Results 301 to 310 of about 412,316 (368)

Ictal tachycardia: The head–heart connection

open access: yesSeizure, 2014
K. Eggleston, B. Olin, R. Fisher
semanticscholar   +1 more source

Development of Electroconductive Polypyrrole‐Polycaprolactone and Poly(3,4‐Ethylenedioxythiophene)‐poly(Styrenesulfonate)‐Polyethylene Oxide Fibrous Scaffolds by Pressurised Gyration for Cardiac Tissue Engineering Applications

open access: yesMacromolecular Materials and Engineering, EarlyView.
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]

open access: yesMethodist Debakey Cardiovasc J
Sharma V   +5 more
europepmc   +1 more source

An X‐Linked Ataxia Syndrome in a Family with Hearing Loss Associated with a Novel Variant in the BCAP31 Gene

open access: yesMovement Disorders, EarlyView.
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

Central Involvement in Pure Autonomic Failure: Insights from Neuromelanin‐Sensitive Magnetic Resonance Imaging and 18F‐Fluorodopa‐Positron Emission Tomography

open access: yesMovement Disorders, EarlyView.
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]

open access: yesClin Case Rep
Mussigbrodt A   +4 more
europepmc   +1 more source

Patients with Allan‐Herndon‐Dudley Syndrome (MCT8 Deficiency) Display Symptoms of Parkinsonism in Childhood and Respond to Levodopa/Carbidopa Treatment

open access: yesMovement Disorders, EarlyView.
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

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