Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Terry Tapscott"'
Autor:
Terry Tapscott, John J. Seger, Oscar Gonzales, Michael H. Gollob, Tanya N. Gollob, Robert Roberts, Linda L. Bachinski
Publikováno v:
Circulation. 104:3030-3033
Background — We recently reported a mutation in the PRKAG2 gene to be responsible for a familial syndrome of ventricular preexcitation, atrial fibrillation, conduction defects, and cardiac hypertrophy. We now report a novel mutation in PRKAG2 causi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbede7e6e3e2d93674b9f5d7266796ac
https://doi.org/10.1161/hc5001.102111
https://doi.org/10.1161/hc5001.102111
Autor:
Jane M. Gregoritch, Miguel A. Quinones, Jean-Bernard Durand, Terry Tapscott, Grazyna Czernuszewicz, Rita Hill, Duanxiang Li, Akihiko Karibe, Jeffrey L. Anderson, Linda L. Bachinski, Robert Roberts, Oscar Gonzalez, Ramon Brugada
Publikováno v:
Circulation. 104:2188-2193
Background Familial dilated cardiomyopathy (FDCM) and hypertrophic cardiomyopathy (FHCM) are the 2 most common forms of primary cardiac muscle diseases. Studies indicate that mutations in sarcomeric proteins are responsible for FHCM and suggest that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9feb32a07413384a26c720b2ef9b2039
https://doi.org/10.1161/hc4301.098285
https://doi.org/10.1161/hc4301.098285
Autor:
Michael H. Gollob, Martin S. Green, Anthony S.-L. Tang, Tanya Gollob, Akihiko Karibe, Al-Sayegh Hassan, Ferhaan Ahmad, Ryan Lozado, Gopi Shah, Lameh Fananapazir, Linda L. Bachinski, Terry Tapscott, Oscar Gonzales, David Begley, Saidi Mohiddin, Robert Roberts
Publikováno v:
New England Journal of Medicine. 344:1823-1831
The Wolff-Parkinson-White syndrome, with a prevalence in Western countries of 1.5 to 3.1 per 1000 persons, causes considerable morbidity and may cause sudden death. We identified two families in which the Wolff-Parkinson-White syndrome segregated as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5635f48407cdb58dfe357e72bba982e7
https://doi.org/10.1056/nejm200106143442403
https://doi.org/10.1056/nejm200106143442403
Autor:
L Brink, J.A. Towbin, Terry Tapscott, J F Hejtmancik, Rita Hill, A Trakhtenbroit, Robert Roberts, P A Brink
Publikováno v:
Circulation. 83:1592-1597
BACKGROUND Familial hypertrophic cardiomyopathy, an inherited primary cardiac abnormality characterized by ventricular hypertrophy, is the leading cause of sudden death in the young. Recent application of restriction fragment length polymorphism mark
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86f48ac104199a5a329dad5a25120c27
https://doi.org/10.1161/01.cir.83.5.1592
https://doi.org/10.1161/01.cir.83.5.1592
Autor:
Jonah Ifegwu, Miguel A. Quinones, Robert Roberts, Qun Tao Yu, Ramon Brugada, Terry Tapscott, Jane M. Gregoritch, Antoine Abchee, S.P. Daiger, Jeffrey L. Anderson, Linda L. Bachinski, Jeffrey A. Towbin, Jean-Bernard Durand, Grazyna Czernuszewicz, Lisa C. Bieling, Rita Hill, Ali J. Marian
Publikováno v:
Circulation. 92:3387-3389
Background Dilated cardiomyopathy, characterized by ventricular dilatation and decreased systolic contraction, is twofold to threefold more common as a cause of heart failure than hypertrophic cardiomyopathy and costs several billion dollars annually
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfef069a4fd986ac2452a62502bbcc3e
https://doi.org/10.1161/01.cir.92.12.3387
https://doi.org/10.1161/01.cir.92.12.3387
Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23
Autor:
Rita Hill, Peter Blackie, Donald G. Weilbaecher, Akihiko Karibe, Ferhaan Ahmad, Robert Roberts, Oscar Gonzalez, Linda L. Bachinski, Terry Tapscott, Michael Furey, Duanxiang Li, Martin J. Gardner
Publikováno v:
Circulation. 98(25)
Background —Arrhythmogenic right ventricular dysplasia (ARVD), a familial cardiomyopathy occurring with a prevalence of 1 in 5000, is characterized by replacement of myocytes with fatty and fibrous tissue. Clinical manifestations include structural
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78cc7cd8e55b8335573c74633d34798b
https://pubmed.ncbi.nlm.nih.gov/9860777
https://pubmed.ncbi.nlm.nih.gov/9860777
Autor:
Ali J. Marian, Grazyna Czernuszewicz, Anna Iglesias, Lluís Mont, Josep Brugada, Terry Tapscott, Linda L. Bachinski, Anna Domingo, Josep Girona, Ramon Brugada, Robert Roberts
Publikováno v:
The New England journal of medicine. 336(13)
Atrial fibrillation, the most common sustained cardiac-rhythm disturbance, affects over 2 million Americans and accounts for one third of all strokes in patients over 65 years of age. The molecular basis for atrial fibrillation is unknown, and pallia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1c5430d5fdf06b852df8f0b93da0b95
https://pubmed.ncbi.nlm.nih.gov/9235505
https://pubmed.ncbi.nlm.nih.gov/9235505
Autor:
Geoffrey P. Sharratt, Donald G. Weilbaecher, Terry Tapscott, Robert Roberts, Oscar Gonzalez, Linda L. Bachinski, Martin J. Gardner, Duanxiang Li, Ferhaan Ahmad, Rita Hill, Akihiko Karibe
Publikováno v:
The American Journal of Human Genetics. (1):148-156
SummaryArrhythmogenic right-ventricular dysplasia (ARVD), a cardiomyopathy inherited as an autosomal-dominant disease, is characterized by fibro-fatty infiltration of the right-ventricular myocardium. Four loci for ARVD have been mapped in the Italia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7c914d0288df7544ed0764bb73ee1a9
Autor:
Rita Hill, Grazyna Z. Czemuszewicz, Lucy Brink, Anatole Trakhtenbrolt, M. Benjamin Perryman, Robert Roberts, Terry Tapscott, Jeffrey A. Towbin, J. Fielding Hejtmancik, Paul A. Brink
Publikováno v:
Journal of the American College of Cardiology. (2):A165
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::034b2c29598425560622c095ed802550