Zobrazeno 1 - 10
of 296
pro vyhledávání: '"Vincent GM"'
Autor:
Geukers, Vincent GM, Oudshoorn, Johanna H, Taminiau, Jan AJM, van der Ent, Cornelis K, Schilte, Piet, Ruiter, An FC, Ackermans, Mariëtte T, Endert, Erik, Jonkers-Schuitema, Cora F, Heymans, Hugo SA, Sauerwein, Hans P
Publikováno v:
In The American Journal of Clinical Nutrition March 2005 81(3):605-610
Autor:
Gardiner Susan E, Norelli John L, Silva Nihal de, Fazio Gennaro, Peil Andreas, Malnoy Mickael, Horner Mary, Bowatte Deepa, Carlisle Charmaine, Wiedow Claudia, Wan Yizhen, Bassett Carole L, Baldo Angela M, Celton Jean-Marc, Richter Klaus, Aldwinckle Herb S, Bus Vincent GM
Publikováno v:
BMC Genetics, Vol 13, Iss 1, p 25 (2012)
Abstract Background Breeding of fire blight resistant scions and rootstocks is a goal of several international apple breeding programs, as options are limited for management of this destructive disease caused by the bacterial pathogen Erwinia amylovo
Externí odkaz:
https://doaj.org/article/82675465f30e48459644bd14c08845f7
Autor:
Vincent Gm, McPeak H
Publikováno v:
The Physician and Sportsmedicine. 28:31-39
IN BRIEF: Commotio cordis is arrhythmia or sudden death from low-impact, blunt trauma to the chest without apparent heart injury. Ventricular fibrillation is the most common associated arrhythmia, and heart block, bundle branch block, and ST-segment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a45473bc3c66b35ba2adf5fd804b7c2
https://doi.org/10.3810/psm.2000.11.1285
https://doi.org/10.3810/psm.2000.11.1285
Autor:
Vincent Gm
Publikováno v:
The Physician and Sportsmedicine. 26:59-62
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=doi_________::39bef80ac12d0d4b072144e1bd09874b
https://doi.org/10.3810/psm.1998.07.1091
https://doi.org/10.3810/psm.1998.07.1091
Autor:
Vincent Gm
Publikováno v:
Annual Review of Medicine. 49:263-274
The congenital long QT syndrome is an autosomal-dominant genetic disorder of cardiac electrical repolarization. It is caused by mutations of at least six genes, of which four, all encoding for cardiac ion channels, have been identified: KVLQT1, HERG,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f42eaa1a4f18480e105d2512f908859
https://doi.org/10.1146/annurev.med.49.1.263
https://doi.org/10.1146/annurev.med.49.1.263
Autor:
Peter J. Schwartz, T. De Jager, Mark E. Curran, M T Keating, J.A. Towbin, J. M. Millholland, Gregory M. Landes, Igor Splawski, Katherine W. Timothy, T. J. VanRaay, Donald L. Atkinson, Timothy C. Burn, Timothy D. Connors, Qing Wang, Vincent Gm, Jiaxiang Shen, Arthur J. Moss
Publikováno v:
Nature Genetics. 12:17-23
Genetic factors contribute to the risk of sudden death from cardiac arrhythmias. Here, positional cloning methods establish KVLQT1 as the chromosome 11-linked LQT1 gene responsible for the most common inherited cardiac arrhythmia. KVLQT1 is strongly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92869456f5ca6916ed214d37ee56ad42
https://doi.org/10.1038/ng0196-17
https://doi.org/10.1038/ng0196-17
Autor:
Arthur J. Moss, Vincent Gm, Katherine W. Timothy, Mark Leppert, Mark T. Keating, M Curran, Donald L. Atkinson
Publikováno v:
Journal of Clinical Investigation. 92:799-803
Autosomal dominant long QT syndrome (LQT) is an inherited disorder that causes syncope and sudden death from cardiac arrhythmias. In genetic linkage studies of seven unrelated families we mapped a gene for LQT to the short arm of chromosome 11 (11p15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::787c1c0540b71f804faa4430c098fba0
https://doi.org/10.1172/jci116653
https://doi.org/10.1172/jci116653
Autor:
Vincent Gm
Publikováno v:
Heart. 86:12-14
In recent years the molecular genetics and pathophysiology of long QT syndrome (LQTS), hypertrophic cardiomyopathy (HCM), and Marfan syndrome have been extensively studied. Each disease shows highly variable expression and reduced penetrance of all k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9918d91752e524f2afc491b4c1330534
https://doi.org/10.1136/heart.86.1.12
https://doi.org/10.1136/heart.86.1.12
Autor:
Chen, S, Zhang, L, Bryant, RM, Vincent, GM, Flippin, M, Lee, JC, Brown, E, Zimmerman, F, Rozich, R, Szafranski, P, Oberti, C, Sterba, R, Marangi, D, Tchou, PJ, Chung, MK, Wang, Q
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=pmid________::ee8c9842ddae2de99b2357e3509577e7
https://europepmc.org/articles/PMC1579805/
https://europepmc.org/articles/PMC1579805/
Autor:
Vincent Gm, Aharon Medina, Mark L. Andrews, Katherine W. Timothy, Jennifer L. Robinson, Peter J. Schwartz, Emanuela H. Locati, Li Zhang, William J. Hall, Arthur J. Moss, Silvia G. Priori, Wojciech Zareba, Jesaia Benhorin, Carlo Napolitano, Richard S. Crampton, J.A. Towbin
Publikováno v:
Circulation. 101(6)
Background —β-blockers are routinely prescribed in congenital long-QT syndrome (LQTS), but the effectiveness and limitations of β-blockers in this disorder have not been evaluated. Methods and Results —The study population comprised 869 LQTS pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16c194cf3f4d1004978be32d0656e655
https://pubmed.ncbi.nlm.nih.gov/12506941
https://pubmed.ncbi.nlm.nih.gov/12506941