Author

Rawda Sunbul

Observed names: Sunbul Rawda, Sunbul, Rawda

Institution: Qatif Central Hospital

Observed institutions: Qatif Central Hospital, Shahid Beheshti University of Medical Sciences

OpenAlex ID: A5039988194

Diagnosis and treatment of late-onset Pompe disease in the Middle East and North Africa region: consensus recommendations from an expert group

2015 · The MENA Pompe Working Group, Fatma Al Jasmi, et al. · BMC Neurology · 44

Lethal variants in humans: lessons learned from a large molecular autopsy cohort

2021 · Hanan E. Shamseldin, Lama AlAbdi, et al. · Genome Medicine · 31

The many faces of peroxisomal disorders: Lessons from a large Arab cohort

2018 · Jumanah Alshenaifi, Nour Ewida, et al. · Clinical Genetics · 24

6-Pyruvoyltetrahydropterin Synthase Deficiency: Review and Report of 28 Arab Subjects

2019 · Mohammed Almannai, Rana Felemban, et al. · Pediatric Neurology · 19

Infantile Serine Biosynthesis Defect Due to Phosphoglycerate Dehydrogenase Deficiency: Variability in Phenotype and Treatment Response, Novel Mutations, and Diagnostic Challenges

2017 · Paul J. Benke, Ryan J. Hidalgo, et al. · Journal of Child Neurology · 19

Consensus-based expert recommendations on the management of MPS IVa and VI in Saudi Arabia

2024 · Moeenaldeen AlSayed, Dia Arafa, et al. · Orphanet Journal of Rare Diseases · 4

Experts’ Opinion in Fabry Disease Management and the Unmet Medical Need: The Saudi Perspective

2024 · Majid Alfadhel, Nouriya Al Sannaa, et al. · Therapeutics and Clinical Risk Management · 1

Facilitating intrafamily communication to enable earlier diagnosis of Fabry disease in relatives: Expert opinion

2024 · Dominique P. Germain, Fathiya Al Murshedi, et al. · Molecular Genetics and Metabolism · 1

The landscape of acid sphingomyelinase deficiency in a new therapeutic era: insights from experts in the Gulf region

2023 · Moeenaldeen AlSayed, Fatma Al-Jasmi, et al. · Journal of Biochemical and Clinical Genetics · 1

Expert opinion on facilitating intrafamily communication in rare diseases—Lessons from Fabry disease

2025 · Dominique P. Germain, Fatma Al-Jasmi, et al. · Genetics in Medicine Open

A case report of a first pregnant woman with late-onset multiple acyl-CoA dehydrogenase deficiency in Saudi Arabia

2022 · Shirin Al Sharfa, Rawda Sunbul, et al. · Journal of Biochemical and Clinical Genetics

Works count: 14

Citation count: 144

H-index: 5

I10-index: 5