Rabab Allam
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 12 publications
Alterations in the Plasma Proteome Induced by SARS-CoV-2 and MERS-CoV Reveal Biomarkers for Disease Outcomes for COVID-19 Patients.
Journal: Journal of inflammation research
Published: June 01, 2021
SLC5A1 Mutations in Saudi Arabian Patients With Congenital Glucose-Galactose Malabsorption.
Journal: Journal of pediatric gastroenterology and nutrition
Published: July 29, 2017
Twenty novel mutations in BCKDHA, BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease.
Journal: Molecular genetics and metabolism reports
Published: January 25, 2017
Clinical, Endocrine, and Molecular Genetic Analysis of a Large Cohort of Saudi Arabian Patients with Laron Syndrome.
Journal: Hormone research in paediatrics
Published: December 16, 2016
Two novel LHX3 mutations in patients with combined pituitary hormone deficiency including cervical rigidity and sensorineural hearing loss.
Journal: BMC endocrine disorders
Published: September 07, 2016
Variation in DNAH1 may contribute to primary ciliary dyskinesia.
Journal: BMC medical genetics
Published: February 08, 2015
Variable expression pattern in Donnai-Barrow syndrome: Report of two novel LRP2 mutations and review of the literature.
Journal: European journal of medical genetics
Published: April 11, 2014
Marshall syndrome: further evidence of a distinct phenotypic entity and report of new findings.
Journal: American journal of medical genetics. Part A
Published: October 27, 2013
Spectrum of Mutations in 60 Saudi Patients with Mut Methylmalonic Acidemia.
Journal: JIMD reports
Published: September 18, 2013
A recessive form of Marshall syndrome is caused by a mutation in the COL11A1 gene.
Journal: Journal of medical genetics
Published: April 14, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026