20 May 2026
Reversible high-fat ketogenic formula-induced hypertriglyceridemia in a child with NALCN mutation on a ketogenic diet: a case reportPublisher siteMolecular Biology Reports, Diet and metabolism studies
Active, last published 2026
In metabolism and genetic disorders
Heba
Dawoud
Scholar“Research focused on Metabolism and Genetic Disorders and adjacent fields.”
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01 · About the work
What I study
eba Dawoud is a researcher working on Metabolism and Genetic Disorders. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Heba's work has been cited 58 times across 3 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
03 · Research focus
Topics
Metabolism and Genetic Disorders×5Diet and metabolism studies×3Epigenetics and DNA Methylation×2Mitochondrial Function and Pathology×2Fatty Acid Research and Health×2
04 · Where I am
Affiliations
Affiliation on published researchTanta University Hospital, EgyptDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
6 works1 Apr 2026Open access
Severe osteogenesis imperfecta due to homozygous glycine substitutions in <i>COL1A1</i> and <i>COL1A2</i>Publisher siteEuropean Journal of Endocrinology, Connective tissue disorders research
29 Nov 2025Open access
A multicenter study on clinico-epidemiological profile of phenylketonuria in Egyptian childrenPublisher siteScientific Reports
30 Jul 2025
Comparing long-term nasal projection and rotation outcomes in rhinoplasty: a systematic review and meta-analysis of columellar strut graft versus septal extension graftPublisher siteEuropean Journal of Plastic Surgery, Nasal Surgery and Airway Studies
20 May 2025Open access2cites
Safety and efficacy of Silodosin as medical expulsive therapy after shock wave lithotripsy in paediatric patients with renal stonesPublisher siteUrolithiasis, Kidney Stones and Urolithiasis Treatments
14 Jun 2024
Clinical and molecular characterization of myotonia congenita using whole-exome sequencing in Egyptian patientsPublisher siteMolecular Biology Reports, Genetic Neurodegenerative Diseases
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