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Author

Mohamed Abdulhay

ORCID: 0000-0001-7745-7103
Observed ORCID: 0000-0001-7745-7103
OpenAlex ID: A5086477291
Homogentisate 1,2-dioxygenase (HGD) gene variants in young Egyptian patients with alkaptonuria
2023 · Zeinab S. Abdelkhalek, Iman G. Mahmoud, et al. · Scientific Reports · 9
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Polymorphisms of Immunoglobulin G Fc Receptors in Pediatric Guillain–Barré Syndrome
2016 · Lobna Mansour, Marian Girgis, et al. · Neuropediatrics · 7
Evaluation of insulin-like growth factor-1 in apparently healthy infants and prepubertal Egyptian children with different nutritional statuses
2024 · Hanan Mina Fouad, Amal Ahmed Mohamed, et al. · BMC Pediatrics · 5
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MRI Findings and Diagnostic Yield in Pediatric Epilepsy: A Cross-Sectional Study.
2026 · Mohamed Abdulhay, Mostafa Ebead Alsayed Alfeky, et al. · La Clinica Terapeutica
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Multiplex PCR-based epidemiology of viral acute respiratory infections in hospitalized children: implications for antibiotic stewardship in Saudi Arabia
2026 · Yasser Sedky, Mohamed Abdulhay, et al. · Frontiers in Pediatrics
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Association of CTLA-4 exon 1(+49 A/G) polymorphism and susceptibility to SLE in Egyptian children and adolescents
2026 · Faika Arab, Sarah A. Saleh, et al. · Lupus
Angiotensin‐Converting Enzyme 2 (G8790A) Gene Polymorphism as a Risk Factor for COVID‐19 in Egyptian Children and Adolescents
2025 · Ahmed A. A. Ibraheem, Sarah A. Saleh, et al. · Pediatric Pulmonology
Mitochondrial Complex I Deficiency among Egyptian Pediatric Patients with Steroid-Resistant Nephrotic Syndrome
2021 · Doaa M. Abdou, AbdelAal Mohamed, et al. · International Journal of Nephrology
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The influence of Immunoglobulin IgG Fc-receptor polymorphisms on susceptibility to Guillain–Barre' syndrome
2017 · Mohamed Abdulhay · European Journal of Paediatric Neurology
Works count: 9
Citation count: 21
H-index: 3
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