Zobrazeno 1 - 6 of 6 pro vyhledávání: '"Anne E. Greene"'
1
Transcutaneous Implantation of an Internal Cardioverter Defibrillator in a Small Infant with Recurrent Myocardial Ischemia and Cardiac Arrest Simulating Sudden Infant Death Syndrome
Autor: Gregory B. Di Russo, Yasser Heshmat, John T. Berger, Karen S. Kuehl, Anne E. Greene, Jeffrey P. Moak
Publikováno v: Pacing and Clinical Electrophysiology. 27:112-116
This report describes the implantation of a transcutaneous ICD system using a small patch electrode in the subscapular position, and an active-can device in a 5.3-kg infant. The indication for ICD implantation was recurrent cardiac arrest in the pres
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70e41e88ef07271a38241a152dcaddec
https://doi.org/10.1111/j.1540-8159.2004.00397.x
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3
Targeted point mutagenesis of mouse Kcnq1: phenotypic analysis of mice with point mutations that cause Romano-Ward syndrome in humans
Autor: Karl Pfeifer, Mathew C. Casimiro, Jay C. Vary, Liping Nie, Alexander Grinberg, Bjoern C. Knollmann, Steven N. Ebert, Anne E. Greene, Sing Ping Huang, Syevda G. Sirenko, Ebenezer N. Yamoah
Publikováno v: Genomics. 84(3)
Inherited long QT syndrome is most frequently associated with mutations in KCNQ1, which encodes the primary subunit of a potassium channel. Patients with mutations in KCNQ1 may show only the cardiac defect (Romano-Ward syndrome or RWS) or may also ha
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d0dd5c87ea1faf19864621da6105c8a
https://pubmed.ncbi.nlm.nih.gov/15498462
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4
Familial hypertrophic cardiomyopathy-linked mutant troponin T causes stress-induced ventricular tachycardia and Ca2+-dependent action potential remodeling
Autor: Paulus Kirchhof, Syevda G. Sirenko, Tilmann Schober, James D. Potter, Anne E. Greene, Jessica C. Mackow, Larissa Fabritz, Martin Morad, Bjorn C. Knollmann, Hubertus Degen
Publikováno v: Circulation research. 92(4)
The cardiac troponin T (TnT) I79N mutation has been linked to familial hypertrophic cardiomyopathy and high incidence of sudden death, despite causing little or no cardiac hypertrophy in patients. Transgenic mice expressing mutant human TnT (I79N-Tg)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0e11e05be72bc1946b896a7170e575e
https://pubmed.ncbi.nlm.nih.gov/12600890
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5
Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange– Nielsen Syndrome
Autor: Jay C. Vary, Mathew C. Casimiro, Sing Ping Huang, Steven N. Ebert, Bjorn C. Knollmann, Michael R. Franz, Anne E. Greene, Karl Pfeifer, Alexander Grinberg
KCNQ1 encodes KCNQ1, which belongs to a family of voltage-dependent K + ion channel proteins. KCNQ1 associates with a regulatory subunit, KCNE1, to produce the cardiac repolarizing current, I Ks . Loss-of-function mutations in the human KCNQ1 gene ha
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9dbfb1a7513cd6b99c0f2976d52082e
https://europepmc.org/articles/PMC30171/
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6
The electrophysiology of atrioventricular nodal reentry tachycardia following the Mustard or Senning procedure and its radiofrequency ablation
Autor: Jonathan R. Skinner, Anne M. Dubin, Kathryn K. Collins, Anne E. Greene, George F. Van Hare
Publikováno v: Cardiology in the Young. 15:611
We describe the electrophysiological studies undertaken in four patients with atrioventricular nodal reentry tachycardia in the setting of concordant atrioventricular and discordant ventriculo-arterial connections (transposition). Radiofrequency abla
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7503605b78c442a6d1be715c64f8847a
https://doi.org/10.1017/s1047951105001782
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Plný text Recenzováno Digitální knihovna AV ČR
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