Search Results - "MOSS, A. J"

Online derivatization for hourly measurements of gas- and particle-phase semi-volatile oxygenated organic compounds by thermal desorption aerosol gas chromatography (SV-TAG) by Isaacman, G, Kreisberg, N. M, Yee, L. D, Worton, D. R, Chan, A. W. H, Moss, J. A, Hering, S. V, Goldstein, A. H

“…Laboratory oxidation studies have identified a large number of oxygenated organic compounds that can be used as tracers to understand sources and oxidation…”
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Design of peptide imaging agents for whole-body and intraoperative molecular imaging by Moss, J A, Vāvere, A L, Azhdarinia, A

“…Due to the growing toolkit of targeted contrast agents, molecular imaging continues to play a prominent role in the clinical care of cancer. Peptide-based…”
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Safety and pharmacokinetics of aciclovir in women following release from a silicone elastomer vaginal ring by KELLER, M. J, MALONE, A. M, GUERRERO, D, MOSS, J. A, BAUM, M. M, SMITH, T. J, HEROLD, B. C, CARPENTER, C. A, LO, Y, HUANG, M, COREY, L, WILLIS, R, NGUYEN, C, KENNEDY, S, GUNAWARDANA, M

“…Systemic aciclovir and its prodrug valaciclovir are effective in treating and reducing recurrences of genital herpes simplex virus (HSV) and reducing…”
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Quantification of relative proportions of intact cells in microbiological samples using the example of Cryptosporidium parvum oocysts by Agulló‐Barceló, M., Moss, J.A., Green, J., Gillespie, S., Codony, F., Lucena, F., Nocker, A.

“…The fast analysis of relative proportions of live and dead cells can be of great value whether for comparing inactivation efficiencies of different biocidal…”
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Pathogens in Crassostrea ariakensis and other Asian oyster species : implications for non-native oyster introduction to Chesapeake Bay by MOSS, J. A, BURRESON, E. M, CORDES, J. F, DUNGAN, C. F, BROWN, G. D, WANG, A, WU, X, REECE, K. S

“…With the drastic decline of eastern oyster Crassostrea virginica populations in the Chesapeake Bay due to over-fishing, diseases and habitat destruction, there…”
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Spectrum of mutations in long-QT syndrome genes : KVLQT1, HERG, SCN5A, KCNE1, and KCNE2 by SPLAWSKI, I, JIAXIANG SHEN, KEATING, M. T, TIMOTHY, K. W, LEHMANN, M. H, PRIORI, S, ROBINSON, J. L, MOSS, A. J, SCHWARTZ, P. J, TOWBIN, J. A, VINCENT, G. M

“…Long-QT Syndrome (LQTS) is a cardiovascular disorder characterized by prolongation of the QT interval on ECG and presence of syncope, seizures, and sudden…”
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Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias by Wang, Q, Curran, M.E, Splawski, I, Burn, T.C, Millholland, J.M, VanRaay, T.J, Shen, J, Timothy, K.W, Vincent, G.M, de Jager, T, Schwartz, P.J, Towbin, J.A, Moss, A.J, Atkinson, D.L, Landes, G.M, Connors, T.D, Keating, M.T

“…Genetic factors contribute to the risk of sudden death from cardiac arrhythmias. Here, positional cloning methods establish KVLQT1 as the chromosome 11-linked…”
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Diagnostic criteria for the long QT syndrome : an update by SCHWARTZ, P. J, MOSS, A. J, VINCENT, G. M, CRAMPTON, R. S

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Effectiveness and limitations of β-blocker therapy in congenital long-QT syndrome by MOSS, A. J, ZAREBA, W, MEDINA, A, LI ZHANG, ROBINSON, J. L, TIMOTHY, K, TOWBIN, J. A, ANDREWS, M. L, HALL, W. J, SCHWARTZ, P. J, CRAMPTON, R. S, BENHORIN, J, VINCENT, G. M, LOCATI, E. H, PRIORI, S. G, NAPOLITANO, C

“…beta-blockers are routinely prescribed in congenital long-QT syndrome (LQTS), but the effectiveness and limitations of beta-blockers in this disorder have not…”
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The QT interval and torsade de pointes by MOSS, A. J

“…The QT interval on the electrocardiogram is the time from the onset of ventricular depolarisation (the Q wave) to completion of repolarisation (the end of the…”
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Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development by Anderson, Louise V. B., Davison, Keith, Moss, Jennifer A., Young, Carol, Cullen, Michael J., Walsh, John, Johnson, Margaret A., Bashir, Rumaisa, Britton, Stephen, Keers, Sharon, Argov, Zohar, Mahjneh, Ibrahim, Fougerousse, Françoise, Beckmann, Jacques S., Bushby, Kate M. D.

“…Recently, a single gene, DYSF, has been identified which is mutated in patients with limb-girdle muscular dystrophy type 2B (LGMD2B) and with Miyoshi myopathy…”
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Heart rate variability : Standards of measurement, physiological interpretation, and clinical use by Malik, M., Bigger, J. T., Camm, A. J., Kleiger, R. E., Malliani, A., Moss, A. J., Schwartz, P. J.

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Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome : ECG findings identify genotypes by LI ZHANG, TIMOTHY, Katherine W, YANOWITZ, Frank, BENHORIN, Jesaia, MOSS, Arthur J, SCHWARTZ, Peter J, ROBINSON, Jennifer L, QING WANG, ZAREBA, Wojciech, KEATING, Mark T, TOWBIN, Jeffrey A, NAPOLITANO, Carlo, VINCENT, G. Michael, MEDINA, Aharon, LEHMANN, Michael H, FOX, Jolene, GIULI, Lisa C, JIAXIANG SHEN, SPLAWSKI, Igor, PRIORI, Silvia G, COMPTON, Steven J

“…Congenital long-QT syndrome (LQTS) is caused by mutations of genes encoding the slow component of the delayed rectifier current (LQT1, LQT5), the rapid…”
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Measurement of the QT interval and the risk associated with QTc interval prolongation : a review by MOSS, A. J

“…The accurate measurement of the QT interval and its correction or adjustment for cycle length, age, and gender have been topics of increasing interest over the…”
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Influence of the Genotype on the Clinical Course of the Long-QT Syndrome by Zareba, Wojciech, Moss, Arthur J, Schwartz, Peter J, Vincent, G. Michael, Robinson, Jennifer L, Priori, Silvia G, Benhorin, Jesaia, Locati, Emanuela H, Towbin, Jeffrey A, Keating, Mark T, Lehmann, Michael H, Hall, W. Jackson, Andrews, Mark L, Napolitano, Carlo, Timothy, Katherine, Zhang, Li, Medina, Aharon, MacCluer, Jean W

“…The hereditary long-QT syndrome is a familial disorder characterized by prolonged ventricular repolarization on the electrocardiogram and a propensity for…”
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Identical Mutation in Patients with Limb Girdle Muscular Dystrophy Type 2B Or Miyoshi Myopathy Suggests a Role for Modifier Gene(s) by Weiler, Tracey, Bashir, Rumaisa, Anderson, Louise V. B., Davison, Keith, Moss, Jennifer A., Britton, Stephen, Nylen, Edward, Keers, Sharon, Vafiadaki, Elizabeth, Greenberg, Cheryl R., Bushby, Kate M. D., Wrogemann, Klaus

“…Limb girdle muscular dystrophy type 2B (LGMD2B) and Miyoshi myopathy (MM), a distal muscular dystrophy, are both caused by mutations in the recently cloned…”
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Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome : Findings from the international LQTS registry by LOCATI, E. H, ZAREBA, W, ANDREWS, M, TIMOTHY, K, HALL, W. J, MOSS, A. J, SCHWARTZ, P. J, VINCENT, G. M, LEHMANN, M. H, TOWBIN, J. A, PRIORI, S. G, NAPOLITANO, C, ROBINSON, J. L

“…Unexplained female predominance is observed in long-QT syndrome (LQTS), a congenital autosomal disorder with prolonged repolarization and syncope or sudden…”
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Conservation in the first internal transcribed spacer region (ITS1) in Hematodinium species infecting crustacean hosts found in the UK and Newfoundland by SMALL, H. J, SHIELDS, J. D, MOSS, J. A, REECE, K. S

“…Parasitic dinoflagellates in the genus Hematodinium infect a number of decapod crustaceans in waters off the UK, including the Norway lobster Nephrops…”
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The Long QT syndrome : prospective longitudinal study of 328 families by MOSS, A. J, SCHWARTZ, P. J, ROBINSON, J. L, BENHORIN, J, SUNGSUB CHOI, CRAMPTON, R. S, TZIVONI, D, LOCATI, E. H, MACCLUER, J, HALL, J, WEITKAMP, L, VINCENT, M, GARSON, A. JR

“…The Long QT Syndrome (LQTS) is an infrequently occurring familial disorder in which affected individuals have electrocardiographic QT interval prolongation and…”
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Electrocardiographic quantitation of ventricular repolarization by MERRI, M, BENHORIN, J, ALBERTI, M, LOCATI, E, MOSS, A. J

“…Quantification of the electrocardiographic ventricular repolarization involving the T-U wave complex is usually performed with reference to the axis of the T…”
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