Salam Massadeh

Riyadh, Saudi Arabia

Last Updated: 09/26/2026

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Found 29 publications

Jagged-1 mutation is associated with congenital heart defects: a case report.

Jagged-1 mutation is associated with congenital heart defects: a case report.

Journal: Journal of medical case reports
Published: May 01, 2025

Tween 80-Based Self-Assembled Mixed Micelles Boost Valsartan Transdermal Delivery.

Tween 80-Based Self-Assembled Mixed Micelles Boost Valsartan Transdermal Delivery.

Journal: Pharmaceuticals (Basel, Switzerland)
Published: October 25, 2023

TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy.

TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy.

Journal: Journal of cardiovascular development and disease
Published: October 11, 2023

Association between human leukocyte antigen alleles and COVID-19 disease severity.

Association between human leukocyte antigen alleles and COVID-19 disease severity.

Journal: Journal of infection and public health
Published: October 05, 2023

Case report: A founder UGDH variant associated with developmental epileptic encephalopathy in Saudi Arabia.

Case report: A founder UGDH variant associated with developmental epileptic encephalopathy in Saudi Arabia.

Journal: Frontiers in genetics
Published: September 14, 2023

Reply to Zandi, M.; Soltani, S. Comment on "Alfassam et al. Development of a Colorimetric Tool for SARS-CoV-2 and Other Respiratory Viruses Detection Using Sialic Acid Fabricated Gold Nanoparticles. Pharmaceutics 2021, 13, 502".

Reply to Zandi, M.; Soltani, S. Comment on "Alfassam et al. Development of a Colorimetric Tool for SARS-CoV-2 and Other Respiratory Viruses Detection Using Sialic Acid Fabricated Gold Nanoparticles. Pharmaceutics 2021, 13, 502".

Journal: Pharmaceutics
Published: August 29, 2022

Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.

Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.

Journal: PLoS genetics
Published: April 06, 2022

Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genes.

Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genes.

Journal: Frontiers in genetics
Published: February 28, 2022

Fast-Dissolving Nifedipine and Atorvastatin Calcium Electrospun Nanofibers as a Potential Buccal Delivery System.

Fast-Dissolving Nifedipine and Atorvastatin Calcium Electrospun Nanofibers as a Potential Buccal Delivery System.

Journal: Pharmaceutics
Published: January 02, 2022

Consanguinity and Congenital Heart Disease Susceptibility: Insights into Rare Genetic Variations in Saudi Arabia.

Consanguinity and Congenital Heart Disease Susceptibility: Insights into Rare Genetic Variations in Saudi Arabia.

Journal: Genes
Published: December 26, 2021

The Role of the Disrupted Podosome Adaptor Protein (SH3PXD2B) in Frank-Ter Haar Syndrome.

The Role of the Disrupted Podosome Adaptor Protein (SH3PXD2B) in Frank-Ter Haar Syndrome.

Journal: Genes
Published: December 05, 2021

Association of KIR gene polymorphisms with COVID-19 disease.

Association of KIR gene polymorphisms with COVID-19 disease.

Journal: Clinical immunology (Orlando, Fla.)
Published: August 11, 2021
Showing 1-12 of 29

Last Updated: 09/26/2026