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Case-Based Clinical Cardiology

1, 2021

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Exploring the role of non-coding RNAs in atrial septal defect pathogenesis: A systematic review

PloS one, 2024-08, Vol.19 (8), p.e0306576

2024

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Multimodal Imaging Atlas of Cardiac Masses

2022

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Practical Cardiology

2017

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Practical Cardiology: Principles and Approaches

Second edition, 2021

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Whole-exome sequencing revealed a likely pathogenic variant in NF1 causing neurofibromatosis type I and Arrhythmogenic Cardiomyopathy

BMC cardiovascular disorders, 2024-04, Vol.24 (1), p.220-220, Article 220

2024

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Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy

BMC medical genomics, 2023-12, Vol.16 (1), p.334-334, Article 334

2023

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Development of a patients' satisfaction analysis system using machine learning and lexicon-based methods

BMC health services research, 2023-03, Vol.23 (1), p.280-280, Article 280

2023

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Associations between low serum levels of ANRIL and some common gene SNPs in Iranian patients with premature coronary artery disease

Scientific reports, 2024-01, Vol.14 (1), p.1244-1244, Article 1244

2024

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A novel likely pathogenic variant in the FBXO32 gene associated with dilated cardiomyopathy according to whole‑exome sequencing

BMC medical genomics, 2022-11, Vol.15 (1), p.1-234, Article 234

2022

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A novel stop-gain pathogenic variant in the KCNQ1 gene causing long QT syndrome 1

European journal of medical research, 2023-01, Vol.28 (1), p.23-23, Article 23

2023

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Detection of a novel pathogenic variant in KCNH2 associated with long QT syndrome 2 using whole exome sequencing

BMC medical genomics, 2024-05, Vol.17 (1), p.126-126, Article 126

2024

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Arrhythmogenic left ventricular cardiomyopathy caused by a novel likely pathogenic DSP mutation, p.K1165Rfs8, in a family with sudden cardiac death

BMC medical genomics, 2023-10, Vol.16 (1), p.1-266, Article 266

2023

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A novel homozygous variant (c.5876T > C: p. Leu1959Pro) in DYSF segregates with limb-girdle muscular dystrophy: a case report

BMC musculoskeletal disorders, 2024-03, Vol.25 (1), p.241-241, Article 241

2024

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Small Molecules with Big Impacts on Cardiovascular Diseases

Biochemical genetics, 2020-06, Vol.58 (3), p.359-383

2020

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Left main and three vessels spontaneous coronary artery dissection as an incidental finding in young man with history of Hodgkin's lymphoma-a case report

BMC cardiovascular disorders, 2024-01, Vol.24 (1), p.14-14, Article 14

2024

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A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects

European journal of medical research, 2022-12, Vol.27 (1), p.286-286, Article 286

2022

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A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy

BMC cardiovascular disorders, 2023-10, Vol.23 (1), p.1-487, Article 487

2023

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Prevention of anthracycline-induced cardiotoxicity: a systematic review and network meta-analysis

International journal of clinical pharmacy, 2021-02, Vol.43 (1), p.25-34

2021

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Exploring TTN variants as genetic insights into cardiomyopathy pathogenesis and potential emerging clues to molecular mechanisms in cardiomyopathies

Scientific reports, 2024-03, Vol.14 (1), p.5313-37, Article 5313

2024

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Deep COVID DeteCT: an international experience on COVID-19 lung detection and prognosis using chest CT

NPJ digital medicine, 2021-01, Vol.4 (1), p.11-11, Article 11

2021

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Combination of FLNC and JUP variants causing arrhythmogenic cardiomyopathy in an Iranian family with different clinical features

BMC cardiovascular disorders, 2024-08, Vol.24 (1), p.442-8

2024

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Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole‐exome sequencing

Journal of arrhythmia, 2023-06, Vol.39 (3), p.430-453

2023

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Microvascular and structural analysis of the retina and choroid in heart failure patients with reduced ejection fraction

Scientific reports, 2023-04, Vol.13 (1), p.5467-5467, Article 5467

2023

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Novel homozygous stop-gain pathogenic variant of PPP1R13L gene leads to arrhythmogenic cardiomyopathy

BMC cardiovascular disorders, 2022-08, Vol.22 (1), p.1-359, Article 359

2022

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Case-Based Clinical Cardiology

Exploring the role of non-coding RNAs in atrial septal defect pathogenesis: A systematic review

Multimodal Imaging Atlas of Cardiac Masses

Practical Cardiology

Practical Cardiology: Principles and Approaches

Whole-exome sequencing revealed a likely pathogenic variant in NF1 causing neurofibromatosis type I and Arrhythmogenic Cardiomyopathy

Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy

Development of a patients' satisfaction analysis system using machine learning and lexicon-based methods

Associations between low serum levels of ANRIL and some common gene SNPs in Iranian patients with premature coronary artery disease

A novel likely pathogenic variant in the FBXO32 gene associated with dilated cardiomyopathy according to whole‑exome sequencing

A novel stop-gain pathogenic variant in the KCNQ1 gene causing long QT syndrome 1

Detection of a novel pathogenic variant in KCNH2 associated with long QT syndrome 2 using whole exome sequencing

Arrhythmogenic left ventricular cardiomyopathy caused by a novel likely pathogenic DSP mutation, p.K1165Rfs8, in a family with sudden cardiac death

A novel homozygous variant (c.5876T > C: p. Leu1959Pro) in DYSF segregates with limb-girdle muscular dystrophy: a case report

Small Molecules with Big Impacts on Cardiovascular Diseases

Left main and three vessels spontaneous coronary artery dissection as an incidental finding in young man with history of Hodgkin's lymphoma-a case report

A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects

A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy

Prevention of anthracycline-induced cardiotoxicity: a systematic review and network meta-analysis

Exploring TTN variants as genetic insights into cardiomyopathy pathogenesis and potential emerging clues to molecular mechanisms in cardiomyopathies

Deep COVID DeteCT: an international experience on COVID-19 lung detection and prognosis using chest CT

Combination of FLNC and JUP variants causing arrhythmogenic cardiomyopathy in an Iranian family with different clinical features

Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole‐exome sequencing

Microvascular and structural analysis of the retina and choroid in heart failure patients with reduced ejection fraction

Novel homozygous stop-gain pathogenic variant of PPP1R13L gene leads to arrhythmogenic cardiomyopathy

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