Detalhe da pesquisa
1.
Mavacamten, a Novel Therapeutic Strategy for Obstructive Hypertrophic Cardiomyopathy.
Curr Cardiol Rep
; 23(7): 79, 2021 06 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34081217
2.
Targeted Medical Therapies for Hypertrophic Cardiomyopathy.
Curr Cardiol Rep
; 22(2): 10, 2020 Jan 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-31993794
3.
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center.
Genet Med
; 21(2): 284-292, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29875424
4.
Impact of pregnancy on the natural history of women with hypertrophic cardiomyopathy.
Eur J Prev Cardiol
; 31(1): 3-10, 2024 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37531614
5.
The evolving paradigm and current perception of hypertrophic cardiomyopathy: Implications for management.
Prog Cardiovasc Dis
; 80: 8-13, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37572782
6.
Prognostic value of cardiopulmonary exercise testing in patients with transthyretin cardiac amyloidosis.
Intern Emerg Med
; 18(2): 585-593, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36396841
7.
Safety and efficacy of ranolazine in hypertrophic cardiomyopathy: Real-world experience in a National Referral Center.
Int J Cardiol
; 370: 271-278, 2023 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36228766
8.
Genetic Testing and Counselling in Hypertrophic Cardiomyopathy: Frequently Asked Questions.
J Clin Med
; 12(7)2023 Mar 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37048573
9.
Real-World Use and Predictors of Response to Disopyramide in Patients with Obstructive Hypertrophic Cardiomyopathy.
J Clin Med
; 12(7)2023 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37048808
10.
Incidence of stroke in patients with hypertrophic cardiomyopathy in stable sinus rhythm during long-term monitoring.
Int J Cardiol
; 381: 70-75, 2023 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37061097
11.
Red flags for the diagnosis of cardiac amyloidosis: simple suggestions to raise suspicion and achieve earlier diagnosis.
J Cardiovasc Med (Hagerstown)
; 23(8): 493-504, 2022 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35904994
12.
Arrhythmic Burden in Cardiac Amyloidosis: What We Know and What We Do Not.
Biomedicines
; 10(11)2022 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36359408
13.
Sex-related differences in clinical presentation and all-cause mortality in patients with cardiac transthyretin amyloidosis and light chain amyloidosis.
Int J Cardiol
; 351: 71-77, 2022 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34990715
14.
Prevalence of anxiety and depression symptoms in a sample of outpatients with ATTR cardiac amyloidosis.
Front Psychol
; 13: 1066224, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36743650
15.
Myocardial blood flow in patients with hypertrophic cardiomyopathy receiving perindopril (CARAPaCE): a pilot study.
J Cardiovasc Med (Hagerstown)
; 22(6): 511-513, 2021 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33186235
16.
Cardiac involvement in eosinophilic granulomatosis with polyangiitis (formerly Churg-Strauss syndrome): Prospective evaluation at a tertiary referral centre.
Eur J Intern Med
; 85: 68-79, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33358337
17.
Early Diagnosis and Outcome in Patients With Wild-Type Transthyretin Cardiac Amyloidosis.
Mayo Clin Proc
; 96(8): 2185-2191, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34353472
18.
Doctor-patient care relationship in genetic cardiomyopathies: An exploratory study on clinical consultations.
PLoS One
; 15(8): e0236814, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32756572
19.
Comprehensive Risk Management in Arrhythmogenic Cardiomyopathy Associated With Autosomal Dominant Carvajal Syndrome: Protecting Families.
JACC Case Rep
; 2(6): 925-929, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-34317383
20.
Prevalence, causes and predictors of cardiovascular hospitalization in patients with hypertrophic cardiomyopathy.
Int J Cardiol
; 318: 94-100, 2020 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32735899