Detalhe da pesquisa
1.
IgG4-Related disease with diffuse myopericardial involvement- value of CMR: a case report and literature review of cardiac involvement.
BMC Cardiovasc Disord
; 24(1): 200, 2024 Apr 06.
Artigo
Inglês
| MEDLINE | ID: mdl-38582827
2.
Whole-exome sequencing revealed a likely pathogenic variant in NF1 causing neurofibromatosis type I and Arrhythmogenic Cardiomyopathy.
BMC Cardiovasc Disord
; 24(1): 220, 2024 Apr 23.
Artigo
Inglês
| MEDLINE | ID: mdl-38654147
3.
A novel homozygous variant (c.5876T > C: p. Leu1959Pro) in DYSF segregates with limb-girdle muscular dystrophy: a case report.
BMC Musculoskelet Disord
; 25(1): 241, 2024 Mar 27.
Artigo
Inglês
| MEDLINE | ID: mdl-38539162
4.
Feature tracking cardiac magnetic resonance imaging to assess cardiac manifestations of systemic diseases.
Heart Fail Rev
; 28(5): 1189-1199, 2023 09.
Artigo
Inglês
| MEDLINE | ID: mdl-37191926
5.
Cardiac magnitude resonance findings of a patient with Kawasaki-giant coronary aneurysm and active myocarditis.
Cardiol Young
; 33(5): 817-818, 2023 May.
Artigo
Inglês
| MEDLINE | ID: mdl-36111600
6.
Left Ventricular Myocardial Dysfunction Evaluation in Thalassemia Patients Using Echocardiographic Radiomic Features and Machine Learning Algorithms.
J Digit Imaging
; 36(6): 2494-2506, 2023 12.
Artigo
Inglês
| MEDLINE | ID: mdl-37735309
7.
Novel homozygous stop-gain pathogenic variant of PPP1R13L gene leads to arrhythmogenic cardiomyopathy.
BMC Cardiovasc Disord
; 22(1): 359, 2022 08 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35933355
8.
Intramyocardial echo-free space with a turbulent flow within, suggestive of an aneurysmal coronary artery.
Echocardiography
; 39(2): 407-412, 2022 02.
Artigo
Inglês
| MEDLINE | ID: mdl-35006613
9.
Case Report of a 33-year-old with Ebstein malformation of tricuspid valve and hypertrophic cardiomyopathy.
Cardiol Young
; 32(4): 674-675, 2022 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-34496998
10.
Whole-exome sequencing identified compound heterozygous variants in the TTN gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family.
Cardiol Young
; : 1-6, 2021 Nov 16.
Artigo
Inglês
| MEDLINE | ID: mdl-34782032
11.
Delayed diffuse inflammatory myocardial damage in a child with a history of systemic inflammatory syndrome related to COVID-19.
Eur Heart J
; 42(16): 1639, 2021 04 21.
Artigo
Inglês
| MEDLINE | ID: mdl-33341878
12.
Whole -exome sequencing identified compound heterozygous variants in the TTN gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family - CORRIGENDUM.
Cardiol Young
; : 1, 2021 Dec 06.
Artigo
Inglês
| MEDLINE | ID: mdl-34865674
13.
A novel likely pathogenic homozygous RBCK1 variant in dilated cardiomyopathy with muscle weakness.
ESC Heart Fail
; 11(3): 1472-1482, 2024 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-38329383
14.
Role of feature tracking cardiac magnetic resonance imaging in early detection of cardiac dysfunction in ß-thalassemia patients recovered from COVID-19: A cross-sectional study.
Health Sci Rep
; 7(1): e1783, 2024 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-38186932
15.
Whole-exome sequencing reveals a likely pathogenic LMNA variant causing hypertrophic cardiomyopathy.
Lab Med
; 55(1): 62-70, 2024 Jan 06.
Artigo
Inglês
| MEDLINE | ID: mdl-37246508
16.
European Association of Cardiovascular Imaging (EACVI) survey on Cardiovascular Multimodality Imaging in Acute Myocarditis.
Eur Heart J Cardiovasc Imaging
; 2024 Apr 03.
Artigo
Inglês
| MEDLINE | ID: mdl-38568982
17.
Paediatric heart transplantation during the COVID-19 pandemic in Iran: single-centre experience.
ESC Heart Fail
; 10(4): 2630-2636, 2023 08.
Artigo
Inglês
| MEDLINE | ID: mdl-37343945
18.
Arrhythmogenic left ventricular cardiomyopathy caused by a novel likely pathogenic DSP mutation, p.K1165Rfs*8, in a family with sudden cardiac death.
BMC Med Genomics
; 16(1): 266, 2023 10 26.
Artigo
Inglês
| MEDLINE | ID: mdl-37885024
19.
Coronary artery involvement in a patient with IgG4-related disease.
Radiol Case Rep
; 18(10): 3699-3703, 2023 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-37609068
20.
Polymorphism of rs599839 in the PSRC1 gene is associated with coronary artery disease in an Iranian population.
J Cardiovasc Thorac Res
; 15(3): 168-173, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-38028723