Khalid M. Harbi-Al

Medina, 41477, Saudi Arabia

Last Updated: 09/26/2026

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Found 15 publications

Cardio-Rheumatic Diseases: Inflammasomes Behaving Badly.

Cardio-Rheumatic Diseases: Inflammasomes Behaving Badly.

Journal: International journal of molecular sciences

Published: January 11, 2025

The Immunomodulatory Role of Microbiota in Rheumatic Heart Disease: What Do We Know and What Can We Learn from Other Rheumatic Diseases?

The Immunomodulatory Role of Microbiota in Rheumatic Heart Disease: What Do We Know and What Can We Learn from Other Rheumatic Diseases?

Journal: Medicina (Kaunas, Lithuania)

Published: July 25, 2023

Cytokine Profiling among Children with Multisystem Inflammatory Syndrome versus Simple COVID-19 Infection: A Study from Northwest Saudi Arabia.

Cytokine Profiling among Children with Multisystem Inflammatory Syndrome versus Simple COVID-19 Infection: A Study from Northwest Saudi Arabia.

Journal: Biology

Published: May 27, 2022

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

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

Journal: European review for medical and pharmacological sciences

Published: August 04, 2020

The Polymorphism at the microRNA-155 Binding Site in the AGTR1 Gene is not Significantly Associated with Rheumatic Heart Disease in Saudi Arabia Population.

The Polymorphism at the microRNA-155 Binding Site in the AGTR1 Gene is not Significantly Associated with Rheumatic Heart Disease in Saudi Arabia Population.

Journal: MicroRNA (Shariqah, United Arab Emirates)

Published: September 12, 2019

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

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

Journal: European review for medical and pharmacological sciences

Published: March 07, 2019

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

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

Journal: Medicina (Kaunas, Lithuania)

Published: November 23, 2018

A novel splice-site mutation in the ASPM gene underlies autosomal recessive primary microcephaly.

A novel splice-site mutation in the ASPM gene underlies autosomal recessive primary microcephaly.

Journal: Annals of Saudi medicine

Published: December 07, 2016

CIT, a gene involved in neurogenic cytokinesis, is mutated in human primary microcephaly.

CIT, a gene involved in neurogenic cytokinesis, is mutated in human primary microcephaly.

Journal: Human genetics

Published: June 18, 2016

LGMD2D syndrome: the importance of clinical and molecular genetics in patient and family management. Case Report.

LGMD2D syndrome: the importance of clinical and molecular genetics in patient and family management. Case Report.

Journal: Neuro endocrinology letters

Published: April 20, 2016

The MTHFR C677T polymorphism is associated with mitral valve rheumatic heart disease.

The MTHFR C677T polymorphism is associated with mitral valve rheumatic heart disease.

Journal: European review for medical and pharmacological sciences

Published: January 28, 2016

Impact of MIF Gene Promoter Variations on Risk of Rheumatic Heart Disease and Its Age of Onset in Saudi Arabian Patients.

Impact of MIF Gene Promoter Variations on Risk of Rheumatic Heart Disease and Its Age of Onset in Saudi Arabian Patients.

Journal: Frontiers in immunology

Published: December 17, 2015

Showing 1-12 of 15

Last Updated: 09/26/2026