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Clinical genetics
Citations 321-330 of 397 total displayed.
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Past content
(since Feb 1999):
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- Clinical Investigations and Reports
Genetic Variation in Coagulation and Fibrinolytic Proteins and Their Relation With Acute Myocardial Infarction: A Systematic Review
- S. Matthijs Boekholdt, Nick R. Bijsterveld, Arno H.M. Moons, Marcel Levi, Harry R. Büller, and Ron J.G. Peters
Circulation 2001;104:3063-3068, doi:10.1161/hc5001.100793
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- Clinical Investigations and Reports
Complete Transposition of the Great Arteries: Patterns of Congenital Heart Disease in Familial Precurrence
- Maria Cristina Digilio, Brett Casey, Alessandra Toscano, Raffaele Calabrò, Giuseppe Pacileo, Maurizio Marasini, Elena Banaudi, Aldo Giannotti, Bruno Dallapiccola, and Bruno Marino
Circulation 2001;104:2809-2814, doi:10.1161/hc4701.099786
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- Clinical Investigations and Reports
NKX2.5 Mutations in Patients With Tetralogy of Fallot
- Elizabeth Goldmuntz, Elizabeth Geiger, and D. Woodrow Benson
Circulation 2001;104:2565-2568, doi:10.1161/hc4601.098427
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- Clinical Investigations and Reports
Novel Cardiac Troponin T Mutation as a Cause of Familial Dilated Cardiomyopathy
- Duanxiang Li, Grazyna Z. Czernuszewicz, Oscar Gonzalez, Terry Tapscott, Akihiko Karibe, Jean-Bernard Durand, Ramon Brugada, Rita Hill, Jane M. Gregoritch, Jeffrey L. Anderson, Miguel Quiñones, Linda L. Bachinski, and Robert Roberts
Circulation 2001;104:2188-2193, doi:10.1161/hc4301.098285
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- Clinical Investigations and Reports
Hypertrophic Cardiomyopathy: Histopathological Features of Sudden Death in Cardiac Troponin T Disease
- Amanda M. Varnava, Perry M. Elliott, Christina Baboonian, Fergus Davison, Michael J. Davies, and William J. McKenna
Circulation 2001;104:1380-1384, doi:10.1161/hc3701.095952
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- Clinical Investigations and Reports
Point Mutation in the Stalk of Angiotensin-Converting Enzyme Causes a Dramatic Increase in Serum Angiotensin-Converting Enzyme But No Cardiovascular Disease
- Cornelis Kramers, Sergei M. Danilov, Jaap Deinum, Irina V. Balyasnikova, Nicole Scharenborg, Maaike Looman, Frans Boomsma, Marinus H. de Keijzer, Cornelia van Duijn, Sabrina Martin, Florent Soubrier, and Gosse J. Adema
Circulation 2001;104:1236-1240, doi:10.1161/hc3601.095932
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- Clinical Investigations and Reports
Platelet Glycoprotein Ib HPA-2 Met/VNTR B Haplotype as a Genetic Predictor of Myocardial Infarction and Sudden Cardiac Death
- Jussi Mikkelsson, Markus Perola, Antti Penttilä, and Pekka J. Karhunen
Circulation 2001;104:876-880, doi:10.1161/hc3301.094907
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- Clinical Investigations and Reports
Clinical Implications for Affected Parents and Siblings of Probands With Long-QT Syndrome
- John Kimbrough, Arthur J. Moss, Wojciech Zareba, Jennifer L. Robinson, W. Jackson Hall, Jesaia Benhorin, Emanuela H. Locati, Aharon Medina, Carlo Napolitano, Silvia Priori, Peter J. Schwartz, Katherine Timothy, Jeffrey A. Towbin, G. Michael Vincent, and Li Zhang
Circulation 2001;104:557-562, doi:10.1161/hc3001.093501
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- Clinical Investigations and Reports
Autosomal Recessive Catecholamine- or Exercise-Induced Polymorphic Ventricular Tachycardia : Clinical Features and Assignment of the Disease Gene to Chromosome 1p13-21
- Hadas Lahat, Michael Eldar, Etgar Levy-Nissenbaum, Tangiz Bahan, Eitan Friedman, Asad Khoury, Avraham Lorber, Daniel L. Kastner, Boleslaw Goldman, and Elon Pras
Circulation 2001;103:2822-2827
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- Clinical Investigations and Reports
G20210A Prothrombin Gene Polymorphism and Prothrombin Activity in Subjects With or Without Angiographically Documented Coronary Artery Disease
- Carla Russo, Domenico Girelli, Oliviero Olivieri, Patrizia Guarini, Franco Manzato, Francesca Pizzolo, Barbara Zaia, Alessandro Mazzucco, and Roberto Corrocher
Circulation 2001;103:2436-2440
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