Showing results (131-140 of 184) with videos related to
Sort By:
Pageof 19
Molecular Cytogenetics|April 2, 2016
Microarray testing in clinical diagnosis: an analysis of 5,300 New Zealand patientsAdrian Mc Cormack, Karen Claxton, Fern Ashton, et al.Cold Spring Harbor Molecular Case Studies|July 12, 2017
Compound heterozygous SLC19A3 mutations further refine the critical promoter region for biotin-thiamine-responsive basal ganglia diseaseWhitney Whitford, Isobel Hawkins, Emma Glamuzina, et al.Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing|January 30, 2024
Ebstein's anomaly: an electrophysiological perspectiveAnunay Gupta, Mukund A Prabhu, Robert D Anderson, et al.Heart, Lung & Circulation|May 19, 2020
Patients With Genetic Heart Disease and COVID-19: A Cardiac Society of Australia and New Zealand (CSANZ) Consensus StatementBelinda Gray, Christopher Semsarian, Diane Fatkin, et al.Annals of Emergency Medicine|March 14, 2009
Misdiagnosis of long QT syndrome as epilepsy at first presentationJudith M MacCormick, Hugh McAlister, Jackie Crawford, et al.Journal of the American College of Cardiology|May 30, 2020
A Population-Based Registry of Patients With Inherited Cardiac Conditions and Resuscitated Cardiac ArrestCynthia Rucinski, Annika Winbo, Luciana Marcondes, et al.Circulation. Heart Failure|March 8, 2024
Genetic Testing Yield and Clinical Characteristics of Hypertrophic Cardiomyopathy in Understudied Ethnic Groups: Insights From a New Zealand National RegistryNikki J Earle, Annika Winbo, Jackie Crawford, et al.JIMD Reports|November 22, 2017
Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q10 Deficiency in a Female Sib-PairJessie C Jacobsen, Whitney Whitford, Brendan Swan, et al.BMC Nephrology|April 22, 2024
A loss-of-function AGTR1 variant in a critically-ill infant with renal tubular dysgenesis: case presentation and literature reviewAljazi Al-Maraghi, Waleed Aamer, Mubarak Ziab, et al.BMJ Paediatrics Open|March 9, 2026
Paediatric inherited arrhythmia clinic: developing a new model of careKaren M Robinson, Hiroko Asakai, Christian Turner, et al.Pageof 19