
October 2010

Differential changes in TGF-β/BMP signaling pathway in the right ventricular myocardium of newborns with hypoplastic left heart syndrome.

J Card Fail 2010 Aug 4;16(8):628-34. Epub 2010 May 4.

Division of Cardiothoracic Surgery, University of Miami Miller School of Medicine and Holtz Children's Hospital, Miami, FL, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.cardfail.2010.03.007DOI Listing
August 2010

Genetic variants and ECG pattern variability in long QT syndrome: how far are we?

Authors:
Matteo Vatta

Heart Rhythm 2010 Jul 18;7(7):904-5. Epub 2010 Apr 18.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.hrthm.2010.04.015DOI Listing
July 2010

LAMP2 microdeletions in patients with Danon disease.

Circ Cardiovasc Genet 2010 Apr 20;3(2):129-37. Epub 2010 Feb 20.

Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1161/CIRCGENETICS.109.901785DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2895413PMC
April 2010

Short-term mechanical unloading and reverse remodeling of failing hearts in children.

J Heart Lung Transplant 2010 Jan 26;29(1):98-104. Epub 2009 Sep 26.

Department of Pediatric Cardiology, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas 77030, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.healun.2009.06.030DOI Listing
January 2010

Genetic modulation of brugada syndrome by a common polymorphism.

J Cardiovasc Electrophysiol 2009 Oct 22;20(10):1137-41. Epub 2009 Jun 22.

Montreal Heart Institute and University of Montreal, Montreal, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1540-8167.2009.01508.xDOI Listing
October 2009

A novel SCN5A mutation V1340I in Brugada syndrome augmenting arrhythmias during febrile illness.

Heart Rhythm 2009 Sep 18;6(9):1318-26. Epub 2009 May 18.

Electrophysiology Research Laboratory, Texas Heart Institute/St. Luke's Episcopal Hospital, Houston, Texas 77030, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.hrthm.2009.05.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2753513PMC
September 2009

A nonsense SCN5A mutation associated with Brugada-type electrocardiogram and intraventricular conduction defects.

Pacing Clin Electrophysiol 2009 Sep;32(9):1231-6

Electrophysiology Research Laboratory, Texas Heart Institute/St. Luke's Episcopal Hospital, Houston, Texas.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1540-8159.2009.02470.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2747666PMC
September 2009

Impaired binding of ZASP/Cypher with phosphoglucomutase 1 is associated with dilated cardiomyopathy.

Cardiovasc Res 2009 Jul 17;83(1):80-8. Epub 2009 Apr 17.

Department of Molecular Pathogenesis, Medical Research Institute, Tokyo Medical and Dental University, 1-5-45 Bunkyo-Ku, Tokyo, Japan.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/cvr/cvp119DOI Listing
July 2009

A novel Alu-mediated Xq28 microdeletion ablates TAZ and partially deletes DNL1L in a patient with Barth syndrome.

Am J Med Genet A 2009 May;149A(5):1082-5

Department of Pediatrics, Division of Cardiology, Children's Hospital of Michigan, The Carman and Ann Adams, Wayne State University School of Medicine, Detroit, Michigan, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.32822DOI Listing
May 2009

Intronic variants and splicing errors in cardiovascular diseases.

Authors:
Matteo Vatta

Heart Rhythm 2009 Feb 6;6(2):219-20. Epub 2008 Dec 6.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.hrthm.2008.12.006DOI Listing
February 2009

Remodeling of dystrophin and sarcomeric Z-band occurs in pediatric cardiomyopathies: a unifying mechanism for force transmission defect.

J Cardiovasc Med (Hagerstown) 2009 Feb;10(2):149-56

Department of Pediatrics (Cardiology), Baylor College of Medicine, Houston, Texas, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.2459/JCM.0b013e328318954cDOI Listing
February 2009

Danon disease as a cause of autophagic vacuolar myopathy.

Congenit Heart Dis 2007 Nov-Dec;2(6):404-9

Baylor College of Medicine, Department of Pediatrics, Houston, TX 77030, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1747-0803.2007.00132.xDOI Listing
June 2008

Myocardial Fas ligand expression increases susceptibility to AZT-induced cardiomyopathy.

Cardiovasc Toxicol 2007 18;7(4):255-63. Epub 2007 Oct 18.

Department of Pediatrics, Section of Cardiology, Baylor College of Medicine, Houston, TX 77030, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s12012-007-9004-9DOI Listing
February 2008

Myocardial infarction, viral infection, and the cytoskeleton final common pathways of a common disease?

J Am Coll Cardiol 2007 Dec 19;50(23):2215-7. Epub 2007 Nov 19.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jacc.2007.08.034DOI Listing
December 2007

A common SCN5A variant alters the responsiveness of human sodium channels to class I antiarrhythmic agents.

J Cardiovasc Electrophysiol 2007 Apr 10;18(4):434-40. Epub 2007 Jan 10.

Electrophysiology Research Laboratory, Texas Heart Institute/St. Luke's Episcopal Hospital, Houston, Texas 77030, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1540-8167.2007.00777.xDOI Listing
April 2007

Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3.

Heart Rhythm 2007 Feb 6;4(2):161-6. Epub 2006 Dec 6.

Mayo Medical School, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.hrthm.2006.11.030DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2836535PMC
February 2007

Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy.

Biochem Biophys Res Commun 2006 Dec 9;351(4):896-902. Epub 2006 Nov 9.

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.bbrc.2006.10.119DOI Listing
December 2006

Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome.

Circulation 2006 Nov 23;114(20):2104-12. Epub 2006 Oct 23.

Department of Pediatrics (Cardiology), Baylor College of Medicine, Texas Children's Hospital, Houston, TX 77030, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1161/CIRCULATIONAHA.106.635268DOI Listing
November 2006

Mutations in KCNE1 in long QT syndrome (LQTS): insights into mechanism of LQTS and drug sensitivity?

Heart Rhythm 2006 Sep 21;3(9):1041-2. Epub 2006 Jul 21.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.hrthm.2006.07.020DOI Listing
September 2006

Cytoskeletal basis of ion channel function in cardiac muscle.

Future Cardiol 2006 Jul;2(4):467-76

Baylor College of Medicine, Pediatrics (Cardiology), Texas Children's Hospital, 6621 Fannin St, FC 430.09, Houston, TX 77030, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.2217/14796678.2.4.467DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2747736PMC
July 2006

Genotype-phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin.

Mol Genet Metab 2006 May 13;88(1):78-85. Epub 2005 Dec 13.

Department of Internal Medicine, Division of Cardiovascular Diseases, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ymgme.2005.10.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2756511PMC
May 2006

Altered expression of dystrophin within the thoracic aorta in coarctation.

Cardiol Young 2005 Feb;15(1):73-4

Department of Pediatrics (Cardiology), Baylor College of Medicine, and Texas Children's Hospital, Houston, Texas 77030, USA.

View Article

Download full-text PDF

Source
http://www.journals.cambridge.org/abstract_S1047951105000144
Publisher Site
http://dx.doi.org/10.1017/S1047951105000144DOI Listing
February 2005

Cardiotropic viruses in the myocardium of children with end-stage heart disease.

J Heart Lung Transplant 2004 Sep;23(9):1046-52

Department of Pathology, Children Hospital Bambino Gesù, Rome, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.healun.2003.08.015DOI Listing
September 2004

Assessment of the CTNNA3 gene encoding human alpha T-catenin regarding its involvement in dilated cardiomyopathy.

Hum Genet 2003 Mar 5;112(3):227-36. Epub 2002 Dec 5.

Department of Molecular Biomedical Research, Flanders Interuniversity Institute for Biotechnology, Ghent University, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00439-002-0857-5DOI Listing
March 2003

Genetics and cardiac arrhythmias.

Adv Pediatr 2002 ;49:87-129

Department of Pediatrics, Texas Children's Hospital and Baylor College of Medicine, Houston, USA.

View Article

Download full-text PDF

Source
January 2003

Novel mutations in domain I of SCN5A cause Brugada syndrome.

Mol Genet Metab 2002 Apr;75(4):317-24

Department of Pediatrics (Cardiology), Baylor College of Medicine, Houston, TX, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/S1096-7192(02)00006-9DOI Listing
April 2002