Alfred L. George

发表

Research conference summary from the 2014 International Task Force on ATP1A3-Related Disorders

Frederick Andermann, Masayuki Sasaki, Allison Brashear, 2017, Neurology: Genetics.

Principles of laser velocimetry with Doppler-pictures

J. Srulijes, Alfred L. George, F. Seiler, 1992, Other Conferences.

Filtering approach based on empirical mode decomposition improves the assessment of short scale complexity in long QT syndrome type 1 population

Sergio Cerutti, A. Porta, Vlasta Bari, 2014, 2014 36th Annual International Conference of the IEEE Engineering in Medicine and Biology Society.

Low-Pass Filtering Approach via Empirical Mode Decomposition Improves Short-Scale Entropy-Based Complexity Estimation of QT Interval Variability in Long QT Syndrome Type 1 Patients

Sergio Cerutti, A. Porta, Vlasta Bari, 2014, Entropy.

Autonomic control of heart rate and QT interval variability influences arrhythmic risk in long QT syndrome type 1.

Alberto Porta, Vlasta Bari, Peter J. Schwartz, 2015, Journal of the American College of Cardiology.

Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

Thomas Meitinger, Peter J. Schwartz, Walter J. Chazin, 2013, Circulation.

Impaired Inactivation Gate Stabilization Predicts Increased Persistent Current for an Epilepsy-Associated SCN1A Mutation

Alfred L. George, Kristopher M. Kahlig, Sunita N. Misra, 2006, The Journal of Neuroscience.

Arrhythmogenic Calmodulin Mutations Disrupt Intracellular Cardiomyocyte Ca2+ Regulation by Distinct Mechanisms

Peter J. Schwartz, Alfred L. George, Lia Crotti, 2014, Journal of the American Heart Association.

Prevalence of Long-QT Syndrome Gene Variants in Sudden Infant Death Syndrome

Peter J. Schwartz, Alfred L. George, Lia Crotti, 2007, Circulation.

A Large Candidate Gene Survey Identifies the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes

Marylyn D. Ritchie, Thomas Meitinger, Dana C. Crawford, 2012, Circulation. Cardiovascular genetics.

Multiscale Complexity Analysis of the Cardiac Control Identifies Asymptomatic and Symptomatic Patients in Long QT Syndrome Type 1

Pere Caminal, Sergio Cerutti, Alberto Porta, 2014, PloS one.

Pharmacogenomics of atrial fibrillation

Nancy J. Brown, Marylyn D. Ritchie, Dan M. Roden, 2005 .

Mechanism of sodium channel NaV1.9 potentiation by G-protein signaling

Carlos G. Vanoye, Alfred L. George, A. George, 2013, The Journal of general physiology.

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B

Samuel F. Berkovic, Ingrid E. Scheffer, Robyn H. Wallace, 1998, Nature Genetics.

Extracellular Sodium Interacts with the HERG Channel at an Outer Pore Site

Reshma R. Desai, Alfred L. George, Jeffrey R. Balser, 2002, The Journal of general physiology.

High-Throughput Functional Evaluation of KCNQ1 Decrypts Variants of Unknown Significance

Jens Meiler, Carlos G. Vanoye, Reshma R. Desai, 2018, Circulation. Genomic and precision medicine.

Erratum: Different flecainide sensitivity of hNav1.4 channels and myotonic mutants explained by state-dependent block (The Journal of Physiology (2004) vol. 554 (321-334))

Alfred L. George, Diana Conte Camerino, Jean-François Desaphy, 2004 .

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

Margaret Robertson, Robert L. Barchi, Robert C. Griggs, 1991, Cell.

Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation

Ming Zhou, Mohamed Chahine, Richard Horn, 1994, Neuron.

Characterization of a KCNB1 variant associated with autism, intellectual disability, and epilepsy

Carlos G. Vanoye, Alfred L. George, A. George, 2017, Neurology: Genetics.