Joseph Galvin
Overview
Explore the profile of Joseph Galvin including associated specialties, affiliations and a list of published articles.
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Articles
44
Citations
329
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Recent Articles
1.
Min K, Galvin J, Chung B, Tamate T, Horng J, McCadden A
JSES Rev Rep Tech
. 2024 Oct;
4(4):779-782.
PMID: 39474164
Background: The partial pectoralis major transfer for the treatment of serratus anterior deficiency and modified Eden-Lange/Triple Tendon Transfer for trapezius deficiency result in improvement in pain and shoulder function. However,...
2.
Ge N, Li R, Liu M, Xia W, OBrien S, McInerney V, et al.
J Am Heart Assoc
. 2024 Oct;
13(20):e034690.
PMID: 39377211
Background: Long-QT syndrome is a primary cardiac ion channelopathy predisposing a patient to ventricular arrhythmia through delayed repolarization on the resting ECG. We aimed to establish a patient-specific, human induced...
3.
4.
OBrien J, Valsecchi S, Seaver F, Rosalejos L, Arellano D, Laurilla K, et al.
Eur Heart J Digit Health
. 2024 Jul;
5(4):483-490.
PMID: 39081948
Aims: Catheter ablation is a widely accepted intervention for atrial fibrillation (AF) management. Prior to undertaking this procedure, thorough patient education on its efficacy and potential complications is crucial. Additionally,...
5.
Kerley R, Fitzpatrick N, Galvin J
J Innov Card Rhythm Manag
. 2024 Apr;
15(3):5813-5818.
PMID: 38584745
The pathogenesis of inappropriate sinus tachycardia is not well understood, and the symptoms of inappropriate sinus tachycardia can be difficult to manage. Here, we present a case of inappropriate sinus...
6.
Murphy J, Kirk C, Lambert D, McGorrian C, Walsh R, McVeigh T, et al.
Ir J Med Sci
. 2024 Mar;
193(4):1775-1785.
PMID: 38489124
Background: Inherited cardiomyopathies (HCM, DCM, ACM) and cardiac ion channelopathies (long QT/Brugada syndromes, CPVT) are associated with significant morbidity and mortality; however, diagnosis of a familial pathogenic variant in a...
7.
Amor-Salamanca A, Santana Rodriguez A, Rasoul H, Rodriguez-Palomares J, Moldovan O, Hey T, et al.
Circ Genom Precis Med
. 2024 Feb;
17(2):e004404.
PMID: 38353104
Background: Less than 40% of patients with dilated cardiomyopathy (DCM) have a pathogenic/likely pathogenic genetic variant identified. has been linked to congenital heart defects; although an association with left ventricular...
8.
Piqueras-Flores J, Villacorta-Arguelles E, Galvin J, Climent-Paya V, Escobar-Lopez L, Amor-Salamanca A, et al.
J Med Genet
. 2023 Dec;
61(5):423-427.
PMID: 38160043
Formin homology 2 domain-containing 3 () gene has emerged as one of the main non-sarcomeric genes associated with hypertrophic cardiomyopathy (HCM), but no cases of biallelic variants associated with disease...
9.
Wagener M, Dolan E, Arnous S, Galvin J, Murphy A, Casserly I, et al.
J Clin Med
. 2023 Sep;
12(17).
PMID: 37685701
Uncontrolled arterial hypertension is a major global health issue. Catheter-based renal denervation has shown to lower blood pressure in sham-controlled trials and represents a device-based, complementary treatment option for hypertension....
10.
Ge N, Liu M, Li R, Allen N, Galvin J, Shen S, et al.
Stem Cell Rev Rep
. 2023 Aug;
19(8):2774-2789.
PMID: 37653182
Human induced pluripotent stem cells (hiPSCs) have been widely used in cardiac disease modelling, drug discovery, and regenerative medicine as they can be differentiated into patient-specific cardiomyocytes. Long QT syndrome...