Browse by UCL people
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Number of items: 20.
Article
Akhtar, MM;
Lorenzini, M;
Cicerchia, M;
Ochoa, JP;
Hey, TM;
Sabater Molina, M;
Restrepo-Cordoba, MA;
... European Genetic Cardiomyopathies Initiative Investigators; + view all
(2020)
Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene.
Circulation: Heart Failure
, 13
(10)
, Article e006832. 10.1161/CIRCHEARTFAILURE.119.006832.
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Akhtar, MM;
Lorenzini, M;
Pavlou, M;
Ochoa, JP;
O'Mahony, C;
Restrepo-Cordoba, MA;
Segura-Rodriguez, D;
... Elliott, PM; + view all
(2021)
Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart Failure.
JAMA Cardiology
10.1001/jamacardio.2021.1106.
(In press).
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Brownrigg, J;
Lorenzini, M;
Lumley, M;
Elliott, P;
(2019)
Diagnostic performance of imaging investigations in detecting and differentiating cardiac amyloidosis: a systematic review and meta-analysis.
ESC Heart Failure
10.1002/ehf2.12511.
(In press).
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Cannie, Douglas E;
Protonotarios, Alexandros;
Bakalakos, Athanasios;
Syrris, Petros;
Lorenzini, Massimiliano;
De Stavola, Bianca;
Bjerregaard, Louise;
... Elliott, Perry M; + view all
(2023)
Risks of Ventricular Arrhythmia and Heart Failure in Carriers of RBM20 Variants.
Circulation: Genomic and Precision Medicine
, Article e004059. 10.1161/CIRCGEN.123.004059.
(In press).
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Ditaranto, R;
Boriani, G;
Biffi, M;
Lorenzini, M;
Graziosi, M;
Ziacchi, M;
Pasquale, F;
... Biagini, E; + view all
(2019)
Differences in cardiac phenotype and natural history of laminopathies with and without neuromuscular onset.
Orphanet Journal of Rare Diseases
, 14
(1)
, Article 263. 10.1186/s13023-019-1245-8.
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Elliott, Perry M;
Lorenzini, Massimiliano;
(2022)
Understanding the Prognostic Significance of Left Ventricular Apical Aneurysms in Hypertrophic Cardiomyopathy.
JACC: Cardiovascular Imaging
, 15
(10)
pp. 1712-1714.
10.1016/j.jcmg.2022.05.022.
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González-López, E;
Gagliardi, C;
Dominguez, F;
Quarta, CC;
Javier de Haro-del Moral, F;
Milandri, A;
Salas, C;
... Garcia-Pavia, P; + view all
(2017)
Clinical characteristics of wild-type transthyretin cardiac amyloidosis: disproving myths.
European Heart Journal
, 38
(24)
pp. 1895-1904.
10.1093/eurheartj/ehx043.
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Heliö, T;
Elliott, P;
Koskenvuo, JW;
Gimeno, JR;
Tavazzi, L;
Tendera, M;
Kaski, JP;
... EORP Cardiomyopathy Registry Investigators Group, .; + view all
(2020)
ESC EORP Cardiomyopathy Registry: real-life practice of genetic counselling and testing in adult cardiomyopathy patients.
ESC Heart Failure
10.1002/ehf2.12925.
(In press).
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Joy, George;
Kelly, Christopher I;
Webber, Matthew;
Pierce, Iain;
Teh, Irvin;
McGrath, Louise;
Velazquez, Paula;
... Lopes, Luis R; + view all
(2023)
Microstructural and Microvascular Phenotype of Sarcomere Mutation Carriers and Overt Hypertrophic Cardiomyopathy.
Circulation
10.1161/CIRCULATIONAHA.123.063835.
(In press).
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Leone, O;
Corsini, A;
Pacini, D;
Corti, B;
Lorenzini, M;
Laus, V;
Foà, A;
... Rapezzi, C; + view all
(2019)
The complex interplay among atherosclerosis, inflammation, and degeneration in ascending thoracic aortic aneurysms.
The Journal of Thoracic and Cardiovascular Surgery
10.1016/j.jtcvs.2019.08.108.
(In press).
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Lopes, LR;
Futema, M;
Akhtar, MM;
Lorenzini, M;
Pittman, A;
Syrris, P;
Elliott, PM;
(2019)
Prevalence of TTR variants detected by whole-exome sequencing in hypertrophic cardiomyopathy.
The Journal of Protein Folding Disorders
, 26
(4)
pp. 243-247.
10.1080/13506129.2019.1665996.
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Lopes, LR;
Garcia-Hernández, S;
Lorenzini, M;
Futema, M;
Chumakova, O;
Zateyshchikov, D;
Isidoro-Garcia, M;
... Elliott, PM; + view all
(2021)
Alpha-protein kinase 3 (ALPK3)-truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy.
European Heart Journal
10.1093/eurheartj/ehab424.
(In press).
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Lopez-Sainz, A;
Dominguez, F;
Lopes, LR;
Ochoa, JP;
Barriales-Villa, R;
Climent, V;
Linschoten, M;
... European Genetic Cardiomyopathies Initiative Investigators; + view all
(2020)
Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis.
Journal of the American College of Cardiology
, 76
(2)
pp. 186-197.
10.1016/j.jacc.2020.05.029.
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Lorenzini, M;
Khanji, MY;
Lopes, LR;
Manisty, C;
Savvatis, K;
(2021)
Cardiac magnetic resonance assessment of progressive myo-pericarditis due to cobalt cardiotoxicity.
European Heart Journal - Cardiovascular Imaging
, 22
(6)
e71.
10.1093/ehjci/jeaa272.
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Lorenzini, Massimiliano;
Elliott, Perry M;
(2023)
Do apical aneurysms predict sudden cardiac death in hypertrophic cardiomyopathy?
European Heart Journal
, 44
(17)
pp. 1519-1521.
10.1093/eurheartj/ehad122.
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Lorenzini, M;
Anastasiou, Z;
O'Mahony, C;
Guttman, OP;
Gimeno, JR;
Monserrat, L;
Anastasakis, A;
... Hypertrophic Cardiomyopathy Outcomes investigators, .; + view all
(2019)
Mortality Among Referral Patients With Hypertrophic Cardiomyopathy vs the General European Population.
JAMA Cardiology
10.1001/jamacardio.2019.4534.
(In press).
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Lorenzini, M;
Elliott, PM;
(2019)
Tafamidis for the treatment of transthyretin amyloidosis.
Future Cardiology
, 15
(2)
pp. 53-61.
10.2217/fca-2018-0078.
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Lorenzini, M;
Guha, N;
Davison, JE;
Pitcher, A;
Pandya, B;
Kemp, H;
Lachmann, R;
... Murphy, E; + view all
(2018)
Isolated aortic root dilation in homocystinuria.
Journal of Inherited Metabolic Disease
, 41
(1)
pp. 109-115.
10.1007/s10545-017-0094-7.
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Lorenzini, M;
Norrish, G;
Field, E;
Ochoa, JP;
Cicerchia, M;
Akhtar, MM;
Syrris, P;
... Elliott, PM; + view all
(2020)
Penetrance of Hypertrophic Cardiomyopathy in Sarcomere Protein Mutation Carriers.
Journal of the American College of Cardiology
, 76
(5)
pp. 550-559.
10.1016/j.jacc.2020.06.011.
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Sengupta, Anshuman;
Akhtar, Mohammed Majid;
Akhtar, Abid Mohammed;
Lorenzini, Massimiliano;
Slater, Thomas;
Syrris, Petros;
Savvatis, Konstantinos;
... Elliott, Perry Mark; + view all
(2025)
Cardiomyopathy caused by mitochondrial DNA 4300A > G variant.
European Heart Journal
, Article ehaf319. 10.1093/eurheartj/ehaf319.
(In press).
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