Moeenaldeen D. Sayed-Alsayed
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
Impact of glycerol phenylbutyrate on biochemistry and outcomes in paediatric patients with urea cycle disorders: a multicentre case series from Saudi Arabia.
Journal: Orphanet journal of rare diseases
Published: March 30, 2025
Consensus-based expert recommendations on the management of MPS IVa and VI in Saudi Arabia.
Journal: Orphanet journal of rare diseases
Published: February 15, 2024
Validation of Ion TorrentTM Inherited Disease Panel with the PGMTM Sequencing Platform for Rapid and Comprehensive Mutation Detection.
Journal: Genes
Published: April 02, 2018
Impact of long-term elosulfase alfa on activities of daily living in patients with Morquio A syndrome in an open-label, multi-center, phase 3 extension study.
Journal: Molecular genetics and metabolism
Published: October 27, 2017
Variation in DNAH1 may contribute to primary ciliary dyskinesia.
Journal: BMC medical genetics
Published: February 08, 2015
Mitochondrial Neurogastrointestinal Encephalomyopathy Treated with Stem Cell Transplantation: A Case Report and Review of Literature.
Journal: Hematology/oncology and stem cell therapy
Published: September 25, 2014
Spectrum of Mutations in 60 Saudi Patients with Mut Methylmalonic Acidemia.
Journal: JIMD reports
Published: September 18, 2013
Mutations underlying 3-hydroxy-3-methylglutaryl CoA lyase deficiency in the Saudi population.
Journal: BMC medical genetics
Published: May 21, 2006
Goldenhar syndrome and hereditary tyrosinemia type 1.
Journal: Saudi medical journal
Published: January 09, 2003
Goldenhar syndrome and hereditary tyrosinemia type 1.
Journal: Neurosciences (Riyadh, Saudi Arabia)
Published: January 01, 2003
Showing 1-10 of 10
Last Updated: 09/26/2026