Sialic acid and anti-ganglioside M1 antibodies are invaluable biomarkers correlated with the severity of autism spectrum disorder
Ashaat, Engy A., Sabry, Sahar, Zaki, Moushira E., Mohamed, Ramy, Abdelsattar, Hoda A., Bawady, Somia A., Ashaat, Neveen A., Elnaggar, Walaa, Ganem, Mona M.F., El-Hariri, Hazem M., El-Bassyouni, Hala T., Saleh, Dina Amin
Published in Brain & development (Tokyo. 1979) (01.04.2023)
Published in Brain & development (Tokyo. 1979) (01.04.2023)
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Short term Neurological Complications After Surgical Correction in Children with Congenital Heart Disease: A Single Center Study
Walaa Elnaggar, Imane A. Yassine, Mohamed S. Abdelwahab, Ahmed Y. Abdelglil, Aya M. Fattouh, Ali Elkazaz
Published in Pediatric Sciences Journal (01.01.2023)
Published in Pediatric Sciences Journal (01.01.2023)
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Neonatal Auditory Screening is a Necessity in The Neonatal Intensive Care Unit: Single Center Study
Hala Ahmed ElGindy, Mohamed Farouk Mohamed, Magd Ahmed Kotb, Zahraa Ezz El Din, Hussein Sherif Hamdy, Mohamed Fetouh Hussein, Walaa M. Elnaggar
Published in Pediatric Sciences Journal (01.07.2022)
Published in Pediatric Sciences Journal (01.07.2022)
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Clinical, biochemical, and molecular characterization of mucopolysaccharidosis type III in 34 Egyptian patients
Almenabawy, Nihal, Ramadan, Manal, Kamel, Mona, Mahmoud, Iman G., Amer, Fawzia, Shaheen, Yara, Elnaggar, Walaa, Selim, Laila
Published in American journal of medical genetics. Part A (01.09.2023)
Published in American journal of medical genetics. Part A (01.09.2023)
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The clinical and genetic landscape of developmental and epileptic encephalopathies in Egyptian children
Elkhateeb, Nour, Issa, Mahmoud Y, Elbendary, Hasnaa M, Elnaggar, Walaa, Ramadan, Areef, Rafat, Karima, Kamel, Mona, Abdel-Ghafar, Sherif F, Amer, Fawzia, Hassaan, Hebatallah M, Trunzo, Roberta, Pereira, Catarina, Abdel-Hamid, Mohamed S, D'Arco, Felice, Bauer, Peter, Bertoli-Avella, Aida M, Girgis, Marian, Gleeson, Joseph G, Zaki, Maha S, Selim, Laila
Published in Clinical genetics (01.05.2024)
Published in Clinical genetics (01.05.2024)
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Journal Article
Late Presenting Central Pontine Myelinolysis Post- tonsillectomy in a Child: Case Report
Magd Ahmed Kotb, Menat-allah Mahmoud Elzabet, Walaa Elnaggar
Published in Pediatric Sciences Journal (01.07.2024)
Published in Pediatric Sciences Journal (01.07.2024)
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Journal Article
Clinical, biomarker and genetic spectrum of Niemann‐Pick type C in Egypt: The detection of nine novel NPC1 mutations
Mahmoud, Iman G., Elmonem, Mohamed A., Elkhateeb, Nour M., Elnaggar, Walaa, Sobhi, Ahmed, Girgis, Marian Y., Kamel, Mona, Shaheen, Yara, Samaha, Mona, Ramadan, Areef, Zaki, Maha S., El‐Hawary, Bahaa, Hassan, Sawsan A., Khalifa, Iman A., Mossad, Fawzya, Al‐Menabawy, Nihal M., Zielke, Susanne, Gleeson, Joseph G., Rolfs, Arndt, Selim, Laila A.
Published in Clinical genetics (01.04.2019)
Published in Clinical genetics (01.04.2019)
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Cerebral Folate Transport Deficiency in 2 Cases with Intractable Myoclonic Epilepsy
Girgis, Marian Y, Mahfouz, Eman, Abdellatif, Alshaimaa, Taha, Farah, ElNaggar, Walaa
Published in Journal of epilepsy research (30.06.2024)
Published in Journal of epilepsy research (30.06.2024)
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