Evaluation of tumorigenesis-related miRNAs in breast cancer in Egyptian women: a retrospective, exploratory analysis von Salum, Ghada M., Elaraby, Nesma M., Ahmed, Hoda A., Abd El Meguid, Mai, Fotouh, Basma E., Ashraf, Muhammed, Elhusseny, Yasmine, Dawood, Reham M.

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Face retrieval system based on elastic web crawler over cloud computing von ElAraby, M. E., Shams, M. Y.

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First LIPA Mutational Analysis in Egyptian Patients Reveals One Novel Variant: Wolman Disease von Elaraby, Nesma M., Galal, Eman Reda, Abdel-Hamid, Mohamed, Elbendary, Hasnaa M., Elbadry, Mohamed, Mekkawy, Mona K., Ashaat, Neveen A., Mounir, Samir M., Ashaat, Engy A.

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The significance of isolated hyperbilirubinemia in detecting asymptomatic common bile duct stones in patients undergoing laparoscopic cholecystectomy von Aljorfi, A, Abdelkarim, M, Elaraby, M, Kotb, A, Morgan, R

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Growth, carcass characteristics, meat quality, and microbial aspects of growing quail fed diets enriched with two different types of probiotics (Bacillus toyonensis and Bifidobacte... von Abou-Kassem, D.E., Elsadek, M.F., Abdel-Moneim, A.E., Mahgoub, S.A., Elaraby, G.M., Taha, A.E., Elshafie, M.M., Alkhawtani, D.M., Abd El-Hack, M.E., Ashour, E.A.

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Immobilization of horseradish peroxidase on cationic microporous starch: Physico-bio-chemical characterization and removal of phenolic compounds von El-Naggar, Mehrez E., Abdel-Aty, Azza M., Wassel, Ahmed R., Elaraby, Nesma M., Mohamed, Saleh A.

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Association of MTR and MTRR polymorphisms with recurrent pregnancy loss: a case control study von Shaker, Mai M., Elaraby, Nesma M., Shalabi, Taghreed A.

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Correction: Association of MTR and MTRR polymorphisms with recurrent pregnancy loss: a case control study von Shaker, Mai M., Elaraby, Nesma M., Shalabi, Taghreed A.

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Elastic Web Crawler Service-Oriented Architecture Over Cloud Computing von ElAraby, M. E., Moftah, Hossam M., Abuelenin, Sherihan M., Rashad, M. Z.

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Expression Levels of PF4, ALOX12, ITGA2B, F131A in Pregnant COVID-19 Survivors von Shaker, Mai M, Abdelghany, Asia E, Elaraby, Nesma M

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A new architecture for improving focused crawling using deep neural network von ElAraby, M.E., Abuelenin, Sherihan M., Moftah, Hossam M., Rashad, M.Z.

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Improvement of enzymatic properties and decolorization of azo dye: immobilization of horseradish peroxidase on cationic maize starch von Mohamed, Saleh A., Elaraby, Nesma M., Abdel-Aty, Azza M., Shaban, Elkhabiry, Abu-Saied, M.A., Kenawy, El-Refaie, El-Naggar, Mehrez E.

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Efficacy of Laser Acupuncture for Children with Autism Spectrum Disorder: Clinical, Molecular and Biochemical Study von Elsheikh, Mai S., Ashaat, Engy A., Ramadan, Abeer, Mohamed, Nagwa H., Elaraby, Nesma M., El-Hariri, Hazem Mohmed, Hashish, Adel F., Nashaat, Neveen Hassan

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The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy von 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

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Correction to: Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene von Elaraby, Nesma M., Ahmed, Hoda A., Ashaat, Neveen A., Tawfik, Sameh, Ahmed, Mahmoud K. H., Hassib, Nehal F., Ashaat, Engy A.

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Pile-up correction algorithm for high count rate gamma ray spectroscopy von Hammad, M.E., Kasban, H., Fikry, R.M., Dessoky, Moawad I., Zahran, O., Elaraby, Sayed M.S., Abd El-Samie, Fathi E.

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Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene von Elaraby, Nesma M., Ahmed, Hoda A., Ashaat, Neveen A., Tawfik, Sameh, Ahmed, Mahmoud K. H., Hassib, Nehal F., Ashaat, Engy A.

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Clinical and molecular characterization of myotonia congenita using whole-exome sequencing in Egyptian patients von Elaraby, Nesma M., Ahmed, Hoda A., Dawoud, Heba, Ashaat, Neveen A., Azmy, Ashraf, Galal, Eman Reda, Elhusseny, Yasmine, Awady, Heba El, Metwally, Ammal M., Ashaat, Engy A.

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Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene and Review of Literature von Elaraby, Nesma M, Ahmed, Hoda A, Ashaat, Neveen A, Tawfik, Sameh, Ahmed, Mahmoud K H, Hassib, Nehal F, Ashaat, Engy A

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Principle component analysis for radiotracer signal separation von Kasban, H., Arafa, H., Elaraby, S.M.S.

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