Badr M. Alsaleem

Riyadh, Saudi Arabia

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 23 publications

Gut virome profile in new onset treatment naïve Saudi children with ulcerative colitis.

Gut virome profile in new onset treatment naïve Saudi children with ulcerative colitis.

Journal: Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association

Published: January 20, 2025

Early diagnosis and follow-up of cerebrotendinous xanthomatosis in infant siblings presenting with congenital diarrhea: A case study from Saudi Arabia.

Early diagnosis and follow-up of cerebrotendinous xanthomatosis in infant siblings presenting with congenital diarrhea: A case study from Saudi Arabia.

Journal: Molecular genetics and metabolism reports

Published: December 11, 2024

Clinical variability in cerebrotendinous xanthomatosis (CTX): Insights from 16 cases across Gulf Cooperation Council's (GCC's) high consanguineous population.

Clinical variability in cerebrotendinous xanthomatosis (CTX): Insights from 16 cases across Gulf Cooperation Council's (GCC's) high consanguineous population.

Journal: Journal of clinical lipidology

Published: November 25, 2024

Gut fungal profile in new onset treatment-naïve ulcerative colitis in Saudi children.

Gut fungal profile in new onset treatment-naïve ulcerative colitis in Saudi children.

Journal: Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association

Published: June 22, 2024

Bacterial dysbiosis in newly diagnosed treatment naïve pediatric ulcerative colitis in Saudi Arabia.

Bacterial dysbiosis in newly diagnosed treatment naïve pediatric ulcerative colitis in Saudi Arabia.

Journal: Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association

Published: February 17, 2024

KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon.

KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon.

Journal: Human genetics

Published: October 17, 2022

Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis.

Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis.

Journal: Nature genetics

Published: October 11, 2021

Tricho-hepato-enteric syndrome: Retrospective multicenter experience in Saudi Arabia.

Tricho-hepato-enteric syndrome: Retrospective multicenter experience in Saudi Arabia.

Journal: Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association

Published: August 20, 2021

Clinical, Biochemical, and Molecular Characterization of Neonatal-Onset Dubin-Johnson Syndrome in a Large Case Series From the Arabs.

Clinical, Biochemical, and Molecular Characterization of Neonatal-Onset Dubin-Johnson Syndrome in a Large Case Series From the Arabs.

Journal: Frontiers in pediatrics

Published: July 15, 2021

Viral dysbiosis in children with new-onset celiac disease.

Viral dysbiosis in children with new-onset celiac disease.

Journal: PloS one

Published: May 27, 2021

Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects.

Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects.

Journal: Human genetics

Published: February 17, 2021

Fungal Dysbiosis in Children with Celiac Disease.

Fungal Dysbiosis in Children with Celiac Disease.

Journal: Digestive diseases and sciences

Published: August 31, 2020

Showing 1-12 of 23

Last Updated: 09/26/2026