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Biofactors (Oxford, England)|January 31, 2020
Beyond cholesterol metabolism: The pleiotropic effects of proprotein convertase subtilisin/kexin type 9 (PCSK9). Genetics, mutations, expression, and perspective for long-term inhibitionArturo Cesaro, Vanessa Bianconi, Felice Gragnano, et al.
Molecular Genetics & Genomic Medicine|May 13, 2020
Genetic analysis resolves differential diagnosis of a familial syndromic dilated cardiomyopathy: A new case of Alström syndromeBarbara Lombardo, Valeria D'Argenio, Emanuele Monda, et al.
Open Heart|November 6, 2014
The influence of aortoseptal angulation on provocable left ventricular outflow tract obstruction in hypertrophic cardiomyopathyChristopher Howell Critoph, Antonios Pantazis, Maria Teresa Tome Esteban, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|August 26, 2006
Noninvasive risk stratification prevents sudden death due to paroxysmal atrial fibrillation in hypertrophic cardiomyopathyGiuseppe Limongelli, Perry Mark Elliott, Giuseppe Pacileo, et al.
European Journal of Heart Failure|March 4, 2026
The Yield and Clinical Impact of Genetic Testing in Older Patients with Dilated CardiomyopathyDouglas E Cannie, Athanasios Bakalakos, Petros Syrris, et al.
Echocardiography (Mount Kisco, N.Y.)|September 20, 2014
Right ventricular cardiomyopathies: a multidisciplinary approach to diagnosisGiuseppe Limongelli, Alessandra Rea, Daniele Masarone, et al.
Cardiology in the Young|February 11, 2021
Rare case of Kawasaki disease with cardiac tamponade and giant coronary artery aneurysmsAndrea Vergara, Emanuele Monda, Cinzia Mautone, et al.
American Journal of Medical Genetics. Part A|September 15, 2023
An atypical Aymé-Gripp phenotype detected by exome sequencingMartina Caiazza, Alberto Budillon, Emanuele Monda, et al.
Biochemistry Research International|September 8, 2012
A novel Myosin essential light chain mutation causes hypertrophic cardiomyopathy with late onset and low expressivityPaal Skytt Andersen, Paula Louise Hedley, Stephen P Page, et al.
Genes|May 14, 2020
Genotype-Phenotype Correlation: A Triple DNA Mutational Event in a Boy Entering Sport Conveys an Additional Pathogenicity RiskGiuseppe Limongelli, Marcella Nunziato, Cristina Mazzaccara, et al.
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