Detalhe da pesquisa
1.
Cardiomyopathies in children and adolescents: aetiology, management, and outcomes in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis Registry.
Eur Heart J
; 45(16): 1443-1454, 2024 Apr 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38427064
2.
The role of genetic testing in Marfan syndrome.
Curr Opin Cardiol
; 39(3): 162-169, 2024 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38386349
3.
An atypical Aymé-Gripp phenotype detected by exome sequencing.
Am J Med Genet A
; 194(1): 70-76, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37712597
4.
The Role of Scintigraphy with Bone Radiotracers in Cardiac Amyloidosis.
Heart Fail Clin
; 20(3): 307-316, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38844301
5.
Genotype-Phenotype Correlations in ATTR Amyloidosis: A Clinical Update.
Heart Fail Clin
; 20(3): 317-323, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38844302
6.
Pathophysiology of Cardiac Amyloidosis.
Heart Fail Clin
; 20(3): 261-270, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38844297
7.
The Role of Echocardiography for the Clinical Diagnosis, Risk Stratification, and Management of Cardiac Amyloidosis.
Heart Fail Clin
; 20(3): 271-282, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38844298
8.
Tafamidis in the Treatment of ATTR-related Cardiomyopathy: Indications and Grey Zones.
Heart Fail Clin
; 20(3): 333-341, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38844304
9.
Clinical application of CMR in cardiomyopathies: evolving concepts and techniques : A position paper of myocardial and pericardial diseases and cardiac magnetic resonance working groups of Italian society of cardiology.
Heart Fail Rev
; 28(1): 77-95, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35536402
10.
Genome Editing and Heart Failure.
Adv Exp Med Biol
; 1396: 75-85, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36454460
11.
Indications and management of implantable cardioverter-defibrillator therapy in childhood hypertrophic cardiomyopathy.
Cardiol Young
; 33(5): 681-698, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-37102324
12.
Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes.
Int J Mol Sci
; 24(10)2023 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37240454
13.
The heart in RASopathies.
Am J Med Genet C Semin Med Genet
; 190(4): 440-451, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36408797
14.
Progressive right ventricular dysfunction and exercise impairment in patients with heart failure and diabetes mellitus: insights from the T.O.S.CA. Registry.
Cardiovasc Diabetol
; 21(1): 108, 2022 06 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35710369
15.
Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry.
J Public Health (Oxf)
; 44(3): 586-594, 2022 08 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-33982102
16.
Transthoracic echocardiography for arrhythmic mitral valve prolapse: Phenotypic characterization as first step.
Echocardiography
; 39(9): 1158-1170, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36029124
17.
Mystery(n) Phenotypic Presentation in Europeans: Report of Three Further Novel Missense RNF213 Variants Leading to Severe Syndromic Forms of Moyamoya Angiopathy and Literature Review.
Int J Mol Sci
; 23(16)2022 Aug 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36012218
18.
The Influence of Genotype on the Phenotype, Clinical Course, and Risk of Adverse Events in Children with Hypertrophic Cardiomyopathy.
Heart Fail Clin
; 18(1): 1-8, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34776071
19.
The Risk of Sudden Unexpected Cardiac Death in Children: Epidemiology, Clinical Causes, and Prevention.
Heart Fail Clin
; 18(1): 115-123, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34776073
20.
Clinical Manifestations of 22q11.2 Deletion Syndrome.
Heart Fail Clin
; 18(1): 155-164, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34776076