Clinical and genetic characterization of ten Egyptian patients with Wolf–Hirschhorn syndrome and review of literature
Mekkawy, Mona K., Kamel, Alaa K., Thomas, Manal M., Ashaat, Engy A., Zaki, Maha S., Eid, Ola M., Ismail, Samira, Hammad, Saida A., Megahed, Hisham, ElAwady, Heba, Refaat, Khaled M., Hussien, Shymaa, Helmy, Nivine, Abd Allah, Sally G., Mohamed, Amal M., El Ruby, Mona O.
Published in Molecular genetics & genomic medicine (01.02.2021)
Published in Molecular genetics & genomic medicine (01.02.2021)
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Congenital anomalies in neonates in Fayoum Governorate, Egypt
ElAwady, Heba, AlGameel, Alkasem, Ragab, Tamer, Hassan, Nasser
Published in Eastern Mediterranean health journal (01.08.2021)
Published in Eastern Mediterranean health journal (01.08.2021)
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Journal Article
Neuroblastoma-associated Opsoclonous Myoclonous Ataxia Syndrome: Profile and Outcome Report on 15 Egyptian Patients
Elzomor, Hossam, El Menawi, Salma, Elawady, Heba, Elkinaai, Naglaa, Elshafie, Maged, Refaat, Amal, Ghareeb, Hany, Fawzy, Mohamed
Published in Journal of pediatric hematology/oncology (01.03.2023)
Published in Journal of pediatric hematology/oncology (01.03.2023)
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Effect of Pyridoxine on the safety of Levetiracetam in a pediatric population with Epilepsy - A Retrospective pharmacovigilance study
Alqweai, Hissa, ElAwady, Heba, Hussein, Sherin, aloudah, Reem, Boushra, Amy
Published in Fayoum University Medical Journal (Online) (01.03.2023)
Published in Fayoum University Medical Journal (Online) (01.03.2023)
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The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy
Ashaat, Engy A., Ahmed, Hoda A., Elaraby, Nesma M., Fayez, Alaaeldin, Metwally, Ammal M., Mekkawy, Mona K., Hussen, Dalia Farouk, Ashaat, Neveen A., Elhossini, Rasha M., ElAwady, Heba Ahmed, Abdelgawad, Randa H. A., Gammal, Mona El, Al Kersh, Mohamed Ahmed, Saleh, Dina Amin
Published in Molecular neurobiology (01.08.2024)
Published in Molecular neurobiology (01.08.2024)
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Diagnostic approach of floppy infants: a study in Fayoum University Hospital, Egypt
Abdel Ghaffar, Hadeer, ElAwady, Heba, Abouleinin, Ihab, Rabie, Eslam
Published in Middle East Journal of Medical Genetics (01.07.2017)
Published in Middle East Journal of Medical Genetics (01.07.2017)
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Xmn I polymorphism in Egyptian patients with β-thalassemia major and its correlation with the HbF level
El Gawhary, Somaya, Farid, Mona, Ezzat, Mostafa, ElAwady, Heba, Mostafa, Heba
Published in Gene reports (01.06.2018)
Published in Gene reports (01.06.2018)
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