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1
Trends in diagnosis, referral, red flag onset, patient profiles and natural outcome of de novo cardiac amyloidosis and their multidisciplinary implications
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Trends in diagnosis, referral, red flag onset, patient profiles and natural outcome of de novo cardiac amyloidosis and their multidisciplinary implications

embargo 640030 ;ISSN: 1784-973X ;ISSN: 0001-5385 ;EISSN: 1784-973X ;DOI: 10.1080/00015385.2021.1976450

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2
Molecular mechanism of triptolide in myocardial fibrosis through the Wnt/β-catenin signaling pathway
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Molecular mechanism of triptolide in myocardial fibrosis through the Wnt/β-catenin signaling pathway

Scandinavian cardiovascular journal : SCJ, 2024-12, Vol.58 (1), p.2295785 [Peer Reviewed Journal]

EISSN: 1651-2006 ;DOI: 10.1080/14017431.2023.2295785 ;PMID: 38164796

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3
Exploration and validation of signature genes and immune associations in septic cardiomyopathy
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Article
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Exploration and validation of signature genes and immune associations in septic cardiomyopathy

Clinical and experimental hypertension (1993), 2024-12, Vol.46 (1), p.2302570-2302570 [Peer Reviewed Journal]

ISSN: 1064-1963 ;EISSN: 1525-6006 ;DOI: 10.1080/10641963.2024.2302570 ;PMID: 38281072

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4
Can native T1 mapping sequence be used as a non-invasive alternative imaging tool to LGE sequence for evaluating DCM patients?
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Can native T1 mapping sequence be used as a non-invasive alternative imaging tool to LGE sequence for evaluating DCM patients?

Egyptian Journal of Radiology and Nuclear Medicine, 2024-12, Vol.55 (1), p.1-10 [Peer Reviewed Journal]

The Author(s) 2024 ;COPYRIGHT 2024 Springer ;ISSN: 0378-603X ;EISSN: 2090-4762 ;DOI: 10.1186/s43055-023-01180-0

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5
Short-term regulation of TSFM level does not alter amyloidogenesis and mitochondrial function in type-specific cells
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Short-term regulation of TSFM level does not alter amyloidogenesis and mitochondrial function in type-specific cells

Molecular biology reports, 2024-12, Vol.51 (1), p.484-484 [Peer Reviewed Journal]

The Author(s), under exclusive licence to Springer Nature B.V. 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. ;2024. The Author(s), under exclusive licence to Springer Nature B.V. ;ISSN: 0301-4851 ;EISSN: 1573-4978 ;DOI: 10.1007/s11033-024-09426-4 ;PMID: 38578353

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6
Ghrelin inhibits myocardial pyroptosis in diabetic cardiomyopathy by regulating ERS and NLRP3 inflammasome crosstalk through the PI3K/AKT pathway
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Ghrelin inhibits myocardial pyroptosis in diabetic cardiomyopathy by regulating ERS and NLRP3 inflammasome crosstalk through the PI3K/AKT pathway

Journal of drug targeting, 2024-12, Vol.32 (2), p.148 [Peer Reviewed Journal]

EISSN: 1029-2330 ;DOI: 10.1080/1061186X.2023.2295268 ;PMID: 38088811

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7
Takotsubo syndrome after bilateral simultaneous total knee arthroplasty - A case report
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Takotsubo syndrome after bilateral simultaneous total knee arthroplasty - A case report

Journal of orthopaedics, 2024-08, Vol.54, p.1-4 [Peer Reviewed Journal]

2024 Professor P K Surendran Memorial Education Foundation ;2024 Professor P K Surendran Memorial Education Foundation. Published by Elsevier B.V. All rights reserved. ;ISSN: 0972-978X ;EISSN: 0972-978X ;DOI: 10.1016/j.jor.2024.03.006 ;PMID: 38496261

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8
Non-dilated left ventricular non-compaction cardiomyopathy with systolic dysfunction is reclassified as non-dilated left ventricular cardiomyopathy with hypertrabeculation
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Non-dilated left ventricular non-compaction cardiomyopathy with systolic dysfunction is reclassified as non-dilated left ventricular cardiomyopathy with hypertrabeculation

International journal of cardiology, 2024-07, Vol.406, p.132077 [Peer Reviewed Journal]

EISSN: 1874-1754 ;DOI: 10.1016/j.ijcard.2024.132077 ;PMID: 38643798

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9
A rare homozygous mutation in the YARS2 gene presents with hypertrophic cardiomyopathy, lactic acidosis and anemia in a Chinese infant
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A rare homozygous mutation in the YARS2 gene presents with hypertrophic cardiomyopathy, lactic acidosis and anemia in a Chinese infant

Gene, 2024-07, Vol.914, p.148379 [Peer Reviewed Journal]

EISSN: 1879-0038 ;DOI: 10.1016/j.gene.2024.148379 ;PMID: 38490507

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10
Levosimendan in cardiac amyloidosis: Unveiling promising paths
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Article
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Levosimendan in cardiac amyloidosis: Unveiling promising paths

International journal of cardiology, 2024-07, Vol.406, p.131994 [Peer Reviewed Journal]

EISSN: 1874-1754 ;DOI: 10.1016/j.ijcard.2024.131994 ;PMID: 38575001

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11
Comparison of electrographic changes, clinical features and outcomes in different variants of Takotsubo syndrome
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Comparison of electrographic changes, clinical features and outcomes in different variants of Takotsubo syndrome

International journal of cardiology, 2024-07, Vol.406, p.132072 [Peer Reviewed Journal]

Copyright © 2024 Elsevier B.V. All rights reserved. ;EISSN: 1874-1754 ;DOI: 10.1016/j.ijcard.2024.132072 ;PMID: 38643795

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12
Emerging concepts in inflammatory cardiomyopathy
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Article
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Emerging concepts in inflammatory cardiomyopathy

International journal of cardiology, 2024-07, Vol.406, p.132058 [Peer Reviewed Journal]

EISSN: 1874-1754 ;DOI: 10.1016/j.ijcard.2024.132058 ;PMID: 38636604

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13
Left atrial strains in cardiac amyloidosis -does its subtype matter?
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Article
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Left atrial strains in cardiac amyloidosis -does its subtype matter?

International journal of cardiology, 2024-07, Vol.406, p.132078 [Peer Reviewed Journal]

EISSN: 1874-1754 ;DOI: 10.1016/j.ijcard.2024.132078 ;PMID: 38643799

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14
Natural history of cardiac involvement in myotonic dystrophy type 1 - Emphasis on the need for lifelong follow-up
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Natural history of cardiac involvement in myotonic dystrophy type 1 - Emphasis on the need for lifelong follow-up

International journal of cardiology, 2024-07, Vol.406, p.132070 [Peer Reviewed Journal]

Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved. ;EISSN: 1874-1754 ;DOI: 10.1016/j.ijcard.2024.132070 ;PMID: 38643802

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15
Reduced Ejection Fraction in Elite Endurance Athletes: Clinical and Genetic Overlap With Dilated Cardiomyopathy
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Article
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Reduced Ejection Fraction in Elite Endurance Athletes: Clinical and Genetic Overlap With Dilated Cardiomyopathy

embargo 742600;All rights reserved ;ISSN: 0009-7322 ;ISSN: 1524-4539 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.122.063777

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16
Gender disparities and predictors of in-hospital mortality with Takotsubo cardiomyopathy
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Article
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Gender disparities and predictors of in-hospital mortality with Takotsubo cardiomyopathy

International journal of cardiology, 2024-06, Vol.405, p.131959 [Peer Reviewed Journal]

Published by Elsevier B.V. ;EISSN: 1874-1754 ;DOI: 10.1016/j.ijcard.2024.131959 ;PMID: 38484803

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17
Safety and efficacy of levosimendan in patients with cardiac amyloidosis
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Article
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Safety and efficacy of levosimendan in patients with cardiac amyloidosis

International journal of cardiology, 2024-06, Vol.405, p.131963 [Peer Reviewed Journal]

Copyright © 2024 Elsevier B.V. All rights reserved. ;EISSN: 1874-1754 ;DOI: 10.1016/j.ijcard.2024.131963 ;PMID: 38479497

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18
Renal impairment and outcome in Takotsubo syndrome: Insights from a national multicentric cohort
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Article
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Renal impairment and outcome in Takotsubo syndrome: Insights from a national multicentric cohort

International journal of cardiology, 2024-06, Vol.405, p.131971 [Peer Reviewed Journal]

Copyright © 2024 Elsevier B.V. All rights reserved. ;EISSN: 1874-1754 ;DOI: 10.1016/j.ijcard.2024.131971 ;PMID: 38490270

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19
Protein phosphatase 2A anchoring disruptor gene therapy for familial dilated cardiomyopathy
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Article
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Protein phosphatase 2A anchoring disruptor gene therapy for familial dilated cardiomyopathy

Molecular therapy. Methods & clinical development, 2024-06, Vol.32 (2), p.101233-101233, Article 101233 [Peer Reviewed Journal]

2024 The Author(s) ;2024 The Author(s). ;2024 The Author(s) 2024 ;ISSN: 2329-0501 ;EISSN: 2329-0501 ;DOI: 10.1016/j.omtm.2024.101233 ;PMID: 38572067

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20
Tail length and E525K dilated cardiomyopathy mutant alter human β-cardiac myosin super-relaxed state
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Tail length and E525K dilated cardiomyopathy mutant alter human β-cardiac myosin super-relaxed state

The Journal of general physiology, 2024-06, Vol.156 (6) [Peer Reviewed Journal]

2024 Duno-Miranda et al. ;EISSN: 1540-7748 ;DOI: 10.1085/jgp.202313522 ;PMID: 38709176

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