Publications by authors named "Sherin A Taha"

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Regulatory T-cells in children with generalized epilepsy: a case-control study.
Khaled Saad, Eman F Gad, Samaher Taha, Mohamed Gamil M Abo-Elela, Sherin A Taha

Eur J Pediatr· November 2025

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Acid β-glucosidase (GBA1) gene mutational spectrum and clinical phenotypes in patients with gaucher disease: seven novel mutations in a multicenter retrospective cohort study from upper Egypt.
Mervat A M Youssef, Solaf M Elsayed, Khalid I Elsayh, Sherin A Taha, Hala S M Abdelmotogaly

Mol Cell Pediatr· October 2025

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Impact of Nutritional Status on Pulmonary Function in Pediatric Cystic Fibrosis: A Retrospective Multicenter Study from Upper Egypt.
Khaled Saad, Eman F Gad, Samaher F Taha, Sherin A Taha, Hamada K Fayed

Med Sci (Basel)· September 2025

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Analysis of gut microbiota variations in patients with Henoch-Schönlein purpura: a comprehensive systematic review.
Khaled Saad, Muhammad Abd-Ellatif, Nehal E Abdel-Hakem, Abdelrahman Ali, Osama Ahmed Khalil, Sherin A Taha

Int Urol Nephrol· July 2025

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FokI polymorphism of the vitamin D receptor gene: Linking COVID-19 risk to genetic susceptibility in children.
Amal Ahmed Mohamed, Abdullah Taher Alanazi, Hoda H Ahmed, Samar Elfiky, Muhammad T Abdel Ghafar, Sherin A Taha

Cytokine· July 2025

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Febrile Infection-Related Epilepsy Syndrome (FIRES) in children: a retrospective cohort study.
Khaled Saad, Amir M Aboelgheet, Yasser Hamed, Thamer A M Alruwaili, Mohamed Fahmy M Ibrahim, Sherin A Taha, Samaher Taha

Eur J Pediatr· February 2025

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Maternal chorioamnionitis and the risk for necrotizing enterocolitis in the United States: A national cohort study.
Mohsen A A Farghaly, Sarah Alzayyat, Daliah Kassim, Sherin A Taha, Hany Aly

Early Hum Dev· October 2024

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Association of CYP3A5*3 and CYP1A1*2C Polymorphism with Development of Acute Myeloid Leukemia in Egyptian Patients.
Nahed Abd El Wahab, Nevine F Shafik, Roxan E Shafik, Sherin A Taha, Hanan E Shafik

Asian Pac J Cancer Prev· March 2017

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