Results 301 to 310 of about 412,316 (368)
Ictal tachycardia: The head–heart connection
K. Eggleston, B. Olin, R. Fisher
semanticscholar +1 more source
2019 HRS/EHRA/APHRS/LAHRS expert consensus statement on catheter ablation of ventricular arrhythmias [PDF]
Cuculich, Phillip, et al,
core +1 more source
Definition and classification of the histamine-release response to drugs in anaesthesia and surgery: studies in the conscious human subject [PDF]
Doenicke, A.+5 more
core +1 more source
This study pioneers the fabrication of electroconductive cardiac scaffolds using pressurised gyration with the conductive polymers PPy and PEDOT:PSS. The resulting scaffolds exhibit optimal electroconductive and physicochemical properties, closely matching those of native cardiac tissue.
Juan Grano de Oro Fernandez+3 more
wiley +1 more source
Heart on Fire: Unmasking <i>RyR2</i> Mutation in Stress-Induced Ventricular Arrhythmias. [PDF]
Sharma V+5 more
europepmc +1 more source
Abstract Objective Pathogenic variants in B‐cell receptor‐associated protein (BCAP31) are associated with X‐linked, deafness, dystonia and cerebral hypomyelination (DDCH) syndrome. DDCH is congenital and non‐progressive, featuring severe intellectual disability (ID), variable dysmorphism, and sometimes associated with shortened survival. BCAP31 encodes
Martin Paucar+10 more
wiley +1 more source
Using a Novel Pulsed Field Ablation Technique to Identify the Critical Isthmus Within a Tachycardia Circuit. [PDF]
Mannion J, Rathore F, David J, Lyne J.
europepmc +1 more source
Abstract Background Central synucleinopathies, including Parkinson's disease (PD), dementia with Lewy bodies (DLB), and multiple system atrophy (MSA), involve alpha‐synuclein accumulation and dopaminergic cell loss in the substantia nigra (SN) and locus coeruleus (LC).
Paula Trujillo+10 more
wiley +1 more source
Leaping to Diagnosis: The Frog Sign as a Key Clue in AVNRT. [PDF]
Mussigbrodt A+4 more
europepmc +1 more source
Abstract Background Patients with mutations in the monocarboxylate transporter 8 (MCT8, SLC16A2) suffer from X‐linked recessive Allan‐Herndon‐Dudley syndrome (AHDS), which is characterized by developmental delay and a severe movement disorder. Current trials using thyroid hormone derivatives to overcome the transporter defect have failed to achieve ...
Nina‐Maria Wilpert+21 more
wiley +1 more source