Zobrazeno 1 - 10
of 29
pro vyhledávání: '"G M, Vincent"'
Autor:
Mina K Chung, G. M. Vincent, Patrick J. Tchou, M. Flippin, J. C. Lee, S. Chen, E. Brown, Randall M. Bryant, R. Rozich, Li Zhang, C. Oberti, F. Zimmerman, R. Sterba, Qing Kenneth Wang, D. Marangi, Przemyslaw Szafranski
Publikováno v:
Clinical Genetics. 63:273-282
Long QT syndrome (LQTS) is the prototype of the cardiac ion channelopathies which cause syncope and sudden death. LQT1, due to mutations of KCNQ1 (KVLQT1), is the most common form. This study describes the genotype-phenotype characteristics in 10 fam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d5d39ffcde79e39ccf1b4e84d59cd18
https://doi.org/10.1034/j.1399-0004.2003.00048.x
https://doi.org/10.1034/j.1399-0004.2003.00048.x
Publikováno v:
Cardiology in Review. 7:44-55
The inherited long QT syndrome is caused by mutations of at least 5 ion channel genes. Mutations of the cardiac sodium ion channel gene and 3 potassium channel genes have been identified to this time. A genetic locus on chromosome 4 has been identifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4128fe88f0c0bd301ca522dcc61c1e19
https://doi.org/10.1097/00045415-199901000-00014
https://doi.org/10.1097/00045415-199901000-00014
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 17:2783-2792
Abstract An interaction between high plasma lipoprotein(a) [Lp(a)], unfavorable plasma lipids, and other risk factors may lead to very high risk for premature CAD. Plasma Lp(a), lipids, and other coronary risk factors were examined in 170 cases with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::695176c8b49a20b49a55543ffa4a3513
https://doi.org/10.1161/01.atv.17.11.2783
https://doi.org/10.1161/01.atv.17.11.2783
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 16:250-255
Abstract Mildly increased serum bilirubin has recently been suggested as a protective factor, possibly reducing the risk of coronary artery disease (CAD) by acting as an antioxidant. We tested this hypothesis by examining serum bilirubin concentratio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8388c6b9a0d6eedcdfc2ee85ed1163e
https://doi.org/10.1161/01.atv.16.2.250
https://doi.org/10.1161/01.atv.16.2.250
Autor:
Roger R. Williams, Steven C. Hunt, Barbara James, G M Vincent, James T. Wu, Paul N. Hopkins, Lily L. Wu
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 15:1314-1320
Abstract To examine the graded risks for coronary artery disease (CAD) associated with plasma homocyst(e)ine [H(e)] and to evaluate the extent to which this risk is mediated by altered vitamin status, we measured plasma concentrations of H(e), vitami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f58cd5863619513d76bbf15ff63abe8e
https://doi.org/10.1161/01.atv.15.9.1314
https://doi.org/10.1161/01.atv.15.9.1314
Autor:
Barbara James, James T. Wu, Paul N. Hopkins, Roger R. Williams, Steven C. Hunt, Lily Wu, G M Vincent
Publikováno v:
Clinical Chemistry. 40:552-561
We measured plasma homocyst(e)ine [H(e)] and other coronary risk factors in 266 patients with early coronary artery disease from 170 families in which two or more siblings were affected and in 168 unmatched controls. The mean H(e) concentration adjus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3dc90f6b69218e91719e192080859ba
https://doi.org/10.1093/clinchem/40.4.552
https://doi.org/10.1093/clinchem/40.4.552
Autor:
G M, Vincent
Publikováno v:
The Physician and sportsmedicine. 26(7)
A 14-year-old girl suffered cardiac arrest, collapsing in midstride while sprinting during a sports event. Her teammates and coaches found her unconscious and gasping for breath. She had no pulse and quickly became cyanotic.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::71235eb70abe590815798753cef8f046
https://pubmed.ncbi.nlm.nih.gov/20086834
https://pubmed.ncbi.nlm.nih.gov/20086834
Autor:
Qing Kenneth Wang, Katherine W. Timothy, S. J. Compton, M. T. Keating, Peter J. Schwartz, L. C. Giuli, J. Shen, Frank G. Yanowitz, A. Medina, Carlo Napolitano, M. H. Lehmann, J. Benhorin, J. L. Robinson, I. Splawski, A. J. Moss, G M Vincent, Li Zhang, Silvia G. Priori, Wojciech Zareba, J. Fox, J. A. Towbin
Publikováno v:
Web of Science
Scopus-Elsevier
ResearcherID
Scopus-Elsevier
ResearcherID
Background —Congenital long-QT syndrome (LQTS) is caused by mutations of genes encoding the slow component of the delayed rectifier current (LQT1, LQT5), the rapid component of the delayed rectifier current (LQT2, LQT6), or the Na + current (LQT3),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71834e5d4d3578083fccc84955fb8b2f
https://pubmed.ncbi.nlm.nih.gov/11104734
https://pubmed.ncbi.nlm.nih.gov/11104734
Publikováno v:
Science. 252:704-706
Genetic factors contribute to heart disease. In this study, linkage analyses have been performed in a family that is predisposed to sudden death from cardiac arrhythmias, the long QT syndrome (LQT). A DNA marker at the Harvey ras-1 locus (H-ras-1) wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::799cb2e34abdfa26cceedfb70b427f11
https://doi.org/10.1126/science.1673802
https://doi.org/10.1126/science.1673802