Search Results - "TAPSCOTT, Terry"

Identification of a Gene Responsible for Familial Wolff–Parkinson–White Syndrome by Gollob, Michael H, Gollob, Tanya, Green, Martin S, Tang, Anthony S.-L, Karibe, Akihiko, Hassan, Al-Sayegh, Ahmad, Ferhaan, Lozado, Ryan, Shah, Gopi, Fananapazir, Lameh, Bachinski, Linda L, Tapscott, Terry, Gonzales, Oscar, Begley, David, Mohiddin, Saidi, Roberts, Robert

“…Probable causative mutation was identified in a protein kinase gene (PRKAG2) on chromosome 7. The Wolff–Parkinson–White syndrome is the second most common…”
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Identification of a Genetic Locus for Familial Atrial Fibrillation by Brugada, Ramon, Brugada, Josep, Tapscott, Terry, Czernuszewicz, Grazyna Z, Marian, A.J, Iglesias, Anna, Mont, Lluis, Girona, Josep, Domingo, Anna, Bachinski, Linda L, Roberts, Robert

“…Atrial fibrillation, the most common sustained cardiac-rhythm disturbance, 1 affects more than 2 million Americans, 2 with an overall prevalence of 0.89…”
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Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23 by AHMAD, F, DUANXIANG LI, BACHINSKI, L. L, ROBERTS, R, KARIBE, A, GONZALEZ, O, TAPSCOTT, T, HILL, R, WEILBAECHER, D, BLACKIE, P, FUREY, M, GARDNER, M

“…Arrhythmogenic right ventricular dysplasia (ARVD), a familial cardiomyopathy occurring with a prevalence of 1 in 5000, is characterized by replacement of…”
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The Locus of a Novel Gene Responsible for Arrhythmogenic Right-Ventricular Dysplasia Characterized by Early Onset and High Penetrance Maps to Chromosome 10p12-p14 by Li, Duanxiang, Ahmad, Ferhaan, Gardner, Martin J., Weilbaecher, Donald, Hill, Rita, Karibe, Akihiko, Gonzalez, Oscar, Tapscott, Terry, Sharratt, Geoffrey P., Bachinski, Linda L., Roberts, Robert

“…Arrhythmogenic right-ventricular dysplasia (ARVD), a cardiomyopathy inherited as an autosomal-dominant disease, is characterized by fibro-fatty infiltration of…”
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Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32 by DURAND, J.-B, BACHINSKI, L. L, BRUGADA, R, DAIGER, S, GREGORITCH, J. M, ANDERSON, J. L, QUINONES, M, TOWBIN, J. A, ROBERTS, R, BIELING, L. C, CZERNUSZEWICZ, G. Z, ABCHEE, A. B, QUN TAO YU, TAPSCOTT, T, HILL, R, IFEGWU, J, MARIAN, A. J

“…Dilated cardiomyopathy, characterized by ventricular dilatation and decreased systolic contraction, is twofold to threefold more common as a cause of heart…”
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Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy by GOLLOB, Michael H, SEGER, John J, GOLLOB, Tanya N, TAPSCOTT, Terry, GONZALES, Oscar, BACHINSKI, Linda, ROBERTS, Robert

“…We recently reported a mutation in the PRKAG2 gene to be responsible for a familial syndrome of ventricular preexcitation, atrial fibrillation, conduction…”
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Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy by DUANXIANG LI, CZERNUSZEWICZ, Grazyna Z, QUINONES, Miguel, BACHINSKI, Linda L, ROBERTS, Robert, GONZALEZ, Oscar, TAPSCOTT, Terry, KARIBE, Akihiko, DURAND, Jean-Bernard, BRUGADA, Ramon, HILL, Rita, GREGORITCH, Jane M, ANDERSON, Jeffrey L

“…Familial dilated cardiomyopathy (FDCM) and hypertrophic cardiomyopathy (FHCM) are the 2 most common forms of primary cardiac muscle diseases. Studies indicate…”
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Localization of gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse US population by HEJTMANCIK, J. F, BRINK, P. A, TOWBIN, J, HILL, R, BRINK, L, TAPSCOTT, T, TRAKHTENBROIT, A, ROBERTS, R

“…Familial hypertrophic cardiomyopathy, an inherited primary cardiac abnormality characterized by ventricular hypertrophy, is the leading cause of sudden death…”
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Localization of the gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse American population by Hejtmancik, J.Fielding, Brink, Paul A., Towbin, Jeffrey, Hill, Rita, Brink, Lucy, Czemuszewicz, Grazyna Z, Tapscott, Terry, Trakhtenbrolt, Anatole, Perryman, M.Benjamin, Roberts, Robert

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