T-Regulatory Cell Subsets in Children with Type 1 Diabetes Mellitus: Relation to Control of the Disease
Ghonaim, Mabrouk M, El-Edel, Rawhia H, Kamal Eldein, Samar M, Abo El Fotoh, Wafaa Moustafa M, Salman, Samar S
Published in Endocrine, metabolic & immune disorders drug targets (01.01.2017)
Published in Endocrine, metabolic & immune disorders drug targets (01.01.2017)
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The genetic variant “C588T” of GABARG2 is linked to childhood idiopathic generalized epilepsy and resistance to antiepileptic drugs
Abou El Ella, Soheir S., Tawfik, Maha Atef, Abo El Fotoh, Wafaa Moustafa M., Soliman, Omar Ahmed M.
Published in Seizure (London, England) (01.08.2018)
Published in Seizure (London, England) (01.08.2018)
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Journal Article
The potential implication of SCN1A and CYP3A5 genetic variants on antiepileptic drug resistance among Egyptian epileptic children
Abo El Fotoh, Wafaa Moustafa M, Abd el naby, Sameh abd Allah, El-din Habib, Mona Salah, Ahmed AL-refai, Abeer, Kasemy, Zeinab A
Published in Seizure (London, England) (01.10.2016)
Published in Seizure (London, England) (01.10.2016)
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Genetic Variants and Haplotypes of Tryptophan Hydroxylase 2 and Reelin Genes May Be Linked with Attention Deficit Hyperactivity Disorder in Egyptian Children
Abo El Fotoh, Wafaa Moustafa M, Bayomy, Noha Rabie, Kasemy, Zeinab A, Barain, Ahmed Moustafa, Shalaby, Basma Mofed, Abd el naby, Sameh Abdallah
Published in ACS chemical neuroscience (15.07.2020)
Published in ACS chemical neuroscience (15.07.2020)
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Journal Article
Autism Spectrum Disorders: The Association with Inherited Metabolic Disorders and Some Trace Elements. A Retrospective Study
El Fotoh, Wafaa Moustafa M Abo, El Naby, Sameh Abdallah Abd, Abd El Hady, Nahla M Said
Published in CNS & neurological disorders drug targets (01.01.2019)
Published in CNS & neurological disorders drug targets (01.01.2019)
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Journal Article
The potential role of incorporating real-time PCR and DNA sequencing for amplification and detection of 16S rRNA gene signatures in neonatal sepsis
Midan, Dina A, Abo El Fotoh, Wafaa Moustafa M, El Shalakany, Abeer H
Published in The journal of maternal-fetal & neonatal medicine (18.06.2017)
Published in The journal of maternal-fetal & neonatal medicine (18.06.2017)
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Biochemical alteration in children with idiopathic nephrotic syndrome associated with an increased risk of sensorineural hearing loss; additional insights in cochlear renal relationship
El Mashad, Ghada Mohamed, Abo El Fotoh, Wafaa Moustafa M, Zein El Abedein, Ahmed Mahmoud, Abd El Sadek, Fatma Abd El raoof
Published in International journal of pediatric otorhinolaryngology (01.06.2017)
Published in International journal of pediatric otorhinolaryngology (01.06.2017)
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Establishment of blood pressure nomograms representative for Egyptian children and adolescents: a cross-sectional study
El-shafie, Ali M, El-Gendy, Fady M, Allhony, Dalia M, Abo El Fotoh, Wafaa Moustafa M, Omar, Zein A, Samir, Mohamed A, Bahbah, Wael A, Abd el naby, Sameh Abdallah, El Zayat, Rania S, Abd El Hady, Nahla M Said, El Gazar, Basim A, Zannoun, Mohamed A, Kasemy, Zeinab A, El-Bazzar, Ahmed N, Abd El-Fattah, Mohamed Abd El-nour, Abd El-monsef, Amir A, Kairallah, Amir M, Raafet, Hythem M, Baz, Ghada M, Salah, Amany Gaber, Galab, Walaa S
Published in BMJ open (25.07.2018)
Published in BMJ open (25.07.2018)
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Children with Down syndrome: association of Bcl-I polymorphism of nuclear receptor subfamily 3 group C member 1 gene with obesity
Abo El-Fotoh, Wafaa Moustafa M., Bahbah, Hebatallah Mohammed Nasser, Elaithy, Manal Abd El-Monem, Ahmed, Rana Khairy Rashad, Bayomy, Noha Rabie
Published in Pediatric research (01.07.2022)
Published in Pediatric research (01.07.2022)
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Molecular study of developmental sex disorders in children
AboElella, Soheir S., Tawfik, Maha A.M., Abo El-fotoh, Wafaa moustafa M.
Published in The Egyptian journal of medical human genetics (01.07.2015)
Published in The Egyptian journal of medical human genetics (01.07.2015)
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Screening for developmental delay in preschool-aged children using parent-completed Ages and Stages Questionnaires: additional insights into child development
Abo El Elella, Soheir S, Tawfik, Maha A M, Abo El Fotoh, Wafaa Moustafa M, Barseem, Naglaa Fathy
Published in Postgraduate medical journal (01.10.2017)
Published in Postgraduate medical journal (01.10.2017)
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A66G and C524T polymorphisms of methionine synthase reductase gene are linked to the development of acyanotic congenital heart diseases in Egyptian children
Hassan, Fahima M., Khattab, Ahmad A., Abo El Fotoh, Wafaa Moustafa M., Zidan, Reham S.
Published in Gene (20.09.2017)
Published in Gene (20.09.2017)
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