Search Results - "LAM, Lien"

Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy by Bagnall, Richard D., Crompton, Douglas E., Petrovski, Slavé, Lam, Lien, Cutmore, Carina, Garry, Sarah I., Sadleir, Lynette G., Dibbens, Leanne M., Cairns, Anita, Kivity, Sara, Afawi, Zaid, Regan, Brigid M., Duflou, Johan, Berkovic, Samuel F., Scheffer, Ingrid E., Semsarian, Christopher

“…Objective The leading cause of epilepsy‐related premature mortality is sudden unexpected death in epilepsy (SUDEP). The cause of SUDEP remains unknown. To…”
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Nonfamilial Hypertrophic Cardiomyopathy by Ingles Jodie, Burns, Charlotte, Bagnall, Richard D, Lam, Lien, Yeates, Laura, Sarina Tanya, Puranik Rajesh, Briffa, Tom, Atherton, John J, Driscoll, Tim, Semsarian Christopher

“…Background—Yield of causative variants in hypertrophic cardiomyopathy (HCM) is increased in some probands, suggesting different clinical subgroups of disease…”
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Meromorphic Extensions of (·,W)-Meromorphic Functions by Quang, Thai Thuan, Lam, Lien Vuong

“…In this paper we establish some classes of subspaces W of the dual F ′ of a locally convex space F such that every F -valued ( F ,  W )-meromorphic function…”
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A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia by Gray, Belinda, BSc (Med), MBBS, Bagnall, Richard D., PhD, Lam, Lien, BMedSc, PhD, Ingles, Jodie, GradDipGenCouns, MPH, PhD, Turner, Christian, MBBS, Haan, Eric, BMedSc, MBBS, Davis, Andrew, MBBS, MD, FHRS, Yang, Pei-Chi, PhD, Clancy, Colleen E., PhD, Sy, Raymond W., MBBS PhD, Semsarian, Christopher, MBBS, MPH, PhD, FHRS

“…Background Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a lethal inherited arrhythmia syndrome characterised by adrenergically stimulated…”
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Study on Domestic Wastewater Treatment of the Horizontal Subsurface Flow Wetlands (HSSF-CWs) Using Brachiaria mutica by Van Thi Thanh Ho, Dang, Minh Pham, Lien, Lam Tu, Huynh, Tai Thien, Van Hung, Tran, Bach, Long Giang

“…This study aimed to evaluate the effect of domestic wastewater treatment on the horizontal subsurface flow-constructed wetlands (HSSF-CWs) using Brachiaria…”
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Cross Theorems for Separately (⋅,W)-meromorphic Functions by Quang, Thai Thuan, Lam, Lien Vuong

“…It is shown that Rothstein's theorem holds for (F, W)-meromorphic functions withFis a sequentially complete locally convex space. We also prove that a…”
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Severe Heart Failure and Early Mortality in a Double-Mutation Mouse Model of Familial Hypertrophic Cardiomyopathy by TSOUTSMAN, Tatiana, KELLY, Matthew, NG, Dominic C. H, TAN, Ju-En, TU, Emily, LAM, Lien, BOGOYEVITCH, Marie A, SEIDMAN, Christine E, SEIDMAN, J. G, SEMSARIAN, Christopher

“…Familial hypertrophic cardiomyopathy (FHC) is characterized by genetic and clinical heterogeneity. Five percent of FHC families have 2 FHC-causing mutations,…”
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Abnormal cardiac response to exercise in a murine model of familial hypertrophic cardiomyopathy by Nguyen, Lan, Chung, Jessica, Lam, Lien, Tsoutsman, Tatiana, Semsarian, Christopher

“…Abstract Clinical outcome in familial hypertrophic cardiomyopathy (FHC) may be influenced by modifying factors such as exercise. Transgenic mice which…”
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Levi Extension Theorems for Meromorphic Functions of Weak Type in Infinite Dimension by Quang, Thai Thuan, Lam, Lien Vuong

“…The aim of paper is to give some results, that prepare for studying the problem on cross theorems for separately ( · , W ) -meromorphic functions. Some general…”
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Exome sequencing identifies a novel mutation in the MYH6 gene in a family with early-onset sinus node dysfunction, ventricular arrhythmias, and cardiac arrest by Lam, Lien, Ingles, Jodie, Turner, Christian, Kilborn, Michael, Bagnall, Richard D., Semsarian, Christopher

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Assessing the impact of a leadership and advocacy elective course in a college of pharmacy curriculum by Young, David, Gadd, Shannon, Ashmead, Payson, Abbinanti, Alan, Pinnock, Emily, Do Lam, Tuyet Lien, Turner, Kyle

“…While the scope of a pharmacist's work has grown, continued advocacy is needed to ensure that their skillset is used to the best advantage of the patient. To…”
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Molecular insights from a novel cardiac troponin I mouse model of familial hypertrophic cardiomyopathy by Tsoutsman, Tatiana, Chung, Jessica, Doolan, Alessandra, Nguyen, Lan, Williams, Iwan A., Tu, Emily, Lam, Lien, Bailey, Charles G., Rasko, John E.J., Allen, David G., Semsarian, Christopher

“…Gene mutations in cardiac troponin I (cTnI) account for up to 5% of genotyped families with familial hypertrophic cardiomyopathy (FHC). Little is known about…”
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On σ(·, W)-Holomorphic Functions and Theorems of Vitali-Type by Quang, Thai Thuan, Lam, Lien Vuong, Van Dai, Nguyen

“…The aim of this paper is to give some criterions for holomorphy of F -valued σ ( F , W )-holomorphic functions which are bounded on bounded sets in a domain D…”
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Multiple Gene Variants in Hypertrophic Cardiomyopathy in the Era of Next-Generation Sequencing by Burns, Charlotte, Bagnall, Richard D, Lam, Lien, Semsarian, Christopher, Ingles, Jodie

“…BACKGROUND—Multiple likely pathogenic/pathogenic (LP/P; ≥2) variants in patients with hypertrophic cardiomyopathy were described 10 years ago with a prevalence…”
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A Prospective Study of Sudden Cardiac Death among Children and Young Adults by Bagnall, Richard D, Weintraub, Robert G, Ingles, Jodie, Duflou, Johan, Yeates, Laura, Lam, Lien, Davis, Andrew M, Thompson, Tina, Connell, Vanessa, Wallace, Jennie, Naylor, Charles, Crawford, Jackie, Love, Donald R, Hallam, Lavinia, White, Jodi, Lawrence, Christopher, Lynch, Matthew, Morgan, Natalie, James, Paul, du Sart, Desirée, Puranik, Rajesh, Langlois, Neil, Vohra, Jitendra, Winship, Ingrid, Atherton, John, McGaughran, Julie, Skinner, Jonathan R, Semsarian, Christopher

“…In 490 cases of sudden cardiac death identified over a 3-year period (annual incidence of 1.3 per 100,000), causes were found in 60% through conventional…”
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Nonfamilial Hypertrophic Cardiomyopathy: Prevalence, Natural History, and Clinical Implications by Ingles, Jodie, Burns, Charlotte, Bagnall, Richard D, Lam, Lien, Yeates, Laura, Sarina, Tanya, Puranik, Rajesh, Briffa, Tom, Atherton, John J, Driscoll, Tim, Semsarian, Christopher

“…BACKGROUND—Yield of causative variants in hypertrophic cardiomyopathy (HCM) is increased in some probands, suggesting different clinical subgroups of disease…”
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Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing by Ito, Kaoru, Patel, Parth N., Gorham, Joshua M., McDonough, Barbara, DePalma, Steven R., Adler, Emily E., Lam, Lien, MacRae, Calum A., Mohiuddin, Syed M., Fatkin, Diane, Seidman, Christine E., Seidman, J. G.

“…Genetic variants that cause haploinsufficiency account for many autosomal dominant (AD) disorders. Gene-based diagnosis classifies variants that alter…”
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A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy by Horvat, Claire, Johnson, Renee, Lam, Lien, Munro, Jacob, Mazzarotto, Francesco, Roberts, Angharad M., Herman, Daniel S., Parfenov, Michael, Haghighi, Alireza, McDonough, Barbara, DePalma, Steven R., Keogh, Anne M., Macdonald, Peter S., Hayward, Christopher S., Roberts, Amy, Barton, Paul J.R., Felkin, Leanne E., Giannoulatou, Eleni, Cook, Stuart A., Seidman, J.G., Seidman, Christine E., Fatkin, Diane

“…We evaluated strategies for identifying disease-causing variants in genetic testing for dilated cardiomyopathy (DCM). Cardiomyopathy gene panel testing was…”
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Mannose-specific lectins modulate ligand binding to AMPA-type glutamate receptors by Hoffman, Keith B, Kessler, Markus, Ta, Joseph, Lam, Lien, Lynch, Gary

“…Binding of [ 3 H] AMPA was increased above control levels in rat brain membranes that had been incubated with concanavalin A (Con A) or a lectin from Lens…”
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NON-FAMILIAL HYPERTROPHIC CARDIOMYOPATHY: PREVALENCE, NATURAL HISTORY AND CLINICAL IMPLICATIONS by Ingles, Jodie, Burns, Charlotte, Bagnall, Richard, Lam, Lien, Yeates, Laura, Sarina, Tanya, Puranik, Raj, Briffa, Tom, Atherton, John, Driscoll, Tim, Semsarian, Christopher

“…Background: The yield of positive sarcomere mutations in hypertrophic cardiomyopathy (HCM) is increased in probands with a family history of disease, younger…”
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