Zobrazeno 1 - 10
of 20
pro vyhledávání: '"David K. Lawrence"'
Autor:
David K. Lawrence, Chenni S. Sriram
Publikováno v:
Journal of Arrhythmia, Vol 37, Iss 5, Pp 1380-1382 (2021)
Externí odkaz:
https://doaj.org/article/f076090e493845d8bbd436f396518936
Autor:
Chenni S. Sriram, Malini Madhavan, Sanjeev Aggarwal, Pezad Doctor, Pooja Gupta, David K. Lawrence, Gautam K. Singh
Publikováno v:
Pacing and Clinical Electrophysiology. 45:302-313
OBJECTIVES To evaluate any association between non-sustained ventricular tachycardia (NSVT) detected by intra-cardiac device and clinical outcomes in repaired adult congenital heart disease (ACHD) without tetralogy of Fallot (TOF). BACKGROUND NSVT po
Autor:
Iqbal El Assaad, Benjamin Hammond, Christopher M. Janson, Elizabeth D. Sherwin, Elizabeth A. Stephenson, Christopher L. Johnsrude, Mary C. Niu, Ira Shetty, David K. Lawrence, Anthony C. McCanta, Seshadri Balaji, Shubhayan Sanatani, Frank A. Fish, Gregory Webster, Peter F. Aziz
Publikováno v:
Heart Rhythm. 19:S337-S338
Autor:
Seshadri Balaji, Iqbal El Assaad, Gregory Webster, Sarah Worley, Shubhayan Sanatani, Elizabeth D. Sherwin, Peter F. Aziz, Christopher L. Johnsrude, Elizabeth A. Stephenson, Anthony C. McCanta, David K. Lawrence, Frank A. Fish, Mary C. Niu, Lukas D. Kost, Ira Shetty, Benjamin H. Hammond, Christopher M. Janson
Publikováno v:
Heart Rhythm
BACKGROUND: Atrial fibrillation (AF) in healthy children and young adults is rare. Risk of recurrence and treatment efficacy are not well-defined. OBJECTIVE: To assess recurrence patterns and treatment efficacy in AF. METHODS: A retrospective multi-c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeec389d3ee75f07ae2044ccf8d79bd4
https://europepmc.org/articles/PMC9364419/
https://europepmc.org/articles/PMC9364419/
Publikováno v:
J Pediatr Genet
Nevoid basal cell carcinoma syndrome (NBCCS), also referred to as Gorlin's syndrome, is an autosomal dominant inherited condition that predisposes affected individuals to various tumors such as cardiac fibromas. Though technically benign, cardiac fib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba26095db08edc79330e8391e7e01eca
https://europepmc.org/articles/PMC10118701/
https://europepmc.org/articles/PMC10118701/
Publikováno v:
Cardiology in the young. 30(12)
Noonan syndrome is the second most common genetic syndrome associated with congenital heart disease after Trisomy 21. The two most common cardiac lesions associated with Noonan syndrome are pulmonary stenosis and hypertrophic cardiomyopathy. Although
Publikováno v:
Journal of electrocardiology. 62
Mutations in the cardiac ryanodine receptor 2 gene (RYR2) are noted in approximately 55% of the patients with catecholaminergic polymorphic ventricular tachycardia (CPVT). However, a high background rate of rare amino acid-altering variants in RYR2 [
Publikováno v:
Journal of Interprofessional Care. 29:445-450
As the evidence supporting the value of well-coordinated healthcare teams continues to grow, so to do the calls from medical educators and policy makers for the development of meaningful interprofessional educational experiences for health profession
Autor:
Mark D. Ayers, David K. Lawrence
Publikováno v:
Congenital Heart Disease. 10:333-339
Objective Neurocardiogenic syncope (NCS) is the most common cause of syncope in children and adolescents. Neurocardiogenic syncope occurs secondary to cerebral hypotension because of bradycardia, hypotension, or both. Head-up tilt-table test (HUTT) i
Autor:
Jamie Wikenheiser, Yong Qiu Doughman, Michiko Watanabe, John B.E. Burch, David K. Lawrence, Laura Barbosky, Richard P. Visconti, Ganga Karunamuni
Publikováno v:
Developmental dynamics : an official publication of the American Association of Anatomists. 235(9)
Apoptosis occurs at high frequency in the myocardium of the developing avian cardiac outflow tract (OFT). Up- or down-regulating apoptosis results in defects resembling human conotruncal heart anomalies. This finding suggested that regulated levels o