Mohammed A. Alomari

Khamis Mushait, Saudi Arabia

Last Updated: 09/26/2026

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Found 12 publications

Incidence and Risk Factors of Retinopathy of Prematurity at the Armed Forces Hospital, Southern Region, Saudi Arabia.

Incidence and Risk Factors of Retinopathy of Prematurity at the Armed Forces Hospital, Southern Region, Saudi Arabia.

Journal: Cureus
Published: September 16, 2025

Incidence and Risk Factors of Intraventricular Hemorrhage in Premature Infants at King Faisal Military Hospital, Southern Region: A Retrospective Review.

Incidence and Risk Factors of Intraventricular Hemorrhage in Premature Infants at King Faisal Military Hospital, Southern Region: A Retrospective Review.

Journal: Cureus
Published: March 26, 2025

Pseudohypoaldosteronism Type 1b in a Saudi Female Infant Due to Homozygous Variant Gene Mutation in SCNN1A: A Case Report.

Pseudohypoaldosteronism Type 1b in a Saudi Female Infant Due to Homozygous Variant Gene Mutation in SCNN1A: A Case Report.

Journal: Cureus
Published: August 18, 2024

Risk Prediction of Severe Bronchopulmonary Dysplasia (BPD) Using the Respiratory Severity Score (RSS) in Extremely Preterm Infants: A Retrospective Study From Saudi Arabia.

Risk Prediction of Severe Bronchopulmonary Dysplasia (BPD) Using the Respiratory Severity Score (RSS) in Extremely Preterm Infants: A Retrospective Study From Saudi Arabia.

Journal: Cureus
Published: March 21, 2024

Retraction: Giant Unruptured Internal Carotid Artery Aneurysm.

Retraction: Giant Unruptured Internal Carotid Artery Aneurysm.

Journal: Cureus
Published: January 26, 2024

LAD-III, a Mild Phenotype Resulting From a Novel Variant of FERMT3 Gene: A Case Report.

LAD-III, a Mild Phenotype Resulting From a Novel Variant of FERMT3 Gene: A Case Report.

Journal: Cureus
Published: December 25, 2023

Congenital Factor X-Riyadh (Stuart-Prower) Deficiency With Isolated Prothrombin Time Prolongation: A Case Report.

Congenital Factor X-Riyadh (Stuart-Prower) Deficiency With Isolated Prothrombin Time Prolongation: A Case Report.

Journal: Cureus
Published: April 12, 2023

Progressive Familial Intrahepatic Cholestasis Type 3 Homozygous Pathogenic Variant c.2906G>A in the ATP Binding Cassette Subfamily B Member 4 (ABCB4) Gene: A Case Report of an Unusual Presentation.

Progressive Familial Intrahepatic Cholestasis Type 3 Homozygous Pathogenic Variant c.2906G>A in the ATP Binding Cassette Subfamily B Member 4 (ABCB4) Gene: A Case Report of an Unusual Presentation.

Journal: Cureus
Published: December 12, 2022

Primary Ciliary Dyskinesia: Phenotype Resulting From a Novel Variant of LRRC56 Gene.

Primary Ciliary Dyskinesia: Phenotype Resulting From a Novel Variant of LRRC56 Gene.

Journal: Cureus
Published: August 27, 2022

Expression of Concern: Giant Unruptured Internal Carotid Artery Aneurysm.

Expression of Concern: Giant Unruptured Internal Carotid Artery Aneurysm.

Journal: Cureus
Published: April 25, 2022

Giant Unruptured Internal Carotid Artery Aneurysm.

Giant Unruptured Internal Carotid Artery Aneurysm.

Journal: Cureus
Published: December 15, 2021

The Use of Epidermal Growth Factor Receptor Type 2-Targeting Tyrosine Kinase Inhibitors in the Management of Epidermal Growth Factor Receptor Type 2-Positive Gastric Cancer: A Narrative Review.

The Use of Epidermal Growth Factor Receptor Type 2-Targeting Tyrosine Kinase Inhibitors in the Management of Epidermal Growth Factor Receptor Type 2-Positive Gastric Cancer: A Narrative Review.

Journal: Cureus
Published: January 16, 2020
Showing 1-12 of 12

Last Updated: 09/26/2026