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Khalid M. Al-Harbi

Taibah University

23

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140

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A novel homozygous TPM1 mutation in familial pediatric hypertrophic cardiomyopathy and in silico screening of potential targeting drugs.

2020 European Review for Medical and Pharmacological Sciences
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Design, click conventional and microwave syntheses, DNA binding, docking and anticancer studies of benzotriazole-1,2,3-triazole molecular hybrids with different pharmacophores

2020 Journal of Molecular Structure
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The polymorphism at the microRNA-155 binding site in AGTR1 gene is not significantly associated with rheumatic heart disease in Saudi Arabia population

2020
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Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy

2019 Medicina-buenos Aires
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Interaction between MTHFR Polymorphisms and Maternal Age Increases the Risk of Congenital Heart Defects in Down Syndrome

2019 Pakistan Journal of Zoology
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Risk factors for prolonged mechanical ventilation after surgical repair of congenital heart disease. Experience from a single cardiac center

2019 Saudi Medical Journal
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Next-generation sequencing identifies a homozygous mutation in ACADVL associated with pediatric familial dilated cardiomyopathy.

2019 European Review for Medical and Pharmacological Sciences
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Types of Surgical Repair and Outcome in Patients with Tetralogy of Fallot: Experience from A Single Center in Saudi Arabia

2018 The Egyptian Journal of Hospital Medicine
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Targeted Next-Generation Sequencing of 406 Genes Identified Genetic Defects Underlying Congenital Heart Disease in Down Syndrome Patients

2018 Pediatric Cardiology
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Rachitic hypocalcemic cardiomyopathy in an infant

2017 Journal of The Saudi Heart Association
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